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3D Printed Assistive Devices for Individuals With Physical Disabilities

Satisfaction of 3D Printed Assistive Devices for Individuals With Physical Disabilities Living in a Long-Term Care Setting

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05519891
Enrollment
10
Registered
2022-08-29
Start date
2022-08-31
Completion date
2022-12-31
Last updated
2023-01-17

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

Conditions

Disability Physical

Brief summary

Our research aims to examine 3D printed device satisfaction when using mobile devices for individuals with physical disabilities in long-term care facilities, and the impact of the 3D printed device integration on overall occupational performance and satisfaction.

Detailed description

This feasibility study will be conducted at Good Shepherd Rehabilitation Network (GSRN) in the collection of data examining 3D printing outcomes. The 3D printed devices are within the current normal and customary care of GSRN services, with the focus on the created 3D printed adaptations for mobile device usage (i.e. smartphone adaptations). The feasibility data will assist in understanding the satisfaction and performance of 3D printed devices for persons with a physical disability.

Interventions

OTHERCustom 3D printed device

A 3D printed adaptation for a mobile device.

Sponsors

Moravian University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Being over the age of 18 2. Self-identified accessibility needs of the mobile device to address secondary to a physical accessibility limitation(s) 3. Accessibility requests of a device that has not already been addressed by 3D printing 4. Ownership or borrowing of a mobile device for personal use Operational definition of mobile devices: Mobile devices are a maximum length and width of 9.4 by 6.8 and must weigh less than 1.03 lb (e.g. dimensions of a standard iPad mini) and should be a one-handed use device with touch-screen capabilities

Exclusion criteria

1. Individuals with severe cognitive impairment (BIMS score of 7 or less) 2. Individuals who were unwilling to use a 3D printed device

Design outcomes

Primary

MeasureTime frameDescription
Canadian Occupational Performance Measure (COPM)3-4 weeksAs a self-reported measure of occupational performance and occupational satisfaction, the scale ranges from 1-10, with 10 indicating a more favorable outcome in self-rated occupational performance and satisfaction.

Secondary

MeasureTime frameDescription
Quebec User Evaluation of Satisfaction with Assistive Technology (QUEST 2.0)3-4 weeksParticipants will self-report satisfaction with the created and printed device and service on a Likert scale from 1-5, with 5 indicating maximum satisfaction.

Countries

United States

Outcome results

None listed

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