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Additive Effect of IVR Program on Pain, Function, and Kinesiophobia in patients with Frozen Shoulder

Additive Effect Of Immersive Virtual Reality Program Along With Conventional exercise On Pain, Function, and Kinesiophobia in Patients with Frozen Shoulder: A Randomized Controlled Trial - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/072644
Enrollment
36
Registered
2024-08-19
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Health Condition 1: M256- Stiffness of joint, not elsewhereclassified

Interventions

Intervention1: Immersive Virtual Reality + Conventional Exercise: The IVR + Conventional exercise will be used for the study. Each exercise session will include 15 repetitions, involving 15 minutes of

Sponsors

Dr Heti Jadav
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Diagnosed Frozen shoulder patients with Stage 2 and 3, where stiffness is more than pain. NPRS would be between 3 to 7 out of 10. Restriction of PROM would be more than 50% in abduction, flexion, and external rotation. Tampa Scale of Kinesiophobia-11 will be more than 23.

Exclusion criteria

Exclusion criteria: Proximal humerus fracture to the affected shoulder. Rotator cuff tear. Subacromial bursitis. Rheumatoid Arthritis of the shoulder. Cervicogenic shoulder pain. Pseudo-frozen shoulder. Locked posterior shoulder dislocation. Proximal humerusbony tumor. People who received additional pain management procedures, such as intra-articular injection during the therapy. Surgical intervention on the affected shoulder for 6 months. Unhealed scar around the shoulder.

Design outcomes

Primary

MeasureTime frame
Shoulder Pain and Disability Index (SPADI)Timepoint: Baseline, 6th week, 12th week, 24th week

Secondary

MeasureTime frame
Hand behind-back measurementTimepoint: Baseline, 6th week, 12th week, 24th week;Numeric Pain Rating Scale (NPRS)Timepoint: Baseline, 6th week, 12th week, 24th week;TAMPA Scale of Kinesiophobia (TSK-11)Timepoint: Baseline, 6th week, 12th week, 24th week;Universal Goniometer measurementTimepoint: Baseline, 6th week, 12th week, 24th week

Countries

India

Contacts

Public ContactHeti Jadav

Institute of Physiotherapy, Srinivas University

kamalakannan.pt@gmail.com9924638398

Outcome results

None listed

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