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ursing intervention to decrease physical pain and psychological distress associated with wearing a shoulder abduction brace in a patient after rotator cuff repair surgery.

Not Applicable
Conditions
Rotator cuff tear
Registration Number
JPRN-UMIN000029733
Lead Sponsor
Kyushu University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
20
Inclusion Criteria

Not provided

Exclusion Criteria

Patients who falls into one of the three. 1.Patients who were diagnosed as a re-tear after rotator cuff repair surgery. 2.Patients were judged by researcher as unable to communicate with cognitive impairment or mental disorder. 3.Patients were judged by their doctor as delays attachment and detachment of their brace by doctor and nurse from 15 days after surgery.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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