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临床试验/NCT06369701
NCT06369701已完成不适用

The Effects of a Compressive Tissue Flossing Program on the Symptoms of Lateral Elbow Tendinopathy in United States Service Members

Brooke Army Medical Center2 个研究点 分布在 1 个国家目标入组 35 人开始时间: 2024年2月13日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
35
试验地点
2
主要终点
Patient-Rated Tennis Elbow Evaluation

研究概览

简要总结

The purpose of this research study will be to assess the effects of a compressive tissue flossing (CTF) program on the symptoms of lateral elbow tendinopathy in United States service members. Dependent variables will be the Defense and Veteran's Pain Rating Scale (DVPRS), decrease their Patient-Rated Tennis Elbow Evaluation (PRTEE) score, increase their maximal grip strength in the affected upper extremity (UE). Measurements will be taken at baseline, immediately after the first CTF intervention, and at the 1-week follow-up, for a total of 3 measurements.

详细描述

The purpose of this research study will be to assess the effects of a compressive tissue flossing (CTF) program on the symptoms of lateral elbow tendinopathy in United States service members. I hypothesize that tissue flossing with a band for a 2-minute session daily will decrease patient's report of pain on the Defense and Veteran's Pain Rating Scale (DVPRS), decrease their Patient-Rated Tennis Elbow Evaluation (PRTEE) score, increase their maximal grip strength in the affected upper extremity (UE). Measurements will be taken at baseline, immediately after the first CTF intervention, and at the 1-week follow-up, for a total of 3 measurements. If this method is shown to acutely decrease the symptoms of LET, it would give occupational therapists a potential home exercise program that is easy to initiate and only takes 2 minutes per day for patients to perform. This could prove to be an effective and low-cost method for service members to treat elbow pain symptoms. This technique could be used in austere environments where traditional musculoskeletal rehabilitation may not be available.

Specific Aim 1: Assess the acute effects of compressive tissue flossing on the symptoms of lateral elbow tendinopathy in United States service members.

I will accomplish this by recording the patient's report of pain on the Defense and Veteran's Pain Rating Scale, their Patient-Rated Tennis Elbow Evaluation outcome measure score, and their maximal grip strength in the affected UE before CTF, immediately after CTF, and at the 1-week follow-up after completing tissue flossing daily for 2 minutes. I will compare the outcomes from each measurement to evaluate the effects of CTF on lateral elbow pain symptoms.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • United States military service members stationed at JBSA between the ages of 18 to 65
  • Report of lateral elbow pain
  • Can perform either a modified push-up or push-up for 1 minute.

排除标准

  • Under 18 years old or over 65 years old
  • Recent surgical treatment of the involved upper extremity
  • Current fracture of the involved upper extremity
  • Open wounds at the treatment area
  • History of skin diseases
  • Tumors at the treatment area
  • History of a peripheral vascular condition
  • History of chronic inflammatory processes
  • Latex allergy
  • History of varicose veins
  • History of vein inflammation
  • History of thrombosis
  • Diagnosed with diabetes
  • Diagnosed with cardiac insufficiency Stage C or D
  • Diagnosed with lymphedema
  • Currently taking blood thinners
  • Currently receiving high-dose corticosteroids
  • Currently receiving other therapy for the elbow pain
  • Presently diagnosed with cervical radiculopathy

结局指标

主要结局

Patient-Rated Tennis Elbow Evaluation

时间窗: 1 week

Minimum value is 0 and maximum value is 100. 0 indicates that lateral elbow pain has no effect on the participant, whereas an increased score indicates the participant's lateral elbow pain has an increased effect on ability to perform activities and a worse outcome.

Patient's report of pain on the Defense and Veteran's Pain Rating Scale

时间窗: 1 week

This pain scale assesses the participant's perceived pain on a scale from 0-10. ) being no pain and 10 being as bad as the pain could possibly be. A participant rating their pain lower post-intervention would indicate a positive outcome.

Maximal grip strength in the affected upper extremity

时间窗: 1 week

Maximal grip strength will be recorded by the participant squeezing a calibrated dynamometer, which is a measurement tool used to calculate grip strength in pounds per square inch. The amount of grip strength generated in pounds per square inch in the affected upper extremity will be compared to maximal grip strength after the intervention is implemented day 1 and after 1 week.

次要结局

未报告次要终点

研究者

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

John Edgar Elam

Army-Baylor Doctor of Science in Occupational Therapy Fellow

Brooke Army Medical Center

研究点 (2)

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