Predict4All: Spelling Mistake Tolerant Word Prediction for Working, Writing and Communicating

Sponsor
Centre d'Investigation Clinique et Technologique 805 (Other)
Overall Status
Completed
CT.gov ID
NCT04210661
Collaborator
(none)
13
2
2
24.8
6.5
0.3

Study Details

Study Description

Brief Summary

The main objective of the PREDICT4ALL project is to provide written communication in a computer, reducing the number of spelling errors for each user.

The effectiveness of written communication is defined in this study by the number of spelling errors for each user. Word prediction (and therefore correction) must be able to be configured by a therapist (speech therapist, occupational therapist).

Adapting the prediction to user errors should also allow it to be more relevant throughout the text input. This software efficiency must increase text input speed, Reduce the cognitive load, establish a classification of spelling errors adapted to the context of text input speed and develop the word prediction module tolerant of these spelling errors.

Condition or Disease Intervention/Treatment Phase
  • Other: prediction software with spell checker
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
13 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Intervention Model Description:
interventionnal, prsopective, randomized, multicentricinterventionnal, prsopective, randomized, multicentric
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Spelling Mistake Tolerant Word Prediction for Working, Writing and Communicating - Predict4All
Actual Study Start Date :
Feb 13, 2020
Actual Primary Completion Date :
Mar 8, 2022
Actual Study Completion Date :
Mar 8, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: classic prediction software

test with classic precition software

Other: prediction software with spell checker
test with prediction software with spell checker

Experimental: prediction software with spell checker

test with prediction software with spell checker

Other: prediction software with spell checker
test with prediction software with spell checker

Outcome Measures

Primary Outcome Measures

  1. number of spelling errors [20 min]

    total of number of spelling errors during the test

Secondary Outcome Measures

  1. Text input speed [20 min]

    Text input speed in the test

  2. Prediction usage rate [20 min]

    number of times the prediction is used

  3. Keystrokes Saving Rate [5 min]

    measured by the percentage of input saved by word prediction versus a keyboard alone

  4. Attentional load [1 min]

    Likert Analog Visual Scale [0-10]

  5. Fatigue [1 min]

    Likert Analog Visual Scale [0-10]

  6. software Satisfaction [1 min]

    Likert Analog Visual Scale [0-10]

Eligibility Criteria

Criteria

Ages Eligible for Study:
6 Years to 25 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Aged between 6 and 25 years old For center 1

  • patient with dysorthographia

  • educational level greater than or equal to CE2

  • A developmental level in reading on the Evalouette test (Evaleo battery) greater than or equal to CE1 For center 2

  • Neurologic disorder impacting communication

Exclusion Criteria:
  • Patient's refusal to participate in the study

  • Persons under guardianship

  • Pregnant women

  • No affiliation to a social security scheme (beneficiary or beneficiary)

  • Having visual disturbances preventing the use of the computer tool

Contacts and Locations

Locations

Site City State Country Postal Code
1 Raymond Poincaré hospital Garches France 92380
2 CMRRF Kerpape Ploemeur France 56270

Sponsors and Collaborators

  • Centre d'Investigation Clinique et Technologique 805

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Centre d'Investigation Clinique et Technologique 805
ClinicalTrials.gov Identifier:
NCT04210661
Other Study ID Numbers:
  • 2019-A01882-55
First Posted:
Dec 26, 2019
Last Update Posted:
Mar 9, 2022
Last Verified:
Feb 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Centre d'Investigation Clinique et Technologique 805
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 9, 2022