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Comparing Two Different Rehabilitation Protochols on Patients With Rotator Cuff Repair

Not Applicable
Completed
Conditions
Rotator Cuff Tear
Interventions
Other: Home-based rehabilitation
Other: Hospitalized rehabilitation
Registration Number
NCT03533088
Lead Sponsor
Hacettepe University
Brief Summary

Rotator cuff (RC) repair is one of the most common treatment approch to relief the pain and improve the shoulder function on patients with rotator cuff rupture. Despite the improved surgical techniques and decreased failure rate, there are still complications after the surgey like shoulder persistant shoulder pain, stiffness even re-tear. Therefore, rehabilitation after the RC repair procedure is crucial for the success of the treatment. However, there is no concencus between the post-operative rehabilitation protochol. The aim of this study is to compare two different rehabilitation protochols on patients with RC repair.

Detailed Description

Rotator cuff (RC) repair is one of the most common treatment approch to relief the pain and improve the shoulder function on patients with rotator cuff rupture. Despite the improved surgical techniques and decreased failure rate, there are still complications after the surgey like shoulder persistant shoulder pain, stiffness even re-tear. Therefore, rehabilitation after the RC repair procedure is crucial for the success of the treatment. However, there is no concencus between the post-operative rehabilitation protochol. The aim of this study is to compare two different rehabilitation protochols in terms of shoulder range of motion, self-reported shoulder function and pain on patients with RC repair.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
54
Inclusion Criteria
  • Having a Rotator Cuff repair surgery
  • Having post-op rehabilitation program at our clinic until post-op 3 months
  • No previous surgery in the shoulder joint
Exclusion Criteria
  • Additional pathology other then RC tear
  • Refusing to participate to the study

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Home-based rehabilitationHome-based rehabilitationPatients in his groups will performed home-based rehabilitation in the early stages of the post-op period. They will com to our clinic once in a two weeks and the recieve the exercise program to perform at home until the 6. weeks of the post-operative period. After the 6. week they will come to our clinic once in a week until the post-operative 12. week.
Hospitalized rehabilitationHospitalized rehabilitationPatients in this group will recieve rehabilitation program twice in a week at our clinic after the surgical procedure until post-operative 12 weeks.
Primary Outcome Measures
NameTimeMethod
scapular kinematics6 months

3-Dimensional scapular kinematics will be assessed

Secondary Outcome Measures
NameTimeMethod
gleno-humeral range of motion6 months

patients' shoulder range of motions will be assessed

Trial Locations

Locations (1)

Hacettepe Univercity, Faculty of Physical Theraphy and Rehablitation

🇹🇷

Altındağ, Ankara, Turkey

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