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Pediatric Powered Wheelchair Standing Devices: An Exploratory Study

Pediatric Powered Wheelchair Standing Devices: An Exploratory Study

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05117827
Enrollment
4
Registered
2021-11-11
Start date
2021-11-12
Completion date
2027-10-31
Last updated
2025-09-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

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

Brief 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.

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.

Sponsors

Grand Valley State University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
5 Years to 17 Years
Healthy volunteers
No

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

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

Design outcomes

Primary

MeasureTime frameDescription
Participation in children2 yearsDoes using a PWSD increase participation in children who have neurodevelopmental conditions other than DMD?

Secondary

MeasureTime frameDescription
Parental/caregiver perceptions2 yearsDoes using a PWSD influence parental/caregiver perceptions of their child's emotional/behavioral status?
Children's perceptions2 yearsFor 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?

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026