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临床试验/NCT07004894
NCT07004894招募中不适用

Effects of Neuromuscular Reeducation Versus Friction Massage in Lateral Epicondylitis: A Randomized Control Trial

Furqan Ahmed Siddiqi1 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2024年7月18日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
42
试验地点
1
主要终点
Lateral Epicondylitis Pain

研究概览

简要总结

This study is a randomised control trial and the purpose of this study is to determine the effects of neuromuscular reeducation versus friction massage in lateral epicondylitis.

详细描述

Participants will be recruited into their respective groups using a coin toss method. Lateral epicondylitis will be assessed using the following tests:

Cozen's test Maudsley's test Mills test

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

入选标准

  • •Diagnosed cases of lateral epicondylitis
  • •Age 25-50 years
  • •Both genders
  • •Postive tests; cozens, maudsley's, mills (at least any of 2)

排除标准

  • •Recent elbow fractures or dislocations
  • •Elbow joint instability
  • •Active joint disease
  • •Open wounds around elbow joints

研究组 & 干预措施

Neuromuscular reeducation

Experimental

Group A will recieve treatment of ultrasound followed by neuromuscular re-education+ strengthning exercises For the 1st two weeks; cross friction massage with active movement will be performed.

For the next two weeks; longitudinal friction massage with active movement will be performed.

干预措施: Neuromuscular re-education(experimental) (Procedure)

Friction massage

Active Comparator

Group B will receive standard treatment of ultrasound followed by friction massage+ strengthning exercises For the 1st two weeks; cross friction massage alone will be performed. For the last two weeks; longitudinal friction massage alone will be performed.

干预措施: Friction massage(standard protocol) (Procedure)

结局指标

主要结局

Lateral Epicondylitis Pain

时间窗: Variable will be assessed at pre and post treatment for the total interval of 4 weeks.

It will be measured using numeric pain rating scale (NPRS) in which the subjects select a number ranging from 0-10 according to their intensity of pain. '0' score indicates no pain while '10' indicates worst pain experienced.

Range of Motion

时间窗: Variable will be assessed at pre and post treatment for the total interval of 4 weeks.

Range of motion will be measured using goniometer. An instrument with movable and stationary arm used to measure range of motion at joint. It will be used to measure range of motion of flexion and extension at elbow joint, forearm pronation and supination, and flexion, extension, radial deviation, ulnar deviation at wrist joint.

次要结局

未报告次要终点

研究者

发起方
Furqan Ahmed Siddiqi
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Furqan Ahmed Siddiqi

Foundation University Islamabad

Foundation University Islamabad

研究点 (1)

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