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Quantified Analysis of Neuronal Recovery Using Myelin Imaging After Robot Assisted Upper Arm Training in Subacute Stroke Patients

NCT04651322 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2020-12-03

No results posted yet for this study

Summary

* Quantitative assessment method developed for brain plasticity through disability rehabilitation using a brain imaging technique.
* Development of brain imaging technology to improve understanding of brain plasticity during rehabilitation and to improve the efficiency of rehabilitation treatment for people with brain injury. ○ Development of the latest brain function image analysis algorithm and data processing technology

* Development of new technology for imaging brain plasticity in addition to existing functional imaging technology and diffuse imaging technology (Example: Myelinated brain imaging technology, susceptibility imaging (SWI) technology)
* Development of image reconstruction software technology using new image technology
* Multi-image and repeated shot data processing technology, wheat analysis technology development (Example: 3D registration technology, automated segmentation technology)
* Conducted clinical research on clinical quantitative evaluation of brain plasticity due to rehabilitation treatment

* Recruitment of a group of patients for pursuing plasticity through rehabilitation among stroke patients (estimating the number of sample patients by setting a specific patient group and analyzing statistical power)
* Image-based brain change analysis through patient rehabilitation and before and after imaging
* Comparative analysis through securing a control group and activating the control group. Derivation of clinical relevance through comparison with rehabilitation process

Conditions

Interventions

DEVICE

upper robot Robot assisted upper arm training(RAT)

The training group received an additional upper robot Robot assisted upper arm training(RAT) with Armeopower® 5 times per week for 4weeks. \*Robot Assisted Arm training + Conventional occupational therapy

BEHAVIORAL

Conventional therapy

The control group received the usual conventional therapy \*Only Conventional occupational therapy

Sponsors & Collaborators

  • Yonsei University

    lead OTHER

Principal Investigators

  • Deog Young Kim · Severance Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-03-01
Primary Completion
2021-06-30
Completion
2021-06-30

Countries

  • South Korea

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04651322 on ClinicalTrials.gov