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EFFECTS OF VIRTUAL REHABILITATION ON UPPER EXTREMITY MOTOR RECOVERY IN PATIENTS WITH SUBACUTE STROKE

EFFECTS OF VIRTUAL REHABILITATION ON UPPER EXTREMITY MOTOR RECOVERY IN PATIENTS WITH SUBACUTE STROKE

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210507051203N1
Enrollment
48
Registered
2021-07-05
Start date
2021-03-05
Completion date
Unknown
Last updated
2021-07-12

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

Conditions

Subacute Stroke. Cerebral infarction, unspecified

Interventions

Intervention 1: Intervention Group 1: In this group patients will be treated with routine physiotherapy combined with virtual rehabilitation. The exercise program consists of stretching, strengthening

Sponsors

Madina Teaching Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 65 Years

Inclusion criteria

Inclusion criteria: • Ischemic or hemorrhagic stroke • Stroke onset with less than 2 weeks and more than 6 months • First-ever ischemic or hemorrhagic stroke confirmed by MRI or CT • Patients with more than 25 years and less than 65 years Old • Unilateral upper extremity weakness, • Patients who could perform the reaching activity with their hemiparetic arm. • Both genders will be included • Voluntary shoulder, elbow and wrist movement which is able to perform In-game commands. • Subjects willing to participate in the study.

Exclusion criteria

Exclusion criteria: • Patients with co-morbidities or neurodegenerative diseases, • Uncontrolled medical condition (e.g., active infection, pulmonary embolism, unstable angina), • Patients who are unable to follow verbal commands due to cognitive impairment or aphasia • Patients who are unable to participate Kinect-based VR due to any reason (e.g., visual impairment, hemi spatial neglect, apraxia) • History of seizures/fits, • Psychological illness, • Bony deformities • Prior history of drugs that could alter balance will be excluded from the study

Design outcomes

Primary

MeasureTime frame
Fugl Meyer Assessment. Timepoint: Before Intervention, 2 Weeks and 4 Weeks. Method of measurement: 226 points multi-item questionnaire used for the evaluation of recovery from stroke.

Secondary

MeasureTime frame
• Brunnstrom Recovery Stages. Timepoint: Baseline, 2 Weeks and after 4 Weeks. Method of measurement: Brunnstrom recovery stages or BRS is 6-stage evaluation tool indicating the recovery after stroke.;Modified Ashworth Scale. Timepoint: Baseline, 2 Weeks and after 4 Weeks. Method of measurement: It is 6 points scale ranging from 0-4 and lower reading indicates the normal tone of muscle and higher score means more resistance to passive movement or spasticity.

Countries

Pakistan

Contacts

Public ContactOsama Saeed

The University of Faisalabad

osama.saeed@tuf.edu.pk+92 41 8750971

Outcome results

None listed

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