Comparing the Effectiveness of Traditional Physiotherapy Combined With Virtual Reality for Post-Stroke Patients

Superior University

Status

Active, not recruiting

Conditions

Stroke

Treatments

Diagnostic Test: Traditional Physiotherapy Group

Combination Product: VR + Traditional Physiotherapy Group

Study type

Interventional

Funder types

Other

Identifiers

NCT06739902

MSRSW/Batch-Fall22/770

Details and patient eligibility

About

This study aims to evaluate the effectiveness of combining virtual reality (VR) therapy with traditional physiotherapy in post-stroke rehabilitation. Post-stroke patients often suffer from impairments in motor function, balance, and overall quality of life. While traditional physiotherapy is a widely accepted method for stroke recovery, incorporating VR technology may enhance treatment outcomes by providing an engaging, immersive environment that motivates patients to perform therapeutic movements.

Full description

This study will compare the functional and quality-of-life improvements in patients undergoing traditional physiotherapy alone versus those receiving a combination of conventional physiotherapy and VR interventions. By assessing changes in motor function, trunk stability, balance, and quality of life, this research will provide valuable insights into whether VR can be an effective adjunctive tool in post-stroke rehabilitation programs.

Enrollment

24 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Stroke, either ischemic or hemorrhagic
Participants who can ambulate independently or with minimal assistance.
Participants who were willing & able to adhere to the study protocol.
Including participants who were attending follow-up appointments & completing outcome measures.
Participants who were able to understand & provide written informed consent

Exclusion criteria

Existence of additional neurological disorders (such as multiple sclerosis or Parkinson's disease) or serious medical conditions that could prevent participants from participating in the study.
Participants receiving rehabilitation or rigorous physical treatment in the previous three months were excluded.
Pregnant women or breastfeeding women.
Participants who refused to participate in the study or provide informed consent.