Ignite Creation Date:
2024-05-06 @ 7:59 PM
Last Modification Date:
2024-10-26 @ 3:17 PM
Study NCT ID:
NCT06204744
Status:
RECRUITING
Last Update Posted:
2024-01-12
First Post:
2023-12-12
Brief Title:
Home-based Arm and Hand Exercise Program for Stroke A Multisite Trial
Sponsor:
Chang Gung Memorial Hospital
Organization:
Chang Gung Memorial Hospital
Study Overview
Official Title:
Scale-out of a Home-based Arm and Hand Exercise Program for Stroke A Multisite Implementation-efficacy Trial
Status:
RECRUITING
Status Verified Date:
2024-01
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:
The goal of this multisite clinal trial is to evaluate the implementation of the home-based Graded Repetitive Arm Supplementary Program GRASP at rehabilitation clinics across several hospitals The main questions it aims to answer is
the efficacy of the home-based GRASP program relative to the conventional occupational therapy intervention on improving health outcomes including UE motor function daily function quality of life and motor control strategies
Stroke participants will be randomly assigned to either the Home-based GRASP group or the conventional occupational therapy home program group Each group will undergo an 4 to 6-week intervention 3 sessionsweek with evaluations conducted before immediately after and 3 months post-trial assessing clinical and kinematic measures Interviews and surveys will be conducted to gain insights into the perspectives of patients regarding the implementation of the home-based GRASP program
the efficacy of the home-based GRASP program relative to the conventional occupational therapy intervention on improving health outcomes including UE motor function daily function quality of life and motor control strategies
Stroke participants will be randomly assigned to either the Home-based GRASP group or the conventional occupational therapy home program group Each group will undergo an 4 to 6-week intervention 3 sessionsweek with evaluations conducted before immediately after and 3 months post-trial assessing clinical and kinematic measures Interviews and surveys will be conducted to gain insights into the perspectives of patients regarding the implementation of the home-based GRASP program
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