- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03364010
Dyslexia, Motor Control and Proprioception
February 17, 2023 updated by: Institut National de la Santé Et de la Recherche Médicale, France
Relationships Between Proprioception, Motor Control and Reading in Children With Dyslexia
The investigators hypothesize that children with dyslexia present proprioceptive disorders and the purpose of the present study is to better understand relationships between motor control, proprioception and academic learnings.
The investigators compare a group of French students with and without dyslexia aged 10-12.
Study Overview
Status
Terminated
Conditions
Detailed Description
2 groups of children (dyslexics and control) will be evaluated on 2 tasks:
- Evaluation of the proprioception: Perception of the speed and Perception of the position
- Evaluation of the motor learning: Estimation of state in the framework of a motor perturbation
Study Type
Interventional
Enrollment (Actual)
56
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Jeremie Gaveau, PH.D
- Phone Number: +33380396772
- Email: jeremie.gaveau@u-bourgogne.fr
Study Contact Backup
- Name: Julie LAPREVOTTE
- Phone Number: 03 80 39 67 67
- Email: Julie.Laprevotte@u-bourgogne.fr
Study Locations
-
-
Bourgogne
-
Dijon, Bourgogne, France, 21000
- Inserm U1093
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
10 years to 12 years (Child)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion criteria for all children
- Child with a French social security
- School child
- Native French speaker
- right-handed
- Normal or corrected vision
- Without neurological or psychiatric histories
- Agree to participate in the study in agreement with parental rights representatives
For the dyslexic group :
- pluridisciplinary diagnostic
- never consulted for proprioception before
- without any other leaning disorders like dysphasia
- attention deficit hyperactivity disorder (ADHD) or developmental coordination disorder (DCD)
For the control group :
- regular school attendance
- never consulted for learning disabilities
- No learning disorders known for their parents or siblings.
Exclusion criteria for all children
- genetic disorder
- neurological or psychiatric history
- Delayed psychomotor development
- Reeducation or current treatment interfering with the evaluation
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Dyslexic and non dyslexic Children
Children aged 10-12 Evaluation of proprioception Evaluation of motor learning Evaluation of written language
|
Velocity perception and Position perception
Motor accurancy and State Estimation with visual perturbations
Text reading, Identifying words and Phonological awareness: phonemic blending and phonemic elision
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Evaluation of proprioception through velocity perception
Time Frame: 1day
|
The ability to perceive motion at 3 different velocities for 3 different joints is assessed using a motorized ergometer.
A passive movement is performed by the ergometer and children are tasked to press a button as soon as they feel the movement.
We calculate the angle of detection for each speed and compare it between Dyslexic and healthy children.
|
1day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Evaluation of proprioception through position perception
Time Frame: 1 day
|
The ability to perceive position is assessed using an ergometer that produces passive movements of 3 different amplitudes on the dominant arm.
In a second time, the ergometer produces a passive movement of the same arm and children are tasked to press a button as soon as they feel they are in the exact previously-experienced position.
We calculate the angular error and compare it between Dyslexic and healthy children.
|
1 day
|
Motor learning
Time Frame: 1 day
|
The ability to learn new motor tasks is assessed using virtual reality and motor acquisition systems.
First we evaluate the motor accuracy and the state estimation by pointing tests.
Then visual perturbations are introduced during pointing.
Finally, we evaluate motor accuracy and state estimation again.
|
1 day
|
Text reading
Time Frame: 1day
|
The ability to read aloud a text is assessed using the French standardized test " Alouette ", which provide accuracy in reading aloud age-normed texts (ratio between words that have been correctly read and all the words that have been read).
|
1day
|
Phonological awareness: phonemic blending and phonemic elision
Time Frame: 1day
|
The ability to derive a phonemic pattern from distinct phonemic units or to substitute a phonemic pattern for another is assessed using the French standardized test " Nepsy2, phonological process " which provide standard deviation in reading aloud by the investigator.
|
1day
|
Identifying words
Time Frame: 1day
|
The ability to identify words is assessed using the French standardized test " Timé3 ", which provide lexical level and delay reading in silent reading age-normed words.
|
1day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Patrick QUERCIA, dr, Unité Inserm d'affiliation : Laboratoire U1093 Cognition, Action et Plasticité Sensorimotrice
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 4, 2018
Primary Completion (Actual)
May 9, 2019
Study Completion (Actual)
June 2, 2021
Study Registration Dates
First Submitted
September 27, 2017
First Submitted That Met QC Criteria
November 30, 2017
First Posted (Actual)
December 6, 2017
Study Record Updates
Last Update Posted (Estimate)
February 21, 2023
Last Update Submitted That Met QC Criteria
February 17, 2023
Last Verified
February 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- C17-14
- 2017-A01547-46 (Registry Identifier: RCB)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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