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Comparing Two Different Rehabilitation Protochols on Patients With Rotator Cuff Repair

Comparing Two Different Rehabilitation Protochols on Patients With Rotator Cuff Repair

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03533088
Enrollment
54
Registered
2018-05-22
Start date
2019-07-15
Completion date
2021-02-15
Last updated
2021-08-25

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

Conditions

Rotator Cuff Tear

Keywords

shoulder, rotator cuff, exercise

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.

Interventions

OTHERHospitalized rehabilitation

Patients will recive a rehabilitation prgram at the clinic twice in a week until the post-operative 12. weeks

Patients will recive a home program once in a two weeks until the 6. weeks of post-operative period. Then will start to recieve a rehabilitation program ar the clinic once in a week auntil the 12. week of the post-operative period.

Sponsors

Hacettepe University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Randomised control trial

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
scapular kinematics6 months3-Dimensional scapular kinematics will be assessed

Secondary

MeasureTime frameDescription
gleno-humeral range of motion6 monthspatients' shoulder range of motions will be assessed

Countries

Turkey (Türkiye)

Outcome results

None listed

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