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Tele-Rehabilitation in Rotator cuff injury

To study the efficacy of Tele-teaching on Therapistsâ?? attitude and Tele-Rehabilitation satisfaction and improvement in patients with Rotator Cuff Tendinopathy.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/12/048210
Enrollment
60
Registered
2022-12-16
Start date
Unknown
Completion date
Unknown
Last updated
2023-01-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M751- Rotator cuff tear or rupture, notspecified as traumatic

Interventions

Intervention1: Group 1 Tele Rehabilitation group: the subjects will be given online rehabilitation exercises along with hot pack at home for 6 weeks via Zoom/ Cisco webex or Google meet Platforms for

Sponsors

Self
Lead Sponsor

Eligibility

Inclusion criteria

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: 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

Design outcomes

Primary

MeasureTime frame
Range of Motion (ROM): The ROM of the Neck, Shoulder and Elbow will be measured as an outcome measure. Shoulder Pain And Disability Index. (SPADI) The readings of SPADI will be taken as an outcome measure. Western Ontario Rotator Cuff (WORC) Index â?? The readings of WORC Index will be taken as an outcome measure. CRP levels (Quantitative) Readings of CRP levels will be taken up on day 0 and after 6 weeks of treatment. Inflammatory markers (IL6) Readings of IL6 will be taken up on day 0 and after 6 weeks of treatment. Ultrasonography (USG) UGs of shoulder will be taken done on day 0 and after 6 weeks of treatment. Timepoint: VAS,ROM, SPADI, WORC at 0,2,4,6 weeks .

Secondary

MeasureTime frame
CRP quantitative, IL6 and Ultrasonography.Timepoint: 0 and 6 weeks

Countries

India

Contacts

Public ContactJitender Munjal

Noth DMC Medical College and Hindu rao hospital.

gbskohli@yahoo.com9811014671

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026