Developement of Stroke Prognosis Predictive Precision Medicine Based on a Digital Twin

NCT ID: NCT06035198

Last Updated: 2023-11-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

1000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-10-05

Study Completion Date

2026-12-31

Brief Summary

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The purpose of this study is to realize customized precision medicine for stroke patients and the visual digitization of patient medical information required in the era of digital transformation.

This study will collect large-scale, high-quality clinical data and daily life exercise pattern data covering the subacute to chronic stages of stroke patients. Based on this, we will use artificial intelligence analysis technology to predict the functional status of stroke patients in the chronic stage after their disability is fixed. We aim to develop the next generation of personalized digital twins by creating a prognostic prediction model.

Detailed Description

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Conditions

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Stroke

Study Design

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Observational Model Type

COHORT

Study Time Perspective

OTHER

Study Groups

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Stroke patients

Patients diagnosed with stroke at four hospitals in Korea

Stroke

Intervention Type OTHER

No intervention

Interventions

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Stroke

No intervention

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Adults over 20 years of age with a history of stroke onset between 2018.01.01 to 2023.07.31.
* Patients who exist rehabilitation medical evaluation after stroke onset
* Patients who voluntarily decide to participate in this study

Exclusion Criteria

* Those who have severe internal diseases such as unstable conditions of the cardiovascular system, digestive system, respiratory system, endocrine system, etc. and are in poor overall condition.
* Those who have impaired ability to consent (MMSE score less than 10 points) and not accompanied by a care-giver.
* In any other cases where the researcher determines that participation in this study is not appropriate.
Minimum Eligible Age

20 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Seyoung Shin

OTHER

Sponsor Role lead

Responsible Party

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Seyoung Shin

Principal Investigator

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Seyoung Shin, MD

Role: PRINCIPAL_INVESTIGATOR

CHA University

Locations

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Bundang CHA Medical Center

Gyeonggi-do, , South Korea

Site Status RECRUITING

Countries

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South Korea

Central Contacts

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Seyoung Shin, MD

Role: CONTACT

+821094113333

Facility Contacts

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Seyoung Shin, MD

Role: primary

+821094113333

Other Identifiers

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RS-2023-00262005

Identifier Type: -

Identifier Source: org_study_id

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