Trials / Terminated
TerminatedNCT04079205
Home Rehabilitation Using Smart Wearable Exercise and Electrical Stimulation Device After Anterior Cruciate Ligament Reconstruction
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
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 10 (actual)
- Sponsor
- Seoul National University Bundang Hospital · Academic / Other
- Sex
- All
- Age
- 19 Years
- Healthy volunteers
- Not accepted
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).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Wearable Device(exoRehab) | rehabilitation program for patients after Anterior Cruciate Ligament Reconstruction using Wearable Device (exoRehab) |
| BEHAVIORAL | Home rehabilitation program | rehabilitation program for patients after Anterior Cruciate Ligament Reconstruction |
Timeline
- Start date
- 2018-12-31
- Primary completion
- 2021-06-30
- Completion
- 2021-06-30
- First posted
- 2019-09-06
- Last updated
- 2021-09-27
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT04079205. Inclusion in this directory is not an endorsement.