Collecting motion data from stroke patients
A Study for Collecting Data on the Motion Analysis of Stroke Patients
Bundang CHA Hospital · NCT05916924
This study is trying to collect movement data from stroke patients to help create personalized rehab goals and improve virtual reality treatments for recovery.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | 20 Years and up |
| Sex | All |
| Sponsor | Bundang CHA Hospital (other) |
| Locations | 1 site (Seongnam) |
| Trial ID | NCT05916924 on ClinicalTrials.gov |
What this trial studies
This observational study aims to gather functional evaluation and daily motion data from stroke patients to create 3D kinematic data. This data will help set personalized rehabilitation goals and develop virtual reality rehabilitation content. The study involves collecting clinical data through various assessments, including manual muscle tests and balance scales, using video shooting techniques. The goal is to enhance rehabilitation strategies for stroke recovery.
Who should consider this trial
Good fit: Ideal candidates are individuals over 20 years old who are more than one month post-stroke and can provide informed consent.
Not a fit: Patients with severe medical conditions or those unable to consent may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to more effective and personalized rehabilitation strategies for stroke patients.
How similar studies have performed: While this approach is observational and may build on existing methodologies, the use of 3D kinematic data in stroke rehabilitation is still relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
1. Inclusion criteria 1. Over 20 years of age 2. More than 1 month after onset of stroke 3. After hearing a detailed explanation of this study and fully understanding it, the subject or legal representative voluntarily decides to participate and agrees in writing to observe the precautions 2. Exclusion criteria 1. Patients who correspond to one or more of the following cannot participate in the study. 2. Patients with systemic infectious symptoms at the time of participation in the study 3. In the case of a person with impaired ability to consent (less than 10 points on the MMSE), a person without a guardian 4. Those with severe medical conditions such as unstable conditions in the cardiovascular system, digestive system, respiratory system, endocrine system, etc., and those with poor general health 5. Other cases where the researcher judges that participation in this study is not suitable (Patients who are participating in other studies or have participated in other studies within the past 30 days can also participate in this study.)
Where this trial is running
Seongnam
- Department of Rehabilitation Medicine, CHA Bundang Medical Center — Seongnam, Korea, Republic of (RECRUITING)
Study contacts
- Study coordinator: Hyun Jung Oh
- Email: a210525@chamc.co.kr
- Phone: +82 031 780 6003
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Stroke