MedPath

Tissue Flossing in Tennis Elbow Patients

Not Applicable
Conditions
Tennis Elbow
Interventions
Other: Tissue flossing
Other: Placebo comparator
Registration Number
NCT03834077
Lead Sponsor
University of Jaén
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.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
50
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.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Tissue flossingTissue flossingConventional physiotherapy consisted in electrotherapy and stretching in addition to tissue flossing.
Placebo comparatorPlacebo comparatorConventional physiotherapy consisted in electrotherapy and stretching in addition with tissue flossing without tension.
Primary Outcome Measures
NameTimeMethod
Patient-related Tennis Elbow Questionnaire changeAt baseline, after 1 week and after 4 week.

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

Secondary Outcome Measures
NameTimeMethod
Numeric rating scale changeAt baseline, after 1 week and after 4 week.

10 point rating scale of pain where 0 is associated with no pain and 10 with greatest pain.

Pressure Pain Threshold changeAt baseline, after 1 week and after 4 week.

Determine the pain free pression with a validated instrument

Trial Locations

Locations (1)

University of Jaen

🇪🇸

Jaen, Spain

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