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临床试验/NCT07207174
NCT07207174招募中不适用

Dual-Language Brief Mindfulness-Oriented Recovery Enhancement (B-MORE) vs Brief Cognitive-Behavioral Therapy (B-CBT) for Chronic Pain

Florida State University1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2025年9月26日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
120
试验地点
1
主要终点
Program Feasibility

研究概览

简要总结

This randomized controlled trial aims to test both English and Spanish versions of two, benign behavioral interventions for adults with chronic pain -- 1) Brief Mindfulness-Oriented Recovery Enhancement (B-MORE), and 2) Brief Cognitive- Behavioral Therapy (B-CBT).

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
Single (Investigator)

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

  • •Having a chronic pain condition
  • •Average pain of > 3 in the last week
  • •Willingness to engage with study assessments and interventions
  • •Understanding English or Spanish instructions fluently
  • •Age 18 and above.

排除标准

  • •Unable to consent because of physical or mental incapacity
  • •Have previous, formal mindfulness or CBT training (e.g., MBSR)
  • •Have pain from a current cancer diagnosis
  • •Unstable illness that may interfere with treatment
  • •Had surgery within the previous three months
  • •Had pain relieving injections, such as cortisone or hyaluronate, within the previous three months.

研究组 & 干预措施

Brief Behavioral Intervention #1

Experimental

Brief Mindfulness Oriented Recovery Enhancement (B-MORE)

干预措施: Brief Mindfulness Oriented Recovery Enhancement (Behavioral)

Brief Behavioral Intervention #2

Experimental

Brief Cognitive-Behavioral Therapy (B-CBT)

干预措施: Brief Cognitive-Behavioral Therapy (Behavioral)

结局指标

主要结局

Program Feasibility

时间窗: At the first treatment session [1 hour] and the final treatment session [1 hour]

Feasibility will be assessed by intervention adherence rates (percentage of treatment sessions completed).

Treatment Acceptability

时间窗: Upon completion of the final treatment session [1 hour]

Treatment acceptability will be assessed by an adaptation of the Theoretical Framework of Acceptability scale (TFA).

次要结局

  • Pain Catastrophizing(Baseline and 2, 6, and 12-week post-treatment follow-ups)
  • Wellbeing(Baseline and 2, 6, and 12-week post-treatment follow-ups)
  • Chronic Pain Symptoms(Baseline and 2, 6, and 12-week post-treatment follow-ups)
  • Depressive Symptoms(Baseline and 2, 6, and 12-week post-treatment follow-ups)
  • Anxiety Symptoms(Baseline and 2, 6, and 12-week post-treatment follow-ups)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Adam Hanley

Assistant Professor

Florida State University

研究点 (1)

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