Virtual Reality Relaxation for Post-Stroke Recovery: A Randomised Controlled Trial

Efficacy of Virtual Reality-Based Relaxation on Post-Stroke Anxiety, Fatigue, and Quality of Life: A Randomized Controlled Trial. - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/10/095835

Enrollment

Registered

2025-10-09

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

None listed

Interventions

Intervention1: Participants will be given the Virtual reality along with conventional physiotherapy.: Virtual reality, along with conventional physiotherapy for 60 minutes, 5 days/week, for 2 weeks, w

each group of muscles is repeatedly trained 3 times in sequence. Each session will last approximately 20 minutes. At the same time, the patient takes a deep breath, inhaling through their nose and e

Eligibility

Inclusion criteria

Inclusion criteria: Chronic Stroke patients who are willing to participate, with all genders of age group 18-65 years, Anxiety score of more than 22 on BAI, Score more than 36 on fatigue severity scale, Able to understand instructions and ability to sit through VR sessions

Exclusion criteria

Exclusion criteria: Subjects who are medically unstable, History of epilepsy or seizure, Vestibular disorders, Impaired vision or hearing

Design outcomes

Primary

Measure	Time frame
Beck Anxiety Inventory (BAI), Fatigue Severity Scale (FSS), Stroke Specific Quality of Life Scale (SS-QOL) Timepoint: assessed on the first day of treatment and on the last day of treatment	—

Secondary

Measure	Time frame
Stroke Specific Quality of Life Scale (SS-QOL) Timepoint: assessed on the last day of treatment	—

Countries

India

Contacts

Public ContactDr Raghavendrasingh Dharwadkar

KLE Institute of Physiotherapy

sanjanamohata2908@gmail.com7028859912

Outcome results