A Study for the Collection of Clinical Data for Stroke Patients and Healthy Subjects

NCT ID: NCT05908994

Last Updated: 2023-06-18

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 100 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2021-10-06
• Study Completion Date: 2024-12-31

Brief Summary

This study aimes to medical data, musculoskeletal data and functional data over time of stroke patients and healthy subjects to compared the clinical differences between stroke and healthy subjects.

Conditions

Stroke; Health Behavior

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Interventions

Examination

Exmainations including imaging, neurophysiological, kinetic and kinematic measurmetns. Behavioral assessments

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Adults over 20 years of age
• More than 1 month after onset of stroke

• 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

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.)
• 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.)

• Minimum Eligible Age: 20 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Bundang CHA Hospital

OTHER

Sponsor Role: lead

Responsible Party

MinYoung Kim, MD, PhD

Principle investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Department of Rehabilitation Medicine, CHA Bundang Medical Center

Seongnam, , South Korea

Site Status: RECRUITING

Countries

South Korea

Central Contacts

Hyun Jung Oh, Bachelor's degree

Role: CONTACT

a210525@chamc.co.kr

+82 031 780 6003

Facility Contacts

MinYoung Kim, MD,PhD

Role: primary

Other Identifiers

2021-05-026

Identifier Type: -

Identifier Source: org_study_id