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Sleep Enhancement Training Study for Novice Shiftworkers
This study is currently recruiting participants.
Verified by University of California, San Francisco, November 2008
First Received: November 4, 2008   No Changes Posted
Sponsors and Collaborators: University of California, San Francisco
National Institute of Nursing Research (NINR)
Information provided by: University of California, San Francisco
ClinicalTrials.gov Identifier: NCT00786266
  Purpose

The purpose of this study is to determine if a modified version of the Sleep Enhancement Fatigue Reduction Training (SEFRT) system can improve sleep and health-related symptoms and quality of life in shiftwork-naive new nurse graduates.


Condition Intervention Phase
Shift-Work Sleep Disorder
Behavioral: Sleep Enhancement Training System
Behavioral: NIOSH shiftwork booklet
Phase I

MedlinePlus related topics: Sleep Disorders
U.S. FDA Resources
Study Type: Interventional
Study Design: Prevention, Randomized, Double Blind (Subject, Outcomes Assessor), Parallel Assignment, Efficacy Study
Official Title: Sleep Enhancement Training Study for Novice Shiftworkers

Further study details as provided by University of California, San Francisco:

Primary Outcome Measures:
  • actigraphy measures of sleep [ Time Frame: 6 weeks ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • subjective measures of sleep and well-being [ Time Frame: 6 weeks ] [ Designated as safety issue: No ]

Estimated Enrollment: 30
Study Start Date: November 2008
Estimated Study Completion Date: May 2009
Estimated Primary Completion Date: April 2009 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
NIOSH shiftwork booklet: Active Comparator Behavioral: NIOSH shiftwork booklet
weekly readings about coping with shiftwork
Sleep Enhancement Training System: Experimental Behavioral: Sleep Enhancement Training System
4 week program of readings and relaxation programs

  Eligibility

Ages Eligible for Study:   18 Years to 30 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • English-speaking, full-time nurses scheduled to work at least 2 consecutive night shifts per week in the next 3 months
  • 18-30 years of age

Exclusion Criteria:

  • prior experience working night-shift
  • history of diagnosed sleep disorder or affective illness
  • sleep disturbance due to environmental factors (e.g., partner, children, or pets)
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00786266

Contacts
Contact: Traci Coggins 415-476-4435 traci.coggins@ucsf.edu
Contact: Caryl Gay, PhD 415-476-4435 caryl.gay@ucsf.edu

Locations
United States, California
University of California, San Francisco Recruiting
San Francisco, California, United States, 94143
Sub-Investigator: Kathryn A. Lee, RN, PhD            
Sponsors and Collaborators
University of California, San Francisco
Investigators
Principal Investigator: Christopher R Alsten, PhD Inner Health, Inc.
  More Information

No publications provided

Responsible Party: Inner Health, Inc. ( Christopher Alsten, PhD, Executive Vice President )
Study ID Numbers: R43-NR010688, R43-NR010688
Study First Received: November 4, 2008
Last Updated: November 4, 2008
ClinicalTrials.gov Identifier: NCT00786266     History of Changes
Health Authority: United States: Institutional Review Board

Keywords provided by University of California, San Francisco:
shift-work
sleep
nurse
relaxation

Study placed in the following topic categories:
Signs and Symptoms
Sleep Disorders, Circadian Rhythm
Mental Disorders
Neurologic Manifestations
Disorders of Environmental Origin
Dyssomnias
Sleep Disorders
Occupational Diseases
Chronobiology Disorders

Additional relevant MeSH terms:
Signs and Symptoms
Sleep Disorders, Circadian Rhythm
Mental Disorders
Nervous System Diseases
Neurologic Manifestations
Disorders of Environmental Origin
Dyssomnias
Sleep Disorders
Occupational Diseases
Chronobiology Disorders

ClinicalTrials.gov processed this record on May 07, 2009