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临床试验/NCT06839690
NCT06839690招募中不适用

Comparison of Sub-maximal Voluntary Isometric Training vs Eccentric Training in Management of De Quervain Tenosynovitis

Foundation University Islamabad2 个研究点 分布在 1 个国家目标入组 58 人开始时间: 2024年7月18日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
58
试验地点
2
主要终点
Grip Strength measurement

研究概览

简要总结

This study is a randomised control trial and the purpose of this study is to compare the effects of Sub-maximal Voluntary Isometric Training vs Eccentric Training in Management of De Quervain Tenosynovitis

详细描述

Participants will be recruited into their respective groups using a coin toss method. De Quervain Tenosynovitis will be assessed using the following tests:

  1. Wrist hyperflexion and abduction of thumb (WHAT) test
  2. Finkelstein's / Eichhoff's test
  3. De Quervain Screening Tool

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
21 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Patients having history of pain, tenderness in thumb region from 3 weeks or more
  • Age 21-50
  • Both genders
  • Individuals meeting the diagnostic criteria i.e.
  • A score of 3 or more out of 7 on De Quervain screening tool.
  • Positive Wrist hyperflexion and abduction of thumb (WHAT) test
  • Positive Finkelstein's / Eichhoff's test

排除标准

  • Diagnosed cases of Osteoarthritis of 1st CMC joint and Rheumatoid arthritis
  • C6 cervical radiculopathy
  • Any systemic inflammatory condition like septic arthritis
  • Carpal Tunnel Syndrome
  • Complex regional pain syndrome
  • Previous surgery impacting the first extensor compartment of the wrist
  • Corticosteroid injection in the radial wrist region within 3 months of enrolment into the study
  • If patient had undergone isometric thumb exercises or any strengthening protocol lasting greater than 2 weeks for the management of their current episode of de Quervain's syndrome

结局指标

主要结局

Grip Strength measurement

时间窗: 4 weeks

Power grip strength will be measured using hand held dynamometer and pinch grip strength will be measured using Modified sphygmomanometer

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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