跳至主要内容
临床试验/NCT05838976
NCT05838976招募中不适用

Validity and Reliability of the Shorter Version of the CTQ-SSS in Patients With Carpal Tunnel Syndrome: A Cross-sectional Study

Ahram Canadian University1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2023年5月最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
50
试验地点
1
主要终点
Validity and Reliability of the Shorter Version of the CTQ-SSS

研究概览

简要总结

To determine the validity and reliability of the shorter version of the CTQ-SSS in patients with carpal tunnel syndrome (CTS) undergoing nonsurgical management.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Cross Sectional

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Patients diagnosed with carpal tunnel syndrome based on clinical presentation and/or nerve conduction studies.
  • Patients aged 18 years to 60 years old.
  • Patients who are undergoing nonsurgical management for carpal tunnel syndrome.

排除标准

  • Patients with a history of hand or wrist surgery within the past 6 months.
  • Patients with severe hand or wrist pain that would prevent completion of the outcome measures or interfere with their ability to participate in the study.
  • Patients with severe cognitive impairment or language barrier that would prevent understanding of the study instructions or interfere with their ability to participate in the study.
  • Patients with any other medical condition that could affect hand function or interfere with test completion.

结局指标

主要结局

Validity and Reliability of the Shorter Version of the CTQ-SSS

时间窗: Outcome measures will be assessed within 2-4 weeks of the initial CTQ-SSS administration.

To determine the validity and reliability of the shorter version of the CTQ-SSS in patients with carpal tunnel syndrome undergoing nonsurgical management. The CTQ-SSS will be administered at baseline and at a follow-up visit within 2-4 weeks to assess test-retest reliability. Internal consistency will be assessed using Cronbach's alpha coefficient. Construct validity will be assessed by comparing the CTQ-SSS scores with other functional measures such as the DASH questionnaire and PRWE using Pearson's correlation coefficient.

次要结局

未报告次要终点

研究者

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

Mohamed Magdy ElMeligie

Lecturer of Physical Therapy and Director of Electromyography Lab

Ahram Canadian University

研究点 (1)

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