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Investigation of Laterality and Sensory Acuity Abilities of Frozen Shoulder Patients

Completed
Conditions
Frozen Shoulder
Laterality Defects
Registration Number
NCT06046430
Lead Sponsor
Harran University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

Frozen Shoulder Group:<br><br>Inclusion Criteria:<br><br>Patients with shoulder pain of at least six months' duration secondary to tendinopathy<br>and/or partial rotator cuff tear; Patients with ability to follow simple orders; iii)<br>Patients with ability to sign to provide informed consent<br><br>Exclusion Criteria:<br><br>Normal passive ROM External ROM < 30 To have received treatment (physiotherapy,<br>intra-articular injection, surgery) related to the existing complaint Pain < 3 according<br>to the numbered pain assessment scale<br><br>Healthy group :<br><br><br><br>No actual shoulder pain or previous history of shoulder complaints including Frozen<br>Shoulder.

Exclusion Criteria

Not provided

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Right-Left Discrimination;Acuity
Secondary Outcome Measures
NameTimeMethod
Pain Intensity;Active Range of Motion (AROM) Assessment;Central sensitization;Pain Catastrophizing;Anxiety and Depression
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