Developing AI-based rehabilitation strategies for pain management
Establishment of Biomechanical-based Rehabilitation Strategies for Pain-inducing Lifestyles in Degenerative Knee/Back Patients and for Artificial Intelligence-based Rehabilitation System
Bundang CHA Hospital · NCT05905029
This study is testing new ways to use artificial intelligence to help manage pain by looking at how lifestyle choices affect people with knee and back pain.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | 19 Years and up |
| Sex | All |
| Sponsor | Bundang CHA Hospital (other) |
| Locations | 2 sites (Seongnam and 1 other locations) |
| Trial ID | NCT05905029 on ClinicalTrials.gov |
What this trial studies
This study aims to create biomechanical indicators for lifestyles that induce pain and to implement lifestyle strategies for patients suffering from degenerative knee and back pain. By confirming the effectiveness of these strategies, the study seeks to enhance the use of artificial intelligence in digital treatment devices. Participants will be normal subjects over 19 years of age who do not report any pain on the Knee/Back Pain Assessment Scale. The study is observational and focuses on understanding the relationship between lifestyle factors and pain management.
Who should consider this trial
Good fit: Ideal candidates for this study are healthy individuals over 19 years old who do not experience knee or back pain.
Not a fit: Patients with existing systemic health issues or those currently experiencing pain will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved rehabilitation strategies that effectively manage pain and enhance quality of life for patients.
How similar studies have performed: While the approach of using biomechanical indicators and AI in rehabilitation is innovative, similar studies have shown promise in related fields, suggesting potential for success.
Eligibility criteria
Show full inclusion / exclusion criteria
1. Normal subjects
* Inclusion criteria
1. Over 19 years of age
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
* Exclusion criteria
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.)
2. Subjects who complain pain by degenrative changes in knee
* Inclusion criteria
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
* Exclusion criteria
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
* Inclusion criteria
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
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.)
Where this trial is running
Seongnam and 1 other locations
- Department of Rehabilitation Medicine, CHA Bundang Medical Center — Seongnam, Korea, Republic of (RECRUITING)
- Department of Rehabilitation Medicine, CHA Bundang Medical Center — Seongnam, Korea, Republic of (NOT_YET_RECRUITING)
Study contacts
- Principal investigator: Minyoung Kim, M.D., Ph.D. — Bundang CHA Hospital
- Study coordinator: Hyun Jung Oh, Bachelor
- 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: Healthy, Degenerative Disease