Other Clinical Trial - Comprehensive Police Fatigue Management Program

Status Completed

Clinical Trial Summary

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.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Factorial Assignment, Masking: Open Label, Primary Purpose: Diagnostic

Related Conditions & MeSH terms

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

Clinical Trial Details

NCT number	NCT00246051
Study type	Interventional
Source	Brigham and Women's Hospital
Contact
Status	Completed
Phase	N/A
Start date	November 2005
Completion date	December 2010

View Details

See also
Status	Clinical Trial	Phase
Terminated	`NCT03605329` - Evaluation of the Severity of Cardiovascular Autonomic Neuropathy in Type 1 Diabetic Patients With OSAS	N/A
Completed	`NCT04912635` - Evaluation of a Health Dashboard Intervention to Improve Engagement With CPAP Therapy in PAP-Naïve Patients: Project Neo	N/A
Not yet recruiting	`NCT05939934` - Impact of the Mandibular Advancement Device on Sleep Apnea During CPAP Withdrawal	N/A
Enrolling by invitation	`NCT02290236` - Monitored Saturation Post-ICU	N/A
Completed	`NCT02088723` - Testing the Elevation as Sleep Apnea Treatment	N/A
Terminated	`NCT02269774` - Origin of Premature Atrial Beats Induced by Simulated Obstructive Sleep Apnea	N/A
Completed	`NCT02261857` - 3D-Printed CPAP Masks for Children With Obstructive Sleep Apnea	Early Phase 1
Completed	`NCT01943708` - Novel Auto-continuous Positive Airway Pressure (CPAP) Validation	Phase 3
Completed	`NCT01181570` - Efficacy and Safety of Adalimumab in Patients With Psoriasis and Obstructive Sleep Apnea	Phase 4
Completed	`NCT00273754` - The Effect of Caffeine on Postextubation Adverse Respiratory Events in Children With Obstructive Sleep Apnea (OSA).	Phase 2
Recruiting	`NCT02166879` - Undetected Sleep Apnea in the Postanesthesia Acute Care Unit (PACU)
Recruiting	`NCT04963192` - Integrated Management of Chronic Respiratory Diseases	N/A
Completed	`NCT05056766` - How Does the Clinical and Paraclinical Efficacy of an Oral Appliance Evolved According to Propulsion: Control With Each mm of Advancement
Completed	`NCT04846400` - Pilot Study of a Self-Supporting Nasopharyngeal Airway in Hypotonia	N/A
Recruiting	`NCT04314492` - Intracapsular Tonsillectomy in the Treatment of Obstructive Sleep Apnea in Adults	N/A
Completed	`NCT05175287` - OSA (oRisk of Obstructive Sleep Apnea and Traffic Accidents Among Bus Drivers in Ecuador: is There a Significant Association
Active, not recruiting	`NCT03431038` - Cross-sectional Study of Prevalence Rate of Abdominal Aortic Aneurysm in OSAHS Patients From BTCH	N/A
Enrolling by invitation	`NCT03075787` - Cardiovascular Variability and Heart Rate Response Associated With Obstructive Sleep Apnea	N/A
Completed	`NCT03300037` - HYpopnea and Apnea Detection and Treatment Performance of a New cardiOreSpiratory Holter Monitor	N/A
Recruiting	`NCT06097949` - AcuPebble to Remotely Monitor Patients With OSA on CPAP Therapy

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.