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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03834077
Other study ID # Ujaenflossing
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date February 20, 2019
Est. completion date April 10, 2019

Study information

Verified date February 2019
Source University of Jaén
Contact David Cruz-Diaz, PhD
Phone 953213408
Email dcruz@ujaen.es
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


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 information / eligibility

Status Not yet recruiting
Enrollment 50
Est. completion date April 10, 2019
Est. primary completion date March 28, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility 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


Related Conditions & MeSH terms


Intervention

Other:
Tissue flossing
Electrotherapy (transcutaneous electrical nerve stimulation) and Ultrasound in addition to tissue flossing.
Placebo comparator
Conventional physiotherapy in addition to flossing without tension

Locations

Country Name City State
Spain University of Jaen Jaen

Sponsors (1)

Lead Sponsor Collaborator
University of Jaén

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Patient-related Tennis Elbow Questionnaire change Self reported questionnaire ranged from 0 to 150 with greater scores associated with severe disability. At baseline, after 1 week and after 4 week.
Secondary Numeric rating scale change 10 point rating scale of pain where 0 is associated with no pain and 10 with greatest pain. At baseline, after 1 week and after 4 week.
Secondary Pressure Pain Threshold change Determine the pain free pression with a validated instrument At baseline, after 1 week and after 4 week.
See also
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