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Tele-Rehabilitation in Rotator cuff injury

Not Applicable
Conditions
Health Condition 1: M751- Rotator cuff tear or rupture, notspecified as traumatic
Registration Number
CTRI/2022/12/048210
Lead Sponsor
Self
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Inclusion Criteria:

1.Age 18 to 40 years.

2.Both males and females.

3.Subjects referred by the orthopaedic surgeon with a diagnosis of rotator cuff tendinopathy.

4.Subjects those are willing to discontinue taking steroid medications.

5.BMI 20 to 30 Kg/m2

Exclusion Criteria

Exclusion Criteria:

1.Participant refusal

2.Pregnant women

3.Patients with RA/OA.

4.Hypersensitivity

5.Past history of steroid injection/surgery of the rotator cuff.

6.Diabetic subjects.

7.the presence of a chronic medical conditions like: malignancy, infection, systemic inflammatory disorders

8. History of Covid 19 vaccination in last 1 month

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Range of Motion (ROM): <br/ ><br>The ROM of the Neck, Shoulder and Elbow will be measured as an outcome measure. <br/ ><br>Shoulder Pain And Disability Index. (SPADI) <br/ ><br>The readings of SPADI will be taken as an outcome measure. <br/ ><br>Western Ontario Rotator Cuff (WORC) Index â?? <br/ ><br>The readings of WORC Index will be taken as an outcome measure. <br/ ><br>CRP levels (Quantitative) <br/ ><br>Readings of CRP levels will be taken up on day 0 and after 6 weeks of treatment. <br/ ><br>Inflammatory markers (IL6) <br/ ><br>Readings of IL6 will be taken up on day 0 and after 6 weeks of treatment. <br/ ><br>Ultrasonography (USG) <br/ ><br>UGs of shoulder will be taken done on day 0 and after 6 weeks of treatment. <br/ ><br>Timepoint: VAS,ROM, SPADI, WORC at 0,2,4,6 weeks .
Secondary Outcome Measures
NameTimeMethod
CRP quantitative, IL6 and Ultrasonography.Timepoint: 0 and 6 weeks
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