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Clinical Trials/NCT01888016
NCT01888016
Completed
Not Applicable

Effectiveness of Fascial Manipulation in Early Rehabilitation Treatment of Rotator's Cuff Surgery Patients. A Randomized Trial.

Istituto Ortopedico Rizzoli1 site in 1 country60 target enrollmentJune 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cuff Rotator Syndrome
Sponsor
Istituto Ortopedico Rizzoli
Enrollment
60
Locations
1
Primary Endpoint
visual analogue scale (VAS)mean
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The purpose is to evaluate the effectiveness of fascial manipulation treatment in terms to reduce pain and improve physical functionality after rotator's cuff surgery. The technique involves deep friction manipulation of fascia's specific spots. Distant from surgical site.

Detailed Description

To evaluate the effectiveness of fascial manipulation treatment associated with standard physiotherapies treatment in rotator's cuff surgery patients, we'll randomize about 60 patients for arm's of study. Both arm's will receive 10 standard physiotherapies treatments in 2 weeks while the experimental arm will receive 3 manual intervention on deep fascial tissues, according to fascial manipulation technique, providing a specific motor and manual assessment, and a deep manual intervention over specific fascial alteration. To evaluate the effectiveness of fascial manipulation treatment we'll use 2 type of outcome measure and we will compare the result of both arms of study.

Registry
clinicaltrials.gov
Start Date
June 2013
End Date
June 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Rotator's cuff surgery patients that have been operated within the past 4/5 weeks
  • Age between 18 to 65 years old

Exclusion Criteria

  • Patients with traumatic shoulder's injury that involved bone's fractures.
  • Severe underlying pathologies like rheumatic, neurological and cardio pathologies that affect the correct shoulder treatment
  • Patients on anticoagulant treatment

Outcomes

Primary Outcomes

visual analogue scale (VAS)mean

Time Frame: Change from baseline in pain at the end of the rehabilitation cycle (two weeks)

we'll compare the baseline data (the first evaluation), with data at the end of the treatment, and with follow up (30 days from surgery)

Secondary Outcomes

  • Constant Murley score(Change from baseline in range of motion at the end of the rehabilitation cycle (two weeks))

Study Sites (1)

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