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Iluminación del lugar de trabajo para mejorar el estado de alerta y el estado de ánimo en los trabajadores diurnos

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References

Referencias de los estudios incluidos en esta revisión

Avery 2001 {published data only}

Avery DH, Kizer D, Bolte MA, Hellekson C. Bright light therapy of subsyndromal seasonal affective disorder in the workplace: morning vs. afternoon exposure. Acta Psychiatrica Scandinavica 2001;103(4):267‐74. CENTRAL

Bragard 2013 {published data only}

Bragard I, Coucke PA. Impact of the use of Luminette(R) on well‐being at work in a radiotherapy department [Impact de l’utilisation de la Luminette® sur le bien‐être au travail dans un service de radiothérapie]. Cancer Radiotherapie 2013;17(8):731‐5. CENTRAL

Fostervold 2008 {published data only}

Fostervold KI, Nersveen J. Proportions of direct and indirect indoor lighting ‐ the effect on health, well‐being and cognitive performance of office workers. Lighting Research and Technology 2008;40(3):175‐97. CENTRAL

Mills 2007 {published data only}

Mills PR, Tomkins SC, Schlangen LJM. The effect of high correlated colour temperature office lighting on employee wellbeing and work performance. Journal of Circadian Rhythms 2007;5:2‐2. CENTRAL

Viola 2008 {published data only}

Viola AU, James LM, Schlangen LJ, Dijk DJ. Blue‐enriched white light in the workplace improves self‐reported alertness, performance and sleep quality. Scandinavian Journal of Work, Environment & Health 2008;34(4):297‐306. CENTRAL

Referencias de los estudios excluidos de esta revisión

Aarås 1998 {published data only}

Aarås A, Horgen G, Bjørset H‐H, Ro O, Thoresen M. Musculoskeletal, visual and psychosocial stress in VDU operators before and after multidisciplinary ergonomic interventions. Applied Ergonomics 1998;29(5):335‐54. CENTRAL

Axarli 2008 {published data only}

Axarli K, Meresi A. Objective and subjective criteria regarding the effect of sunlight and daylight in classrooms. 25th Conference on Passive and Low Energy Architecture; 2008 Oct 22‐24; Dublin, Republic of Ireland. 2008. CENTRAL

Buffoli 2007 {published data only}

Buffoli M, Capolongo S, Cattaneo M, Signorelli C. Project, natural lighting and comfort indoor. Annali di Igiene 2007;19(5):429‐41. CENTRAL

Chen 2004 {published data only}

Chen MT, Lin CC. Comparison of TFT‐LCD and CRT on visual recognition and subjective preference. International Journal of Industrial Ergonomics 2004;34(3):167‐74. CENTRAL

Gray 2012 {published data only}

Gray WA, Kesten KS, Hurst S, Day TD, Anderko L. Using clinical simulation centers to test design interventions: a pilot study of lighting and color modifications. HERD 2012;5(3):46‐65. CENTRAL

Haans 2014 {published data only}

Haans A. The natural preference in people's appraisal of light. Journal of Environmental Psychology 2014;39:51‐61. CENTRAL

Hadi 2015 {published data only}

Hadi K, DuBose JR, Ryherd E. Lighting and nurses at medical‐surgical units: impact of lighting conditions on nurses' performance and satisfaction. Health Environments Research and Design Journal 2015;9(3):17‐30. CENTRAL

Hawes 2012 {published data only}

Hawes BK, Brunyé TT, Mahoney CR, Sullivan JM, Aall CD. Effects of four workplace lighting technologies on perception, cognition and affective state. International Journal of Industrial Ergonomics 2012;42(1):122‐8. CENTRAL

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Hedge A. The effects of direct and indirect office lighting on VDT workers. Proceedings of the Human Factors Society 35th Annual Meeting. 1991:536‐40. CENTRAL

Huiberts 2016 {published data only}

Huiberts LM, Smolders KCHJ, de Kort YAW. Non‐image forming effects of illuminance level: exploring parallel effects on physiological arousal and task performance. Physiology and Behavior 2016;164:129‐39. CENTRAL

Janardana 2010 {published data only}

Janardana IGN. Effect of intensity on the wall color information room for getting work ergonomic. International Joint Conference APCHI‐ERGOFUTURE. 2010:346‐8. CENTRAL

Kaida 2006b {published data only}

Kaida K, Takahashi M, Haratani T, Otsuka Y, Fukasawa K, Nakata A. Indoor exposure to natural bright light prevents afternoon sleepiness. Sleep 2006;29(4):462‐9. CENTRAL

Kraneburg 2017 {published data only}

Kraneburg A, Franke S, Methling R, Griefahn B. Effect of color temperature on melatonin production for illumination of working environments. Applied Ergonomics 2017;58:446‐53. CENTRAL

Lehrl 2007 {published data only}

Lehrl S, Gerstmeyer K, Jacob JH, Frieling H, Henkel AW, Meyrer R, et al. Blue light improves cognitive performance. Journal of Neural Transmission 2007;114(4):457‐60. CENTRAL

Leichtfried 2015 {published data only}

Leichtfried V, Mair‐Raggautz M, Schaeffer V, Hammerer‐Lercher A, Mair G, Bartenbach C, et al. Intense illumination in the morning hours improved mood and alertness but not mental performance. Applied Ergonomics 2015;46:54‐9. CENTRAL

Lerchl 2009 {published data only}

Lerchl A, Schindler C, Eichhorn K, Kley F, Erren TC. Indirect blue light does not suppress nocturnal salivary melatonin in humans in an automobile setting. Journal of Pineal Research 2009;47(2):143‐6. CENTRAL

Münch 2012 {published data only}

Münch M, Linhart F, Borisuit A, Jaeggi SM, Scartezzini J‐L. Effects of prior light exposure on early evening performance, subjective sleepiness, and hormonal secretion. Behavioral Neuroscience 2012;126(1):196‐203. CENTRAL

NCT02858765 {unpublished data only}

Bourgin P. Influence of light on sleep, awakening, electroencephalogram (EEG) and cognitive performances. clinicaltrials.gov/ct2/show/NCT02858765. CENTRAL

Noell‐Waggoner 2008 {published data only}

Noell‐Waggoner E. Eye on the boomers. Lighting Design and Application 2008;38(10):23‐4. CENTRAL

Partonen 2000 {published data only}

Partonen T, Lönnqvist J. Bright light improves vitality and alleviates distress in healthy people. Journal of Affective Disorders 2000;57:55‐61. CENTRAL

Pathak 2014 {published data only}

Pathak PM, Dongre AR, Shiwalkar JP. Impact of spatial, thermal and lighting parameters on the efficiency and comfort of users in Indian workspaces. Journal of Sustainable Development 2014;7(4):111‐23. CENTRAL

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Robertson AS, McInnes M, Glass D, Dalton G, Burge PS. Building sickness, are symptoms related to the office lighting?. Annals of Occupational Hygiene 1989;33(1):47‐59. CENTRAL

Singh 2010 {published data only}

Singh A, Syal M, Grady SC, Korkmaz S. Effects of green buildings on employee health and productivity. American Journal of Public Health 2010;100(9):1665‐8. CENTRAL

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van Bommel 2006 {published data only}

van Bommel, MWJ. Non‐visual biological effect of lighting and the practical meaning for lighting for work. Applied Ergonomics 2006;37:461‐6. CENTRAL

Vimalanathan 2014 {published data only}

Vimalanathan K, Ramesh BT. The effect of indoor office environment on the work performance, health and well‐being of office workers. Journal of Environmental Health Science & Engineering 2014;12:113. CENTRAL

Vossen 2016 {published data only}

Vossen FM, Aarts MPJ, Debije M. Visual performance of red luminescent solar concentrating windows in an office environment. Energy and Buildings 2016;113:123‐32. CENTRAL

Weiss 2013 {published data only}

Weiss EM, Canazei M. The influence of light on mood and emotion. In: Mohiyeddini C, Eysenck M, Bauer S editor(s). Handbook of Psychology of Emotions. 1st Edition. Nova Science Publishers, Inc., 2013:297‐306. CENTRAL

Berson 2002

Berson DM, Dunn FA, Takao M. Phototransduction by retinal ganglion cells that set the circadian clock. Science 2002;295(5557):1070‐3.

Bonmati‐Carrion 2014

Bonmati‐Carrion M, Arguelles‐Prieto R, Martinez‐Madrid M, Reiter R, Hardeland R, Rol M, et al. Protecting the melatonin rhythm through circadian healthy light exposure. International Journal of Molecular Sciences 2014;15(12):23448‐500.

Borisuit 2015

Borisuit A, Linhart F, Scartezzini J‐L, Münch M. Effects of realistic office daylighting and electric lighting conditions on visual comfort, alertness and mood. Lighting Research and Technology 2015;47:192‐209.

Boubekri 2014

Boubekri M, Cheung IN, Reid KJ, Wang CH, Zee PC. Impact of windows and daylight exposure on overall health and sleep quality of office workers: a case‐control pilot study. Journal of Clinical Sleep Medicine 2014;10(6):603‐11.

Boyce 1997

Boyce PR, Beckstead JW, Eklund NH, Rea MS. Lighting the graveyard shift: the influence of a daylight‐simulating skylight on the task performance and mood of night‐shift workers. Lighting Research & Technology 1997;29(3):105‐34.

Cajochen 2000

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Cajochen C. Alerting effects of light. Sleep Medicine Reviews 2007;11(6):453‐64.

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Chang 2013

Chang AM, Scheer FA, Czeisler CA, Aeschbach D. Direct effects of light on alertness, vigilance, and the waking electroencephalogram in humans depend on prior light history. Sleep 2013;36(8):1239‐46.

Chellappa 2011

Chellappa SL, Steiner R, Blattner P, Oelhafen P, Gotz T, Cajochen C. Non‐visual effects of light on melatonin, alertness and cognitive performance: can blue‐enriched light keep us alert?. PloS One 2011;6(1):e16429.

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Drake 2010

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Espiritu RC, Kripke DF, Ancoli‐Israel S, Mowen MA, Mason WJ, Fell RL, et al. Low illumination experienced by San Diego adults: association with atypical depressive symptoms. Biological Psychiatry 1994;35(6):403‐7.

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Hoffmann 2008

Hoffmann G, Gufler V, Griesmacher A, Bartenbach C, Canazei M, Staggl S, et al. Effects of variable lighting intensities and colour temperatures on sulphatoxymelatonin and subjective mood in an experimental office workplace. Applied Ergonomics 2008;39(6):719‐28.

Hubbard 2013

Hubbard J, Ruppert E, Gropp CM, Bourgin P. Non‐circadian direct effects of light on sleep and alertness: lessons from transgenic mouse models. Sleep Medicine Reviews 2013;17(6):445‐52.

Hébert 1998

Hébert M, Dumont M, Paquet J. Seasonal and diurnal patterns of human illumination under natural conditions. Chronobiology International 1998;15(1):59‐70.

Iskra‐Golec 2012

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Kort 2010

Kort YAW, Smolders KCHJ. Effects of dynamic lighting on office workers: first results of a field study with monthly alternating settings. Lighting Research and Technology 2010;42:345‐60.

Kuller 1993

Kuller R, Wetterberg L. Melatonin, cortisol, EEG, ECG and subjective comfort in healthy humans: impact of two fluorescent lamp types at two light intensities. Lighting Research and Technology 1993;25(2):71‐80.

Lanfumey 2013

Lanfumey L, Mongeau R, Hamon M. Biological rhythms and melatonin in mood disorders and their treatments. Pharmacology & Therapeutics 2013;138(2):176‐84.

Liu 2000

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Lucas 2014

Lucas RJ, Peirson SN, Berson DM, Brown TM, Cooper HM, Czeisler CA, et al. Measuring and using light in the melanopsin age. Trends in Neurosciences 2014;37(1):1‐9.

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Sahin L, Figueiro MG. Alerting effects of short‐wavelength (blue) and long‐wavelength (red) lights in the afternoon. Physiology & Behavior 2013;116‐117:1‐7.

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Referencias de otras versiones publicadas de esta revisión

Pachito 2016

Pachito DV, Eckeli AL, Desouky AS, Corbett MA, Partonen T, Wilson Rajaratnam SM, et al. Workplace lighting for improving mood and alertness in daytime workers. Cochrane Database of Systematic Reviews 2016, Issue 6. [DOI: 10.1002/14651858.CD012243]

Characteristics of studies

Characteristics of included studies [ordered by study ID]

Jump to:

Avery 2001

Methods

Randomised controlled trial with a parallel design and individual allocation.

Comparison: exposure to morning bright light vs afternoon bright light.

Participants

Volunteers presenting seasonal problems recruited by advertisement, with a regular daytime work schedule (n = 30).

Morning light group: n = 16, all female, mean (SD) age 37 ± 11 years.

Afternoon light group: n = 14, 12 females, mean (SD) age 43 ± 9 years.

Interventions

Morning light group: 2 hours of bright light in the morning (during the first 2 available hours between 07:00 a.m. and 12:00 a.m.).

Afternoon light group: 2 hours of bright light in the afternoon (between the last 2 available hours between 12:00 a.m. to 17:00 p.m.). The bright light source was the Philips Bright Light, 2500 Lux.

No inactive controlled employed.

Outcomes

Alertness assessed by VAS 100‐mm line.

Mood assessed by 5 measures: SIGH‐SAD, HDRS‐21, HDRS‐17, SAD subscale, VAS 100‐mm line.

Adverse effects.

Notes

Risk of bias

Bias

Authors' judgement

Support for judgement

Random sequence generation (selection bias)

Unclear risk

Quote: "At the end of the first week, the subjects were assigned randomly to 2 weeks of bright light treatment: either 2 hours of bright light in the morning (during the first 2 available hours between 0700 and 1200) or 2 hours of bright light in the afternoon (between the last 2 available hours between 1200 to 1700)."

Comment: methods for randomisation not reported.

Allocation concealment (selection bias)

Unclear risk

Comment: methods for allocation concealment not reported.

Blinding of participants and personnel (performance bias)
All outcomes

High risk

Comment: intervention applied at different times of day.

Blinding of outcome assessment (detection bias)
All outcomes

Low risk

Quote: "At the end of both the baseline week and the second treatment week, the subjects were assessed blindly by a psychiatrist using the SIGH‐SAD, the primary measure of improvement."

Comment: participants assessed blindly by a psychiatrist using SIGH‐SAD.

Incomplete outcome data (attrition bias)
All outcomes

Low risk

Quote: "One patient assigned to afternoon light used the light in the afternoon during the first week, but mistakenly used the bright light in the morning during the second week. His data are excluded from the analyses."

Comment: 1 loss due to protocol deviation in the afternoon light group (< 10% of randomised participants).

Selective reporting (reporting bias)

Low risk

Comment: no evidence of selective reporting identified.

Other bias

Unclear risk

Quote: "The VAS scales were missing baseline values for two subjects in the a.m. group and five in the p.m. group, but still showed clear evidence of improvement over time."

Comment: there were missing data for baseline values of VAS for 2 participants in the a.m. group and 5 in the p.m. group. We could not assess whether this could mask baseline imbalance.

Bragard 2013

Methods

Randomised controlled trial with cross‐over design and individual allocation.

Comparison: individually applied blue‐enriched light vs no treatment.

Participants allocated into 2 blocks: ABAB and BABA, where 2 × 4‐week periods of using intervention A were alternated with 2 × 4‐week periods of not using (intervention B).

Participants

Staff members (secretaries, nurses, doctors, psychologists, physicians) working in a hospital with no access to natural light; n = 25. Only 25% of the staff participated in the study. Mean (SD) age 36.6 ± 7.7 years.

Interventions

Intervention A: blue‐enriched light emitted by 8 LEDs mounted in spectacles (Luminette), which were directed on the lower part of the retina. Participants used Luminette at work between 07:00 a.m. and 09:00 a.m. for a maximum of 30 minutes a day, at least 5 days a week.

Intervention B: no treatment.

Outcomes

Alertness assessed using Epworth Sleepiness Scale.

Mood assessed and reported using Beck Depression Inventory‐II.

Notes

Risk of bias

Bias

Authors' judgement

Support for judgement

Random sequence generation (selection bias)

Low risk

Comment: randomisation performed by random draw.

Allocation concealment (selection bias)

Unclear risk

Comment: methods for allocation concealment not reported.

Blinding of participants and personnel (performance bias)
All outcomes

High risk

Comment: intervention compared to no treatment.

Blinding of outcome assessment (detection bias)
All outcomes

High risk

Comment: outcomes derived from questionnaires answered by participants not blind for interventions.

Incomplete outcome data (attrition bias)
All outcomes

High risk

Quote: "Fourteen employees participated in all assessment phases. No significant scoring difference was noted at time in the questionnaires between subjects who continued (n = 14) and those who stopped (n = 11). Reasons for stopping the use of Luminette® were multiple: negative side effects (e.g. migraines, nausea), decreased interest in the study, exclusion of pregnant women, and holidays (including Christmas)."

Comment: only 14/25 participants finished study protocol. Reasons not fully reported. High rate of attrition (44%). Unclear if there was imbalance between groups regarding number of losses and reasons for dropping out.

Selective reporting (reporting bias)

High risk

Comment: data from SIGH‐HDRS, planned in Methods section, was not reported.

Other bias

Low risk

Comment: no other bias identified.

Carry‐over effect

Unclear risk

Comment: carry‐over effect could not be ruled out.

Availability of 2‐period data

Low risk

Comment: data reported from first and second intervention period and for first control period.

Incorrect analysis

Low risk

Comment: paired analyses presented.

Comparability of results with those from parallel‐group trials

Unclear risk

Comment: no results from parallel‐group trials available for same intervention.

Fostervold 2008

Methods

Randomised controlled trial with a parallel design and individual allocation.

Comparison: different proportions of direct and indirect indoor lighting.

Participants

Employees at 2 public service departments in a municipality near Oslo (n = 64, 23 women and 41 men), working in private offices.

Age: 29 to 62 years (mean ± SD: 47.5 ± 9.7 years).

Random assignment was used to form 4 groups of 16 participants.

Interventions

Lighting scheme 1 (LSI.1): 100% indirect lighting.

Lighting scheme 2 (LSID.2): 70% indirect and 30% direct lighting.

Lighting scheme 3 (LSDI.3): 30% indirect and 70% direct lighting.

Lighting scheme 4 (LSD.4): 100% direct lighting.

Each office was equipped with 2 independently controlled sources of light, the overhead light specific to each intervention scheme and a desk lamp identical for all offices.

Outcomes

Somatic health assessed with a modified version of a subjective symptom questionnaire, containing background variables, such as ocular and visual symptoms, musculoskeletal symptoms and systemic body symptoms.

Well‐being measured by job satisfaction, job stress, anxiety and depression.

Notes

Risk of bias

Bias

Authors' judgement

Support for judgement

Random sequence generation (selection bias)

Low risk

Quote: "The randomization procedure was a stratified randomization procedure. Building and gender were used as strata which means that the four lighting concepts were distributed evenly among the two buildings used in the study and gender."

Comment: Email correspondence with author.

Allocation concealment (selection bias)

Unclear risk

Comment: methods for allocation concealment not reported.

Blinding of participants and personnel (performance bias)
All outcomes

High risk

Comment: different types of lighting systems compared.

Blinding of outcome assessment (detection bias)
All outcomes

High risk

Quote: "Depression was measured with the Norwegian edition of Becks Depression Inventory (BDI). The BDI is a self‐rating scale comprising 21 items. Each item has four response choices in the form of statements ranked in order of severity. The respondent selects the statement that suits the feelings at the moment."

Comment: self‐assessment questionnaires. Participants not blind to interventions.

Incomplete outcome data (attrition bias)
All outcomes

High risk

Quote: "The attrition was thirteen participants, representing 25% of the original sample. Attrition was mainly caused by change of employment and long‐term sick leave, while pregnancy and higher education was stated in some instances. There was no indication of any association between the intervention factors and stated causes for sick leave. Two participants were excluded from the study because their new lighting installations did not meet the technical specifications. The attrition for each lighting scheme was three from LSI.1 (100% indirect lighting), one from LSID.2 (70% indirect and 30% direct), two from LSDI.3 (30% indirect and 70% direct lighting) and seven from LSD.4 (100% direct lighting). Separate statistical analyses conducted on the baseline measures showed no indication of bias regarding any of the dependent variables for any of the groups."

Comment: reasons for attrition were presented; however, there was considerable imbalance of attrition across interventions groups, with greater rates of attrition for the group exposed to 100% direct lighting.

Selective reporting (reporting bias)

Low risk

Comment: data reported for all outcomes.

Other bias

Low risk

Comment: no other bias identified.

Mills 2007

Methods

Controlled before‐after study with cluster allocation.

Comparison: high CCT vs standard illumination.

Participants

Participants working as call‐handlers on two different floors of call centre offices in the UK (n = 69, 23 participants on the control floor and 46 on the intervention floor). Work schedule spanned from 8 a.m. to 8 p.m.

Interventions

Intervention: lamp change to the entire lighting system, with replacement of existing lighting system by new high CCT fluorescent lamps (ActiViva Active, Philips), yielding an enhanced amount of short wavelength light with colour temperature of 17,000 K.

Control: lights with a CCT of 2900 K.

Outcomes

Alertness assessed by two items of the Columbia Jet Lag Scale and by one non‐validated question for self‐assessment of overall alertness and concentration.

Notes

Risk of bias

Bias

Authors' judgement

Support for judgement

Random sequence generation (selection bias)

High risk

Comment: non‐randomised study.

Allocation concealment (selection bias)

High risk

Comment: non‐randomised study.

Blinding of participants and personnel (performance bias)
All outcomes

High risk

Comment: different lighting conditions.

Blinding of outcome assessment (detection bias)
All outcomes

High risk

Quote: "Individuals' alertness, performance, concentration and health related quality of life were assessed by means of two online questionnaires."

Comment: self‐assessment questionnaires. Participants were not blind to interventions.

Incomplete outcome data (attrition bias)
All outcomes

Low risk

Comment: no attrition identified.

Selective reporting (reporting bias)

Low risk

Comment: data reported for all outcomes.

Other bias

Low risk

Comment: no other bias identified.

Recruitment bias

High risk

Quote: "Sixty‐nine individuals agreed to take part in the study (23 on the control floor and 46 on the intervention floor), representing 49% of the total eligible population during the study period."

Comment: low rate of acceptance of participation (49%).

Baseline imbalance

Low risk

Comment: no imbalance between groups identified.

Loss of clusters

Low risk

Comment: no loss of clusters.

Incorrect analysis

High risk

Comment: unity of analysis (individual) different from unit of allocation (cluster).

Comparability with individually randomised trials

Unclear risk

Comment: no individually randomised trial focusing on same type of intervention identified.

Viola 2008

Methods

Controlled before‐after study with cluster allocation and cross‐over design.

Comparison: high CCT vs standard illumination.

Participants

94 white‐collar workers, working at a distribution company in northern England, at latitude of 52º north. Two floors of a large office building, which housed the company, were selected and used. Each floor was the same with regard to layout of desks and environmental light exposure. The two floors were also very similar with respect to nature of work carried out. The habitual start was 08:30 a.m. and end time was 16:45 p.m. of work on both floors.

First floor: 52 participants (26 women, aged: mean ± SD: 34.6 ± 1.4 years).

Second floor: 42 participants (19 women, aged mean ± SD: 37.4 ± 1.5 years).

Interventions

Two periods of four weeks under different light conditions (17,000 and 4000 K).

Intervention 1: newly developed fluorescent light source with a highly CCT (17,000 K, Philip Master TL‐D ActiViva Active, Philips, Roozendaal, the Netherlands).

Intervention 2: similar light source with a lower CCT (4000 K, Philips Master TL‐D super 80).

Both types of fluorescent tubes were 18 W and had a similar spectral power distribution in the medium and long wavelength ranges, but the 17,000 K light source produced more output between 420 nm and 480 nm.

Outcomes

Alertness assessed by Karolinska Sleepiness Scale. Questionnaires were completed on a weekly basis.

Positive and negative mood assessed by PANAS scale.

Adverse events (irritability, headache, eye strain, eyes discomfort, eye fatigue, difficult focusing, difficult concentrating and blurred vision) assessed by questionnaire. Symptoms were rated from 1 to 4 (severe).

Outcomes reported as means of all measurements performed in different time points.

Notes

Risk of bias

Bias

Authors' judgement

Support for judgement

Random sequence generation (selection bias)

High risk

Comment: non‐randomised study.

Allocation concealment (selection bias)

High risk

Comment: non‐randomised study.

Blinding of participants and personnel (performance bias)
All outcomes

High risk

Comment: different lighting conditions.

Blinding of outcome assessment (detection bias)
All outcomes

High risk

Quote: "During the two 4‐week periods of exposure to experimental lighting conditions, the participants completed questionnaires in the morning, midday, and late afternoon on the Tuesday of every week. They were requested to complete the morning measures in the hour after their arrival at work and to consider only the time since their arrival at work."

Comments: self‐assessment questionnaires. Participants were not blind to interventions.

Incomplete outcome data (attrition bias)
All outcomes

High risk

Quote: "Ten participants withdrew from the study. The reasons for withdrawal included loss of interest in the study, change of floor during the study, and time off work during the study. The analyses presented in this report are therefore based on 94 participants."

Comments: attrition rate 10.6%. Reasons justifying withdrawal included loss of interest in study, change of floor during study and time off during study. Withdrawals in each group were not reported.

Selective reporting (reporting bias)

Low risk

Comment: data reported for all outcomes.

Other bias

Low risk

Comment: no other bias identified.

Recruitment bias

Unclear risk

Comment: rate of acceptance of participation not reported.

Baseline imbalance

Low risk

Comment: cross‐over design

Loss of clusters

Low risk

Comment: no loss of clusters.

Incorrect analysis

High risk

Comment: unit of allocation (cluster) not taken into account in statistical analysis.

Comparability with individually randomised trials

Unclear risk

Comment: no individually randomised trial focusing on the same type of intervention was identified.

Carry‐over effect

Unclear risk

Comments: no washout period. Carry‐over effect influencing mood could not be disregarded.

Availability of 2‐period data

Low risk

Comment: data from both periods presented.

Incorrect analysis

Low risk

Comment: comparisons of repeated measures were made between the light condition using mixed‐models analyses of variance for repeated measures.

Comparability of results with those from parallel‐group trials

Low risk

Comment: results were in accordance with those from parallel‐group trials (Mills 2007).

CCT: correlated colour temperature; CI: confidence interval; HDRS‐17: 17‐item Hamilton Depressive Rating Scale; HDRS‐21: 21‐item Hamilton Depressive Rating Scale; LED: light‐emitting diode; n: number of participants; PANAS: Positive and Negative Affect Schedule; SAD: seasonal affective disorder; SD: standard deviation; SIGH‐HDRS: Structured Interview Guide for the Hamilton Depressive Rating Scale; SIGH‐SAD: Structured Interview Guide for the Hamilton Depression Rating Scale‐Seasonal Affective Disorders Version; SMD: standardised mean difference; VAS: visual analogue scale.

Characteristics of excluded studies [ordered by study ID]

Jump to:

Study

Reason for exclusion

Aarås 1998

This study assessed preferred lighting conditions, symptoms of visual discomfort, headache and somatic pain, but not alertness or mood.

Axarli 2008

This study employed a cross‐sectional design to assess the influence of different lighting conditions on classroom occupants' behaviour and subjective perception.

Buffoli 2007

This study was conducted in residential and not occupational settings.

Chen 2004

This study was conducted in a laboratory, enrolling college students, not employees.

Gray 2012

This study enrolled undergraduate and graduate students, not employees.

Haans 2014

This study assessed perceived naturalness of light emitted by different light sources, but not alertness or mood.

Hadi 2015

This study assessed nurses' satisfaction related to lighting conditions at different hospital locations, but not alertness or mood.

Hawes 2012

This study was conducted in a laboratory and not in a real work setting.

Hegde 1991

This study reported the effects of the modification of lighting system in the long term. Attempts to contact the author for data prior to the modification were unsuccessful.

Huiberts 2016

This study was conducted in a laboratory and not in a real work setting.

Janardana 2010

The intervention of interest was the change of the colours of walls, rather than the modification of light source.

Kaida 2006b

This study was conducted in a laboratory and not in a real work setting.

Kraneburg 2017

This study was conducted in a laboratory and not in a real work setting.

Lehrl 2007

This study did not employ a control group.

Leichtfried 2015

This study was conducted in a laboratory and not in a real work setting.

Lerchl 2009

This study was conducted in a laboratory and not in a real work setting.

Münch 2012

This study was conducted in laboratory.

NCT02858765

Attempts to contact the author for determining eligibility were unsuccessful.

Noell‐Waggoner 2008

This publication is a narrative review on illumination effects.

Partonen 2000

Lighting exposure took place in both residential and work settings.

Pathak 2014

This study employed a cross‐sectional design.

Robertson 1985

This study employed a cross‐sectional design to assess the effects of different ventilation conditions.

Robertson 1989

This study employed a cross‐sectional design.

Singh 2010

This study did not employ a control group.

Stammerjohn 1981

This study employed a cross‐sectional design.

van Bommel 2006

This publication is a narrative review.

Vimalanathan 2014

This study was conducted in a laboratory and not in a real work setting.

Vossen 2016

This study was conducted in a laboratory and not in a real work setting.

Weiss 2013

This publication is a narrative review.

Data and analyses

Open in table viewer
Comparison 1. High correlated colour temperature light versus standard illumination

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Alertness ‐ Item Decreased Daytime Alertness from Columbia Jet Lag Scale 14 weeks Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 1.1

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 1 Alertness ‐ Item Decreased Daytime Alertness from Columbia Jet Lag Scale 14 weeks.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 1 Alertness ‐ Item Decreased Daytime Alertness from Columbia Jet Lag Scale 14 weeks.

2 Alertness ‐ Item Sleepiness in Day from Columbia Jet Lag Scale 14 weeks Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 1.2

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 2 Alertness ‐ Item Sleepiness in Day from Columbia Jet Lag Scale 14 weeks.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 2 Alertness ‐ Item Sleepiness in Day from Columbia Jet Lag Scale 14 weeks.

3 Alertness ‐ Karolinska Sleepiness Scale: mean of all time points Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 1.3

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 3 Alertness ‐ Karolinska Sleepiness Scale: mean of all time points.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 3 Alertness ‐ Karolinska Sleepiness Scale: mean of all time points.

4 Alertness ‐ meta‐analysis Show forest plot

2

50

Std. Mean Difference (IV, Fixed, 95% CI)

‐0.69 [‐1.28, ‐0.10]

Analysis 1.4

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 4 Alertness ‐ meta‐analysis.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 4 Alertness ‐ meta‐analysis.

5 Mood ‐ Positive Mood PANAS Scale: mean of all time points Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 1.5

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 5 Mood ‐ Positive Mood PANAS Scale: mean of all time points.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 5 Mood ‐ Positive Mood PANAS Scale: mean of all time points.

6 Mood ‐ Negative Mood PANAS Scale: mean of all time points Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 1.6

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 6 Mood ‐ Negative Mood PANAS Scale: mean of all time points.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 6 Mood ‐ Negative Mood PANAS Scale: mean of all time points.

7 Adverse events ‐ eye discomfort: mean of all time points Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 1.7

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 7 Adverse events ‐ eye discomfort: mean of all time points.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 7 Adverse events ‐ eye discomfort: mean of all time points.

8 Adverse events ‐ irritability: mean of all time points Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 1.8

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 8 Adverse events ‐ irritability: mean of all time points.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 8 Adverse events ‐ irritability: mean of all time points.

9 Adverse events ‐ headache: mean of all time points Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 1.9

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 9 Adverse events ‐ headache: mean of all time points.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 9 Adverse events ‐ headache: mean of all time points.

10 Adverse events ‐ eye strain: mean of all time points Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 1.10

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 10 Adverse events ‐ eye strain: mean of all time points.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 10 Adverse events ‐ eye strain: mean of all time points.

11 Adverse events ‐ eye fatigue: mean of all time points Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 1.11

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 11 Adverse events ‐ eye fatigue: mean of all time points.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 11 Adverse events ‐ eye fatigue: mean of all time points.

12 Adverse events ‐ difficult focusing: mean of all time points Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 1.12

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 12 Adverse events ‐ difficult focusing: mean of all time points.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 12 Adverse events ‐ difficult focusing: mean of all time points.

13 Adverse events ‐ difficulty concentrating: mean of all time points Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 1.13

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 13 Adverse events ‐ difficulty concentrating: mean of all time points.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 13 Adverse events ‐ difficulty concentrating: mean of all time points.

14 Adverse events ‐ blurred vision: mean of all time points Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 1.14

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 14 Adverse events ‐ blurred vision: mean of all time points.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 14 Adverse events ‐ blurred vision: mean of all time points.

Open in table viewer
Comparison 2. Different proportions of direct and indirect indoor lighting

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Mood BDI: indirect lighting versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.1

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 1 Mood BDI: indirect lighting versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 1 Mood BDI: indirect lighting versus direct lighting.

1.1 Mood BDI after 2 months: indirect lighting versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

1.2 Mood BDI after 5 months: indirect lighting versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

2 Adverse events ‐ ocular problems indirect versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.2

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 2 Adverse events ‐ ocular problems indirect versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 2 Adverse events ‐ ocular problems indirect versus direct lighting.

2.1 Adverse events after 2 months ‐ ocular problems indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

2.2 Adverse events after 5 months ‐ ocular problems indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

3 Mood Beck Depression Inventory (BDI): indirect lighting versus 70% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.3

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 3 Mood Beck Depression Inventory (BDI): indirect lighting versus 70% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 3 Mood Beck Depression Inventory (BDI): indirect lighting versus 70% indirect lighting.

3.1 Mood BDI after 2 months: indirect lighting versus 70% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

3.2 Mood BDI after 5 months: indirect lighting versus 70% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

4 Mood BDI: indirect lighting versus 30% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.4

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 4 Mood BDI: indirect lighting versus 30% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 4 Mood BDI: indirect lighting versus 30% indirect lighting.

4.1 Mood BDI after 2 months: indirect lighting versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

4.2 Mood BDI after 5 months: indirect lighting versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

5 Mood BDI: 70% indirect lighting versus 30% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.5

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 5 Mood BDI: 70% indirect lighting versus 30% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 5 Mood BDI: 70% indirect lighting versus 30% indirect lighting.

5.1 Mood BDI after 2 months: 70% indirect lighting versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

5.2 Mood BDI after 5 months: 70% indirect lighting versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

6 Mood BDI: 70% indirect lighting versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.6

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 6 Mood BDI: 70% indirect lighting versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 6 Mood BDI: 70% indirect lighting versus direct lighting.

6.1 Mood BDI after 2 months: 70% indirect lighting versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

6.2 Mood BDI after 5 months: 70% indirect lighting versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

7 Mood BDI: 30% indirect lighting versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.7

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 7 Mood BDI: 30% indirect lighting versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 7 Mood BDI: 30% indirect lighting versus direct lighting.

7.1 Mood BDI after 2 months: 30% indirect lighting versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

7.2 Mood BDI after 5 months: 30% indirect lighting versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

8 Adverse events ‐ reading problems indirect versus 30% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.8

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 8 Adverse events ‐ reading problems indirect versus 30% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 8 Adverse events ‐ reading problems indirect versus 30% indirect lighting.

8.1 Adverse events after 2 months ‐ reading problems indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

8.2 Adverse events after 5 months ‐ reading problems indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

9 Adverse events ‐ ocular problems indirect versus 70% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.9

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 9 Adverse events ‐ ocular problems indirect versus 70% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 9 Adverse events ‐ ocular problems indirect versus 70% indirect lighting.

9.1 Adverse events after 2 months ‐ ocular problems indirect versus 70% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

9.2 Adverse events after 5 months ‐ ocular problems indirect versus 70% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

10 Adverse events ‐ ocular problems indirect versus 30% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.10

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 10 Adverse events ‐ ocular problems indirect versus 30% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 10 Adverse events ‐ ocular problems indirect versus 30% indirect lighting.

10.1 Adverse events after 2 months ‐ ocular problems indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

10.2 Adverse events after 5 months ‐ ocular problems indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

11 Adverse events ‐ ocular problems 70% indirect versus 30% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.11

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 11 Adverse events ‐ ocular problems 70% indirect versus 30% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 11 Adverse events ‐ ocular problems 70% indirect versus 30% indirect lighting.

11.1 Adverse events after 2 months ‐ ocular problems 70% indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

11.2 Adverse events after 5 months ‐ ocular problems 70% indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

12 Adverse events ‐ ocular problems 70% indirect versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.12

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 12 Adverse events ‐ ocular problems 70% indirect versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 12 Adverse events ‐ ocular problems 70% indirect versus direct lighting.

12.1 Adverse events after 2 months ‐ ocular problems 70% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

12.2 Adverse events after 5 months ‐ ocular problems 70% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

13 Adverse events ‐ ocular problems 30% indirect versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.13

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 13 Adverse events ‐ ocular problems 30% indirect versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 13 Adverse events ‐ ocular problems 30% indirect versus direct lighting.

13.1 Adverse events after 2 months ‐ ocular problems 30% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

13.2 Adverse events after 5 months ‐ ocular problems 30% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

14 Adverse events ‐ reading problems indirect versus 70% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.14

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 14 Adverse events ‐ reading problems indirect versus 70% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 14 Adverse events ‐ reading problems indirect versus 70% indirect lighting.

14.1 Adverse events after 2 months ‐ reading problems indirect versus 70% indirect lightning

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

14.2 Adverse events after 5 months ‐ reading problems indirect versus 70% indirect lightning

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

15 Adverse events ‐ reading problems indirect versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.15

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 15 Adverse events ‐ reading problems indirect versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 15 Adverse events ‐ reading problems indirect versus direct lighting.

15.1 Adverse events after 2 months ‐ reading problems indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

15.2 Adverse events after 5 months ‐ reading problems indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

16 Adverse events ‐ reading problems 70% indirect versus 30% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.16

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 16 Adverse events ‐ reading problems 70% indirect versus 30% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 16 Adverse events ‐ reading problems 70% indirect versus 30% indirect lighting.

16.1 Adverse events after 2 months ‐ reading problems 70% indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

16.2 Adverse events after 5 months ‐ reading problems 70% indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

17 Adverse events ‐ reading problems 70% indirect versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.17

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 17 Adverse events ‐ reading problems 70% indirect versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 17 Adverse events ‐ reading problems 70% indirect versus direct lighting.

17.1 Adverse events after 2 months ‐ reading problems 70% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

17.2 Adverse events after 5 months ‐ reading problems 70% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

18 Adverse events ‐ reading problems 30% indirect versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.18

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 18 Adverse events ‐ reading problems 30% indirect versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 18 Adverse events ‐ reading problems 30% indirect versus direct lighting.

18.1 Adverse events after 2 months ‐ reading problems 30% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

18.2 Adverse events after 5 months ‐ reading problems 30% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

19 Adverse events ‐ concentration problems indirect versus 70% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.19

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 19 Adverse events ‐ concentration problems indirect versus 70% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 19 Adverse events ‐ concentration problems indirect versus 70% indirect lighting.

19.1 Adverse events after 2 months ‐ concentration problems indirect versus 70% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

19.2 Adverse events after 5 months ‐ concentration problems indirect versus 70% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

20 Adverse events ‐ concentration problems indirect versus 30% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.20

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 20 Adverse events ‐ concentration problems indirect versus 30% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 20 Adverse events ‐ concentration problems indirect versus 30% indirect lighting.

20.1 Adverse events after 2 months ‐ concentration problems indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

20.2 Adverse events after 5 months ‐ concentration problems indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

21 Adverse events ‐ concentration problems indirect versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.21

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 21 Adverse events ‐ concentration problems indirect versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 21 Adverse events ‐ concentration problems indirect versus direct lighting.

21.1 Adverse events after 2 months ‐ concentration problems indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

21.2 Adverse events after 5 months ‐ concentration problems indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

22 Adverse events ‐ concentration problems 70% indirect versus 30% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.22

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 22 Adverse events ‐ concentration problems 70% indirect versus 30% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 22 Adverse events ‐ concentration problems 70% indirect versus 30% indirect lighting.

22.1 Adverse events after 2 months ‐ concentration problems 70% indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

22.2 Adverse events after 5 months ‐ concentration problems 70% indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

23 Adverse events ‐ concentration problems 70% indirect versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.23

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 23 Adverse events ‐ concentration problems 70% indirect versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 23 Adverse events ‐ concentration problems 70% indirect versus direct lighting.

23.1 Adverse events after 2 months ‐ concentration problems 70% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

23.2 Adverse events after 5 months ‐ concentration problems 70% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

24 Adverse events ‐ concentration problems 30% indirect versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.24

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 24 Adverse events ‐ concentration problems 30% indirect versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 24 Adverse events ‐ concentration problems 30% indirect versus direct lighting.

24.1 Adverse events after 2 months ‐ concentration problems 30% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

24.2 Adverse events after 5 months ‐ concentration problems 30% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

25 Adverse events ‐ musculoskeletal symptoms indirect versus 70% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.25

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 25 Adverse events ‐ musculoskeletal symptoms indirect versus 70% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 25 Adverse events ‐ musculoskeletal symptoms indirect versus 70% indirect lighting.

25.1 Adverse events after 2 months ‐ musculoskeletal symptoms indirect versus 70% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

25.2 Adverse events after 5 months ‐ musculoskeletal symptoms indirect versus 70% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

26 Adverse events ‐ musculoskeletal symptoms indirect versus 30% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.26

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 26 Adverse events ‐ musculoskeletal symptoms indirect versus 30% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 26 Adverse events ‐ musculoskeletal symptoms indirect versus 30% indirect lighting.

26.1 Adverse events after 2 months ‐ musculoskeletal symptoms indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

26.2 Adverse events after 5 months ‐ musculoskeletal symptoms indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

27 Adverse events ‐ musculoskeletal symptoms indirect versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.27

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 27 Adverse events ‐ musculoskeletal symptoms indirect versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 27 Adverse events ‐ musculoskeletal symptoms indirect versus direct lighting.

27.1 Adverse events after 2 months ‐ musculoskeletal symptoms indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

27.2 Adverse events after 5 months ‐ musculoskeletal symptoms indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

28 Adverse events ‐ musculoskeletal symptoms 70% indirect versus 30% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.28

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 28 Adverse events ‐ musculoskeletal symptoms 70% indirect versus 30% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 28 Adverse events ‐ musculoskeletal symptoms 70% indirect versus 30% indirect lighting.

28.1 Adverse events after 2 months ‐ musculoskeletal symptoms 70% indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

28.2 Adverse events after 5 months ‐ musculoskeletal symptoms 70% indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

29 Adverse events ‐ musculoskeletal symptoms 70% indirect versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.29

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 29 Adverse events ‐ musculoskeletal symptoms 70% indirect versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 29 Adverse events ‐ musculoskeletal symptoms 70% indirect versus direct lighting.

29.1 Adverse events after 2 months ‐ musculoskeletal symptoms 70% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

29.2 Adverse events after 5 months ‐ musculoskeletal symptoms 70% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

30 Adverse events ‐ musculoskeletal symptoms 30% indirect versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 2.30

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 30 Adverse events ‐ musculoskeletal symptoms 30% indirect versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 30 Adverse events ‐ musculoskeletal symptoms 30% indirect versus direct lighting.

30.1 Adverse events after 2 months ‐ musculoskeletal symptoms 30% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

30.2 Adverse events after 5 months ‐ musculoskeletal symptoms 30% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

Open in table viewer
Comparison 3. Individually applied blue‐enriched light versus no treatment

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Alertness ‐ Epworth Sleepiness Scale Show forest plot

1

Mean Difference (Fixed, 95% CI)

Totals not selected

Analysis 3.1

Comparison 3 Individually applied blue‐enriched light versus no treatment, Outcome 1 Alertness ‐ Epworth Sleepiness Scale.

Comparison 3 Individually applied blue‐enriched light versus no treatment, Outcome 1 Alertness ‐ Epworth Sleepiness Scale.

2 Mood Beck Depression Inventory‐II Show forest plot

1

Mean Difference (Fixed, 95% CI)

Totals not selected

Analysis 3.2

Comparison 3 Individually applied blue‐enriched light versus no treatment, Outcome 2 Mood Beck Depression Inventory‐II.

Comparison 3 Individually applied blue‐enriched light versus no treatment, Outcome 2 Mood Beck Depression Inventory‐II.

Open in table viewer
Comparison 4. Morning bright light versus afternoon bright light

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Alertness (visual analogue scale (VAS)) after 2 weeks of intervention Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 4.1

Comparison 4 Morning bright light versus afternoon bright light, Outcome 1 Alertness (visual analogue scale (VAS)) after 2 weeks of intervention.

Comparison 4 Morning bright light versus afternoon bright light, Outcome 1 Alertness (visual analogue scale (VAS)) after 2 weeks of intervention.

2 Mood (≥ 50% of reduction of Structured Interview Guide for the Hamilton Depression Rating Scale‐Seasonal Affective Disorders Version (SIGH‐SAD) scores from baseline after 2 weeks of treatment)) Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

Analysis 4.2

Comparison 4 Morning bright light versus afternoon bright light, Outcome 2 Mood (≥ 50% of reduction of Structured Interview Guide for the Hamilton Depression Rating Scale‐Seasonal Affective Disorders Version (SIGH‐SAD) scores from baseline after 2 weeks of treatment)).

Comparison 4 Morning bright light versus afternoon bright light, Outcome 2 Mood (≥ 50% of reduction of Structured Interview Guide for the Hamilton Depression Rating Scale‐Seasonal Affective Disorders Version (SIGH‐SAD) scores from baseline after 2 weeks of treatment)).

3 Mood SIGH‐SAD after 2 weeks of intervention Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 4.3

Comparison 4 Morning bright light versus afternoon bright light, Outcome 3 Mood SIGH‐SAD after 2 weeks of intervention.

Comparison 4 Morning bright light versus afternoon bright light, Outcome 3 Mood SIGH‐SAD after 2 weeks of intervention.

4 Mood 21‐item Hamilton Depressive Rating Scale after 2 weeks of interventions Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 4.4

Comparison 4 Morning bright light versus afternoon bright light, Outcome 4 Mood 21‐item Hamilton Depressive Rating Scale after 2 weeks of interventions.

Comparison 4 Morning bright light versus afternoon bright light, Outcome 4 Mood 21‐item Hamilton Depressive Rating Scale after 2 weeks of interventions.

5 Mood 17‐item Hamilton Depressive Rating Scale after 2 weeks of intervention Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 4.5

Comparison 4 Morning bright light versus afternoon bright light, Outcome 5 Mood 17‐item Hamilton Depressive Rating Scale after 2 weeks of intervention.

Comparison 4 Morning bright light versus afternoon bright light, Outcome 5 Mood 17‐item Hamilton Depressive Rating Scale after 2 weeks of intervention.

6 Mood Seasonal Affective Disorders subscale after 2 weeks of intervention Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 4.6

Comparison 4 Morning bright light versus afternoon bright light, Outcome 6 Mood Seasonal Affective Disorders subscale after 2 weeks of intervention.

Comparison 4 Morning bright light versus afternoon bright light, Outcome 6 Mood Seasonal Affective Disorders subscale after 2 weeks of intervention.

7 Mood VAS after 2 weeks of intervention Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Analysis 4.7

Comparison 4 Morning bright light versus afternoon bright light, Outcome 7 Mood VAS after 2 weeks of intervention.

Comparison 4 Morning bright light versus afternoon bright light, Outcome 7 Mood VAS after 2 weeks of intervention.

8 Frequency of adverse events after 2 weeks of intervention Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

Analysis 4.8

Comparison 4 Morning bright light versus afternoon bright light, Outcome 8 Frequency of adverse events after 2 weeks of intervention.

Comparison 4 Morning bright light versus afternoon bright light, Outcome 8 Frequency of adverse events after 2 weeks of intervention.

PRISMA study flow diagram.
Figures and Tables -
Figure 1

PRISMA study flow diagram.

Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.
Figures and Tables -
Figure 2

Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.

Risk of bias summary: review authors' judgements about each risk of bias item for each included study.
Figures and Tables -
Figure 3

Risk of bias summary: review authors' judgements about each risk of bias item for each included study.

Forest plot of comparison: 4 High correlated colour temperature light versus standard illumination, outcome: alertness.
Figures and Tables -
Figure 4

Forest plot of comparison: 4 High correlated colour temperature light versus standard illumination, outcome: alertness.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 1 Alertness ‐ Item Decreased Daytime Alertness from Columbia Jet Lag Scale 14 weeks.
Figures and Tables -
Analysis 1.1

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 1 Alertness ‐ Item Decreased Daytime Alertness from Columbia Jet Lag Scale 14 weeks.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 2 Alertness ‐ Item Sleepiness in Day from Columbia Jet Lag Scale 14 weeks.
Figures and Tables -
Analysis 1.2

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 2 Alertness ‐ Item Sleepiness in Day from Columbia Jet Lag Scale 14 weeks.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 3 Alertness ‐ Karolinska Sleepiness Scale: mean of all time points.
Figures and Tables -
Analysis 1.3

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 3 Alertness ‐ Karolinska Sleepiness Scale: mean of all time points.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 4 Alertness ‐ meta‐analysis.
Figures and Tables -
Analysis 1.4

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 4 Alertness ‐ meta‐analysis.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 5 Mood ‐ Positive Mood PANAS Scale: mean of all time points.
Figures and Tables -
Analysis 1.5

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 5 Mood ‐ Positive Mood PANAS Scale: mean of all time points.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 6 Mood ‐ Negative Mood PANAS Scale: mean of all time points.
Figures and Tables -
Analysis 1.6

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 6 Mood ‐ Negative Mood PANAS Scale: mean of all time points.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 7 Adverse events ‐ eye discomfort: mean of all time points.
Figures and Tables -
Analysis 1.7

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 7 Adverse events ‐ eye discomfort: mean of all time points.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 8 Adverse events ‐ irritability: mean of all time points.
Figures and Tables -
Analysis 1.8

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 8 Adverse events ‐ irritability: mean of all time points.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 9 Adverse events ‐ headache: mean of all time points.
Figures and Tables -
Analysis 1.9

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 9 Adverse events ‐ headache: mean of all time points.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 10 Adverse events ‐ eye strain: mean of all time points.
Figures and Tables -
Analysis 1.10

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 10 Adverse events ‐ eye strain: mean of all time points.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 11 Adverse events ‐ eye fatigue: mean of all time points.
Figures and Tables -
Analysis 1.11

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 11 Adverse events ‐ eye fatigue: mean of all time points.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 12 Adverse events ‐ difficult focusing: mean of all time points.
Figures and Tables -
Analysis 1.12

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 12 Adverse events ‐ difficult focusing: mean of all time points.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 13 Adverse events ‐ difficulty concentrating: mean of all time points.
Figures and Tables -
Analysis 1.13

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 13 Adverse events ‐ difficulty concentrating: mean of all time points.

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 14 Adverse events ‐ blurred vision: mean of all time points.
Figures and Tables -
Analysis 1.14

Comparison 1 High correlated colour temperature light versus standard illumination, Outcome 14 Adverse events ‐ blurred vision: mean of all time points.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 1 Mood BDI: indirect lighting versus direct lighting.
Figures and Tables -
Analysis 2.1

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 1 Mood BDI: indirect lighting versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 2 Adverse events ‐ ocular problems indirect versus direct lighting.
Figures and Tables -
Analysis 2.2

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 2 Adverse events ‐ ocular problems indirect versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 3 Mood Beck Depression Inventory (BDI): indirect lighting versus 70% indirect lighting.
Figures and Tables -
Analysis 2.3

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 3 Mood Beck Depression Inventory (BDI): indirect lighting versus 70% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 4 Mood BDI: indirect lighting versus 30% indirect lighting.
Figures and Tables -
Analysis 2.4

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 4 Mood BDI: indirect lighting versus 30% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 5 Mood BDI: 70% indirect lighting versus 30% indirect lighting.
Figures and Tables -
Analysis 2.5

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 5 Mood BDI: 70% indirect lighting versus 30% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 6 Mood BDI: 70% indirect lighting versus direct lighting.
Figures and Tables -
Analysis 2.6

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 6 Mood BDI: 70% indirect lighting versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 7 Mood BDI: 30% indirect lighting versus direct lighting.
Figures and Tables -
Analysis 2.7

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 7 Mood BDI: 30% indirect lighting versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 8 Adverse events ‐ reading problems indirect versus 30% indirect lighting.
Figures and Tables -
Analysis 2.8

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 8 Adverse events ‐ reading problems indirect versus 30% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 9 Adverse events ‐ ocular problems indirect versus 70% indirect lighting.
Figures and Tables -
Analysis 2.9

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 9 Adverse events ‐ ocular problems indirect versus 70% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 10 Adverse events ‐ ocular problems indirect versus 30% indirect lighting.
Figures and Tables -
Analysis 2.10

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 10 Adverse events ‐ ocular problems indirect versus 30% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 11 Adverse events ‐ ocular problems 70% indirect versus 30% indirect lighting.
Figures and Tables -
Analysis 2.11

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 11 Adverse events ‐ ocular problems 70% indirect versus 30% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 12 Adverse events ‐ ocular problems 70% indirect versus direct lighting.
Figures and Tables -
Analysis 2.12

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 12 Adverse events ‐ ocular problems 70% indirect versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 13 Adverse events ‐ ocular problems 30% indirect versus direct lighting.
Figures and Tables -
Analysis 2.13

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 13 Adverse events ‐ ocular problems 30% indirect versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 14 Adverse events ‐ reading problems indirect versus 70% indirect lighting.
Figures and Tables -
Analysis 2.14

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 14 Adverse events ‐ reading problems indirect versus 70% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 15 Adverse events ‐ reading problems indirect versus direct lighting.
Figures and Tables -
Analysis 2.15

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 15 Adverse events ‐ reading problems indirect versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 16 Adverse events ‐ reading problems 70% indirect versus 30% indirect lighting.
Figures and Tables -
Analysis 2.16

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 16 Adverse events ‐ reading problems 70% indirect versus 30% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 17 Adverse events ‐ reading problems 70% indirect versus direct lighting.
Figures and Tables -
Analysis 2.17

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 17 Adverse events ‐ reading problems 70% indirect versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 18 Adverse events ‐ reading problems 30% indirect versus direct lighting.
Figures and Tables -
Analysis 2.18

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 18 Adverse events ‐ reading problems 30% indirect versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 19 Adverse events ‐ concentration problems indirect versus 70% indirect lighting.
Figures and Tables -
Analysis 2.19

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 19 Adverse events ‐ concentration problems indirect versus 70% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 20 Adverse events ‐ concentration problems indirect versus 30% indirect lighting.
Figures and Tables -
Analysis 2.20

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 20 Adverse events ‐ concentration problems indirect versus 30% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 21 Adverse events ‐ concentration problems indirect versus direct lighting.
Figures and Tables -
Analysis 2.21

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 21 Adverse events ‐ concentration problems indirect versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 22 Adverse events ‐ concentration problems 70% indirect versus 30% indirect lighting.
Figures and Tables -
Analysis 2.22

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 22 Adverse events ‐ concentration problems 70% indirect versus 30% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 23 Adverse events ‐ concentration problems 70% indirect versus direct lighting.
Figures and Tables -
Analysis 2.23

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 23 Adverse events ‐ concentration problems 70% indirect versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 24 Adverse events ‐ concentration problems 30% indirect versus direct lighting.
Figures and Tables -
Analysis 2.24

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 24 Adverse events ‐ concentration problems 30% indirect versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 25 Adverse events ‐ musculoskeletal symptoms indirect versus 70% indirect lighting.
Figures and Tables -
Analysis 2.25

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 25 Adverse events ‐ musculoskeletal symptoms indirect versus 70% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 26 Adverse events ‐ musculoskeletal symptoms indirect versus 30% indirect lighting.
Figures and Tables -
Analysis 2.26

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 26 Adverse events ‐ musculoskeletal symptoms indirect versus 30% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 27 Adverse events ‐ musculoskeletal symptoms indirect versus direct lighting.
Figures and Tables -
Analysis 2.27

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 27 Adverse events ‐ musculoskeletal symptoms indirect versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 28 Adverse events ‐ musculoskeletal symptoms 70% indirect versus 30% indirect lighting.
Figures and Tables -
Analysis 2.28

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 28 Adverse events ‐ musculoskeletal symptoms 70% indirect versus 30% indirect lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 29 Adverse events ‐ musculoskeletal symptoms 70% indirect versus direct lighting.
Figures and Tables -
Analysis 2.29

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 29 Adverse events ‐ musculoskeletal symptoms 70% indirect versus direct lighting.

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 30 Adverse events ‐ musculoskeletal symptoms 30% indirect versus direct lighting.
Figures and Tables -
Analysis 2.30

Comparison 2 Different proportions of direct and indirect indoor lighting, Outcome 30 Adverse events ‐ musculoskeletal symptoms 30% indirect versus direct lighting.

Comparison 3 Individually applied blue‐enriched light versus no treatment, Outcome 1 Alertness ‐ Epworth Sleepiness Scale.
Figures and Tables -
Analysis 3.1

Comparison 3 Individually applied blue‐enriched light versus no treatment, Outcome 1 Alertness ‐ Epworth Sleepiness Scale.

Comparison 3 Individually applied blue‐enriched light versus no treatment, Outcome 2 Mood Beck Depression Inventory‐II.
Figures and Tables -
Analysis 3.2

Comparison 3 Individually applied blue‐enriched light versus no treatment, Outcome 2 Mood Beck Depression Inventory‐II.

Comparison 4 Morning bright light versus afternoon bright light, Outcome 1 Alertness (visual analogue scale (VAS)) after 2 weeks of intervention.
Figures and Tables -
Analysis 4.1

Comparison 4 Morning bright light versus afternoon bright light, Outcome 1 Alertness (visual analogue scale (VAS)) after 2 weeks of intervention.

Comparison 4 Morning bright light versus afternoon bright light, Outcome 2 Mood (≥ 50% of reduction of Structured Interview Guide for the Hamilton Depression Rating Scale‐Seasonal Affective Disorders Version (SIGH‐SAD) scores from baseline after 2 weeks of treatment)).
Figures and Tables -
Analysis 4.2

Comparison 4 Morning bright light versus afternoon bright light, Outcome 2 Mood (≥ 50% of reduction of Structured Interview Guide for the Hamilton Depression Rating Scale‐Seasonal Affective Disorders Version (SIGH‐SAD) scores from baseline after 2 weeks of treatment)).

Comparison 4 Morning bright light versus afternoon bright light, Outcome 3 Mood SIGH‐SAD after 2 weeks of intervention.
Figures and Tables -
Analysis 4.3

Comparison 4 Morning bright light versus afternoon bright light, Outcome 3 Mood SIGH‐SAD after 2 weeks of intervention.

Comparison 4 Morning bright light versus afternoon bright light, Outcome 4 Mood 21‐item Hamilton Depressive Rating Scale after 2 weeks of interventions.
Figures and Tables -
Analysis 4.4

Comparison 4 Morning bright light versus afternoon bright light, Outcome 4 Mood 21‐item Hamilton Depressive Rating Scale after 2 weeks of interventions.

Comparison 4 Morning bright light versus afternoon bright light, Outcome 5 Mood 17‐item Hamilton Depressive Rating Scale after 2 weeks of intervention.
Figures and Tables -
Analysis 4.5

Comparison 4 Morning bright light versus afternoon bright light, Outcome 5 Mood 17‐item Hamilton Depressive Rating Scale after 2 weeks of intervention.

Comparison 4 Morning bright light versus afternoon bright light, Outcome 6 Mood Seasonal Affective Disorders subscale after 2 weeks of intervention.
Figures and Tables -
Analysis 4.6

Comparison 4 Morning bright light versus afternoon bright light, Outcome 6 Mood Seasonal Affective Disorders subscale after 2 weeks of intervention.

Comparison 4 Morning bright light versus afternoon bright light, Outcome 7 Mood VAS after 2 weeks of intervention.
Figures and Tables -
Analysis 4.7

Comparison 4 Morning bright light versus afternoon bright light, Outcome 7 Mood VAS after 2 weeks of intervention.

Comparison 4 Morning bright light versus afternoon bright light, Outcome 8 Frequency of adverse events after 2 weeks of intervention.
Figures and Tables -
Analysis 4.8

Comparison 4 Morning bright light versus afternoon bright light, Outcome 8 Frequency of adverse events after 2 weeks of intervention.

Summary of findings for the main comparison. High correlated colour temperature light versus standard illumination for improving mood and alertness in daytime workers

High correlated colour temperature light versus standard illumination for improving mood and alertness in daytime workers

Patient or population: daytime workers
Setting: offices
Intervention: high correlated colour temperature light
Comparison: standard illumination

Outcomes

Anticipated absolute effects (95% CI)

№ of participants
Effective sample size*

(studies)

Quality of the evidence
(GRADE)

Risk with standard illumination

Risk with CCT light

Alertness
assessed with: CJL and KS Scale
CLJ range 1 to 5

KS range 1 to 9 (worst)
follow‐up: range 1‐3 months

‐‐

SMD** 0.69 lower
(1.28 lower to 0.1 lower)

163

Effective sample size = 50
(2 CBA studies)

⊕⊝⊝⊝
Very low1

Mood (positive)
assessed with: PANAS
Scale from: 10 (worst) to 50 (best)
follow‐up: 1 month

Mean standard positive mood 25.9

MD 2.08 higher
(0.1 lower to 4.26 higher)

94

Effective sample size = 34
(1 CBA study)

⊕⊝⊝⊝
Very low1,2

Mood (negative)
assessed with: PANAS
Scale from: 10 (best) to 50 (worst)
follow‐up: 1 month

Mean standard negative mood 13.7

MD 0.45 lower
(1.84 lower to 0.94 higher)

94

Effective sample size = 34
(1 CBA study)

⊕⊝⊝⊝
Very low1,2

Adverse events ‐ eye discomfort
follow‐up: 1 month

Mean standard adverse events 1.7

MD 0.23 lower
(0.37 lower to 0.09 lower)

94

Effective sample size = 34
(1 CBA study)

⊕⊝⊝⊝
Very low1

* Effective sample sizes applied to correct for the unit‐of‐analysis error.

** As a rule of thumb, 0.2 Standard Deviations represents a small difference, 0.5 a moderate difference, and 0.8 a large difference.

CI: confidence interval; CCT: correlated colour temperature; MD: mean difference; PANAS: Positive and Negative Affect Schedule; SMD: standardised mean difference.

GRADE Working Group grades of evidence
High quality: We are very confident that the true effect lies close to that of the estimate of the effect.
Moderate quality: We are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different.
Low quality: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of the effect.
Very low quality: We have very little confidence in the effect estimate: The true effect is likely to be substantially different from the estimate of effect.

1 The assessment of risk of bias for non‐randomised studies starts at low‐quality evidence. We downgraded the level of evidence with one level, i.e. to very low quality, due to imprecision caused by a small sample size.

2 We would have downgraded the level of evidence with one more level due to imprecision caused by wide confidence intervals that include a null effect but we had already reached a judgment of very low‐quality evidence.

Figures and Tables -
Summary of findings for the main comparison. High correlated colour temperature light versus standard illumination for improving mood and alertness in daytime workers
Summary of findings 2. Indirect light versus direct light for improving mood and alertness in daytime workers

Indirect light versus direct light for improving mood and alertness in daytime workers

Patient or population: daytime workers
Setting: offices
Intervention: indirect lighting
Comparison: direct lighting

Outcomes

Anticipated absolute effects (95% CI)

№ of participants
(studies)

Quality of the evidence
(GRADE)

Risk with direct light

Risk with indirect light

Alertness

Not assessed

Not assessed

Not assessed

Not assessed

Mood
assessed with: BDI
Scale: 0 (best) to 63 (worst)
follow‐up: 5 months

Mean mood 5.8

MD 1 higher
(2.86 lower to 4.86 higher)

22
(1 RCT)

⊕⊕⊝⊝
Low1,2

Adverse events

(ocular problems)
follow‐up: 5 months

Mean adverse events 0.4

MD 0.1 lower
(0.92 lower to 0.72 higher)

22
(1 RCT)

⊕⊕⊝⊝
Low1,2

CI: confidence interval; MD: mean difference; RCT: randomised controlled trial.

GRADE Working Group grades of evidence
High quality: We are very confident that the true effect lies close to that of the estimate of the effect.
Moderate quality: We are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different.
Low quality: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of the effect.
Very low quality: We have very little confidence in the effect estimate: The true effect is likely to be substantially different from the estimate of effect.

1 We downgraded the level of evidence with one level, i.e. from high to moderate quality, due to risk of bias (the authors did not fully describe how or if they employed allocation concealment, outcome assessors were not blinded and there was a high and unbalanced attrition rate).

2 We downgraded the level of evidence with one level, i.e. from moderate to low quality, due to imprecision (a small sample size and a wide confidence interval including a null effect).

Figures and Tables -
Summary of findings 2. Indirect light versus direct light for improving mood and alertness in daytime workers
Summary of findings 3. Individually applied blue‐enriched light versus no treatment for improving mood and alertness in daytime workers

Individually applied blue‐enriched light versus no treatment for improving mood and alertness in daytime workers

Patient or population: daytime workers
Setting: hospital
Intervention: individually applied blue‐enriched light
Comparison: no treatment

Outcomes

Anticipated absolute effects (95% CI)

№ of participants
(studies)

Quality of the evidence
(GRADE)

Risk with light as usual

Risk with blue‐enriched light

Alertness
assessed with: Epworth Sleepiness Scale
Scale from: 0 to 24 (worst)
follow‐up: 16 weeks

Mean alertness

MD 3.3 lower
(6.28 lower to 0.32 lower)

25
(1 RCT)

⊕⊝⊝⊝
Very low1,2

Mood
assessed with: Beck Depression Inventory‐II
Scale from: 0 to 63 (worst)
follow‐up: 16 weeks

Mean mood

MD 4.8 lower
(9.46 lower to 0.14 lower)

25
(1 RCT)

⊕⊝⊝⊝
Very low1,2

Adverse events

Not assessed

Not assessed

Not assessed

Not assessed

CI: confidence interval; MD: mean difference; RCT: randomised controlled trial.

GRADE Working Group grades of evidence
High quality: We are very confident that the true effect lies close to that of the estimate of the effect.
Moderate quality: We are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different.
Low quality: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of the effect.
Very low quality: We have very little confidence in the effect estimate: The true effect is likely to be substantially different from the estimate of effect.

1 We downgraded the level of evidence with two levels, i.e. from high to low quality, due to risk of bias (the authors did not fully describe how or if they employed allocation concealment, outcome assessors were not blinded, results for SIGH‐HDRS were not reported and there was a high attrition rate).

2 We downgraded the level of evidence with one level, i.e. from low to very low quality, due to imprecision (a small sample size and a wide confidence interval).

Figures and Tables -
Summary of findings 3. Individually applied blue‐enriched light versus no treatment for improving mood and alertness in daytime workers
Summary of findings 4. Morning bright light versus afternoon bright light for improving mood and alertness in daytime workers

Morning bright light versus afternoon bright light for improving mood and alertness in daytime workers

Patient or population: daytime workers
Setting: offices
Intervention: morning bright light
Comparison: afternoon bright light

Outcomes

Anticipated absolute effects* (95% CI)

Relative effect with morning bright light
(95% CI)

№ of participants
(studies)

Quality of the evidence
(GRADE)

Risk with afternoon bright light

Risk with morning bright light

Alertness
assessed with: visual analogue scale
Scale from: 0 to 100 (better)
follow‐up: 2 weeks

Mean 59 (SD 23)

Mean 66 (SD 25)

MD 7 higher
(−10.18 lower to 24.18 higher)

30
(1 RCT)

⊕⊕⊝⊝
Low1,2

Mood
assessed with: SIGH‐SAD (≥ 50% reduction of SIGH‐SAD)
follow‐up: 2 weeks

426 per 1000

688 per 1000
(345 to 1376)

RR 1.60
(0.81 to 3.20)

30
(1 RCT)

⊕⊕⊝⊝
Low1,2

Adverse events (frequency)
follow‐up: 2 weeks

712 per 1000

375 per 1000
(349 to 1000)

RR 0.53
(0.26 to 1.07)

30
(1 RCT)

⊕⊕⊝⊝
Low1,2

*The risk in the intervention group (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).

CI: confidence interval; MD: mean difference; RCT: randomised controlled trial; RR: risk ratio; SIGH‐SAD: Structured Interview Guide for the Hamilton Depression Rating Scale‐Seasonal Affective Disorders Version.

GRADE Working Group grades of evidence
High quality: We are very confident that the true effect lies close to that of the estimate of the effect.
Moderate quality: We are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different.
Low quality: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of the effect.
Very low quality: We have very little confidence in the effect estimate: The true effect is likely to be substantially different from the estimate of effect.

1 We downgraded the level of evidence with one level, i.e. from high to moderate quality, due to risk of bias (the authors did not fully describe their randomisation method nor how or if they employed allocation concealment).

2 We downgraded the level of evidence with one level, i.e. from moderate to low quality, due to imprecision (a small sample size and a wide confidence interval including a null effect).

Figures and Tables -
Summary of findings 4. Morning bright light versus afternoon bright light for improving mood and alertness in daytime workers
Comparison 1. High correlated colour temperature light versus standard illumination

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Alertness ‐ Item Decreased Daytime Alertness from Columbia Jet Lag Scale 14 weeks Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

2 Alertness ‐ Item Sleepiness in Day from Columbia Jet Lag Scale 14 weeks Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

3 Alertness ‐ Karolinska Sleepiness Scale: mean of all time points Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

4 Alertness ‐ meta‐analysis Show forest plot

2

50

Std. Mean Difference (IV, Fixed, 95% CI)

‐0.69 [‐1.28, ‐0.10]

5 Mood ‐ Positive Mood PANAS Scale: mean of all time points Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

6 Mood ‐ Negative Mood PANAS Scale: mean of all time points Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

7 Adverse events ‐ eye discomfort: mean of all time points Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

8 Adverse events ‐ irritability: mean of all time points Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

9 Adverse events ‐ headache: mean of all time points Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

10 Adverse events ‐ eye strain: mean of all time points Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

11 Adverse events ‐ eye fatigue: mean of all time points Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

12 Adverse events ‐ difficult focusing: mean of all time points Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

13 Adverse events ‐ difficulty concentrating: mean of all time points Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

14 Adverse events ‐ blurred vision: mean of all time points Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

Figures and Tables -
Comparison 1. High correlated colour temperature light versus standard illumination
Comparison 2. Different proportions of direct and indirect indoor lighting

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Mood BDI: indirect lighting versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

1.1 Mood BDI after 2 months: indirect lighting versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

1.2 Mood BDI after 5 months: indirect lighting versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

2 Adverse events ‐ ocular problems indirect versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

2.1 Adverse events after 2 months ‐ ocular problems indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

2.2 Adverse events after 5 months ‐ ocular problems indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

3 Mood Beck Depression Inventory (BDI): indirect lighting versus 70% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

3.1 Mood BDI after 2 months: indirect lighting versus 70% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

3.2 Mood BDI after 5 months: indirect lighting versus 70% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

4 Mood BDI: indirect lighting versus 30% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

4.1 Mood BDI after 2 months: indirect lighting versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

4.2 Mood BDI after 5 months: indirect lighting versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

5 Mood BDI: 70% indirect lighting versus 30% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

5.1 Mood BDI after 2 months: 70% indirect lighting versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

5.2 Mood BDI after 5 months: 70% indirect lighting versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

6 Mood BDI: 70% indirect lighting versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

6.1 Mood BDI after 2 months: 70% indirect lighting versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

6.2 Mood BDI after 5 months: 70% indirect lighting versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

7 Mood BDI: 30% indirect lighting versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

7.1 Mood BDI after 2 months: 30% indirect lighting versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

7.2 Mood BDI after 5 months: 30% indirect lighting versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

8 Adverse events ‐ reading problems indirect versus 30% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

8.1 Adverse events after 2 months ‐ reading problems indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

8.2 Adverse events after 5 months ‐ reading problems indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

9 Adverse events ‐ ocular problems indirect versus 70% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

9.1 Adverse events after 2 months ‐ ocular problems indirect versus 70% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

9.2 Adverse events after 5 months ‐ ocular problems indirect versus 70% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

10 Adverse events ‐ ocular problems indirect versus 30% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

10.1 Adverse events after 2 months ‐ ocular problems indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

10.2 Adverse events after 5 months ‐ ocular problems indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

11 Adverse events ‐ ocular problems 70% indirect versus 30% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

11.1 Adverse events after 2 months ‐ ocular problems 70% indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

11.2 Adverse events after 5 months ‐ ocular problems 70% indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

12 Adverse events ‐ ocular problems 70% indirect versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

12.1 Adverse events after 2 months ‐ ocular problems 70% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

12.2 Adverse events after 5 months ‐ ocular problems 70% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

13 Adverse events ‐ ocular problems 30% indirect versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

13.1 Adverse events after 2 months ‐ ocular problems 30% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

13.2 Adverse events after 5 months ‐ ocular problems 30% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

14 Adverse events ‐ reading problems indirect versus 70% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

14.1 Adverse events after 2 months ‐ reading problems indirect versus 70% indirect lightning

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

14.2 Adverse events after 5 months ‐ reading problems indirect versus 70% indirect lightning

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

15 Adverse events ‐ reading problems indirect versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

15.1 Adverse events after 2 months ‐ reading problems indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

15.2 Adverse events after 5 months ‐ reading problems indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

16 Adverse events ‐ reading problems 70% indirect versus 30% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

16.1 Adverse events after 2 months ‐ reading problems 70% indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

16.2 Adverse events after 5 months ‐ reading problems 70% indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

17 Adverse events ‐ reading problems 70% indirect versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

17.1 Adverse events after 2 months ‐ reading problems 70% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

17.2 Adverse events after 5 months ‐ reading problems 70% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

18 Adverse events ‐ reading problems 30% indirect versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

18.1 Adverse events after 2 months ‐ reading problems 30% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

18.2 Adverse events after 5 months ‐ reading problems 30% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

19 Adverse events ‐ concentration problems indirect versus 70% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

19.1 Adverse events after 2 months ‐ concentration problems indirect versus 70% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

19.2 Adverse events after 5 months ‐ concentration problems indirect versus 70% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

20 Adverse events ‐ concentration problems indirect versus 30% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

20.1 Adverse events after 2 months ‐ concentration problems indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

20.2 Adverse events after 5 months ‐ concentration problems indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

21 Adverse events ‐ concentration problems indirect versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

21.1 Adverse events after 2 months ‐ concentration problems indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

21.2 Adverse events after 5 months ‐ concentration problems indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

22 Adverse events ‐ concentration problems 70% indirect versus 30% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

22.1 Adverse events after 2 months ‐ concentration problems 70% indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

22.2 Adverse events after 5 months ‐ concentration problems 70% indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

23 Adverse events ‐ concentration problems 70% indirect versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

23.1 Adverse events after 2 months ‐ concentration problems 70% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

23.2 Adverse events after 5 months ‐ concentration problems 70% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

24 Adverse events ‐ concentration problems 30% indirect versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

24.1 Adverse events after 2 months ‐ concentration problems 30% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

24.2 Adverse events after 5 months ‐ concentration problems 30% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

25 Adverse events ‐ musculoskeletal symptoms indirect versus 70% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

25.1 Adverse events after 2 months ‐ musculoskeletal symptoms indirect versus 70% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

25.2 Adverse events after 5 months ‐ musculoskeletal symptoms indirect versus 70% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

26 Adverse events ‐ musculoskeletal symptoms indirect versus 30% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

26.1 Adverse events after 2 months ‐ musculoskeletal symptoms indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

26.2 Adverse events after 5 months ‐ musculoskeletal symptoms indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

27 Adverse events ‐ musculoskeletal symptoms indirect versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

27.1 Adverse events after 2 months ‐ musculoskeletal symptoms indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

27.2 Adverse events after 5 months ‐ musculoskeletal symptoms indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

28 Adverse events ‐ musculoskeletal symptoms 70% indirect versus 30% indirect lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

28.1 Adverse events after 2 months ‐ musculoskeletal symptoms 70% indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

28.2 Adverse events after 5 months ‐ musculoskeletal symptoms 70% indirect versus 30% indirect lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

29 Adverse events ‐ musculoskeletal symptoms 70% indirect versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

29.1 Adverse events after 2 months ‐ musculoskeletal symptoms 70% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

29.2 Adverse events after 5 months ‐ musculoskeletal symptoms 70% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

30 Adverse events ‐ musculoskeletal symptoms 30% indirect versus direct lighting Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

30.1 Adverse events after 2 months ‐ musculoskeletal symptoms 30% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

30.2 Adverse events after 5 months ‐ musculoskeletal symptoms 30% indirect versus direct lighting

1

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

Figures and Tables -
Comparison 2. Different proportions of direct and indirect indoor lighting
Comparison 3. Individually applied blue‐enriched light versus no treatment

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Alertness ‐ Epworth Sleepiness Scale Show forest plot

1

Mean Difference (Fixed, 95% CI)

Totals not selected

2 Mood Beck Depression Inventory‐II Show forest plot

1

Mean Difference (Fixed, 95% CI)

Totals not selected

Figures and Tables -
Comparison 3. Individually applied blue‐enriched light versus no treatment
Comparison 4. Morning bright light versus afternoon bright light

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Alertness (visual analogue scale (VAS)) after 2 weeks of intervention Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

2 Mood (≥ 50% of reduction of Structured Interview Guide for the Hamilton Depression Rating Scale‐Seasonal Affective Disorders Version (SIGH‐SAD) scores from baseline after 2 weeks of treatment)) Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

3 Mood SIGH‐SAD after 2 weeks of intervention Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

4 Mood 21‐item Hamilton Depressive Rating Scale after 2 weeks of interventions Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

5 Mood 17‐item Hamilton Depressive Rating Scale after 2 weeks of intervention Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

6 Mood Seasonal Affective Disorders subscale after 2 weeks of intervention Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

7 Mood VAS after 2 weeks of intervention Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

8 Frequency of adverse events after 2 weeks of intervention Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

Figures and Tables -
Comparison 4. Morning bright light versus afternoon bright light