Physical Activity Pain Resilience
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- Acceptability of Intervention
研究概览
简要总结
The purpose of this research study is to test a new program called Pain REsilience Promotion for Youth (PREP-Y). This program is designed to help adolescents with chronic musculoskeletal pain (pain in muscles, bones, or joints that lasts more than 3 months) become more physically active and better able to manage their pain. The program includes four weekly virtual sessions that teach skills related to resilience, such as how to stay motivated, build confidence, and cope with pain.
Participants will complete surveys and physical activity tests before and after the program. Participants will also wear physical activity monitors to track their activity levels. The goal of this study is to learn whether the program is practical, helpful, and acceptable to participants, and to prepare for a future larger study.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 12 Years 至 17 Years（Child）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Between the ages of 12 and 17
- •History of chronic musculoskeletal pain for more than 3 months assessed by a pediatric rheumatologist or pain physician
- •Diagnosis of a primary pain disorder (e.g., juvenile fibromyalgia and other widespread pain conditions, lower back pain, complex regional pain and amplified pain syndrome)
- •Speaks English as primary language
排除标准
- •Chronic pain secondary to disease (e.g., sickle cell disease or rheumatic disease such as juvenile arthritis, systemic lupus erythematosus)
- •Presence of an untreated major psychiatric diagnosis (e.g., major depression, bi-polar disorder, psychoses)
- •History or diagnosis of developmental delay.
研究组 & 干预措施
PREP-Y
干预措施: PREP-Y (Behavioral)
结局指标
主要结局
Acceptability of Intervention
时间窗: From enrollment to the post-treatment visit, for a total of 6 weeks
Number of intervention visits completed by participants will be used to determine how acceptable the intervention is to the target population.
Feasibility of Intervention
时间窗: From enrollment to the post-treatment visit, for a total of 6 weeks
Fidelity checklists detailing content areas of the intervention adequately conveyed during the study visit will be used to measure intervention feasibility.
次要结局
- Accelerometry Data(From baseline to 3-month follow-up, for a total of 18 weeks)
- Functional Disability Inventory(From baseline to 3-month follow-up, for a total of 18 weeks)
研究者
William Black
Principal Investigator
Nationwide Children's Hospital