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临床试验/NCT06316713
NCT06316713招募中不适用

Spanish Language Adaptation of One MORE for Chronic Pain in Latinos

University of Utah2 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2024年4月8日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
34
试验地点
2
主要终点
Pain Intensity & Interference

研究概览

简要总结

This study will be a single-site, two-arm randomized controlled trial conducted among Spanish-speaking chronic pain patients. Chronic pain patients will be randomized by a computer-generated randomization schedule with simple random allocation (1:1) to either One MORE or a wait-list control condition (WLC). One MORE will be delivered individually either in-person or via a HIPAA compliant virtual meeting platform.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
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

入选标准

  • Spanish-speaking
  • Diagnosed with a chronic pain condition
  • Average pain in the previous week > or = 3
  • Willingness to participate in study interventions and assessments.

排除标准

  • Non Spanish-speaking
  • Score of 10 or greater ('high risk') on the suicidality subsection of the MINI
  • Psychotic episode within the last 12 months as deemed by the corresponding subsection of the MINI
  • Presence of clinically unstable illness judged to interfere with treatment or study procedures
  • Unable or unlikely to complete study procedures (e.g., planned major surgery, anticipated move, travel barrier)
  • Communication or cognitive impairment that limits participation in treatment or study procedures.

结局指标

主要结局

Pain Intensity & Interference

时间窗: Will be completed at baseline, week 2, and week 6.

Change in pain intensity and interference from baseline through 6-week follow-up will be assessed with the Pain, Enjoyment, and General Activity scale. Scores range from 0 to 30, with higher scores reflecting greater pain intensity/interference.

次要结局

  • Acceptability(Will be completed immediately after the second of the two, 1-hour sessions of the One MORE intervention.)
  • Acute Pain(Will be completed immediately before and after each of the two, 1-hour sessions of the One MORE intervention.)

研究者

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

Eric Garland

Professor

University of Utah

研究点 (2)

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