Viewing Study NCT04750746



Ignite Creation Date: 2024-05-06 @ 3:47 PM
Last Modification Date: 2024-10-26 @ 1:56 PM
Study NCT ID: NCT04750746
Status: COMPLETED
Last Update Posted: 2021-05-06
First Post: 2021-02-10

Brief Title: Exer-gaming on Upper Extremity Function and Activities of Daily Living in Sub-acute Stroke Patient
Sponsor: Riphah International University
Organization: Riphah International University

Study Overview

Official Title: Effects of Exer-gaming on Upper Extremity Function and Activities of Daily Living in Sub-acute Stroke Patient
Status: COMPLETED
Status Verified Date: 2021-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Stroke is one of the leading cause of death in adult stroke causes permanent disability Stoke impact the life of a person significantly including the quality of life of an individual and especially performing the task of daily activities independently About 50 survival of stroke have daily life activity limitation which is affecting their quality of life Among stroke patients 69 experience functional motor disturbance in their upper extremity

The aim of this study is to evaluate the effect of Exer-gaming by using the Xbox Kinect game system on upper extremity motor functions and the ability to perform ADLs in sub-acute stroke Various treatment methods are used for the rehabilitation of stroke This study will be a randomized controlled trial used to compare the effectiveness of Exer gaming on upper extremity function and activities of daily living in sub-acute stroke patient Subjects with Sub-acute stroke meeting the predetermined inclusion exclusion criteria will be divided into two groups using simple random sampling technique Pre assessment will be done using FMA SIS measurements Subjects in one group will be treated with Conventional therapy and exer gaming and the other will be treated with conventional therapy and activities training session Each subject will be received a total 18 treatment sessions with 3 treatment sessions per week for 6 weeks Post treatment reading for FMA and SIS will be recorded after the end of treatment session Recorded values will be analyzed for any change using SPSS
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None