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临床试验/NCT04124289
NCT04124289已完成不适用

A Pilot Study to Validate a Functional Pain Scale in Order to Improve the Patient Experience

The Guthrie Clinic1 个研究点 分布在 1 个国家目标入组 49 人开始时间: 2019年10月29日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
49
试验地点
1
主要终点
Change in pain score using functional pain scale questionnaire

研究概览

简要总结

This will be an observational cohort study to evaluate pain measurement after surgery using a new functional pain scale.

详细描述

Patients admitted for orthopedic surgery may take part in this research. Participants will be assessed using three different pain scales: numeric rating scale (NRS), FACES pain scale and a new functional pain scale (FPS).

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

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

  • Completed orthopedic (hip or knee) surgery
  • English as primary language and able to read
  • Low risk as assessed by Opioid Risk Assessment Tool (ORAT)
  • No history of opioid abuse
  • Patients with a diagnosis of chronic pain other than the scheduled hip or knee meeting the above criteria may be included.

排除标准

  • Previous diagnosis of cognitive impairment

结局指标

主要结局

Change in pain score using functional pain scale questionnaire

时间窗: Through study completion, an average of 4 days.

Change in pain measurement using new functional pain scale from baseline postoperatively until discharge. The functional pain scale is a scale of 10 descriptive words related to pain and ability to function, ranging from minimal to immobilizing

Change in pain score using FACES pain scale

时间窗: Through study completion, an average of 4 days.

Change in pain measurement using FACES pain scale from baseline postoperatively until discharge. The scale includes pictures of facial expressions with correlating numerical scale of 0-10, 0 being no hurt and 10 being the worst hurt.

Change in pain score using numeric 0-10 rating scale

时间窗: Through study completion, an average of 4 days.

Change in pain measurement using standard numeric rating scale from baseline postoperatively until discharge. The numeric rating scale is 0-10 where 0 is no pain, 5 is moderate pain and 10 is the worst pain.

Change in functionality

时间窗: Through study completion, an average of 4 days.

Change in patient's ability to complete daily functions from baseline postoperatively until discharge. Physical therapy and occupational therapy reports will be reviewed to see if pain appears to interfere with the ability to participate in rehabilitation therapy.

次要结局

  • Patient preference for ease of use of the three pain scales (functional, FACES or numerical)(Through study completion, an average of 4 days.)
  • Provider preference for ease of use of the three pain scales (functional, FACES or numerical)(Through study completion, an average of 4 days.)
  • Opioid administration(Through study completion, an average of 4 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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