Move in Mind: Program for Reducing Musculoskeletal Pain
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 主要终点
- Difference in quality and intensity of pain at the end of treatment/waitlist period.
研究概览
简要总结
The present pilot study will explore the range of mental and physical health benefits associated with a Rolfing®-based intervention program ("Move in Mind"). To assess the effects of this program on pain management and various psychological outcomes, the investigator's study will be offered to individuals with mild chronic musculoskeletal pain (e.g., lower back pain, neck pain, shoulder pain, knee pain, arthritic pain). Shortened from ten to six sessions and adapted to a group setting by Rolfing® instructor Monica Canducci, the intervention will be delivered weekly by Ms. Canducci, who is certified in Rolfing®. The program will target the potential associations of the Move in Mind program with better pain management (primary outcome) as well as increased body awareness and presence, increased well-being, and better stress management (secondary outcomes). Interested participants will be asked to complete a battery of questionnaires and psychometric scales to assess the variables of interest before (baseline) and after their participation in the Move in Mind program (six-week follow-up). A waitlist control group will also be assessed at baseline and follow-up and will then receive the Move in Mind sessions subsequently and also assessed after their participation.
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
- 否
入选标准
- •18 or older
- •experiencing a type of mild musculoskeletal pain (e.g., pain related to the muscles, ligaments, bones, joints, or nerve compression)
排除标准
- •receiving treatment for severe chronic pain
- •have had recent concussions or fractures as a result of accidents
结局指标
主要结局
Difference in quality and intensity of pain at the end of treatment/waitlist period.
时间窗: 7 days after last intervention session in week six
The short-form McGill Pain Questionaire (SF-MPQ) is a 15-item self-report measure that assesses the quality and intensity of a patient's pain. Descriptors either represent the sensory dimension (items 1-11; e.g., "Stabbing") or the affective dimension of pain experience (items 12-15; e.g., "Punishing-Cruel"). Patients respond to the SF-MPQ using an intensity scale ranging from 0 (none) to 3 (severe).
次要结局
- Difference in changes in physical and mental health at the end of treatment/waitlist period.(7 days after last intervention session in week six)
- Difference in perceived stress at the end of treatment/waitlist period.(7 days after last intervention session in week six)
- Difference in depressive disorder diagnoses and depressive symptom severity at the end of treatment/waitlist period.(7 days after last intervention session in week six)
- Difference in positive and negative affect at the end of treatment/waitlist period.(7 days after last intervention session in week six)
- Difference in satisfaction with Move in Mind program at the end of treatment/waitlist period.(7 days after last intervention session in week six)
研究者
Barbel Knauper
James McGill Professor of Psychology
McGill University