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A clinical trial to study the effect of Radial shockwave therapy and Ultrasound therapy in Adhesive Capsulitis patients

Comparative efficacy of Radial Shockwave Therapy and Ultrasound Therapy on pain, range of motion and function in subjects with Adhesive Capsulitis: A Randomized Clinical Trial - NIL

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/070584
Enrollment
34
Registered
2024-07-15
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: M958- Other specified acquired deformities of musculoskeletal system

Interventions

Intervention1: Radial Shockwave Therapy: Radial Shockwave Therapy (RSWT) for 4 sessions [2 sessions per week (on 1st, 4th, 7th and 10th day)].Glenohumeral joint mobilization, Supervised Exercise Progr

Sponsors

Deepak Sharma
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Both male and female subjects. 2.Age between 40-60 years. 3.Subjects with Adhesive Capsulitis stage II and III. 4.VAS score between 3-7.

Exclusion criteria

Exclusion criteria: 1.Surgical history of shoulder joint or cervical spine. 2.Diagnosed cases of musculoskeletal conditions like Rotator cuff tendinitis or injury, fracture around shoulder, Shoulder impingement syndrome, upper limb deformity etc. 3.Diagnosed cases of neurological conditions like Stroke, Parkinson’s disease etc. 4.Rheumatological diseases like Rheumatoid Arthritis, Ankylosing Spondylitis. 5.Red flag sign like Malignancy, Vascular disorders. 6.History of oral steroid in last 1 month and intraarticular corticosteroid injection for Adhesive Capsulitis in last 3 months. 7.Implanted Pacemaker.[27] 8.Non-cooperative subjects.

Design outcomes

Primary

MeasureTime frame
1.Pain by Visual Analogue Scale (VAS). 2.Active Abduction, External and Internal rotation ROM by Universal half circle goniometer. 3.Function by Shoulder Pain and Disability Index (SPADI)Timepoint: 2 times - on day 0 and after 2 weeks of interventions

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDeepak Sharma

National Institute for Locomotor Disabilities (Divyangjan)

m.amrita007@gmail.com7384361511

Outcome results

None listed

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