跳至主要内容
临床试验/NCT00643695
NCT00643695已完成不适用

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

Portland VA Medical Center2 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2008年3月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
14
试验地点
2
主要终点
Reduction of symptoms of depression as measured by the Beck Depression Inventory II (BDI-II)

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male or female, age 18 or older
  • Documentation of positive hepatitis C status as indicated by a detectable HCV viral load by polymerase chain reaction
  • Mild to moderate depressive symptoms as evidenced by a BDI II score of ≥ 14
  • Able to read and understand English
  • Written/signed informed consent specific to this protocol
  • Being sedentary that is , less than 30 minutes of planned low to moderate intensity exercise 2 days per week

排除标准

  • Suicidal ideations
  • Current interferon therapy or planning to begin interferon therapy during the next three months
  • Diagnosis of Bipolar disorder, Schizophrenia, or Post Traumatic Stress Disorder
  • Any medical condition, disorder, or medication that contraindicates participation in a mild to moderate intensity walking program

结局指标

主要结局

Reduction of symptoms of depression as measured by the Beck Depression Inventory II (BDI-II)

时间窗: 12 weeks

次要结局

  • Reduction in symptoms of fatigue as measured by the Brief Fatigue Inventory (BFI)(12 weeks)
  • reduce the reported level of chronic pain(12 weeks)

研究者

申办方类型
Fed
责任方
Principal Investigator
主要研究者

Patricia Taylor-Young

Nurse Scientist

Portland VA Medical Center

研究点 (2)

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