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CompletedNCT00207285Updated Mar 17, 2016

Sleep Disorders Management, Health and Safety in Police

An interventional study of Sleep Hygiene Education and Screening and Treatment of Sleep Disorders in Sleep Disorders, Sleep Apnea, Obstructive and Restless Legs Syndrome, sponsored by Brigham and Women's Hospital. Completed at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-03-17.

Sponsored by Brigham and Women's Hospital · Not applicable, Interventional, and Diagnostic

Phase
Not applicable
Study type
Interventional
Enrollment
731
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of the study is to test the effect of a sleep disorders detection and treatment program for police officers on their safety, quality of life, and job performance. The program is called Operation Healthy Sleep. We will develop and test a sleep health detection and treatment program that we aim to apply nationwide to reduce police officer fatigue and stress; enhance the ability of officers and their families to cope with police work; improve the health, safety and performance of law enforcement officers; and thereby improve public safety. Part of this program will include a questionnaire asking about about work hours and health related issues. We will then look at how these survey data relate with data on police officer safety and job performance that we are collecting through police department's databases.

Sleep disorders are common and treatable, but often remain undiagnosed and untreated. Police officers work some of the most demanding schedules known, which increases their risk of sleep disorders. The public expects officers to perform flawlessly, but unrecognized sleep disorders lead to severe disruption of sleep, which significantly reduces an individual's ability to think clearly and perform well. In addition, sleep loss and sleep disruption affect personal health, increasing the risk of gastrointestinal and cardiovascular. We also know that sleep loss increases the risk of injury due to motor vehicle crashes.

The goals of Operation Healthy Sleep are to improve officers' health, safety, and performance by reducing the impact of fatigue.

The study will take place over two years. In the first year, half of the police officers will take part in Operation Healthy Sleep, and in the second year, the second half will participate. We will carefully select the year 1 and year 2 groups so that the data collected across the two years can be validly compared.

Read the detailed description

Information Session and Surveys We will visit police stations and present an information session about Operation Healthy Sleep. The session will take place during work time. During this session, we will also provide a short education session aimed to help officers to improve their sleep habits and alertness. During the session, we will invite officers to take part in Operation Healthy Sleep.

If the officer agrees to take part, he/she will be asked to provide informed consent, and then complete a survey. The survey is comprehensive and includes questions regarding work schedules, past medical history, health habits, accidents, quality of life, and mood. The survey will also include a screening test to see if they might have a sleeping disorder. The total time commitment involved in attending the information/education session and completing the survey will be about 1 to 2 hours.

Officers will be asked to provide email address and other contact information. Officers will then receive information on how to link to our monthly web-based nationwide survey. The brief monthly surveys include questions regarding work schedules, accidents and injuries, health, quality of life, and mood. The survey should take about 10-15 minutes to complete each month.

Finally, a version of the survey will be completed at the end of each year until the study is completed (i.e. at most, two years). These yearly surveys will be completed during regular work time.

During the study, we will be tracking work hours, accidents, and job performance of all officers using the police department's computerized and paper records. Data collected through this system may be compared with other data we collect from officers directly. Protection of officers' confidentiality will be our highest priority.

Assessment and Treatment of Sleep Disorders After the initial information/education session is completed, we will review responses to the survey to check whether officers are at risk of having a sleep disorder. If officers are found to be at risk, we will contact them and recommend that they undergo assessment and, if necessary, treatment by a physician or sleep specialist. We will provide the officer with referrals to local sleep disorders testing and treatment centers and physicians. Officers are free to choose another sleep disorders specialist or another physician if they prefer.

02

Conditions studied

  • Sleep Disorders
  • Sleep Apnea, Obstructive
  • Restless Legs Syndrome
  • Sleep Disorders, Circadian Rhythm
  • Sleep Initiation and Maintenance Disorders

Keywords

  • Police
  • Sleep
  • Fatigue
  • Work Hours
  • Sleep disorder
  • Performance
03

In context

Sleep Apnea, Obstructive

2,198 studies on the registry are indexed under Sleep Apnea, Obstructive; 469 are open to participants now.

This study's enrollment of 731 is above the median of 53 across 1,448 interventional studies indexed under Sleep Apnea, Obstructive.

Browse Sleep Apnea, Obstructive studies →

Lead sponsor

Brigham and Women's Hospital is the lead sponsor of 1,236 studies on the registry; 224 are open to participants now.

Of its 116 completed or terminated interventional studies of FDA-regulated products, 64 (55%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Active sworn police officers

Exclusion criteria

Exclusion Criteria:

  • none
05

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Randomized
Intervention model
Factorial assignment
Masking
None (open label)
Enrollment
731 participants (actual)

Study arms

  • Other
    In Person Training

    These firefighters received the sleep education and sleep disorders screening in person by one of our research staff.

    Behavioral: Sleep Hygiene Education · Procedure: Screening and Treatment of Sleep Disorders

  • Other
    Train the Trainer

    These firefighters received the education and sleep disorder screening in person with someone taught by our research staff.

    Behavioral: Sleep Hygiene Education · Procedure: Screening and Treatment of Sleep Disorders

  • Other
    Online Group

    These firefighters took the sleep disorder screening and education online.

    Behavioral: Sleep Hygiene Education · Procedure: Screening and Treatment of Sleep Disorders

Interventions

  • BehavioralSleep Hygiene Education

    Baseline general meetings with officers in intervention districts, in which we will provide an introductory program on optimal caffeine use (caffeine re-education) and sleep hygiene, as these are cost-effective measures that may effectively address difficulties adjusting to night work, and low-grade sleep disorders such as mild shift work sleep disorder across the cohort as a whole.

  • ProcedureScreening and Treatment of Sleep Disorders

    All individuals who screen positive in the questionnaires on the baseline survey will be referred to one of the physicians at Sleep HealthCenters® or other sleep clinics in Massachusetts. Individuals will be paid $40 for attending an initial consultation visit with a sleep clinician and $400 if they are then asked to undergo an overnight sleep study and they complete the sleep study. Individuals will also be asked to wear an ApneaLink device for 2 nights at home and for 1 night during the overnight visit at Sleep HealthCenters®. Subjects may be asked to wear the ApneaLink device for more than 2 nights if there are not 4 hours of usable data each night. If the data is inadequate, subjects will be asked to wear the device until 4 hours of usable data on 2 nights is achieved. The ApneaLink device is an FDA approved sleep-screening tool that is used to identify individuals that are at risk for Obstructive Sleep Apnea Syndrome.

06

What researchers measure

Primary outcomes

  1. Motor vehicle accidents as a function of miles traveled

    Time frame: 05/2005 - 07/2009

  2. Number of on-the-job injuries

    Time frame: 05/2005 - 07/2009

  3. Number of citations issued

    Time frame: 05/2005 - 07/2009

  4. Number of arrests made

    Time frame: 05/2005 - 07/2009

  5. Number of warnings issued

    Time frame: 05/2005 - 07/2009

  6. Number of officer-initiated vehicle assists

    Time frame: 05/2005 - 07/2009

  7. Number of sick leave days

    Time frame: 05/2005 - 07/2009

  8. Sleep duration

    Time frame: 05/2005 - 07/2009

  9. Sleep quality

    Time frame: 05/2005 - 07/2009

  10. Alertness

    Time frame: 05/2005 - 07/2009

  11. Performance

    Time frame: 05/2005 - 07/2009

Secondary outcomes

  1. Job satisfaction

    Time frame: 05/2005 - 07/2009

  2. Burnout

    Time frame: 05/2005 - 07/2009

  3. Works hours

    Time frame: 05/2005 - 07/2009

07

Study locations

1 site
  • Brigham and Women's Hospital
    Boston, Massachusetts 02115, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 17, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00207285
Lead sponsor
Brigham and Women's Hospital
Responsible party
Charles Andrew Czeisler, MD, PhD (Charles A Czeisler, Ph.D., M.D.,, Brigham and Women's Hospital) — Principal investigator
First posted
Sep 21, 2005
Start date
May 2005
Primary completion
Sep 2010
Completion
Sep 2010
Last update
Mar 17, 2016

Study contacts

Charles A Czeisler, Ph.D., M.D.
principal investigator · Brigham and Women's Hospital, Harvard Medical School
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Mar 2016. You cannot join it, but the record below documents what was studied.

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