Clinical Trials Directory

Trials / Active Not Recruiting

Active Not RecruitingNCT06582394

Effect of Virtual BASRD Reality Training Versus Conservative Treatment In Chronic Hemipretic Stroke Survivors

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
30 (actual)
Sponsor
Superior University · Academic / Other
Sex
All
Age
35 Years – 85 Years
Healthy volunteers
Not accepted

Summary

In hemiparetic stroke patient's VR is very useful. Due to hemiparesis one side muscle weakness occurs because of disruption in brain, spinal cord and nervous system technologies improvs motor activities of patients, by improvement in motor activities patients perform activities in better way.

Detailed description

The study's main aim is to check virtual reality's effect on conservative treatment in hemiparetic stroke patients.

Conditions

Interventions

TypeNameDescription
COMBINATION_PRODUCTExp GroupBalance and coordination were targeted through virtual stepping tasks, where participants practiced stepping in various directions to improve postural control and lower limb function. Additionally, they performed virtual balance exercises by standing on simulated platforms of varying stability. For gait and mobility, participants practiced walking in a virtual environment with real-time feedback to correct gait abnormalities. They also encountered virtual obstacles, which required them to adapt their walking patterns and improve mobility. In this study, both the intervention and control groups underwent a 6-week treatment plan consisting of 5 sessions per week, with each session lasting 45 minutes.
OTHERControl groupFor gait training, participants practiced walking on flat surfaces, sometimes with the assistance of parallel bars or walking aids, to improve their walking speed, step length, and rhythm. They also performed sit-to-stand exercises to strengthen the lower limbs and improve mobility for daily activities. Additionally, manual therapy techniques, such as joint mobilizations and stretching, were applied to reduce spasticity and increase range of motion in the affected limbs. Both treatment groups progressed based on individual capabilities, with therapists adjusting exercises accordingly throughout the study. In this study, both the intervention and control groups underwent a 6-week treatment plan consisting of 5 sessions per week, with each session lasting 45 minutes.

Timeline

Start date
2023-11-01
Primary completion
2024-05-01
Completion
2024-10-30
First posted
2024-09-03
Last updated
2024-09-03

Locations

1 site across 1 country: Pakistan

Source: ClinicalTrials.gov record NCT06582394. Inclusion in this directory is not an endorsement.