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. 2019 Mar 18;2019(3):CD011269. doi: 10.1002/14651858.CD011269.pub3

Summary of findings for the main comparison. Bright white light therapy compared with no light therapy for prevention of SAD.

Bright white light therapy compared with no light therapy for prevention of SAD
Patient or population: all participants were known SAD patients who had been successfully treated with conventional light therapy in previous winters
 Settings: this was an outpatient field study. Participants chose when (between 6 am and 9 am) and where they would use the visors
 Intervention: bright white light therapy
 Comparison: no light therapy
Outcomes Illustrative comparative risks* (95% CI) Relative effect
 (95% CI) Number of participants
 (studies) Quality of the evidence
 (GRADE) Comments
Assumed risk Corresponding risk
No light therapy Light therapy
Incidence of SAD (SIGH‐SAD score ≥ 20)
(follow‐up 26 weeks)
Low RR 0.64
 (0.30 to 1.38) 23
 (1 RCT) ⊕⊝⊝⊝
 Very lowa,b  
300 per 1000 192 per 1000
 (90 to 414)
Moderate
500 per 1000 320 per 1000
(150 to 690)
High
600 per 1000 276 per 1000
(210 to 966)
Incidence of severe SAD (SIGH‐SAD‐SR (≥ 40))
(follow‐up 26 weeks)
Study population RR 0.21
 (0.03 to 1.75) 23
 (1 RCT) ⊕⊝⊝⊝
 Very lowa,b  
333 per 1000 70 per 1000
 (10 to 583)
Overall discontinuation
(follow‐up 26 weeks)
Study population RR 2.22
 (0.29 to 17.27) 28
 (1 RCT) ⊕⊝⊝⊝
 Very lowa,b  
100 per 1000 222 per 1000
 (29 to 1000)
*The basis for the assumed risk (e.g. median control group risk across studies) is provided in footnotes. The corresponding risk (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; RCT: randomised controlled trial; RR: risk ratio; SIGH‐SAD‐SR: Structured Interview Guide for the Hamilton Depression Rating Scale‐Seasonal Affective Disorders self‐rating version
GRADE Working Group grades of evidence
 High quality: further research is very unlikely to change our confidence in the estimate of effect
 Moderate quality: further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate
 Low quality: further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate
 Very low quality: we are very uncertain about the estimate

aDowngraded two levels because of severe risk of bias due to non‐blinding and unclear randomisation process and allocation concealment; no intention‐to‐treat analysis was reported, outcomes were self‐rated, compliance throughout study duration was not checked and participant characteristics were not reported comprehensively.
 bDowngraded one level because of small sample size (lack of power and random error could have influenced results).