Comprehensive Police Fatigue Management Program

August 13, 2013 updated by: Charles Andrew Czeisler, MD, PhD, Brigham and Women's Hospital

Testing the Effectiveness of a Comprehensive Fatigue Management for the Police

Police officers work some of the most demanding schedules known, which increases their risk of sleep deprivation and sleep disorders. The need to work frequent overnight shifts and long work weeks leads to acute and chronic partial sleep deprivation as well as misalignment of circadian phase. The public expects officers to perform flawlessly, but sleep deprivation and unrecognized sleep disorders significantly degrade cognition, alertness, reaction time and performance. In addition, both acute and chronic sleep deprivation adversely affect personal health, increasing the risk of gastrointestinal and heart disease, impairing glucose metabolism, and substantially increasing the risk of injury due to motor vehicle crashes.

We propose to conduct a randomized, prospective study of the effect on the safety, health, and performance of a police department of a Comprehensive Police Fatigue Management Program (CPFMP) consisting of the following interventions:

  1. identification and treatment of police with sleep disorders;
  2. caffeine re-education; and
  3. initiation of a sleep, health and safety educational program.

These interventions were chosen because we believe them most likely to lead to measurable improvements on work hours, health, safety, and job performance, and because they are cost effective. The success of the CPFMP will be assessed through an experimental comparison with a standard treatment group that will receive sleep education in the absence of any accompanying interventions. The overall goal of our team will be sleep health detection and treatment program that can be disseminated to practitioners, policymakers and researchers nationwide to reduce police officer fatigue and stress; enhance the ability of officers to cope with shift schedules; improve the health, safety and performance of law enforcement officers; and thereby improve public safety.

Study Overview

Study Type

Interventional

Enrollment (Actual)

683

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

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

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Active Sworn Police Officers

Exclusion Criteria:

  • None

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Diagnostic
  • Allocation: Randomized
  • Interventional Model: Factorial Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Sleep Hygiene Education
An education program, consisting of materials from experts in the field of fatigue management, will be provided to all police officers in the intervention group. Videotapes, slides, handouts and other educational material will be compiled to create a variety of information sources for police officers. Examples of materials to be incorporated into this training program would be the Operation Healthy Sleep Training Video, powerpoint created by the Harvard Work Hours, Health and Safety Group and pamphlets provided by the American Academy of Sleep Medicine.
Other: Expert-Led Sleep Disorders Screening and Treatment

Expert-led sleep disorder screening and treatment will consist of visiting police stations and presenting an information session about Operation Healthy Sleep. The session will take place during work time. During the session, we will invite officers to take the Operation Healthy Sleep survey. All subjects that answer the survey indicating that they are at high risk on the Berlin Questionnaire will be contacted to arrange an initial appointment at our OSA research clinic. If they don't meet the criteria they will be disempanelled.

  1. Positive on the Berlin Questionnaire
  2. Clinic visit, exam with a physician, given a home diagnostic device (HDD)
  3. High risk on HDD, seen by physician, given a CPAP machine
  4. Follow up visit after 2-3 weeks, CPAP data downloaded and reviewed
  5. Contacted by a sleep health clinic at 3, 6, 12 months
  6. After 12 months subject will be referred to their primary care physician
Other: Online Sleep Disorders Screening
Online sleep disorder screening will be available to all police officers nation-wide through the Operation Healthy Sleep survey. All subjects that answer the survey questions indicating that they are at high risk of a sleep disorder will be notified either online following the completion of the survey or by email or a letter. Treatment and follow up will not be conducted for individuals who screen positive on the online version of the Operation Healthy Sleep survey.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Motor vehicle accidents as a function of miles traveled
Time Frame: 05/2005 - 07/2009
05/2005 - 07/2009
Number of on-the-job injuries
Time Frame: 05/2005 - 07/2009
05/2005 - 07/2009
Number of citations issued
Time Frame: 05/2005 - 07/2009
05/2005 - 07/2009
Number of arrests made
Time Frame: 05/2005 - 07/2009
05/2005 - 07/2009
Number of warnings issued
Time Frame: 05/2005 - 07/2009
05/2005 - 07/2009
Number of officer-initiated vehicle assists
Time Frame: 05/2005 - 07/2009
05/2005 - 07/2009
Number of sick leave days
Time Frame: 05/2005 - 07/2009
05/2005 - 07/2009
Sleep duration
Time Frame: 05/2005 - 07/2009
05/2005 - 07/2009
Sleep quality
Time Frame: 05/2005 - 07/2009
05/2005 - 07/2009
Alertness
Time Frame: 05/2005 - 07/2009
05/2005 - 07/2009
Performance
Time Frame: 05/2005 - 07/2009
05/2005 - 07/2009

Secondary Outcome Measures

Outcome Measure
Time Frame
Job satisfaction
Time Frame: 05/2005 - 07/2009
05/2005 - 07/2009
Burnout
Time Frame: 05/2005 - 07/2009
05/2005 - 07/2009
Works hours
Time Frame: 05/2005 - 07/2009
05/2005 - 07/2009

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Charles A. Czeisler, Ph.D., M.D., Brigham and Women's Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

November 1, 2005

Primary Completion (Actual)

December 1, 2009

Study Completion (Actual)

December 1, 2010

Study Registration Dates

First Submitted

September 13, 2005

First Submitted That Met QC Criteria

October 27, 2005

First Posted (Estimate)

October 30, 2005

Study Record Updates

Last Update Posted (Estimate)

August 15, 2013

Last Update Submitted That Met QC Criteria

August 13, 2013

Last Verified

August 1, 2013

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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