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The Efficacy of Myofascial Release at the Cervicothoracic Region in Patients With Rotator Cuff Repairs

The Efficacy of Myofascial Release at the Cervicothoracic Region in Patients With Rotator Cuff Repairs: A Randomized Controlled Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05064774
Enrollment
20
Registered
2021-10-01
Start date
2018-08-01
Completion date
2021-04-01
Last updated
2023-05-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rotator Cuff Tears

Keywords

myofascial release, rotator cuff tears, physiotherapy, rotator cuff repair

Brief 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.

Detailed 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.

Interventions

OTHERmyofascial 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.

OTHERphysiotherapy

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.

Sponsors

Pamukkale University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

randomised controlled study this study was conducted with rotator cuff tear patients who underwent arthroscopic rotator cuff treatment. The patients' pain intensity, joint range of motion, flexibility of shoulder muscles, grip and muscle strength, shoulder function evaluations and physical characteristics, age, differences between body mass index were evaluated with Mann Whitney-U test.Measurements before and after treatment were evaluated with the Wilcoxon test. Friedman test was performed for the measurements made at postoperative 3, 7, and 12 weeks before in-group treatment. Bonferoni correction was done for possible differences.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
pain intensity12 weeksvisual analog scale (pain during night, rest, activity), preoperative, post operative 3-7-12 weeks.
function12 weeksConstant 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.
quality of life ındex12 weeksshort form-36 (SF-36) This scale is used in preoperative and pos operative 12 weeks.Higher score means better results.

Secondary

MeasureTime frameDescription
grip strength12 weeksGrip strength has been measured with dynamometer in preoperative, post operative 7-12 weeks.
flexibility12 weekspectoralis minor flexibility was measured and saved as centimeter.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026