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临床试验/NCT03506685
NCT03506685撤回不适用

The Effectiveness of Dry Needling and Soft Tissue Mobilization in the Management of Pain Post Anterior Cruciate Ligament (ACL) Reconstruction: A Randomized Controlled Trial

Keller Army Community Hospital2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2018年6月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
入组人数
40
试验地点
2
主要终点
Numerical pain rating scale

研究概览

简要总结

The purpose of this study is to determine if dry needling (DN) and soft tissue mobilization (STM) is superior to standard treatment protocol for affecting pain, pain medication usage and measurements of range of motion (ROM) after ACL reconstruction surgery compared to a standard treatment protocol. Measurements of pain, pain medication usage, lower extremity functional scale (LEFS) and ROM will be taken day 2 post op and 1 week, 2 weeks, 3 weeks, and 4 weeks post op. It is hypothesized that the inclusion of DN and STM will acutely decrease the demand for pain medication and improve objective measurements when compared to a standard treatment protocol. Findings will potentially lead to insights as to the benefit of applying these interventions to help decrease the demand for pain medication post-surgery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18-40 Department of Defense( DOD) beneficiaries (17 if Cadet)
  • Scheduled for ACL Reconstruction Surgery

排除标准

  • Self-Reported Pregnancy
  • History of blood borne pathogens/infectious disease/active infection/metal allergy
  • Bleeding disorders or currently taking anti-coagulant medications
  • Participants who are not fluent in English

研究组 & 干预措施

control group Standard ACL protocol

No Intervention

This group will receive the standard ACL protocol rehab

Dry needling and STM group

Experimental

This group will also receive the standard ACL protocol in addition to STM and DN

干预措施: Dry needling and STM (Other)

结局指标

主要结局

Numerical pain rating scale

时间窗: change from baseline, 2 days post-op, 1 week, 2 week, 3 week, 4 week

validated outcome measure for pain ranging from 0-10

次要结局

  • Lower extremity functional scale(change from baseline, 2 days post-op, 1 week, 2 week, 3 week, 4 week)
  • Global rate of change(change from baseline, 2 days post-op, 1 week, 2 week, 3 week, 4 week)
  • knee range of motion(change from baseline, 2 days post-op, 1 week, 2 week, 3 week, 4 week)

研究者

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

Jamie Morris

principal Investigator

Keller Army Community Hospital

研究点 (2)

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