Comparing Two Different Rehabilitation Protochols on Patients With Rotator Cuff Repair

Rotator Cuff Tear Clinical Trial

Official title:

Comparing Two Different Rehabilitation Protochols on Patients With Rotator Cuff Repair

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03533088
• Other study ID #: 1233412334
• Status: Completed
• Phase: N/A
• Start date: July 15, 2019
• Est. completion date: February 15, 2021

Study information

• Verified date: August 2021
• Source: Hacettepe University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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 information / eligibility

• Status: Completed
• Enrollment: 54
• Est. completion date: February 15, 2021
• Est. primary completion date: September 30, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

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

Related Conditions & MeSH terms

• Rotator Cuff Injuries
• Rotator Cuff Tear

Intervention

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

Locations

Country	Name	City	State
Turkey	Hacettepe Univercity, Faculty of Physical Theraphy and Rehablitation	Altindag	Ankara

Sponsors (1)

Lead Sponsor	Collaborator
Hacettepe University

Country where clinical trial is conducted

Turkey, 

References & Publications (2)

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. Review. — View Citation

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. Review. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	scapular kinematics	3-Dimensional scapular kinematics will be assessed	6 months
Secondary	gleno-humeral range of motion	patients' shoulder range of motions will be assessed	6 months