ClinicalTrials.gg
Active, not recruitingNCT05117827Updated Sep 15, 2025

Pediatric Powered Wheelchair Standing Devices: An Exploratory Study

An interventional study of Power Wheelchair Standing Device in Cerebral Palsy, Spinal Muscular Atrophy and Spinal Cord Injuries, sponsored by Grand Valley State University. Active, not recruiting at 1 site in United States. Open to participants aged 5 Years to 17 Years. Per ClinicalTrials.gov, last updated 2025-09-15.

Sponsored by Grand Valley State University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
4
Allocation
Not applicable
Ages
5 Years to 17 Years
Sex
All
01

Study summary

For children who use a power wheelchair, a powered wheelchair standing device (PWSD) may be considered for daily use. A PWSD allows a child to electronically move between sitting and standing and can be driven in either position. Existing published PWSD research in pediatrics is limited to boys with Duchenne muscular dystrophy (DMD).(1, 2) While these studies provide some insights into PWSD use in boys with DMD, they do not reflect PWSD use in children with other conditions. The purpose of this exploratory study is to determine the feasibility of a research protocol exploring use of a PWSD in children who have neurodevelopmental conditions other than DMD.

02

Conditions studied

  • Cerebral Palsy
  • Spinal Muscular Atrophy
  • Spinal Cord Injuries
  • Spina Bifida
  • Development Delay
  • Genetic Disease
03

In context

Cerebral Palsy

1,936 studies on the registry are indexed under Cerebral Palsy; 458 are open to participants now.

This study's enrollment of 4 is below the median of 34 across 1,431 interventional studies indexed under Cerebral Palsy.

Browse Cerebral Palsy studies →

Lead sponsor

Grand Valley State University is the lead sponsor of 11 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
5 Years to 17 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Is 5-17 years of age. NOTE: Participants must be under 18 for the duration of the study.
  2. Diagnosed with a neurodevelopmental condition resulting in an inability to functionally ambulate.
  3. Can safely assume and maintain a supported standing position
  4. Has sufficient upper extremity and function to safely use a PWSD
  5. Can communicate pain or discomfort through verbalization, vocalization, use of augmented communication, etc.
  6. Can safely use the PWSD in areas of their home
  7. Has at least one parent/caregiver who is able to converse in English and actively participate in a device-use education provided in English
  8. The PerMobil PWSD can be set up to meet the child's specific needs
  9. Medical Clearance to trial the PWSD
  10. Participants must reside in Michigan

Exclusion criteria

Exclusion Criteria:

  1. Has a diagnosis of Duchenne muscular dystrophy.
  2. Any reason that it would not be safe for the child to use a PWSD
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
4 participants (actual)

Study arms

  • Experimental
    Power Wheelchair Standing Device User

    Device: Power Wheelchair Standing Device

Interventions

  • DevicePower Wheelchair Standing Device

    A power wheelchair standing device is a power wheelchair that allows a child to electronically move between sitting and standing. It can be driven in either position. The Permobil F5 Corpus VS is the specific power wheelchair standing device to be used in this study.

06

What researchers measure

Primary outcomes

  1. Participation in children

    Does using a PWSD increase participation in children who have neurodevelopmental conditions other than DMD?

    Time frame: 2 years

Secondary outcomes

  1. Parental/caregiver perceptions

    Does using a PWSD influence parental/caregiver perceptions of their child's emotional/behavioral status?

    Time frame: 2 years

  2. Children's perceptions

    For children who are able to respond to questions and participate in an interview using either verbal or augmented communication, does using a PWSD influence their own perceptions of their emotional/behavioral status?

    Time frame: 2 years

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: Yes — The research team may share research data related to study outcomes from this study with other investigators. If this occurs, the data will not contain identifiable data.

Supporting information: Study protocol

Time frame: 2 years

Access criteria: Contact PI

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 15, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05117827
Lead sponsor
Grand Valley State University
Responsible party
Lisa Kenyon (Professor, Grand Valley State University) — Principal investigator
First posted
Nov 11, 2021
Start date
Nov 12, 2021
Primary completion
Oct 31, 2026 (estimated)
Completion
Oct 31, 2027 (estimated)
Last update
Sep 15, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Sep 2025. You cannot join it, but the record below documents what was studied.

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Discussion

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