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Virtual Reality for paretic upper limb recovery in stroke survivors

A COMPARATIVE STUDY ON THE EFFECTIVENESS OF VIRTUAL REALITY VERSUS CONVENTIONAL EXERCISE THERAPY FOR REHABILITATION OF UPPER LIMB IN STROKE SURVIVORS - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/085163
Enrollment
30
Registered
2025-04-21
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: G819- Hemiplegia, unspecified Health Condition 2: G968- Other specified disorders of central nervous system

Interventions

Intervention1: Experimental Group: Participants in the experimental group will receive a 30-minute session of virtual reality (VR)-based exercise therapy along with 30-minute session of conventional

Sponsors

nil
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Individuals who were willing to participate 2 Individuals with Confirmed Diagnosis of Stroke. 3 Both male and female 4 Individuals aged between 30-60 years. 5 Individuals who were in the sub-acute stage of Stroke. Both hemorrhagic and ischemic types of strokes. Individuals with MMSE score more than 23 Individuals With Modified Ashworth Scale score between 0-1+ for upper limb Individuals with mild upper limb pain VAS Score 5 or lower than 5

Exclusion criteria

Exclusion criteria: 1 Individuals With any other neurological Disorder 2 Non-cooperative individuals. 3 Individuals with Significant cognitive deficits (MMSE Score less than 22) 4 Individuals with fixed joint contractures and deformities in the upper limb. Individuals with severe Pain in hand (VAS Score more than 5) Individuals with a History of any type of Seizures.

Design outcomes

Primary

MeasureTime frame
Fugl Meyer Assement-UE (FMA-UE)- (Motor Functions) Timepoint: At Baseline (DAY 0) At Post Intervention (DAY 30)

Secondary

MeasureTime frame
Montreal Cognitive Assessment (MoCA) - (Cognitive functions) Stroke Impact Scale (SIS) - (Quality of Life) Beck Depression Inventory (BDI) - (Post-stroke Depression) Timepoint: At Baseline (DAY 0) At Post Intervention (DAY 30)

Countries

India

Contacts

Public ContactGurbhej Singh

Punjabi University

13gurbhej2001@gmail.com7814493371

Outcome results

None listed

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