Sleep Disturbance in Deployed Soldiers

Status unconfirmed · Early Phase 1

Conditions studied: Sleep Disturbance

In brief

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.

Key facts

Study ID

NCT00860756

Run by

Brooke Army Medical Center

People needed

150

Starts

2007-09-01

Expected to finish

2009-07-01

Last updated by the study team

2009-03-12

Who can join

Age: 18 and older, up to 50. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 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.

You may not qualify if…

• 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.

Where it is running

• Evans Army Community Hospital — Fort Carson, Colorado, United States (enrolling)
• Brooke Army Medical Center — Fort Sam Houston, Texas, United States (enrolling)
• Carl R. Darnall Army Medical Center — Fort Hood, Texas, United States

Full record on ClinicalTrials.gov

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