Actively Recruiting
Impact Study on Users of Upper Limb Assistive Devices
Led by Association APPROCHE · Updated on 2026-02-24
150
Participants Needed
2
Research Sites
63 weeks
Total Duration
On this page
Sponsors
A
Association APPROCHE
Lead Sponsor
C
Centre Mutualiste de Rééducation et de Réadaptation Fonctionnelles de Kerpape
Collaborating Sponsor
AI-Summary
What this Trial Is About
This impact study of upper limb (UL) assistance devices is part of the Exploratory PEPR O2R "Robotic assistance for human movements." The integrated project PI3 "ASSISTMOV," composed of a multidisciplinary team in engineering and Human and Social Sciences (HSS), targets the use case of employing robotic assistance for the movement of persons with disabilities (PWD). Through the development of a range of exoskeletons (lower and upper limbs), this project aims for a breakthrough technology enabling fluid and robust interaction with a variety of environments and uses (from rehabilitation to daily life). The proposed study contributes to this objective by exploring the clinical and psychosocial dimensions of the daily use of UL assistance devices. Through interviews and questionnaires, it aims to collect data on their impact in terms of independence in activities of daily living (ADL), satisfaction, quality of life, social participation, as well as social perceptions related to the use of these technical aids. It will make it possible to document the benefits and limitations of existing devices from the users' point of view (patients and informal and/or professional caregivers), by identifying the factors that facilitate or hinder their adoption and by exploring the care pathway, from prescription to daily use. The questionnaires will also allow examination of economic dimensions. The participants included in this study will be recruited among users already using, in their daily life, an UL movement assistance device. All will be regular users of their device, functionally integrated into their usual environment for at least two months. Only devices benefiting from CE marking, guaranteeing their compliance with European regulations, will be eligible. No equipment will be specifically provided within the framework of this research: each participant will share their experience with their own device, as it is integrated into their ADL. A preliminary literature review helped identify the main categories of UL movement assistance devices, grouped according to the following typologies: grasping gloves, mealtime aids, robotic manipulation arms, and arm supports (electric or mechanical). The purpose of the approach is both diagnostic and forward-looking. It is diagnostic in that it makes it possible to analyze current practices, real activity, and users' viewpoints, in order to identify elements likely to be improved in the recommendation and use of the devices. It is also forward-looking, since it aims to identify new opportunities, needs, or potential developments, in order to support the thinking of roboticists based on field observations.
CONDITIONS
Official Title
Impact Study on Users of Upper Limb Assistive Devices
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Effective use of a CE-marked upper-limb assistance device for at least 60 days
- Access to a computer with an internet connection and ability to participate in videoconferences
- Provided free and informed non-opposition or consent, or legal representative consent if applicable
- Cognitive abilities sufficient to complete questionnaires and interviews
- Medically stable without ongoing medical events likely to affect study participation
- For caregiver-users: age 18 or older
- Caregivers must live with or regularly interact with a patient-user of an upper-limb assistance device
- Caregivers must have access to a computer with internet and ability to participate in videoconferences
- Caregivers must have provided free and informed non-opposition
You will not qualify if you...
- Enrollment in another protocol evaluating a technical aid (for patient-users)
- Insufficient mastery of the French language (for patient-users and caregiver-users)
- Cognitive impairments preventing understanding of the questions (for caregiver-users)
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Centre Bouffard Vercelli
Perpignan, France, 66962
Actively Recruiting
2
Centre de Kerpape
Ploemeur, France, 56270
Actively Recruiting
Research Team
C
Charlotte LE GOFF, PhD Student
CONTACT
C
Charline LONGUET, CRA
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
5
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