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Clinical Trials/NCT03834077
NCT03834077
Unknown
Not Applicable

The Effect of Tissue Flossing in Patients With Tennis Elbow

University of Jaén1 site in 1 country50 target enrollmentFebruary 20, 2019
ConditionsTennis Elbow

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Tennis Elbow
Sponsor
University of Jaén
Enrollment
50
Locations
1
Primary Endpoint
Patient-related Tennis Elbow Questionnaire change
Last Updated
7 years ago

Overview

Brief Summary

The aim of the present intervention is to determine the effectiveness of the application of tissue flossing in patients with tennis elbow

Detailed Description

The application of tissue flossing has been deemed to provide beneficial results in patients with ankle range of motion limitation. Although, tissue flossing is widely extended among athletes due to its effectiveness in pain, function and range of motion, the evidence is limited. The aim of the present protocol is to determine the effectiveness of tissue flossing in patients with tennis elbow.

Registry
clinicaltrials.gov
Start Date
February 20, 2019
End Date
April 10, 2019
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University of Jaén
Responsible Party
Principal Investigator
Principal Investigator

DAVID CRUZ DÍAZ

Vice Dean

University of Jaén

Eligibility Criteria

Inclusion Criteria

  • Elbow pain for at least 6 weeks and satisfy the widely accepted diagnostic criteria of lateral epicondylalgia.
  • Diagnostic criteria are pain over the lateral humeral epicondyle that is provoked by gripping activities.
  • Reduced grip strength and increased sensitivity to manual palpation over the lateral epicondyle.
  • Pain with stretching or contraction of the wrist extensor muscles.

Exclusion Criteria

  • Upper limb fractures, surgery or concomitant disease.
  • Red flags presence.
  • Mental disorders.

Outcomes

Primary Outcomes

Patient-related Tennis Elbow Questionnaire change

Time Frame: At baseline, after 1 week and after 4 week.

Self reported questionnaire ranged from 0 to 150 with greater scores associated with severe disability.

Secondary Outcomes

  • Numeric rating scale change(At baseline, after 1 week and after 4 week.)
  • Pressure Pain Threshold change(At baseline, after 1 week and after 4 week.)

Study Sites (1)

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