Status:
UNKNOWN
Sleep Disturbance in Deployed Soldiers
Lead Sponsor:
Brooke Army Medical Center
Conditions:
Sleep Disturbance
Eligibility:
All Genders
18-50 years
Phase:
EARLY_PHASE1
Brief Summary
Hypotheses: * Hypothesis 1 - Sleep can be measured in Theater using actigraph technology. * Hypothesis 2 - Standard sleep measures in Soldiers randomized to a sleep intervention group will more close...
Eligibility Criteria
Inclusion
- All study participants must be on Active Duty, or be Reserve or National Guard Service Members notified of impending deployment.
- Recruited prior to deployment in order to obtain baseline measures before deployment.
- Have been stateside at least one full year.
- Able to read and speak English and consent themselves.
Exclusion
- Subjects with self-identified sleep disorder (for example restless leg syndrome or sleep apnea)
- Pregnancy. Pregnant women will be excluded from the study since pregnancy places women in a non-deployable status and pregnant Soldiers will not be deploying.
Key Trial Info
Start Date :
September 1 2007
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
July 1 2009
Estimated Enrollment :
150 Patients enrolled
Trial Details
Trial ID
NCT00860756
Start Date
September 1 2007
End Date
July 1 2009
Last Update
March 12 2009
Active Locations (3)
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1
Evans Army Community Hospital
Fort Carson, Colorado, United States, 80913
2
Carl R. Darnall Army Medical Center
Fort Hood, Texas, United States, 76544
3
Brooke Army Medical Center
Fort Sam Houston, Texas, United States, 78234