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Clinical Trials/NCT04187287
NCT04187287
Completed
Not Applicable

Comparison of Effects of Radial Extracorporeal Shock Wave Therapy and Deep Friction Massage on Individuals With Chronic Lateral Epicondylitis

Eastern Mediterranean University1 site in 1 country30 target enrollmentDecember 9, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Tennis Elbow
Sponsor
Eastern Mediterranean University
Enrollment
30
Locations
1
Primary Endpoint
Elbow and Forearm Pain
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The aim of this study is to compare the effects of Radial Extracorporeal Shockwave Therapy (rESWT) treatment and Deep Friction Massage (DFM) treatment on pain, functionality, grip strength (GS), edema, range of motion (ROM) of the elbow and quality of life in individuals with chronic lateral epicondylitis (CLE).

36 individuals diagnosed with CLE will be randomly divided into two equal groups. rESWT treatment will be applied to Group 1 and DFM treatment to Group 2. Visual analogue scale will be used to assess pain severity, functionality with Patient-Rated Elbow Evaluation Turkish version (PRTEE-T), GS with digital dynamometer, ROM of the elbow joint with goniometer, edema with environmental measurement, and quality of life with Short Form 36 (SF-36).

Registry
clinicaltrials.gov
Start Date
December 9, 2019
End Date
January 31, 2020
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Berkiye Kırmızıgil

Director

Eastern Mediterranean University

Eligibility Criteria

Inclusion Criteria

  • Individuals with pain on the lateral epicondyle or proximal musculotendinous area of the forearm extensor muscles for at least 3 months,
  • Individuals with a positive Thomsen Test ,
  • Individuals who have not received physical therapy for lateral epicondylitis,
  • Individuals with a positive Maudsley Test will be included.

Exclusion Criteria

  • Individuals who have received any physical therapy,
  • Individuals with reflected pain due to cervical and shoulder pathologies,
  • Individuals with elbow osteoarthritis,
  • Individuals with previous elbow fractures or elbow joint operations,
  • Individuals with a history of systemic inflammatory disease,
  • Individuals with osteoporosis,
  • Individuals with cardiovascular problems will not be included in the study.

Outcomes

Primary Outcomes

Elbow and Forearm Pain

Time Frame: Change from Baseline elbow and forearm pain at 3 weeks

will assessed using by visual analog scale

Secondary Outcomes

  • Grip Strength(Change from baseline grip strength at 3 weeks)
  • Change in the level of quality of life(Change from baseline quality of life level at 3 weeks)
  • Functionality(Change from baseline functionality at 3 weeks)
  • Change in the level of elbow and forearm edema(Change from baseline edema at 3 weeks)
  • Range of motion of elbow joint(Change from baseline range of motion at 3 weeks)

Study Sites (1)

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