Ignite Creation Date:
2024-10-26 @ 3:41 PM
Last Modification Date:
2024-10-26 @ 3:41 PM
Study NCT ID:
NCT06615141
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-09-15
Brief Title:
Immersive vs Non-immersive Virtual Reality in Enhancing Upper Limb Functions Among Individuals With Subacute Stage Hemiplegia
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Immersive Versus Non-immersive Virtual Reality in Enhancing Upper Limb Functions Among Individuals With Subacute Stage Hemiplegia - A Randomized Controlled Trial
Status:
RECRUITING
Status Verified Date:
2024-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The goal of this randomized controlled trial is to compare the effectiveness of immersive virtual reality combined with conventional therapy to the effectiveness of non-immersive virtual reality combined with conventional therapy in enhancing upper limb function in subacute hemiplegic stroke patients
Detailed Description:
The study is a single blinded randomized controlled trial in which the assessor will be blinded Male and female participants aged between 28-55 years are included in the study Participants are selected based on inclusion and exclusion criteria and are later randomly assigned to Group 1 and Group 2
Group 1 - Conventional therapy and Immersive Virtual Reality Group 2 - Conventional therapy and Non-Immersive Virtual Reality
Primary Outcome measures include the Fugl Meyer Assessment for Upper limb and Graded Wolf Motor Function test for upper limb
Secondary Outcome measure is the Stroke Specific Quality of Life Scale SS-QOL Questionnaire
Therapy session starts with 15 minutes of stretching and strengthening exercises of the affected arm followed by 45 minutes of Immersive Non Immersive virtual reality training
Follow up assessment is done 6 weeks post intervention
The baseline assessment score and follow up assessment scores will be compared
Group 1 - Conventional therapy and Immersive Virtual Reality Group 2 - Conventional therapy and Non-Immersive Virtual Reality
Primary Outcome measures include the Fugl Meyer Assessment for Upper limb and Graded Wolf Motor Function test for upper limb
Secondary Outcome measure is the Stroke Specific Quality of Life Scale SS-QOL Questionnaire
Therapy session starts with 15 minutes of stretching and strengthening exercises of the affected arm followed by 45 minutes of Immersive Non Immersive virtual reality training
Follow up assessment is done 6 weeks post intervention
The baseline assessment score and follow up assessment scores will be compared
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None