跳至主要内容
临床试验/ISRCTN10412631
ISRCTN10412631进行中(未招募)Unknown

Optimal duration of a single session of dry needling to the common extensor mass of the forearm in adults with lateral epicondylalgia (tennis elbow) for functional outcomes of pain, muscle extensibility, and strength

Franklin Pierce University0 个研究点目标入组 80 人开始时间: 2024年9月26日最近更新:
适应症

试验速览

阶段
Unknown
状态
进行中(未招募)
入组人数
80
主要终点
The following primary outcome measures are assessed at baseline, 5 minutes, and 30 minutes post-intervention: 1. Pain measured via the pain pressure threshold using a dolorimeter2. Grip strength measured using a handheld grip dynamometer3. Wrist flexion passive range of motion measured using a goniometer

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • •Over the age of 18 years old
  • •Diagnosis of lateral epicondylalgia per positive provocation using Cozen's and Maudsley's special tests

排除标准

  • •Those who have received dry needling or physical therapy within the last 6 months for lateral epicondylalgia
  • •Allergy to metals
  • •Needle phobia
  • •Blood clotting disorders
  • •Recent infections
  • •Peripheral neuropathy

结局指标

主要结局

The following primary outcome measures are assessed at baseline, 5 minutes, and 30 minutes post-intervention: 1. Pain measured via the pain pressure threshold using a dolorimeter2. Grip strength measured using a handheld grip dynamometer3. Wrist flexion passive range of motion measured using a goniometer

次要结局

  • Self-perceived disability measured using the QuickDash self-reported outcome survey before the intervention to establish a baseline level of functional impairment

研究者

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