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Effect of immersive 360 virtual reality video-viewing on hand and arm activity in individuals with stroke.

Effect of immersive 360 virtual reality video-viewing on hand and arm activity in individuals with stroke A randomized control trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/112838
Enrollment
80
Registered
2026-06-16
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: I639- Cerebral infarction, unspecified

Interventions

Intervention1: 360 degree virtual viewing video viewing: Prerequisite: To minimize the risk of any VR sickness short stints of VR intervention with breaks will be given. Patients will also be requeste

Sponsors

Dr Archana Gore
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Brunstromm Voluntary Control for Hand 2 to 5 2 Upper extremity pain 1 to 6 on NPRS 3 MOCA score greater than or equal to 26 4 Stroke patients between the ages of 30 to 60 who are medically stable 5 Patients of both genders with incidence of first stroke 6 Patients willing to participate in the study

Exclusion criteria

Exclusion criteria: 1 Presence of severe cognitive impairment (MOCA less than 26) 2 Presence of severe forms of unilateral spatial neglect, screened using the Bell s Test (cut off score greater than or equal to 50%) 3 Presence of severe ideomotor apraxia screened using the Apraxia Screen of TULIA (AST) (cut off score less than 5) 4 Presence of severe anosognosia, screened using the Visual-Analogue Test Assessing Anosognosia for Motor Impairment (VATA-M) (cut off score for lower limb greater than or equal to +6) 5 Presence of severe visual field of view deficits screened using Confrontation Visual Fields method 6 VAS for pain during upper limb activity is greater than 6 7 Drug resistant epilepsy or hypertension

Design outcomes

Primary

MeasureTime frame
1. Fugl Meyer Assessment of Upper Extremity (FMA UE) 2. Action Research Arm Test (ARAT) 3. Wolf Motor Function Test 4. Motor Activity LogTimepoint: Pre intervention and post intervention at completion of 12 weeks (4 weeks)

Secondary

MeasureTime frame
NilTimepoint: Nil

Countries

India

Contacts

Public ContactDr Yash Shinde

Physiotherapy School and Centre Seth G.S. Medical College and KEM hospital

archanagore@kem.edu9082621220

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026