Trying ViBandz for children with neurologic movement problems
Official title: ViBandz Feasibility Study in the Neurological Pediatric Population
Run by Children's Mercy Hospital Kansas City · NCT07458568 · Data updated 2026-11-12
We will try the ViBandz vibration device with children aged 6 months to 17 years who have neurologic movement problems during their regular PT/OT clinic visit.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 6 Months to 17 Years |
| Sex | All |
| Enrollment | 30 (estimated) |
| Sponsor | Children's Mercy Hospital Kansas City Academic / other |
| Locations | 1 site (Kansas City, Missouri) |
| Status | Recruiting |
| Started | April 7, 2026 |
| Main results expected | October 31, 2026 |
| Study ends | December 31, 2026 |
| Registry record updated | April 27, 2026 |
| Trial ID | NCT07458568 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Children aged 6 months to 17 years with neurologic conditions causing abnormal movement of at least one extremity who have a scheduled PT/OT clinic visit including targeted focal vibration and whose parent or LAR speaks English are ideal candidates.
✕Probably not a fit
Children who are wards of the state, whose parent or LAR is not English-speaking, or who are not scheduled for targeted focal vibration in the CM PT/OT clinic are excluded and therefore unlikely to benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This single-site feasibility project will test the ViBandz wearable vibration device with children who receive targeted focal vibration as part of their routine physical or occupational therapy at a Midwest pediatric tertiary care hospital. The design uses a mixed-methods approach with quantitative parent surveys completed immediately in clinic (or by email afterward) and secondary qualitative review of audio and optional video recorded during device use. All participants will receive their standard clinical targeted vibration first and then complete use of the ViBandz after their visit. The collected data will focus on feasibility, usability, and contextual feedback to guide future larger trials.
Why it matters
Potential benefit: If successful, ViBandz could provide a simple adjunct vibration tool to support targeted therapy for improving extremity movement in children with neurologic conditions.
How similar studies have gone: Targeted focal vibration has shown promising results in small pediatric and adult studies, but ViBandz as a specific device is novel and has limited prior clinical data.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria (Children): * Children of ages 6 months to 17 years old * Neurologic conditions resulting in abnormal movement of at least one extremity * Appointment scheduled in CM PT/OT clinic that would include targeted focal vibration as a standard of care Exclusion Criteria (Children): * Wards of the state Inclusion Criteria (Parent/LAR): * Parent or Legally Authorized Representative of a child with inclusion criteria above * English-speaking Exclusion Criteria (Parent/LAR): * Non-English speaking
Where it's running
-
Children's Mercy Hospital
Kansas City, Missouri, United States Recruiting
Study contacts
- Study coordinator: Megan Blaufuss, OTR/L, MS, CPAM
- Email: mmblaufuss@cmh.edu
- Phone: 913-696-5028
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.