Comparing Two Different Rehabilitation Protochols on Patients With Rotator Cuff Repair

NCT ID: NCT03533088

Last Updated: 2021-08-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

54 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-07-15

Study Completion Date

2021-02-15

Brief Summary

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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

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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.

Conditions

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Rotator Cuff Tear

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Randomised control trial
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Hospitalized rehabilitation

Patients in this group will recieve rehabilitation program twice in a week at our clinic after the surgical procedure until post-operative 12 weeks.

Group Type EXPERIMENTAL

Hospitalized rehabilitation

Intervention Type OTHER

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

Home-based rehabilitation

Patients 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.

Group Type EXPERIMENTAL

Home-based rehabilitation

Intervention Type OTHER

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.

Interventions

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Hospitalized rehabilitation

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

Intervention Type OTHER

Home-based rehabilitation

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.

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Hacettepe University

OTHER

Sponsor Role lead

Responsible Party

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Irem Duzgun

Doç. Dr. İrem Düzgün

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Taha Yıdız, Msc

Role: STUDY_CHAIR

İnvestigator

Locations

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Hacettepe Univercity, Faculty of Physical Theraphy and Rehablitation

Altındağ, Ankara, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

References

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Gallagher BP, Bishop ME, Tjoumakaris FP, Freedman KB. Early versus delayed rehabilitation following arthroscopic rotator cuff repair: A systematic review. Phys Sportsmed. 2015 May;43(2):178-87. doi: 10.1080/00913847.2015.1025683. Epub 2015 Mar 22.

Reference Type RESULT
PMID: 25797067 (View on PubMed)

Thomson S, Jukes C, Lewis J. Rehabilitation following surgical repair of the rotator cuff: a systematic review. Physiotherapy. 2016 Mar;102(1):20-8. doi: 10.1016/j.physio.2015.08.003. Epub 2015 Sep 8.

Reference Type RESULT
PMID: 26510584 (View on PubMed)

Other Identifiers

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1233412334

Identifier Type: -

Identifier Source: org_study_id

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