Comparing Two Different Rehabilitation Protochols on Patients With Rotator Cuff Repair

Not Applicable

Completed

• Conditions: Rotator Cuff Tear

• 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.

Study Timeline

• Study First Submitted: 2018-05-10
• Study First Submitted QC: 2018-05-10
• Study First Posted: 2018-05-22
• Study Start: 2019-07-15
• Primary Completion: 2020-09-30
• Study Completion: 2021-02-15
• Status Verified: 2021-08
• Last Update Submitted: 2021-08-24
• Last Update Posted: 2021-08-25

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

Primary Outcome Measures

Name	Time	Method
scapular kinematics	6 months	3-Dimensional scapular kinematics will be assessed

Secondary Outcome Measures

Name	Time	Method
gleno-humeral range of motion	6 months	patients' shoulder range of motions will be assessed

Trial Locations

Locations (1)

Hacettepe Univercity, Faculty of Physical Theraphy and Rehablitation; 🇹🇷 Altındağ, Ankara, Turkey

Hacettepe Univercity, Faculty of Physical Theraphy and Rehablitation

🇹🇷Altındağ, Ankara, Turkey