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. 2016 Aug 23;2016(8):CD010641. doi: 10.1002/14651858.CD010641.pub2

Boivin 2012.

Methods Trial design: Randomised controlled trial
Intervention setting: Police patrol cars
Shift system: 35‐day roster. Succession of 8‐8.5 hr shifts according to a predetermined sequence:
 3 evening shifts; 2 rest days; 4 day shifts; 2 rest days
 7 night shifts (starting at 22:00, 22:30, 23:00, or 23:30 and lasted 8 to 8.5 hr)
 6 rest days; 4 evening shifts; 2 rest days; 3 day shifts; 2 rest days
Follow‐up period (intervention plus follow‐up): approx. 18 days (5‐7 day preparatory phase; first 48‐hour in‐laboratory assessment; 7 nights of intervention/control; second 48‐hour in‐laboratory assessment)
(Washout period): Not relevant*
Participants Inclusion criteria: None reported
Exclusion criteria: None reported
Number screened: Not reported
Number eligible: Not reported
Number included in our analysis: n = 17 (this includes both RCT participants (n = 15) and RXO participants (n = 2))
Industry: Police officers on patrol
Age in years (mean ± SD): 29.8 ± 6.5 (intervention); 30.3 ± 4.1 (control) (n = 17*)
Gender: 53% female
Country: Canada
Month(s) study conducted: not reported, but "season of study...comparable between groups"
"Chronotype" score: 49 ± 9 (intervention); 47 ± 12 (control) (mean ± SD; n = 17)
*data analysis includes two male police officers who completed both intervention and control conditions, at a 1‐year interval
Interventions Intervention: Exposure to full‐spectrum bright, white light via a portable lamp; wearing of orange‐tinted goggles; instructed to keep stable 8 hour daytime sleep episode from 2 hours after the end of the night shift; darkened bedroom windows
Shift‐based timing:
Light: Night (on‐shift)
Goggles: Morning, from sunrise until beginning of daytime sleep episode at home
Hours of intervention: Between 22:00 and 05:30
Dose/frequency/duration: Unclear lux, "intermittently" over 8 to 8.5 hour period, "intermittent" exposure per night for 7 nights
Control/comparison intervention: No light; no goggles; no sleep instructions (but darkened bedroom windows)
Outcomes Outcomes (measurement tool and timing), relevant to current review:
Sleep length off‐shift: Outcome not examined
Sleep quality off‐shift: Outcome not examined
Sleepiness on‐shift:
  • subjective: VAS for alertness at the start, middle, and end of every shift

  • objective: Psychomotor vigilance task at the start and end of every shift (median reaction time, median reaction speed and 10% fastest reaction speed)

Notes Funding: Institute de recherche Robert‐Sauvé en santé et en sécurité du travail; Canadian Institutes for Health Research
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Unclear risk No information available
Allocation concealment (selection bias) Unclear risk No information available
Blinding of participants and personnel (performance bias) 
 All outcomes Unclear risk No information on blinding
Blinding of outcome assessment (detection bias) 
 All outcomes Unclear risk No information available
Incomplete outcome data (attrition bias) 
 All outcomes Unclear risk Sleepiness: PVT data: intervention group (n = 8), control group (n = 9). "Nine missing data points were estimated in order to include all police officers in the statistical analysis"
 "Light exposure during the ambulatory period was analysed independently based on data collected from the actiwatch and the light sensor. Periods during which the device was removed when data were lost due to technical problems for ≥ 3.5 consecutive hours were discarded. For the actiwatch, all data were retained except for two participants (1i, a period of 5 hr and 7i, a period of 5 and 9 hr). For the light sensor, data from eight participants were discarded, for periods ranging from 3.5 to 39 consecutive hours, leaving ≥ 72.9% of data for each participant"
Selective reporting (reporting bias) Low risk P values given for all statistically significant outcomes but not all of those without statistical significance; detailed data not presented
Outcome reliably or objectively measured Low risk Sleepiness measured through Psychomotor Vigilance Task and through a VAS
Other potential sources of bias High risk Mixed study type ‐ 2 participants participated in both groups, in a cross‐over fashion, with a one‐year interval between the two conditions