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NCT00786357 Clinical Trial

Sleep Enhancement Training Study for Experienced Shiftworkers

Shift-Work Sleep Disorder Clinical Trial

— SETS-exp  

Official title:
Sleep Enhancement Training Study for Experienced Shiftworkers

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00786357
Other study ID # SETS-exp
Secondary ID
Status Completed
Phase Phase 1
First received November 4, 2008
Last updated June 22, 2010
Start date November 2008
Est. completion date January 2010

Study information
Verified date June 2010
Source University of California, San Francisco
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

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 experienced shift-working nurses.

Recruitment information / eligibility
Status Completed
Enrollment 32
Est. completion date January 2010
Est. primary completion date January 2010
Accepts healthy volunteers No
Gender Both
Age group 40 Years and older
Eligibility Inclusion Criteria:

- English-speaking nurses

- scheduled to work at least 2 consecutive night shifts per week during the next 3 months

- =40 years of age

- experiencing disturbed sleep related to night-shift

Exclusion Criteria:

- current diagnosis of sleep disorder or affective illness

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Behavioral:
• NIOSH shiftwork booklet
weekly readings about coping with shiftwork
• Sleep Enhancement Training System
4 week program of readings and relaxation programs

Locations
Country Name City State
United States University of California, San Francisco San Francisco California

Sponsors (2)
Lead Sponsor Collaborator
University of California, San Francisco National Heart, Lung, and Blood Institute (NHLBI)

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary actigraphy measures of sleep 3 months No
Secondary subjective measures of sleep and well-being 3 months No
See also
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Terminated NCT01264913 - Cardiometabolic Risk of Shiftwork N/A
Completed NCT03813654 - Sleep and Circadian Treatments for Shift Workers N/A