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Clinical Trials/NCT01249573
NCT01249573
Completed
Not Applicable

The Effect of Fascia Therapy and Transcutaneous Fibrolysis on Acute Ankle Sprain in Young Adults.

University Ghent1 site in 1 country60 target enrollmentOctober 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Acute Ankle Distortion
Sponsor
University Ghent
Enrollment
60
Locations
1
Primary Endpoint
effect of fascia therapy
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

This study investigates the immediate effect of fascia therapy and transcutaneous fibrolysis in the treatment of an acute ankle sprain. These treatments will be compared to a placebo group.

Detailed Description

Ankle sprain is the most occurring sport related injury. In spite of the high prevalence of this injury and the often residual symptoms, there is a large variety in diagnostic approach and therapeutic protocols. Concerning the treatment of an acute ankle sprain, it remains a challenge to minimize injury consequences on short and long term. In this study we investigate the immediate effect of two therapeutic techniques: fascia therapy and transcutaneous fibrolysis. They will be compared to a third group, who receives a placebo treatment. Muscle strength, muscle vascularisation, muscle tenderness and joint position sense are measured before and after treatment. The purpose of this study is to contribute to the knowledge of treating acute ankle sprains.

Registry
clinicaltrials.gov
Start Date
October 2010
End Date
May 2011
Last Updated
14 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • acute ankle sprain

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

effect of fascia therapy

Time Frame: baseline measurements and within 1 hour after treatment

The effect of fascia therapy on an acute ankle distortion. Measurement of muscle power, muscle saturation, joint position sense, tenderness and disability questionnaires.

Secondary Outcomes

  • complaints registration(baseline, 1 hour after treatment and 3 days later)

Study Sites (1)

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