- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04210661
Spelling Mistake Tolerant Word Prediction for Working, Writing and Communicating (Predict4All)
Spelling Mistake Tolerant Word Prediction for Working, Writing and Communicating - Predict4All
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.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Garches, France, 92380
- Raymond Poincaré Hospital
-
Ploemeur, France, 56270
- CMRRF Kerpape
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: SUPPORTIVE_CARE
- Allocation: RANDOMIZED
- Interventional Model: CROSSOVER
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
ACTIVE_COMPARATOR: classic prediction software
test with classic precition software
|
test with prediction software with spell checker
|
EXPERIMENTAL: prediction software with spell checker
test with prediction software with spell checker
|
test with prediction software with spell checker
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
number of spelling errors
Time Frame: 20 min
|
total of number of spelling errors during the test
|
20 min
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Text input speed
Time Frame: 20 min
|
Text input speed in the test
|
20 min
|
Prediction usage rate
Time Frame: 20 min
|
number of times the prediction is used
|
20 min
|
Keystrokes Saving Rate
Time Frame: 5 min
|
measured by the percentage of input saved by word prediction versus a keyboard alone
|
5 min
|
Attentional load
Time Frame: 1 min
|
Likert Analog Visual Scale [0-10]
|
1 min
|
Fatigue
Time Frame: 1 min
|
Likert Analog Visual Scale [0-10]
|
1 min
|
software Satisfaction
Time Frame: 1 min
|
Likert Analog Visual Scale [0-10]
|
1 min
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2019-A01882-55
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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