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Physical Therapy Interventions Following Arthroscopic Rotator Cuff Repair

Primary Purpose

Rotator Cuff Injuries, Pain, Postoperative, Kinesiophobia

Status
Completed
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
physical therapy intervention
Sponsored by
Sahmyook University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Rotator Cuff Injuries

Eligibility Criteria

19 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • The Better Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

physical therapy intervention

Arm Description

Outcomes

Primary Outcome Measures

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.

Secondary Outcome Measures

Full Information

First Posted
January 13, 2021
Last Updated
September 10, 2021
Sponsor
Sahmyook University
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1. Study Identification

Unique Protocol Identification Number
NCT04711616
Brief Title
Physical Therapy Interventions Following Arthroscopic Rotator Cuff Repair
Official Title
Physical Therapy Interventions Following Arthroscopic Rotator Cuff Repair: A Prospective Single Group Interventional Study
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Completed
Study Start Date
March 17, 2021 (Actual)
Primary Completion Date
September 3, 2021 (Actual)
Study Completion Date
September 3, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sahmyook University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rotator Cuff Injuries, Pain, Postoperative, Kinesiophobia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
physical therapy intervention
Arm Type
Experimental
Intervention Type
Behavioral
Intervention Name(s)
physical therapy intervention
Intervention Description
physical therapy interventions include thermal therapy, electrical therapy, manual therapy, and therapeutic exercise.
Primary Outcome Measure Information:
Title
Pain intensity
Description
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.
Time Frame
Change from baseline pain intensity at 12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Facility Information:
Facility Name
The Better Hospital
City
Gwangju
ZIP/Postal Code
61085
Country
Korea, Republic of

12. IPD Sharing Statement

Plan to Share IPD
Yes

Learn more about this trial

Physical Therapy Interventions Following Arthroscopic Rotator Cuff Repair

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