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临床试验/NCT02438384
NCT02438384已完成不适用

Patient Education to Improve Pain Management in Older Adults With Acute Musculoskeletal Pain: A Pilot Randomized Trial

University of North Carolina, Chapel Hill2 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2015年9月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
75
试验地点
2
主要终点
Change in Pain Score

研究概览

简要总结

This is a three arm pilot randomized trial. Patients will be assigned to:

  1. Usual care
  2. Video education in the Emergency Department (ED)
  3. Video education in the ED plus phone follow-up at three days with geriatric pain management specialist for all patients with pain >=4/10

详细描述

This is a three arm pilot randomized trial. Patients will be assigned to:

  1. Usual care
  2. Video education in the ED (10 minute interactive video)
  3. Video education in the ED plus phone follow-up at three days with geriatric pain management specialist for all patients with pain >=4/10

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
None

入排标准

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

入选标准

  • Age 50 and older; ED visit for acute musculoskeletal pain

排除标准

  • Cognitively impaired; chronic pain (daily opioid use prior to onset of pain or pain symptoms more than one month); prison; injury or pain condition requiring hospital admission.

结局指标

主要结局

Change in Pain Score

时间窗: ED visit and 30 days post-ED visit

Change in Pain from emergency department (ED) visit to 30 day follow-up phone call will be measured by calculating the difference between the maximum pain score in the ED and the patient reported average overall pain severity in the past week using the 0-10 numeric rating scale for both measures.Change in pain will be reported as a negative number if the pain decreases (i.e., 10 to 8 = -2). Higher scores indicate a worse outcome.

次要结局

  • Average Overall Pain at One Month(30 days after ED visit)
  • Mean Physical Function Scores(30 days after ED visit)
  • Number of Participants Experiencing Medication Side Effects(30 days after ED visit)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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