Intelligent robotics to assist elderly mobility in Hong Kong
Intelligent Robotics for Elderly Assistance in Hong Kong
This study is testing new robotic devices to help older adults with muscle loss move around better and stay safe, while also making sure these devices meet their needs.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 180 (estimated) |
| Ages | 65 Years to 75 Years |
| Sex | All |
| Sponsor | The University of Hong Kong Academic / other |
| Locations | 1 site (Hong Kong) |
| Trial ID | NCT05327335 on ClinicalTrials.gov |
What this trial studies
This study aims to develop innovative intelligent robotic systems to enhance mobility and manipulability for older adults suffering from sarcopenia. Utilizing a User-Centric Co-creation (UC3) approach, the research will begin with a psycho-social study to identify the specific needs of elderly users. The project will create personalized wearable robotic devices designed to improve independence and quality of life, while also preventing falls. An integrated testing system will be established to evaluate the performance and safety of these robotic solutions in real-world scenarios.
Who should consider this trial
Good fit: Ideal candidates for this study are older adults aged 65 and over with a SARC-F score of 4 or higher, indicating sarcopenia.
Not a fit: Patients with osteoporosis or a history of significant joint surgeries may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could significantly improve the mobility and quality of life for elderly patients with sarcopenia.
How similar studies have performed: Other studies have shown promise in using robotics for elderly assistance, but this specific approach with a UC3 methodology is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Reference group participants: Inclusion Criteria: * Aged 65 or older * SARC-F score (measurement of sarcopenia) below 4 * Capable of clear communication * No cognitive impairment Exclusion Criteria: * Osteoporosis * A history of the spine, knee, hip, and ankle joint surgery Intervention group participants: Inclusion Criteria: * Aged 65 or older * SARC-F score (measurement of sarcopenia) equal to or over 4 * Able to perform the experiment in a laboratory setting independently * Capable of clear communication * No cognitive impairment Exclusion Criteria: * Osteoporosis * A history of the spine, knee, hip, and ankle joint surgery.
Where this trial is running
Hong Kong
- The University of Hong Kong — Hong Kong, Hong Kong (Recruiting)
Study contacts
- Study coordinator: Vivian W.Q. Lou, PhD
- Email: wlou@hku.hk
- Phone: 2831-5334/3917-4835
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.