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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04711616
Other study ID # 2-1040781-A-N-012021012HR
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 17, 2021
Est. completion date September 3, 2021

Study information

Verified date September 2021
Source Sahmyook University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In the post-arthroscopic rotator cuff repair (ARCR) management, physical therapy intervention is an important factor in bringing about a clinically positive prognosis. However, no conclusive therapeutic evidence has been found for various physical therapy interventions. In this study, the investigators would like to investigate the effects of physical therapy interventions on ARCR patients.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date September 3, 2021
Est. primary completion date September 3, 2021
Accepts healthy volunteers No
Gender All
Age group 19 Years to 65 Years
Eligibility Inclusion Criteria: - Adults over 18 years old - In case of 2 weeks after receiving arthroscopic rotator cuff repair - When the participants wishes to enroll in the study Exclusion Criteria: - 65 years old or older - If the tear area is large and augmentation is performed - If there is a previous surgical history at the surgical site - Osteoarthritis in the shoulder joint

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
physical therapy intervention
physical therapy interventions include thermal therapy, electrical therapy, manual therapy, and therapeutic exercise.

Locations

Country Name City State
Korea, Republic of The Better Hospital Gwangju

Sponsors (1)

Lead Sponsor Collaborator
Sahmyook University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain intensity A numeric pain rating scale (NPRS) consisting of 11 points in total from 0 points (no pain) to 10 points (the most severe pain imaginable) is used. The lower the score, the less the pain. Change from baseline pain intensity at 12 weeks
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