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Observing the changes a wearable device creates on the movement of outward turning of the shoulder joint with clients having Frozen Shoulder.

Not Applicable
Conditions
Health Condition 1: M750- Adhesive capsulitis of shoulder
Registration Number
CTRI/2018/10/016203
Lead Sponsor
School of Allied Health Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Limited external rotation range

2.Age range 30 years and above

3.Ending of stage 1 and complete stage 2 (in consultation with the orthopedic surgeon)

4.Patients referred for splint as a part of standard of care by the physician

Exclusion Criteria

1.Secondary frozen shoulder

2.Associated injuries of the upper limb

3.Reflex sympathetic dystrophy (RSD)

4.Patients undergoing regular physical therapy

5.Osteoporotic changes

Study & Design

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