Ignite Creation Date:
2025-12-25 @ 3:20 AM
Ignite Modification Date:
2025-12-26 @ 1:58 AM
Study NCT ID:
NCT04079205
Status:
TERMINATED
Last Update Posted:
2021-09-27
First Post:
2019-05-08
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
Home Rehabilitation Using Smart Wearable Exercise and Electrical Stimulation Device After Anterior Cruciate Ligament Reconstruction
Sponsor:
Seoul National University Bundang Hospital
Organization:
Study Overview
Official Title:
Home-based Rehabilitation Using Smart Wearable Knee Exercise Device With Electrical Stimulation After Anterior Cruciate Ligament Reconstruction: A Study Protocol for a Randomized Controlled Trial
Status:
TERMINATED
Status Verified Date:
2021-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Due to difficulty in patient enrollment
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of this study is to develop and apply a rehabilitation program for patients who are discharged after ACL reconstruction using a wearable joint rehabilitation exercise device (exoRehab).
Detailed Description:
This randomized, single-blind, controlled trial included 40 patients who are discharged after ACL reconstruction.
The intervention group(n=20) was instructed and educated about 6 week home rehabilitation program using a wearable device(exoRehab)
The controls(n=20) was instructed and educated about 6 week conventional home rehabilitation program
Two weeks after surgery and six weeks after discharge, evaluation is performed.
The purpose of this study is to develop and apply a rehabilitation program for patients who are discharged after ACL reconstruction using a wearable joint rehabilitation exercise device (exoRehab).
The intervention group(n=20) was instructed and educated about 6 week home rehabilitation program using a wearable device(exoRehab)
The controls(n=20) was instructed and educated about 6 week conventional home rehabilitation program
Two weeks after surgery and six weeks after discharge, evaluation is performed.
The purpose of this study is to develop and apply a rehabilitation program for patients who are discharged after ACL reconstruction using a wearable joint rehabilitation exercise device (exoRehab).
Study Oversight
Has Oversight DMC:
False
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?: