NCT05837351已完成不适用
The CARE Project: Collaborative Adolescent Running Experience
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 4
- 试验地点
- 1
- 主要终点
- The number of completed running sessions
研究概览
简要总结
This study is being completed to see if participants activity levels may have an impact as a treatment for depression, or depressive symptoms.
Eligible participants will be enrolled and have an 8-week running intervention three times each week.
The study hypothesizes that adolescents with Psychiatric disorders that are experiencing depressive symptoms will participate in a supported running intervention.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 13 Years 至 17 Years（Child）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Psychiatric disorders that are experiencing depressive symptoms (defined by the protocol)
- •Must have a smart phone
- •Parents/guardians will be advised to discuss their child's participation in the intervention with the participant's primary care physician
排除标准
- •Adolescents with unstable cardiac, pulmonary, endocrine or renal disorders
- •Adolescents with previous injuries or other conditions that may impact the safety of a running intervention
研究组 & 干预措施
Exercise -Running
Experimental
干预措施: Exercise -Running (Behavioral)
结局指标
主要结局
The number of completed running sessions
时间窗: weeks 1-8 during treatment period
Feasibility and acceptability of the study will be the completion of running sessions based on the Fitbit and or self-report.
次要结局
- Change in depression severity as reported by The Patient Health Questionnaire for Adolescents (PHQ-A)(Baseline (prior to treatment), 8 weeks (post intervention))
研究者
Richard Dopp
Associate Professor of Psychiatry
University of Michigan
研究点 (1)
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