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Clinical Trials/NCT02374073
NCT02374073
Completed
Not Applicable

Effectiveness of Functional Massage of the Teres Major Muscle in Patients With Subacromial Impingement Syndrome. A Randomized Controlled Pilot Study

Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina0 sites58 target enrollmentJanuary 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Subacromial Impingement Syndrome
Sponsor
Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina
Enrollment
58
Primary Endpoint
Change in Pain Intensity (visual analogue scale)
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

Purpose: Subacromial impingement syndrome is the most common shoulder condition. Myofascial trigger points in teres major muscle can be associated with this syndrome. The investigators objective is to find out if adding manual therapy specifically for teres major trigger points can produce better results in these patients.

Method: A randomized controlled pilot study was carried out. Fifty people were randomly assigned to one of two groups: intervention group or control group. Both groups received a protocolized physical therapy treatment while the intervention group additionally received manual therapy for teres major trigger points.

Registry
clinicaltrials.gov
Start Date
January 2014
End Date
March 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age 18 years and over
  • Clinical diagnosis of Subacromial Impingement Syndrome.
  • Detectable trigger points in teres major muscle.
  • Sign informed consent form.

Exclusion Criteria

  • Presence of wounds or cutaneous alterations in the shoulder region
  • Previous surgery in the shoulder
  • Presence of acute inflammatory process in the shoulder (\< 7 days),
  • Being involved in litigation or compensation processes
  • Not having a domain of the language that could make the informed consent not understandable.

Outcomes

Primary Outcomes

Change in Pain Intensity (visual analogue scale)

Time Frame: Change from baseline to 3 weeks

Using a Visual analogue scale

Secondary Outcomes

  • Change in Active Range of Motion(Change from baseline to 3 weeks)
  • Change in Function (Abbreviated Constant-Murley score)(Change from baseline to 3 weeks)

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