Viewing Study NCT06412237



Ignite Creation Date: 2024-05-19 @ 5:33 PM
Last Modification Date: 2024-10-26 @ 3:29 PM
Study NCT ID: NCT06412237
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-06-20
First Post: 2024-05-08

Brief Title: An Exploratory Study of a Wearable Robotic Hand Orthosis
Sponsor: Tan Tock Seng Hospital
Organization: Tan Tock Seng Hospital

Study Overview

Official Title: An Exploratory Study of a Wearable Robotic Hand Orthosis in the Chronic Stroke Population in Singapore A Clinic to Home Feasibility Trial
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-06
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: Upper limb deficits usually remain in 75 of the stroke survivors despite completing full rehabilitation This is due to lack of effectiveness of rehabilitation and the degree of support and resources available

In this study the investigators plan to study the use of assistive technologies in chronic stroke survivors
Detailed Description: Assistive technologies have shown promising results in immediate improvement in functional abilities

RELab tenoexo is a fully wearable and portable robotic hand orthoses RHO used for functional training Its design support end users with functional hand opening and closing and can be applied in therapy exercises or during functional activities While prior research demonstrated its effectiveness for spinal cord injury it hasnt been tailored for multi-ethnic stroke populations

This study aims to determine the feasibility and extent to which the RELab tenoexo can complement therapy training in clinic and further be used as both a training and assistive device in the home environment In addition it also aims to investigate the amount of upper limb usage before during and after the training period

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