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Complex Sensorimotor DisabilitiesSK4AllNCT06876480

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

A study testing Keyboard in people with Complex Sensorimotor Disabilities, run by Assistance Publique - Hôpitaux de Paris at 1 site in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

comparison of different visual keyboard configurations Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Complex Sensorimotor Disabilities
What is being tested?
Keyboard
Could I receive a placebo?
No, everyone receives an active treatment
How many people
10 participants
Where
1 siteFrance
Study dates
17 Mar 2025to 16 Oct 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • 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
Show all 9Show fewer
  • 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).

Who cannot join

  • 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.

Trial locations and contacts

1 site in 1 country.

France1 site
  • CHU Raymond Poincaré - APHP

    Garches, 92380

Other trials in France

About this study

Official title: Evaluate of Different Visual Keyboard Organizations on People With Complex Sensorimotor Disabilities

comparison of different visual keyboard configurations

Read the detailed description

Information and communication technologies (ICT) occupy an increasingly important place in our daily lives (CREDOC, 2021). Similarly, for the general population faced with these information and communication technologies, people with sensorimotor disabilities want and can claim socio-professional integration, access to knowledge through school integration facilitated by the Internet, access to leisure activities and social participation (Folan et al., 2015) (Picard, 2007) (Angelo et al., 2007) (Cornes \& Bochel, 1987). Consequently, information and communication technologies are essential for people with sensorimotor disabilities and restoring this communication is fundamental.

Regarding access to digital tools, people with sensorimotor disabilities have difficulty accessing the pointing device (moving the mouse cursor, but also the various clicks) and input text (accessing the standard keyboard). Many assistive devices exist depending on the disabilities and abilities of the people, but also on their life habits, environmental constraints and expected uses of the computer tool (LoPresti and Brienza, 2004) (DeVries et al., 1998) (Yu-Luen Chen et al., 2003) (Y.-L. Chen et al., 2003) (Biard et al., 2011).

However, for people with complex sensorimotor disabilities, when few functional movements are possible, scanning access on a visual keyboard is preferred. At this stage, the movement of the mouse cursor, mouse clicks and text input are grouped under the same interface (visual keyboard) controlled by one or two switches. The visual keyboard presents the letters, the arrows for the direction of the mouse cursor and the different clicks (Figure 1).

In aims to increase people's text input speed, several studies have shown that the addition of linguistic prediction modules (of words or characters) would, in theory, make input text faster (Schadle \& Poirier, 2004) (Trnka et al., 2007):

Word prediction (or completion) enables words or completions to be proposed in order to reduce the number of characters to be entered. By reducing the entry of certains characters, the text input speed should theoretically be increased. In fact, this is not necessarily the case (Raynal \& Badr, 2022) (Pouplin et al., 2014).

Character prediction rearranges the layout of characters after each input, according to the probability of each one being selected. In this way, the most likely character becomes the one that can be accessed most quickly, with the least scanning. It has been shown that in the case of a pointing keyboard, this prediction does not satisfy users any more than word prediction (MacKenzie, 2008). Nevertheless, for scanning keyboards, which we are interested in here, even though there are few studies with real users, we can see that in some cases, character prediction seems interesting (Pouplin et al., 2014). Nevertheless, the main drawback of character prediction is that it results to a dynamic display of the keyboard. Indeed, the integration of character prediction seems to take place in much the same way from one study to the next, meaning a reorganization of the character set and therefore of the entire display. This prevents any memorization of the character layout for the user, and thus a certain amount of learning.

Therefore, we propose to integrate character prediction while keeping the display as static as possible.

Being tested
Keyboard
Keywords
Complex sensorimotor disabilities, ScanningKeyboard

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • KeyboardOther

    Day 0 : Collection of the general data required for the study, installation of the computer device including the LifeCompanion software with the different scanning keyboards configurations and organizations. Day 0 to Day 8 : write, in copy, a text using each of the virtual keyboard configurations. Day 8 : copying a text proposed by the investigator of identical difficulty for each condition, for a duration of 15 minutes, per experimental condition. This copying exercise, with the recording of measurements, will be done for each experimental condition. Day 8 to Day 16 : write a copy of a text of his/her choice for 10 minutes, using each of the virtual keyboard configurations. Day 16 : in a text-entry evaluation situation, copying a text proposed by the investigator, of identical difficulty for each condition.

Study groups in NCT06876480
Study groupRoleWhat they receive
Arm with virtual keyboardExperimentalArm with virtual keyboard: 16 days for each participant
Receives: Other: Keyboard

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Text input speed evaluation

    To evaluate the influence of different visual keyboard organizations on text input speed in people with complex sensorimotor disabilities.

    Evaluation criteria: Text input speed (characters/minutes).

    Measured: at 16 days

Secondary outcomes (4)
  1. Evaluate the influence of visual keyboard organizations on fatigue

    To evaluate the influence of different visual keyboard organizations on fatigue in people with complex sensorimotor disabilities.

    Evaluation criteria: Self-assessment of fatigue (Visual Analog Scale (VAS)).

    Measured: at 16 days

  2. Evaluation of usability efficiency

    To evaluate the influence of different visual keyboard organizations on the usability efficiency of the system by people with complex sensorimotor disabilities.

    Evaluation criteria: Input validity (percentage), System use strategy efficiency score (percentage).

    Measured: at 16 days

  3. Self-assessment of satisfaction

    To evaluaSelf-aste the influence of different visual keyboard organizations on text input system satisfaction in people with complex sensorimotor impairments.

    Self-assessment of satisfaction (Visual Analogue Scale (VAS)).

    Measured: at 16 days

  4. Oculometric data evaluation

    To evaluate the influence of different visual keyboard organizations on the distance covered by users' gaze.

    Evaluation criteria: Oculometric data (raw value).

    Measured: at 16 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted14 Mar 2025
  2. Study start17 Mar 2025
  3. Primary completion16 Oct 2025
  4. Study completion16 Oct 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
10 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06876480
Sponsor's protocol ID
APHP240703
Other IDs
2024-A01067-40
Acronym
SK4All
Status last verified
Jul 2026
First submitted
10 Mar 2025
Last updated
16 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Keyboard in people with Complex Sensorimotor Disabilities, run by Assistance Publique - Hôpitaux de Paris at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 9 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 16 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Text input speed evaluation (time frame: at 16 days). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Jul 2026.

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