Sleep Disturbance in Deployed Soldiers
Early Phase 1
- Conditions
- Sleep Disturbance
- Interventions
- Other: Relaxation CD
- Registration Number
- NCT00860756
- Lead Sponsor
- Brooke Army Medical Center
- 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 closely approximate normal as compared to sleep measures of Soldiers randomized to the control group.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 150
Inclusion Criteria
- 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 Criteria
- 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.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description 1 Relaxation CD Intervention Group
- Primary Outcome Measures
Name Time Method Actigraph and self report questionnaires baseline, 6 months, 18 months
- Secondary Outcome Measures
Name Time Method Self report questionnaires baseline, 6 months, 18 months
Trial Locations
- Locations (3)
Carl R. Darnall Army Medical Center
🇺🇸Fort Hood, Texas, United States
Brooke Army Medical Center
🇺🇸Fort Sam Houston, Texas, United States
Evans Army Community Hospital
🇺🇸Fort Carson, Colorado, United States