Actively Recruiting
Impact Evaluation of Breizh Fabribus Intervention for Personalized Assistive Technology Creation or Adaptation
Led by Fondation Ildys · Updated on 2026-01-02
70
Participants Needed
1
Research Sites
26 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the impact of Breizh Fabribus, a mobile workshop in the Finistère region of France that uses 3D printing and laser-cutting to create and customize assistive devices. This study focuses on people with disabilities who experience severe functional limitations or difficulty with essential daily activities. It aims to measure changes in users' ability to perform targeted activities three months after receiving personalized assistive devices, along with user satisfaction and device use. This retrospective, single-center study includes all individuals who received at least one assistive device from Breizh Fabribus between January 2024 and December 2025. Data is collected from routine service records and participant feedback through questionnaires at device delivery and three months later. An optional follow-up at twelve months is also offered to examine longer-term benefits. Participants and caregivers provide consent and complete initial questionnaires capturing demographics, medical history, and satisfaction with the device. Follow-up surveys assess device use frequency, changes in activity exposure, satisfaction, and barriers to use. Data collection runs from October 2025 to May 2026, with analysis planned for June 2026 and results expected in the second half of 2026. The study is monitored continuously to ensure protocol adherence and timely follow-up.
CONDITIONS
Brief Title
Impact Evaluation of Breizh Fabribus Intervention for Personalized Assistive Technology Creation or Adaptation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Any person who has received assistance from BFB for the creation or adaptation of assistive technology
You will not qualify if you...
- Objection to the use of their data
- Solicitation but no delivery of technical assistance by BFB
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - Ongoing based on receipt of assistive devices between January 1, 2024, and December 31, 2025.
Participants are screened for eligibility to participate in the trial.
/ Participants are contacted by phone or mail for consent and eligibility confirmation.
Duration - At or shortly after device request and intake.
Baseline information including demographics, medical history, and activity difficulties is collected from initial request forms.
1 data collection event (remote via forms or records)
Duration - At the time of device delivery.
Participants receive their personalized assistive device and complete a satisfaction questionnaire regarding device fit, usability, and co-creation experience.
1 visit (can be remote or in-person)
Duration - Three months following device delivery.
Participants complete a standardized follow-up questionnaire about device use frequency, changes in activity exposure, satisfaction, and barriers to utilization.
1 follow-up questionnaire (remote via online survey or postal form)
Duration - Up to twelve months after device delivery, within data collection window (October 2025 to May 2026).
An optional follow-up is offered to assess longer-term durability of benefits from the assistive device.
1 optional follow-up questionnaire (remote)
Trial Site Locations
Total: 1 location
1
Fondation ILDYS
Brest, Finistère, France, 29200
Actively Recruiting
Research Team
M
Matthieu PICHELIN
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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