Study on Pain Management Groups in Occupational Health Settings
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 60
- 主要终点
- Pain self-efficacy
研究概览
简要总结
This cluster randomized waiting-list controlled study will evaluate the effectiveness of pain management group activity organized by the OH on pain intensity and associated disability, and co-occurrence of mental or sleep problem in patients with chronic pain.
详细描述
Pain is very prevalent among the working population causing a considerable amount of work disability days. Pain management group therapy has shown to have a significant effect on chronic pain. However, little is known of the effect of such therapy on work disability. There are especially very few studies prescribing the effectiveness of pain management groups provided by the occupational health service.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •chronic pain + increased risk of work disability (based on a screening survey)
排除标准
- •a malignant disease such as cancer, or severe mental illness such as depression causing significant functional disability.
- •participating in another pain group elsewhere.
- •in the middle of a major life crises such as divorce.
研究组 & 干预措施
Pain management group
6 + 1 meetings 2 hours each
干预措施: Pain management group (Behavioral)
Treatment as usual
Waiting list - will receive treatment as usual
结局指标
主要结局
Pain self-efficacy
时间窗: Change in pain self-efficacy from before intervention to immediately after intervention and at 6 months
self-reported questionnaire, set of 10 questions, item response scale 0 - 6, n=60
Sleep problems
时间窗: Change in sleep problems from before intervention to immediately after intervention and at 6 months
self-reported questionnaire, 1-item question, response scale 0-10, n=60
Work ability
时间窗: Change in work ability from before intervention to immediately after intervention and at 6 months
self-reported questionnaire, 1-item question, response scale 0-10, n=60
Pain intensity
时间窗: Change in pain intensity from before intervention to immediately after intervention and at 6 months
self-reported questionnaire, 1-item question, scale 0-10, n=60
Chronic pain acceptance
时间窗: Change in chronic pain acceptance from before intervention to immediately after intervention and at 6 months
self-reported questionnaire, set of 8 questions, item response scale 0 - 6, n=60
Fear-avoidance beliefs
时间窗: Change in fear-avoidance beliefs from before intervention to immediately after intervention and at 6 months
self-reported questionnaire, set of 3 questions, item response scale 0 - 6, n=18
Depressive symptoms
时间窗: Change in depressive symptoms from before intervention to immediately after intervention and at 6 months
self-reported questionnaire, 1-item question, response scale 0-10, n=60
次要结局
- health care contacts(6 months before and 6 months after intervention)
- sickness absence(6 months before and 6 months after intervention)
研究者
Helena Miranda
Project coordinator
Finnish Institute of Occupational Health