Collecting clinical data from stroke patients and healthy individuals
A Study for the Collection of Clinical Data for Stroke Patients and Healthy Subjects
This study is trying to collect health information from stroke patients and healthy people to see how their health and abilities differ over time.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | 20 Years and up |
| Sex | All |
| Sponsor | Bundang CHA Hospital Academic / other |
| Locations | 1 site (Seongnam) |
| Trial ID | NCT05908994 on ClinicalTrials.gov |
What this trial studies
This observational study aims to gather and analyze medical, musculoskeletal, and functional data over time from stroke patients and healthy subjects. By comparing these data sets, the study seeks to identify clinical differences between the two groups. The research will involve examinations to assess various health parameters. The findings could provide insights into the impact of stroke on health and functionality.
Who should consider this trial
Good fit: Ideal candidates include adults over 20 years of age who are more than one month post-stroke.
Not a fit: Patients with severe medical conditions or those unable to provide consent may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance understanding of stroke's effects and improve patient care strategies.
How similar studies have performed: While similar observational studies have been conducted, the specific focus on comparing stroke patients with healthy subjects in this manner may provide novel insights.
Eligibility criteria
Show full inclusion / exclusion criteria
1. For stroke patients 1) Inclusion Criteria:
* Adults over 20 years of age
* More than 1 month after onset of stroke
* 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:
* Patients who correspond to one or more of the following cannot participate in the study.
* Patients with systemic infectious symptoms at the time of participation in the study
* In the case of a person with impaired ability to consent (less than 10 points on the MMSE), a person who is not accompanied by a guardian
* 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
* Other cases where the researcher judges that participation in this study is not suitable(Patients who are participating in other clinical trials or studies, or who have participated in other clinical trials or studies within the past 30 days can also participate in this study.)
2. For healthy voluteers 1) Inclusion Criteria:
* Over 20 years of age
* A person who is performing an independent daily life
* A person who voluntarily decides to participate and agrees in writing to abide by the precautions after hearing a detailed explanation of this study and fully understanding it
2) Exclusion criteria:
* Patients who correspond to one or more of the following cannot participate in the study.
* MMSE score less than 20 points (from 19 points onwards excluded from study)
* Those who remain disabled due to brain disease (stroke, brain tumor, cerebral palsy, dementia, Parkinson's disease, etc.)
* 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
* Other cases where the researcher judges that participation in this study is not suitable (Patients who are participating in other clinical trials or studies, or who have participated in other clinical trials or 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, Bachelor's degree
- 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.