Skip to content

A study in stroke patients to compare virtual reality based rehabilitation with routine physical therapy for improving hand and arm movements.

Comparison of stroke population getting virtual reality rehabilitation versus stroke population getting physical rehabilitation. - STROKE

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/10/095870
Enrollment
30
Registered
2025-10-10
Start date
Unknown
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

Health Condition 1: G94- Other disorders of brain in diseases classified elsewhere

Interventions

Intervention1: Virtual Reality based rehabilitation for upper extremity post stroke: Non invasive device assisted therapy. 30 minutes/day session for 5-7 days Control Intervention1: Coventional physic

Sponsors

Saveetha Institute of Medical and Technical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: (1) Participants must be aged 18 years or above. (2) Diagnosis of acute stroke confirmed by neurological assessment including neuroimaging (MRI or computed tomography) within the last 12 months (3) Absence of cognitive impairments / seizures. (4) Able to follow verbal instructions related to the use of VR devices (5) Patients with either of upper limbs affected.

Exclusion criteria

Exclusion criteria: (1)Patients who are below 18 years of age. (2) Patients who aren t willing to give consent for the study. (3) Patients with both upper limbs affected. (4) Patient who have no attention or Power 0 has been excluded.

Design outcomes

Primary

MeasureTime frame
Improvement in upper limb motor function assessed using Fugl Meyer Assessment- Upper Extremity (FMA-UE)Timepoint: At baseline and after 1 week of intervention.

Secondary

MeasureTime frame
Change in upper limb motor function of stroke patients with rehabilitation using Fugl Meyer Assessment- upper extremityTimepoint: At the end of intervention (day 5-7)

Countries

India

Contacts

Public ContactDr Selva Balaji R

Saveetha Institute of Medical and Technical Sciences

endork@yahoo.com9710071284

Outcome results

None listed

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