Establishment of Biomechanical- and AI- Based Rehabilitation Strategies for Pain Inducing Lifestyles
NCT ID: NCT05905029
Last Updated: 2023-11-18
Study Results
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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RECRUITING
100 participants
OBSERVATIONAL
2023-08-04
2025-02-28
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
2. Those who scored '0' on the Knee/Back Pain Assessment Scale (VAS)
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
1. Over 19 years of age
2. Those who scored '1' or higher on the Knee Pain Assessment Scale (VAS)
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
1. Over 19 years of age
2. Those with a back pain rating scale (VAS) of '1' or higher
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
Exclusion Criteria
2. Those with systemic infectious symptoms at the time of participation in the study
3. Persons with poor systemic conditions such as unstable conditions of the cardiovascular system, digestive system, respiratory system, endocrine system, etc., and those with cerebrovascular disease
4. Other cases where the researcher judges that participation in this study is not suitable (Patients who are participating in other studies or who have participated in other studies within the past 30 days can also participate in this study.)
2. Subjects who complain pain by degenrative changes in knee
1. Patients who correspond to one or more of the following cannot participate in the study.
2. Those with systemic infectious symptoms at the time of participation in the study
3. Persons with poor systemic conditions such as unstable conditions of the cardiovascular system, digestive system, respiratory system, endocrine system, etc., and those with cerebrovascular disease
4. Other cases where the researcher judges that participation in this study is not suitable (Patients who are participating in other studies or who have participated in other studies within the past 30 days can also participate in this study.)
3. Subjects who complain pain by degenrative changes in back
1. Patients who correspond to one or more of the following cannot participate in the study.
2. Those with systemic infectious symptoms at the time of participation in the study
3. Persons with poor systemic conditions such as unstable conditions of the cardiovascular system, digestive system, respiratory system, endocrine system, etc., and those with cerebrovascular disease
4. Other cases where the researcher judges that participation in this study is not suitable (Patients who are participating in other studies or who have participated in other studies within the past 30 days can also participate in this study.)
19 Years
ALL
Yes
Sponsors
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Bundang CHA Hospital
OTHER
Responsible Party
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MinYoung Kim, MD, PhD
Principle investigator
Principal Investigators
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Minyoung Kim, M.D., Ph.D.
Role: PRINCIPAL_INVESTIGATOR
Bundang CHA Hospital
Locations
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Department of Rehabilitation Medicine, CHA Bundang Medical Center
Seongnam, , South Korea
Department of Rehabilitation Medicine, CHA Bundang Medical Center
Seongnam, , South Korea
Countries
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Central Contacts
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Facility Contacts
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MinYoung Kim, MD,PhD
Role: primary
Other Identifiers
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2022-11-015
Identifier Type: -
Identifier Source: org_study_id
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