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临床试验/NCT06688864
NCT06688864招募中不适用

Delivery of an eHealth Intervention for Under-resourced Adults With Chronic Pain (Flourish Study)

Mayo Clinic1 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2024年7月25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
发起方
Mayo Clinic
入组人数
300
试验地点
1
主要终点
Change in West Haven Yale Multiphasic Pain Inventory (WHYMPI) score

研究概览

简要总结

The purpose of this study is to examine the feasibility of the dissemination of a cognitive-behavioral eHealth application (app) for pain self-management with Black and LGBTQ+ adults with high-impact chronic pain lasting at least 3 months and disrupting daily functioning (Implementation aim).

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
Single (Outcomes Assessor)

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

  • •Identify as Black and/or LGBTQ+
  • •Reside in USA
  • •Chronic pain diagnosis for at least 3 months.
  • •Experience chronic pain that makes it harder to do their day-to-day activities
  • •Have daily access to a smart mobile device (smartphone or table) and are willing to use the EPIO app.

排除标准

  • •Unable or unwilling to use the digital app for the study
  • •Do not have daily access to a smart mobile device (smartphone or tablet)
  • •Self-report cancer related pain, or severe untreated psychological illness (e.g., psychosis); and/or do not fit into one of the demographic categories listed in #1-3 for inclusion criteria.

研究组 & 干预措施

Black adults with chronic pain

Experimental

干预措施: EPIO App (Behavioral)

LGBTQIA+ adults with chronic pain

Experimental

干预措施: EPIO App (Behavioral)

结局指标

主要结局

Change in West Haven Yale Multiphasic Pain Inventory (WHYMPI) score

时间窗: Baseline, 6 weeks

The West Haven Yale Multiphasic Pain Inventory (WHYMPI) is a 52-item measure of various domains of the experience of pain, including pain interference (primary intervention outcome) and pain severity with daily functioning.

次要结局

  • Change in Concerns About Pain-Short Form (CAP)(Baseline, 6 weeks)
  • Change in Pain Self-Efficacy Questionnaire (PSEQ) score(Baseline, 6 weeks)
  • Change in Chronic Pain Acceptance Questionnaire-Revised (CPAQ-R) score(Baseline, 6 weeks)
  • Change in Hospital Anxiety and Depression Scale (HADS) score(Baseline, 6 weeks)
  • Change in Short Form-36 score(Baseline, 6 weeks)
  • Change in Alcohol Use Disorders Identification Test-Concise (AUDIT-C) score(Baseline, 6 weeks)
  • Change in Perceived Stress Scale (PSS) score(Baseline, 6 weeks)
  • System Usability Scale score (SUS)(6 weeks)
  • Everyday Discrimination Scale-Expanded (EDS-E) score(Baseline)

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

Eleshia Morrison

Principal Investigator

Mayo Clinic

研究点 (1)

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