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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05064774
Other study ID # 60116787-020/41785
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 1, 2018
Est. completion date April 1, 2021

Study information

Verified date May 2023
Source Pamukkale University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

this study was conducted the patients with rotator cuff tears who underwent rotator cuff repair surger.The patients were randomly divided into 2 groups and a total of 20 subjects were randomized in a single block order using RandomAllocation Software 1.0.0 by simple randomization.All evaluation and treatment was done by the same physiotherapist.The first group was included in the traditional treatment program after rotator cuff repair, while the second group was included in the myofascial release program, 2 sessions a week between the 4th and 7th weeks, in addition to the traditional treatment.


Description:

Patients in the 2 groups undergoing rc repair were also included in a similar physiotherapy program.Immobilization with a sling was made for 4-6 weeks after surgery. In addition to physiotherapy in group 2, myofascial release therapy was applied to the upper trapezius, sternocloidomastoideus, pectoral muscles (major, minor) 2 days a week between the 4th and 7th weeks after surgery, in addition to the conventional treatment. Myofascial treatment took 30-45 minutes per session.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date April 1, 2021
Est. primary completion date March 20, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - aged betweeen 18-65 - diagnosed with RC tear Exclusion Criteria: - wanting to leave the study - not participating in assessments and/or treatments - presence of massive tears - accompanying nerve injuries, - presence of labral lesion, - diagnosed psychological problems, - central nervous system problems - those with any rheumatological and orthopedic diseases - individuals who have had previous surgery on the same shoulder

Study Design


Related Conditions & MeSH terms


Intervention

Other:
myofascial release technique
myofascial release group took myofascial release (MFR) therapy sessions twice a week for 4 weeks between 4 and 7 weeks. MFR was applied to upper trapezius, SCM, pectoralis major-minor and sternocostal fascia. muscle was replaced elongated position and pressure was applied for 60-120 second.
physiotherapy
patients used sling up to 4 weeks. They did first 4 weeks passive/ assistive range of motion exercise. In 6-8 weeks they did active exercises. 8-12 weeks they did progressive resistive exercises.

Locations

Country Name City State
Turkey Pamukkale University Denizli Pamukkale

Sponsors (1)

Lead Sponsor Collaborator
Pamukkale University

Country where clinical trial is conducted

Turkey, 

References & Publications (3)

LeBauer A, Brtalik R, Stowe K. The effect of myofascial release (MFR) on an adult with idiopathic scoliosis. J Bodyw Mov Ther. 2008 Oct;12(4):356-63. doi: 10.1016/j.jbmt.2008.03.008. Epub 2008 Jun 4. — View Citation

Neer CS 2nd. Anterior acromioplasty for the chronic impingement syndrome in the shoulder: a preliminary report. J Bone Joint Surg Am. 1972 Jan;54(1):41-50. No abstract available. — View Citation

Page P. Shoulder muscle imbalance and subacromial impingement syndrome in overhead athletes. Int J Sports Phys Ther. 2011 Mar;6(1):51-8. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary pain intensity visual analog scale (pain during night, rest, activity), preoperative, post operative 3-7-12 weeks. 12 weeks
Primary function Constant Murley's score. This score has been used in preoperative, post operative 7-12 weeks. Higher score means better results. total point changes between 0-100. 12 weeks
Primary quality of life index short form-36 (SF-36) This scale is used in preoperative and pos operative 12 weeks.Higher score means better results. 12 weeks
Secondary grip strength Grip strength has been measured with dynamometer in preoperative, post operative 7-12 weeks. 12 weeks
Secondary flexibility pectoralis minor flexibility was measured and saved as centimeter. 12 weeks
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