Actively Recruiting

Age: 7Years - 13Years
All Genders
Healthy Volunteers
ID06330090

Cognitive Dynamics in Early Childhood

Led by Radboud University Medical Center · Updated on 2025-04-11

600

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating cognitive variability in children aged 7 to 10 at their first assessment. This observational study aims to understand how cognitive differences vary between individuals, explore the brain, psychological, and environmental factors influencing these differences, and examine the long-term effects and outcomes related to cognitive variability. The study uses advanced methods including experience sampling, longitudinal designs, and deep phenotyping to answer these questions. Participants may take part in either a behavioural or a behavioural with imaging arm. The behavioural arm includes children aged 7 to 10, while the imaging arm is for children aged 8 to 10 at the first assessment. The imaging arm involves MRI scans such as MP-RAGE, diffusion weighted imaging, and functional MRI during cognitive tasks. Assessments are done at baseline and followed up two years later for imaging, with cognitive task reaction times and questionnaire scores tracked through an average of three years. During the study, children will complete various cognitive tasks measuring reaction times in vocabulary, working memory, speed, fluid reasoning, and exploration. Mood and sleep scores are also tracked using smiley sliders. Imaging participants will undergo baseline and follow-up MRI scans with naturalistic viewing and reasoning tasks. Parents will provide questionnaire data and reaction times on cognitive tasks. Researchers will assess cognitive performance, brain activity, psychological traits, and environmental factors to understand cognitive variability and its outcomes over time.

CONDITIONS

Brief Title

COgnitive Dynamics in Early Childhood

Who Can Participate

Age: 7Years - 13Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Children between 7 and 10 years old for the behavioural part of the study
  • Children between 8 and 10 years old for the imaging part of the study
Not Eligible

You will not qualify if you...

  • Not understanding instructions for behavioural tasks due to a language barrier
  • History of neurological or psychiatric illness (imaging arm)
  • History of using psychotropic medications (imaging arm)
  • Contraindications for MRI (imaging arm)
  • Presence of metal parts on or in the upper body that cannot be removed (except dental fillings, crowns, metal wire behind teeth, tattoos, contraceptive coils) (imaging arm)
  • Metal fragments in the body, especially in the eye (imaging arm)
  • History of brain surgery (imaging arm)
  • Having active implants such as pacemaker, neurostimulator, insulin pump, or ossicle prosthesis (imaging arm)
  • Using medical plasters that cannot or should not be removed (e.g., nicotine plaster) (imaging arm)

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Approximately 1 year

Participants undergo baseline cognitive and imaging assessments including MRI scans and behavioral tests.

1 baseline visit (in-person)

Long-term Monitoring

Duration - Up to 3 years

Participants are observed over time with repeated cognitive assessments and questionnaires to track changes.

Repeated assessments throughout the study period

Diagnostic Evaluation

Duration - 1 day

Participants complete follow-up cognitive and imaging assessments two years after baseline.

1 follow-up visit (in-person) at two years after baseline

Trial Site Locations

Total: 1 location

1

Radboudumc Department of Cognitive Neuroscience

Nijmegen, Netherlands, 6525 EN

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Research Team

R

Rogier Kievit

I

Ilse Coolen

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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Published Research Related To This Trial

Protocol and preregistration for the CODEC project: measuring, modelling and mechanistically understanding the nature of cognitive variability in early childhood.

Ilse E J I Coolen, Jordy van Langen, Sophie Hofman...

https://pubmed.ncbi.nlm.nih.gov/39060934