A Multicenter Study of Retrospective Rehabilitation Medical Data for the Development for Medical Twins

June 1, 2023 updated by: MinYoung Kim, MD, PhD, Bundang CHA Hospital
Based on previous studies, when medical digital twin-based convergence medical contents are applied to degenerative musculoskeletal and central nervous system diseases, it is possible to more accurately evaluate the subject's motor function and neurological function to predict the subject's disease. In order to create an effective ICT application protocol and clinically apply a treatment program that can improve the subject's kinematic function and neurological function, etc.

Study Overview

Status

Recruiting

Study Type

Observational

Enrollment (Estimated)

150

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

  • Name: Hyun Jung Oh, Bachelor's degree
  • Phone Number: +82 031 780 6003
  • Email: a210525@chamc.co.kr

Study Locations

      • Seongnam, Korea, Republic of, 13496
        • Recruiting
        • Department of Rehabilitation Medicine, CHA Bundang Medical Center
        • Contact:
          • MinYoung Kim, MD,PhD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

N/A

Sampling Method

Non-Probability Sample

Study Population

Healthy and stroke patients

Description

  1. Inclusion Criteria:

    • Healthy subjects : who underwent imaging examination at Bundang CHA hospital from January 1, 2010 to December 31, 2021
    • Stroke patients : who underwent imaging examination at Bundang CHA hospital from January 1, 2010 to December 31, 2021
  2. Exclusion criteria - Who cannot meet the inclusion criteria

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Healthy subjects and stroke patients
Medical record collection

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Imaging examination
Time Frame: A time point at which imaging was performed between January 1, 2010 and December 31, 2021
The results of X-ray measurement in whole spin AP and lateral, low extremty AP & lateral, foot AP & lateral, The results of multispine computed tomography of C-spine, T-spin and L-spine without CM, The results of magnetic resonance imaging of brain MRI and diffusion tensor imaging tractography
A time point at which imaging was performed between January 1, 2010 and December 31, 2021

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Basic characteristics
Time Frame: A time point at which imaging was performed between January 1, 2010 and December 31, 2021
Sex, age, stroke onset, stroke diagnosis, history
A time point at which imaging was performed between January 1, 2010 and December 31, 2021

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 22, 2021

Primary Completion (Estimated)

December 31, 2024

Study Completion (Estimated)

December 31, 2024

Study Registration Dates

First Submitted

May 23, 2023

First Submitted That Met QC Criteria

June 1, 2023

First Posted (Actual)

June 12, 2023

Study Record Updates

Last Update Posted (Actual)

June 12, 2023

Last Update Submitted That Met QC Criteria

June 1, 2023

Last Verified

June 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 2021-11-020

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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