Co-development and Assessment of the Feasibility and Potential Effects of an Online Self-management Program for Chronic Non-cancer Pain
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 63
- 试验地点
- 2
- 主要终点
- Feasibility of the recruitment
研究概览
简要总结
Based on a mixed-methods design, the objective of this trial is to assess the feasibility and acceptability of the "Agir pour moi" program, an 8-week online self-management program for chronic non-cancer pain (CNCP). The investigators will also explore its potential effects on self-efficacy, pain interference, pain severity, anxiety, depression, catastrophizing, and global impression of change in adults with CNCP awaiting services from a chronic pain multidisciplinary treatment center.
详细描述
The mixed-methods sequential explanatory design combines a quantitative questionnaire-based study with a subsequent in depth qualitative approach.
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
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age ≥ 18 years;
- •live with CNCP for more than 3 months;
- •read and understand French easily;
- •have access to a computer and high-speed Internet;
- •be available to take part in the project for 6 to 8 months;
- •not having started a new treatment for pain within the last month;
- •agree to notify the team before starting a new treatment;
- •be able to give informed consent.
排除标准
- •be supported by a multidisciplinary treatment center or be likely to be in the short term;
- •having participated in a CNCP self-management program within the last year;
- •be awaiting scheduled surgical treatment within six months.
结局指标
主要结局
Feasibility of the recruitment
时间窗: Baseline
* Number of potentially eligible adults referred by the multidisciplinary treatment center over the recruitment period * Number of referred adults who respond to the invitation * Number of referred adults who consent to participate in the study * Number of interested adults excluded based on inclusion/exclusion criteria
Feasibility of data collection
时间窗: 3 months post-intervention
* Rate of response to the questionnaires * Rate of completed questionnaires (no missing data)
Acceptability
时间窗: 4 months post-intervention
Qualitative data from semi-structured interviews
Adherence to the program
时间窗: Post-intervention (8 weeks)
Completion rate of the program (completion is following ≥ 75% of the lessons)
次要结局
- Change in pain severity and pain interference: French version of the Brief Pain Inventory (BPI)(Baseline; Post-intervention (8 weeks); 3 months post-intervention)
- Patient Global Impression of Change Scale (PGIC)(Post-intervention (8 weeks); 3 months post-intervention)
- Change in anxiety and depression: French version of the Hospital Anxiety and Depression Scale (HADS)(Baseline; Post-intervention (8 weeks); 3 months post-intervention)
- Change in self-efficacy: French version of the Pain Self-Efficacy Questionnaire (PSEQ)(Baseline; Post-intervention (8 weeks); 3 months post-intervention)
- Change in pain catastrophizing: French version of the Pain Catastrophizing Scale (PCS)(Baseline; Post-intervention (8 weeks); 3 months post-intervention)
研究者
Anne-Marie-Pinard
Anesthesiologist
CHU de Quebec-Universite Laval