Trials / Completed
CompletedNCT03714256
Human Factor Validation of Pediatric Mobility Device
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 33 (actual)
- Sponsor
- Permobil, Inc. · Industry
- Sex
- All
- Age
- 6 Months – 36 Months
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to validate the user interface of a pediatric power mobility device by establishing that the product is safe and effective use for the intended users.
Detailed description
The purpose of this study is to validate the user interface of a pediatric power mobility device by establishing that the product is safe and effective use for the intended users. The human factors validation study will be conducted in children with mobility impairments as categorised by Hays (1987) in the age range of 6 months to 36 months under realistic use conditions.The study is an open label, un-blinded, non-randomized study which consists of one visit.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Device, patient mobility, powered | Pediatric mobility device |
Timeline
- Start date
- 2018-09-21
- Primary completion
- 2018-11-19
- Completion
- 2018-11-19
- First posted
- 2018-10-22
- Last updated
- 2021-01-14
- Results posted
- 2021-01-14
Locations
3 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT03714256. Inclusion in this directory is not an endorsement.