RecruitingNot Applicable

Evaluation of Different Visual Keyboard Organizations on People With Complex Sensorimotor Disabilities

France12 participantsStarted 2025-03-17

Plain-language summary

comparison of different visual keyboard configurations

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * People with complex sensorimotor disabilities who are unable to communicate in standard written and digital form. * Persons aged 18 or over * Ability to read and write French * Patient who own and use IT tool * Patient who has used or used a virtual scanning keyboard to access IT Tools * Health insurance beneficiary or rightful dependent * Patient who has signed an informed and written consent. or * Adult patient under guardianship who has signed an informed and written consent with the assistance of their guardian. * Person agreeing to the terms of the protocol (home visits by the investigator). Exclusion Criteria: * Having visual impairments preventing the use of the IT Tools * Patient under State Medical Aid (except in cases of exemption from affiliation). * Persons deprived of liberty * Pregnant or breastfeeding women.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Text input speed evaluation

Timeframe: at 16 days

Trial details

NCT IDNCT06876480

SponsorAssistance Publique - Hôpitaux de Paris

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-03

Contact for this trial

SAMUEL POUPLIN, PhD

+33171144921 samuel.pouplin@aphp.fr

View on ClinicalTrials.gov More Complex Sensorimotor Disabilities trials

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.