Home-based gait rehabilitation for children with cerebral palsy
Development and Feasibility Study of the Home-based Gait Rehabilitation Service by Using the Insole-type Gait Analysis Device for Children With Cerebral Palsy
This study tests a new insole device to see if it helps children with cerebral palsy improve their walking through a home exercise program.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 10 (estimated) |
| Ages | 7 Years to 18 Years |
| Sex | All |
| Sponsor | Yonsei University Academic / other |
| Locations | 1 site (Seoul, Seodaemun-gu) |
| Trial ID | NCT06461923 on ClinicalTrials.gov |
What this trial studies
This study evaluates the usability and satisfaction of an insole-type gait analysis device for children with cerebral palsy who have walking impairments. Participants will undergo a screening test to ensure they can walk independently for more than 10 meters. Those who qualify will engage in a 6-week home exercise program while using the device, which records their walking patterns. Feedback will be provided during the program, and satisfaction will be assessed after completion.
Who should consider this trial
Good fit: Ideal candidates are children aged 7 to 18 years with cerebral palsy classified as Gross Motor Function Classification System level 1 or 2.
Not a fit: Patients with severe foot deformities or other significant medical issues that affect their ability to use the insole device may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could enhance gait rehabilitation and improve mobility for children with cerebral palsy.
How similar studies have performed: Other studies have shown promise in using technology for gait analysis and rehabilitation, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Patients diagnosed with cerebral palsy aged 7 to 18 years old 2. Patients classified as Gross Motor Function Classification System level 1 or 2 3. Individuals who visited Severance Hospital, comprehended the study, agreed to participate, and submitted the informed consent form Exclusion Criteria: 1. Individuals with complications such as severe foot deformities where the sensors of the insole gait analysis device cannot be recognized 2. In addition to above, individuals with clinically significant findings deemed inappropriate for this study by the study director or person in charge based on medical judgment
Where this trial is running
Seoul, Seodaemun-gu
- Severance Hospital — Seoul, Seodaemun-gu, South Korea (Recruiting)
Study contacts
- Principal investigator: Na Young Kim — Severance Hospital
- Study coordinator: Juntaek Hong
- Email: GHDWNSXOR@yuhs.ac
- Phone: +82 010 6517 7526
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.