基于网络的单次会议授权缓解慢性疼痛患者服用甲或布普伦诺芬的可行性:单臂试验的协议
Morgan R Klein1, Beth D Darnall1, Dokyoung S You1
1Department of Anesthesiology, Perioperative and Pain Medicine, Stanford University School of Medicine, Palo Alto, CA, United States.
JMIR research protocols
|June 6, 2024
概括
这项研究测试了基于网络的疼痛缓解课程,用于治疗美沙或布普伦诺芬的慢性疼痛患者. 结果将指导未来对这种可访问的阿片类药物使用障碍 (OUD) 和疼痛治疗的试验.
科学领域:
- 疼痛管理 疼痛管理
- 行为健康 行为健康
- 数字治疗学数字治疗学
背景情况:
- 慢性疼痛影响数以百万计的人,无法获得非药物治疗.
- 处方阿片类药物被优先考虑,创造了对可访问替代品的需求.
- 这项研究针对的是接受美沙或布普伦诺芬治疗的慢性疼痛患者,这群人群往往服务不足.
研究的目的:
- 评估实时讲师,基于网络的,为期一届会议的止痛技能课程的可行性.
- 评估这种干预措施在特定风险人群中的可接受性和初步有效性.
- 为未来慢性疼痛和阿片类药物使用障碍 (OUD) 随机对照试验的设计提供信息.
主要方法:
- 一个全国性的,前性的,单臂的,不受控制的可行性试验.
- 从门诊疼痛诊所和研究数据库招募至少45名参与者.
- 通过网络,纸质或电话在6个时间点收集患者报告的措施,包括定性访谈.
主要成果:
- 招生于2021年9月开始,招聘于2023年10月完成,数据收集于2024年2月.
- 预计结果将于2024年底公布.
- 可行性值设置为整体组治疗满意度评级为8/10.
结论:
- 该试验将确定授权救援计划的可行性和初步有效性.
- 这些发现将指导未来随机对照试验的设计.
- 这种方法为服务不足的人群提供了可访问的疼痛管理的潜在解决方案.
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