Collecting movement and health data from stroke patients to build digital models
Gathers movement, daily activity and genetic data from people recovering from stroke.
Plain-language title generated from the registry record
Registry title: Development of Stroke Prognosis Predictive Precision Medicine Based on a Digital Twin
Key facts
- Where
- Gyeonggi-do, South KoreaSee the site
Where in South Korea
- Bundang CHA Medical CenterGyeonggi-do, South KoreaTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Seyoung Shin
- Trial code
- NCT07482579
- Record updated
- 25 March 2026
- Original description
To collect large-scale, high-quality clinical data, daily activity and movement patterns, and genomic information from stroke patients spanning the subacute to chronic stages.Read full original descriptionShow less
A Study for the Development of Prognosis Predictive Precision Medicine Based on a Digital Twin Reflexing the Motor Patterns in Stroke Patients: a Prospective Study
To collect large-scale, high-quality clinical data, daily activity and movement patterns, and genomic information from stroke patients spanning the subacute to chronic stages.
This study aims to establish the foundation for personalized precision medicine in stroke care and to develop a visual and digital transformation of patient medical information in the era of digital healthcare.
Inclusion: Adults aged 20 years or older with a confirmed diagnosis of stroke; Within 1 month after stroke onset; Patients scoring between 0 and 3 points on the Functional Ambulatory Category (FAC) test; Patients or their legally authorized representatives who have fully understood the details of this study, voluntarily decided to participate, and provided written informed consent to comply with the study instructions.
Exclusion: Patients with impaired ability to provide consent (MMSE score less than 10) who are not accompanied by a caregiver; Any other cases deemed inappropriate for participation by the investigator. (This study is non-interventional; therefore, patients who are currently participating in or have participated in another clinical study or research within the past 30 days may still be included.).