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临床试验/NCT06394765
NCT06394765已完成不适用

5-minute Mindful Pain Management Strategy

Florida State University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年6月13日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
1
主要终点
Intervention Adherence

研究概览

简要总结

This project is a single-site, two-arm, pilot study assessing the feasibility and preliminary efficacy of a 5-minute Mindful Mapping intervention for adults with chronic musculoskeletal pain (n=60) relative to a time- and attention-matched control condition.

详细描述

This was a two-arm (Mindful Mapping vs. Serial Sevens), remotely delivered, parallel-group, pilot RCT. All procedures were approval by the local IRB and preregistered (NCT06394765). Written informed consent was obtained from all participants prior to their inclusion in the study. Participants were randomly assigned (1:1) to either the Mindful Mapping intervention (n=30) or a control condition, Serial Sevens (n=30). Randomization was performed using a computer-generated sequence.

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 (Participant)

盲法说明

Participants will be randomized (1:1) using a computer-generated randomization sequence created by the PI prior to the study start date.

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •having a chronic pain diagnosis
  • •being able not to commit to another (new) treatment during the course of the study
  • •understanding English instructions fluently
  • •Being 18 and above

排除标准

  • •having learned to practice mindfulness meditation any time in the past
  • •being unable to perform most basic tasks due to pain or pain treatment

研究组 & 干预措施

Mindful Mapping

Experimental

干预措施: Mindful Mapping (Behavioral)

Serial Sevens

Active Comparator

干预措施: Serial Sevens (Behavioral)

结局指标

主要结局

Intervention Adherence

时间窗: 5 minutes

Examine the percentage of participants completing their 5-minute intervention session

Randomization Feasibility

时间窗: 3 months

Examine randomization rates during the 3 months planned for recruitment.

Therapeutic Skill Use Adherence

时间窗: 2 weeks

Examine the frequency of therapeutic skill use during the 2-week, post-intervention, self-management period.

Recruitment Feasibility

时间窗: 3 months

Examine recruitment rates during the 3 months planned for recruitment.

次要结局

  • Treatment Acceptability(Completed at 2- and 6-week follow-ups)
  • Global Impression of Change(Completed at 2- and 6-week follow-ups)

研究者

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

Adam Hanley

Associate Professor

Florida State University

研究点 (1)

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