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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04705311
Other study ID # 2-1040781-A-N-012021010HR
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 10, 2021
Est. completion date August 31, 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

During the rehabilitation process after rotator cuff repair surgery, patients suffer from increased pain and discomfort due to dysfunction. Pain neuroscience education, a more modern educational method, has been reported to be effective in controlling pain by reducing the fear of movement based on an understanding of neurophysiology.


Recruitment information / eligibility

Status Completed
Enrollment 34
Est. completion date August 31, 2021
Est. primary completion date August 31, 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 4 weeks after receiving arthroscopic rotator cuff repair - If you wish to participate in research Exclusion Criteria: - 65 years old or older - Those who are limited in conducting education remotely - 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 - If you cannot understand the guidelines for evaluation or intervention - Mental health and cognitive problems

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Pain neuroscience education
Neurophysiological education of pain allows patients to explore a wider contribution to pain through the knowledge that pain is often an unreliable indicator of the extent or extent of tissue damage. This aims at reconceptualization from biomedical or structural models to actual biological psychosocial pain models.
Behavioral:
Rotator cuff repair rehabilitation
Postoperative rehabilitation programs 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 in pain intensity from baseline to weeks 2, 4, and 6
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