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CompletedNCT06876480SK4AllUpdated Jul 16, 2026

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

An interventional study of Keyboard in Complex Sensorimotor Disabilities, sponsored by Assistance Publique - Hôpitaux de Paris. Completed at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-07-16.

Sponsored by Assistance Publique - Hôpitaux de Paris · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
10
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

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.

02

Conditions studied

  • Complex Sensorimotor Disabilities

Keywords

  • Complex sensorimotor disabilities
  • ScanningKeyboard
03

In context

Lead sponsor

Assistance Publique - Hôpitaux de Paris is the lead sponsor of 3,505 studies on the registry; 1,006 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

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

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.
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
10 participants (actual)

Study arms

  • Experimental
    Arm with virtual keyboard

    Arm with virtual keyboard: 16 days for each participant

    Other: Keyboard

Interventions

  • OtherKeyboard

    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.

06

What researchers measure

Primary outcomes

  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).

    Time frame: at 16 days

Secondary outcomes

  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)).

    Time frame: 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).

    Time frame: 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)).

    Time frame: 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).

    Time frame: at 16 days

07

Study locations

1 site
  • CHU Raymond Poincaré - APHP
    Garches, 92380, France
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 16, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06876480
Lead sponsor
Assistance Publique - Hôpitaux de Paris
Responsible party
Sponsor
First posted
Mar 14, 2025
Start date
Mar 17, 2025
Primary completion
Oct 16, 2025
Completion
Oct 16, 2025
Last update
Jul 16, 2026

Study contacts

SAMUEL POUPLIN, PhD
principal investigator · PFNT DEPARTMENT, Raymon Pincaré Hospital - APHP
Mathieu THEBAUD
study director · Laboratoire d'Assistances Technologiques, CMRRF Kerpape

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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