Breizh Fabribus mobile workshop for on-site personalized assistive devices
Official title: Évaluation d'Impact de l'Intervention du Breizh Fabribus Pour la création ou l'Adaptation d'Aide Technique personnalisée (BFB-IMPACT)
Run by Fondation Ildys · NCT07314099 · Data updated 2026-11-12
This project tests whether on-site 3D‑printed and laser‑cut devices made by the Breizh Fabribus mobile workshop help people with disabilities in Finistère perform targeted daily activities better within three months.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 70 (estimated) |
| Sponsor | Fondation Ildys Academic / other |
| Locations | 1 site (Brest, Finistère) |
| Status | Recruiting |
| Started | December 2025 |
| Main results expected | May 2026 |
| Study ends | November 2026 |
| Registry record updated | January 2, 2026 |
| Trial ID | NCT07314099 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
People of any age in Finistère who received at least one assistive device from Breizh Fabribus between January 1, 2024 and December 31, 2025 and consent to use of their data are eligible.
✕Probably not a fit
Individuals who were only solicited but did not receive a device, those who object to use of their data, or people whose needs require complex institutional equipment rather than small personalized devices are unlikely to benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
BFB-IMPACT is a retrospective, mixed-methods evaluation of a mobile fabrication service that creates or adapts assistive devices using 3D printing and laser cutting. All individuals who received at least one device from Breizh Fabribus between January 1, 2024 and December 31, 2025 are identified from routine service records, contacted for consent, and have baseline information extracted from initial request forms. Immediate device satisfaction is recorded with the CSQ-8 at delivery and a standardized follow-up at three months collects device use, a five-point rating of change in the targeted activity, and free-text comments, with an optional 12-month follow-up. Data collection occurs October 2025–May 2026 with planned analysis in June 2026.
Why it matters
Potential benefit: If successful, this approach could provide faster, lower‑cost, better‑fitting assistive devices that increase independence and user satisfaction.
How similar studies have gone: Previous pilot and small-scale programs using 3D-printed personalized assistive devices report improved fit, satisfaction, and use, though mobile on-site delivery models like Breizh Fabribus are less studied at scale.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Any person who has received assistance from BFB for the creation or adaptation of assistive technology Exclusion Criteria: * objection to the use of their data * Sollicitation but no delivery of technical assistance by BFB
Where it's running
-
Fondation ILDYS
Brest, Finistère, France Recruiting
Study contacts
- Study coordinator: Matthieu PICHELIN
- Email: rcpromotion@ildys.org
- Phone: 02 98 02 11 36
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Comparing powered and mechanical prosthetic knees for K2-level amputees
This study is testing whether powered prosthetic knees work better than mechanical ones for K2-level amputees to help improve their mobility and make better choices for future prosthetic designs.
-
Effect of EMG sensor number and placement on control of below-elbow prosthetic arms
This project will test whether changing the number and placement of myoelectric sensors helps adults with below-elbow limb absence control a prosthetic arm better while wearing a real device.
-
Microprocessor-controlled prosthetic knees for limited community ambulators with above-knee amputation.
This test will see if switching to a microprocessor-controlled prosthetic knee reduces fall-related health problems and improves walking speed, mobility, and quality of life for adults with above-knee amputations who are limited community ambulators compared with non-microprocessor knees.
-
Understanding the impact of powered prosthetics on walking for transfemoral amputees
This study is testing whether powered knee and ankle prosthetics can help transfemoral amputees walk better, especially when combined with special training.
-
Evaluation of a new myoelectric prosthesis for transradial amputees
This study is testing a new type of prosthetic arm that uses a special implant to help people with below-the-elbow amputations control it more easily and naturally.
-
Hand prosthesis usability and performance evaluation for people with upper limb absence
This study tests a new multi-articulating hand prosthesis to see if it performs better or differently than a participant’s own prosthesis.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.