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Effects of Acute Exercise on Motor Learning and Brain Activity in Children With DCD

Study Protocol to Examine the Effects of Acute Exercise on Motor Learning and Brain Activity in Children With Developmental Coordination Disorder (ExLe-Brain-DCD)

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05936372
Acronym
ExLeBrainDCD
Enrollment
120
Registered
2023-07-07
Start date
2024-02-05
Completion date
2025-06-30
Last updated
2024-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Developmental Coordination Disorder

Keywords

Visuomotor adaptation, Attention, Physical exercise, Functional near-infrared spectroscopy (fNIRS), Cortical activation, Prefrontal cortex, Children

Brief summary

The aim of this study is to investigate the impact of an acute intense physical exercise bout on the learning ability of children with typical motor development (TD) and children with developmental coordination disorder (DCD). The effects will be studied during the learning and in the short- (1 hour), medium- (24 hours), and long-terms (7 days) after the initial learning. Participants will be divided into 4 groups: children with typical development who will exercise (EX-TD), children with developmental coordination disorder who will exercise (EX-DCD), children with typical development who will not exercise (CON-TD), and children with developmental coordination disorder who will not exercise (CON-DCD). Participants will be enrolled for 4 different sessions: Session 1: First, participants will do a test to asses their cognitive ability and their height and weight will be measured. Then, participants will run a race test to assess their level of physical condition and to calculate high and moderate intensities of the exercise bout. The test will consist of running from one side to the other of a 20 m long track, while following the rhythm set by a sound. Session 2: at least 48 hours after the first one, the participants will do an exercise bout running from side to side of a 20 m long track alternating high and moderate intensities during 13 min. The members of the control groups (CON-TD and CON-DCD) will not perform this exercise and, instead, will remain at rest for a time equivalent to the exercise of the other groups. On the other hand, participants will perform a learning task involving hand-eye coordination, in which participants will control the movements of a circle on a computer screen using a joystick. The objective of this task will be to move the circle to target points that will appear on the screen with the maximum accuracy and speed possible. Participants will be asked to practice this task for approximately 8 min. Then, after a 1-hour rest period, the participants will be asked to perform the learning task again (only 3.5 min) to check the level of retention of the initial learning. A headcap will be adjusted on the head of the participants during the motor task performance to measure the activity of the brain through infrared light. Sessions 3 and 4: participants will complete two retention tests of the learning task (one in each session) 24 hours and 7 days after the second session, respectively. Participants will also wear the headcap for the brain activity measurements.

Interventions

BEHAVIORALAcute intense aerobic exercise

The acute intense aerobic exercise bout (iE) will consist of a 13-minute 20-meter shuttle run. During this exercise bout two speeds, based on a percentage of the estimated maximal oxygen consumption (VO2max), will be combined: a fast-paced speed (fast: 85% of VO2max) and a slow-paced speed (slow: 60% VO2max). A total of 3 series of 3 min of the fast-paced speed will be carried interspersed with 2 series of 2 min of the slow-paced speed. Prior to the iE start, a warm-up protocol consisting of 2 min slow and 1 min fast will be done with the objective to familiarize participants with the iE speeds. A 5-minute rest period will be guaranteed before starting the iE. Transition time between iE and the rotational visuomotor adaptation task (rVMA) will be 4 min.

Sponsors

ICFO - The Institute of Photonic Sciences
CollaboratorUNKNOWN
Ministerio de Ciencia e Innovación, Spain
CollaboratorOTHER_GOV
University of Stuttgart
CollaboratorOTHER
The University of Texas at Arlington
CollaboratorOTHER
Institut Nacional d'Educacio Fisica de Catalunya
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
90 Months to 126 Months
Healthy volunteers
Yes

Inclusion criteria

* Movement assessment battery for children - second edition (MABC-2) score: developmental coordination disorder (DCD) group score \<15% and typically developed (TD) group score \>25% * An average or better cognitive ability tested through the Test of Nonverbal Intelligence version 4 (TONI-4) * A parent-report history to confirm that, according to the child's pediatrician, motor difficulties showed by their child cannot be explained by any other neurological, developmental, and/or severe psychosocial problem. Comorbid attention deficit hyperactivity disorder, attention deficit disorder, and dyslexia will be acceptable in order to better represent the DCD population since data population-based studies suggest that almost 40% of the children with DCD have combined problems related to learning and/or attentional disorders.

Exclusion criteria

* Participant health status do not allow hem/her to participate in physical activities (Physical Activity Readiness Questionnaire, PAR-Q) * Other comorbidities than attention deficit hyperactivity disorder, attention deficit disorder, and/or dyslexia * Reported neurological, developmental, and/or severe psychosocial problem that could explain the motor development problem * Participant that takes medication that could affect results * Uncorrected 20/20 vision

Design outcomes

Primary

MeasureTime frameDescription
relative deoxyhemoglobin concentration ([HHb]) in the dorsolateral prefrontal cortex0, 1, and 24 hours, and 7 daysNeural activation of each cortical area will be expressed as a relative decrease of deoxyhemoglobin concentration (\[HHb\]) measured by functional near-infrared spectroscopy (fNIRS).
relative oxyhemoglobin concentration ([02Hb]) in the ventrolateral prefrontal cortex0, 1, and 24 hours, and 7 daysNeural activation of each cortical area will be expressed as a relative increase of oxyhemoglobin concentration (\[02Hb\]) measured by functional near-infrared spectroscopy (fNIRS).
relative oxyhemoglobin concentration ([02Hb]) in the dorsolateral prefrontal cortex0, 1, and 24 hours, and 7 daysNeural activation of each cortical area will be expressed as a relative increase of oxyhemoglobin concentration (\[02Hb\]) measured by functional near-infrared spectroscopy (fNIRS).
relative deoxyhemoglobin concentration ([HHb]) in the ventrolateral prefrontal cortex0, 1, and 24 hours, and 7 daysNeural activation of each cortical area will be expressed as a relative decrease of deoxyhemoglobin concentration (\[HHb\]) measured by functional near-infrared spectroscopy (fNIRS).
initial directional error0, 1, and 24 hours, and 7 daysInitial directional error (IDE) will be calculated as the absolute angular difference between the ideal trajectory, a linear vector from the center to the target, and the early real trajectory, defined by the linear vector from the center to the cursor position at the time of 80 ms after movement onset.
root mean square error0, 1, and 24 hours, and 7 daysRoot mean square error (RMSE) will be calculated to represent the straightness of the movement between the ideal trajectory and the real joystick trajectory.
initial rate of learning0, 1, and 24 hours, and 7 daysThe initial rate of learning (RL) will be computed as the first derivative of the first half of the function and evaluated at epoch 1 for both error variables initial directional error (RL-IDE) and root mean square error (RL-RMSE).

Secondary

MeasureTime frameDescription
travel distance0, 1, and 24 hours, and 7 daysDisplacement of the cursor from its initial position to its final position
reaction time0, 1, and 24 hours, and 7 daysReaction time will be defined as the time between target appearance and movement onset.
movement time0, 1, and 24 hours, and 7 daysTime spend moving the cursor from its initial position to its final position

Countries

Spain

Contacts

Primary ContactAlbert Busquets Faciaben, PhD
albert.busquets@gencat.cat+34934255445
Backup ContactBlai Ferrer Uris, PhD
bferrer@gencat.cat+34934255445

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026