临床试验/NCT07755527

NCT07755527尚未招募不适用

An Adaptive Psychological Intervention to Improve Pain and Reduce Opioid Use Following an Injury

Henry Ford Health System0 个研究点目标入组 10 人开始时间: 2026年9月1日最近更新: 2026年9月23日

适应症

干预措施

试验速览

阶段: 不适用
状态: 尚未招募
发起方: Henry Ford Health System
入组人数: 10
主要终点: Acceptability of the intervention

研究概览研究设计入排标准研究组 & 干预措施结局指标研究者记录与标识符相似试验

研究概览

简要总结

The goal of this project is to refine the adaptive psychological intervention and assess initial feasibility and acceptability. Results will be used to inform a pilot randomized trial.

研究设计

研究类型: Interventional
分配方式: Na
干预模型: Single Group
主要目的: Prevention
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: 否

入选标准

•Admitted to Henry Ford Hospital
•Has an acute musculoskeletal injury
•Prescribed opioids during the admission

排除标准

•Under age 18
•Cognitive impairment (i.e., diagnosis of delirium, dementia, or traumatic brain injury/Glasgow Coma Scale less than 13)
•Chronic pain condition (i.e., pain most of the day, nearly every day for the past 3 months or longer)
•Taking opioids 30 days or more prior to this hospitalization

研究组 & 干预措施

Psychological Intervention

Experimental

Participants will receive a computerized brief intervention followed by four weekly psychological treatment sessions.

干预措施: Psychological Intervention (Behavioral)

结局指标

主要结局

Acceptability of the intervention

时间窗: Post-intervention (40-day follow-up)

Percentage of participants that agreed/strongly agreed with items on the acceptability of intervention measure (AIM), intervention appropriateness measure (IAM), and feasibility of intervention measure (FIM).

次要结局

Treatment adherence(Post-intervention (40-day follow-up))
Study adherence(Post-intervention (40-day follow-up))

研究者

发起方

Henry Ford Health System

申办方类型

Other

责任方

Principal Investigator

主要研究者

Lisa Matero

Associate Scientist

Henry Ford Health System

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