Developmental Coordination Disorder (DYSENS)

February 6, 2024 updated by: Hospices Civils de Lyon

Developmental Coordination Disorder: Role of Perceptual Deficits and Body Representation

Developmental Coordination Disorder (DCD) corresponds to a clumsiness, a slowness and an inaccuracy of motor performance. This neurodevelopmental disorder affects 6% of school-aged children, and disturbs daily life activities and academic performances. The etiology of DCD is still unknown. An understanding of this disorder is necessary to improve interventions and therefore quality of life of these people.

A deficit of the so-called internal models is the most commonly described hypothesis of DCD. Indeed, children with DCD exhibit difficulties in predictive control. Internal models, useful for motor control, are closely related to the sensory system, as they are elaborated on and constantly fed by sensory feedback. Deficits in sensory performance are described in DCD, mostly in the visual system, which could in turn partly explain poor motor performance. However, visuo-perceptual deficits cannot explain the entire motor difficulties because some activities in daily life, as buttoning a shirt, are often performed without visual control. Although the integrity of proprioceptive and tactile systems is necessary for the building of internal models, and therefore for a stable motor control, these sensory systems have been very little investigated in DCD.

Moreover, using a tool is often disturbed in children with DCD. In neurotypical subjects, tool use induces a plasticity of body representation, as reflected by modifications of movement kinematics after tool use. Proprioceptive abilities are necessary for this update of the body schema. Thus, potential deficits of the proprioceptive system in children with DCD could impair the plastic modification of the body schema, and hence of motor performance, when using a tool. The aim of this study is to identify the main cause of the DCD, both by evaluating the tactile and proprioceptive abilities and by assessing the body schema updating abilities in children with DCD.

While some daily life activities improve with age, some motor difficulties persist in adults with DCD. To our knowledge, perceptual abilities have never been investigated in adults with DCD and it is thus unknown whether perceptual deficits are still present in adulthood. This information could allow us to understand if motor difficulties in adult DCD are caused by enduring perceptual deficits and/or impaired plasticity of body schema. The second aim of this study is to evaluate abilities of perception and of body schema plasticity in adults with DCD.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

280

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

Study Contact Backup

Study Locations

    • Rhone Alpes
      • Bron, Rhone Alpes, France, 69676
        • Recruiting
        • Equipe IMPACT du CRNL INSERM U1028, CNRS UMR 5292
        • Contact:

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

9 years to 40 years (Child, Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Male or female
  • Aged 9 to 11 or 18 to 40
  • Affiliated to a health care organism
  • Signed written informed consent (adult subjects)
  • One of the legal guardians of children subjects providing their free, informed and written consent to participate in the study; With the child also giving orally his consent to participate.

For participants with Developmental coordination disorder:

  • Subjects fulfilling the diagnostic criteria for dyspraxia of DSM-5 (these criteria will be verified by the principal investigator)
  • Total MABC-2 score below the 15th percentile (if this MABC-2 assessment is already available).

Exclusion Criteria:

  • Prematurity
  • Known neurological pathology (other than dyspraxia)
  • Intellectual disability
  • Visual impairment
  • Surgery or trauma to the upper limbs that has occurred too recently to allow proper testing
  • Subject under tutorship or curatorship
  • Subject deprived of liberty by a judicial or administrative decision

For healthy volunteers only:

- History of developmental coordination disorder in close relatives (parents, children, siblings).

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: Randomized
  • Interventional Model: Factorial Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Dyspraxic children
Children with Developmental coordination disorder

In the first part of the study, the subject must designate a target in 2 ways: manual pointing or ocular saccadic response.

In the second part of the study the subject will have to reach and grasp a rectangular block of wood placed on the table at a distance of 35 cm. He will have to catch the wooden block, lift it a few centimeters and put it back on the table. Tool use and control phases: the subject grasps the wooden block with a tool or without the tool but with a weighted bracelet loading his wrist by the same amount as the tool.

Experimental: Control children
Healthy children

In the first part of the study, the subject must designate a target in 2 ways: manual pointing or ocular saccadic response.

In the second part of the study the subject will have to reach and grasp a rectangular block of wood placed on the table at a distance of 35 cm. He will have to catch the wooden block, lift it a few centimeters and put it back on the table. Tool use and control phases: the subject grasps the wooden block with a tool or without the tool but with a weighted bracelet loading his wrist by the same amount as the tool.

Experimental: Dyspraxic adults
Adults with with Developmental coordination disorder

In the first part of the study, the subject must designate a target in 2 ways: manual pointing or ocular saccadic response.

In the second part of the study the subject will have to reach and grasp a rectangular block of wood placed on the table at a distance of 35 cm. He will have to catch the wooden block, lift it a few centimeters and put it back on the table. Tool use and control phases: the subject grasps the wooden block with a tool or without the tool but with a weighted bracelet loading his wrist by the same amount as the tool.

Experimental: Control adults

In the first part of the study, the subject must designate a target in 2 ways: manual pointing or ocular saccadic response.

In the second part of the study the subject will have to reach and grasp a rectangular block of wood placed on the table at a distance of 35 cm. He will have to catch the wooden block, lift it a few centimeters and put it back on the table. Tool use and control phases: the subject grasps the wooden block with a tool or without the tool but with a weighted bracelet loading his wrist by the same amount as the tool.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Localization error distance
Time Frame: At day 1

Difference in localization error distance between manual response and ocular response: measure in mm between the target and the response of the subject.

Task 1 : proprioceptive localization with manual response Task 2 : proprioceptive localization with ocular response Task 3: tactile localization with manual response Task 4: tactile localization with ocular response

In the 4 tests, we will measure the deviation (in mm) between the localization response of the subject and the reference point.

For tasks 1 and 2, the reference point is the position of the hidden index finger of the subject.

For tasks 3 and 4, the reference point is the position of the tactile stimulation applied to the hidden arm of the subject.

For the manual response, the subject must designate with his other index finger where he considers the target to be.

For the ocular saccadic response, the subject must shift his gaze and look where he considers the target to be.

At day 1

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Reaction time of motor localization response
Time Frame: At day 1
A difference between 'go signal' and initiation of localization motor responses (Tasks 1-4) measured in msec
At day 1
change related to tool-use of amplitude of velocity peak and the peak opening of the thumb-index grip of free reach-to-grasp limb movements
Time Frame: At day 1
the subject will perform free reach-to-grasp limb movements before and after a tool-use phase (grasping a wooden block with a mechanical clamp) or a control phase (grasping the block without tool but with a bracelet loading the wrist by the same amount as the tool). For both tool-use and control conditions, the pre- versus post- difference of trajectory of free reach-to-grasp limb movements will be computed with amplitude in mm/sec of velocity peak and the peak opening of the thumb-index grip.
At day 1
change related to tool-use of latency of velocity peak and the peak opening of the thumb-index grip of free reach-to-grasp limb movements
Time Frame: At day 1
the subject will perform free reach-to-grasp limb movements before and after a tool-use phase (grasping a wooden block with a mechanical clamp) or a control phase (grasping the block without tool but with a bracelet loading the wrist by the same amount as the tool). For both tool-use and control conditions, the pre- versus post- difference of trajectory of free reach-to-grasp limb movements will be computed with latency in msec of velocity peak and the peak opening of the thumb-index grip.
At day 1
change related to tool-use of acceleration peak of the upper limb of free reach-to-grasp limb movements
Time Frame: At day 1
the subject will perform free reach-to-grasp limb movements before and after a tool-use phase (grasping a wooden block with a mechanical clamp) or a control phase (grasping the block without tool but with a bracelet loading the wrist by the same amount as the tool). For both tool-use and control conditions, the pre- versus post- difference of trajectory of free reach-to-grasp limb movements will be computed with acceleration peak in mm/sec2 of the upper limb.
At day 1
change related to tool-use of deceleration peak of the upper limb of free reach-to-grasp limb movements
Time Frame: At day 1
the subject will perform free reach-to-grasp limb movements before and after a tool-use phase (grasping a wooden block with a mechanical clamp) or a control phase (grasping the block without tool but with a bracelet loading the wrist by the same amount as the tool). For both tool-use and control conditions, the pre- versus post- difference of trajectory of free reach-to-grasp limb movements will be computed with deceleration peak in mm/sec2 of the upper limb.
At day 1

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Denis PELISSON, Dr, Centre de Recherche en Neurosciences de Lyon

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)

December 21, 2021

Primary Completion (Estimated)

January 21, 2025

Study Completion (Estimated)

January 21, 2025

Study Registration Dates

First Submitted

July 8, 2021

First Submitted That Met QC Criteria

December 10, 2021

First Posted (Actual)

December 13, 2021

Study Record Updates

Last Update Posted (Actual)

February 7, 2024

Last Update Submitted That Met QC Criteria

February 6, 2024

Last Verified

February 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 69HCL21_0338

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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