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Efficacy of an Exercise Intervention to Decrease Depressive Symptoms in Veterans With Hepatitis C

Depression Clinical Trial

Official title:
Efficacy of an Exercise Intervention to Decrease Depressive Symptoms in Veterans With Hepatitis C

Clinical Trial Summary

In this study, depressed veterans with hepatitis C will be randomly assigned to the control group or to the exercise intervention group. The exercise intervention is designed to begin slowly for most participants and to progress within each participant's target heart rate range for moderate intensity exercise. The exercise intervention is a 12 week home based walking program. Ideally individuals will walk for 30 minutes, at a moderate intensity, a minimum of three times per week. However, the duration and relative intensity will be tailored for each individual.

Central Hypothesis Veterans who receive the exercise intervention will be significantly less symptomatic for depression than veterans in the control group.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00643695
Study type Interventional
Source Portland VA Medical Center
Contact
Status Completed
Phase N/A
Start date March 2008
Completion date October 2014
View Details
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