3D-Transition: Challenges and Resources of Children and Their Families During the Transition From Preschool to School

May 6, 2022 updated by: Jean Séguin, St. Justine's Hospital

3D-Transition Study: Challenges and Resources of Children and Their Families During the Transition From Preschool to School, in a Pregnancy Cohort

The 3D-Transition study is a follow-up of the 3D Cohort pregnancy study (NCT03113331, which covered from the 1st trimester of pregnancy to age 2 years) as the children transition into kindergarten and first grade. It aims at clarifying prenatal and preschool predictors of challenging and successful transitions to school as measured by mental health and academic outcomes.

Study Overview

Detailed Description

Broad goal: This study seeks to understand how early vulnerabilities (externalizing or internalizing symptoms, or low neurodevelopmental/academic skills) turn into a rate of 10-15% of externalizing and internalizing mental health problems in school-aged children.

Rationale: Several lines of research guide this study. Functional impairments emerge for some children challenged by the transition to kindergarten and grade school. This risk is also thought to be programmed very early in life through cumulative early perinatal and psychosocial adversity. Further, interactions between the child, family and school environment during the transition may mitigate future impairments and this may be different for boys and girls. Finally, stress regulation mechanisms during the transition seem linked to early child vulnerabilities. This design allows us to contrast any combination of these mechanisms.

Aims: This study will clarify the role of:

  1. a mismatch between some child preschool vulnerability (externalizing, or internalizing symptoms, or low neurodevelopmental/academic skills) and the challenges of the transition from preschool to formal schooling;
  2. the experience of perinatal adversity and home chaos during child first years;
  3. supportive environments (high quality families or schools) during the school transition, and child sex; and
  4. the child stress response to the school transition, as assessed through salivary cortisol.

Method: Building on an existing pregnancy cohort (NCT03113331, which was structured around a triadic (mother-partner-child) framework, and which covered from the 1st trimester of pregnancy to age 2 years), the investigators have followed at least once 939 of 1551 families that agreed to a further follow-up past the initial study. Children in this cohort, who were seen in 3 waves based on age on September 30th, entered kindergarten in the fall of 2016, 2017, and 2018, respectively. A cohort-sequential longitudinal research design spanning pre-kindergarten to 2nd grade (ages 4 to 8 years), was implemented to follow each wave 6 times over 4 years. Cascade models will be used to address aims 1-3. The stress hormone cortisol will be examined on 11 days spread over a 16 months period for a subsample of 384 children to address aim 4, using growth curves models. This design is well suited and sufficiently powered to examine change processes over time, controlling for potential differences in waves and time of measurement effects.

Additional data: The Research Ethics Committee authorized two Corona Virus (COVID-19) supplemental data collections without additional consent for the spring of 2020 and the spring of 2021. However, cohorts 1 and 2, which had completed participation in 2019 and 2020, were re-consented, and this extended the maximum age range to 10 and 9 years, respectively. As of 2022-05-03 investigators are in the process of requesting approval for an additional COVID-19 follow-up.

Expected outcomes: Public health interventions are being put in place to help children manage the transition to school on the basis of little evidence. This longitudinal research will provide a greater understanding of individual and environmental factors linked to children's adaptation during the perinatal period and transitions to school. As such, mental health prevention research will be better informed on the developmental timing of individual and environmental targets that need to be considered in a developmental framework.

Study Type

Observational

Enrollment (Actual)

939

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Quebec
      • Montréal, Quebec, Canada, H3T 1C5
        • CHU Ste-Justine Research Center
      • Québec, Quebec, Canada, G1V 4G2
        • CHU de Quebec-Universite Laval
      • Sherbrooke, Quebec, Canada, J1H 5N4
        • Universite de Sherbrooke

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

4 years to 10 years (Child)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

General population sample from the main university hospitals affiliated with the province of Québec, Canada's 4 faculties of medicine between November 2010 and March 2013, included.

Description

Inclusion Criteria:

  • All participating families from Clinical Trials NCT03113331 who had accepted a follow-up past the original pregnancy to age 2-years time span of that protocol.

Exclusion Criteria:

  • None for this follow up. See Clinical Trials NCT03113331 for original exclusion criteria.

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

Cohorts and Interventions

Group / Cohort
Cohort 1
These are the eldest children who entered kindergarten in September 2016.
Cohort 2
These children entered kindergarten in September 2017.
Cohort 3
These are the youngest children who entered kindergarten in September 2018

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Mental health: Change in child mental health represented by one latent symptom score of the overarching category: externalizing symptoms.
Time Frame: Six times across 4 years, in the spring during Pre-Kindergarten, then in the fall and spring of Kindergarten and Grade 1, then in the spring of Grade 2

The latent factor will be based on three informants which provide these mental health symptom ratings: mother-, father-, and teacher-reports as measured with age-appropriate non-overlapping items from the externalizing symptoms scales of:

i) the Strengths and Difficulties Questionnaire (SDQ) ii) the Child Behavior Checklist (CBCL) iii) the Behavior scale of the Quebec Longitudinal Study of Child Development (QLSCD).

Six times across 4 years, in the spring during Pre-Kindergarten, then in the fall and spring of Kindergarten and Grade 1, then in the spring of Grade 2
Mental health: Change in child mental health represented by one latent symptom score of the overarching category: internalizing symptoms.
Time Frame: Six times across 4 years, in the spring during Pre-Kindergarten, then in the fall and spring of Kindergarten and Grade 1, then in the spring of Grade 2

The latent factor will be based on three informants which provide these mental health symptom ratings: mother-, father-, and teacher-reports as measured with age-appropriate non-overlapping items from the externalizing symptoms scales of:

i) the Strengths and Difficulties Questionnaire (SDQ) ii) the Child Behavior Checklist (CBCL) iii) the Behavior scale of the Quebec Longitudinal Study of Child Development (QLSCD).

Six times across 4 years, in the spring during Pre-Kindergarten, then in the fall and spring of Kindergarten and Grade 1, then in the spring of Grade 2
Neurodevelopment - Change in executive function
Time Frame: Yearly, across 3 years: in Pre-Kindergarten, Kindergarten and Grade 1

Change in one latent factor score of executive function based on the following tasks:

  1. Dimensional Change Card Sort (DCCS) measuring degree of cognitive flexibility
  2. Random Object Span Task (ROST), a child version of the Self-Ordered Pointing (SOP) test measuring degree of working memory.
  3. Wechsler's Digit Span subtest measuring degree of working memory.
Yearly, across 3 years: in Pre-Kindergarten, Kindergarten and Grade 1
Neurodevelopment - Change in visuo-spatial ability
Time Frame: Yearly, across 3 years: in Pre-Kindergarten, Kindergarten and Grade 1
Change in visuo-spatial ability based on the Wechsler's Block Design subtest.
Yearly, across 3 years: in Pre-Kindergarten, Kindergarten and Grade 1
Neurodevelopment - Change in visuo-motor integration
Time Frame: Yearly, across 2 years: in Pre-Kindergarten and in Kindergarten
Change on the Beery Visuo-Motor integration subtest.
Yearly, across 2 years: in Pre-Kindergarten and in Kindergarten
Neurodevelopment - Change in social cognition
Time Frame: Yearly, across 3 years: in Pre-Kindergarten, Kindergarten and Grade 1
Change in social cognition based on a latent factor of 1st and 2nd order Theory Of Mind (TOM) tests.
Yearly, across 3 years: in Pre-Kindergarten, Kindergarten and Grade 1
Neurodevelopment - Change in emotional development
Time Frame: Yearly, across 3 years: in Pre-Kindergarten, Kindergarten and Grade 1
Change on the Pons and Harris (2000) Test of Emotion Comprehension (TEC) score.
Yearly, across 3 years: in Pre-Kindergarten, Kindergarten and Grade 1
Academic skills scores - Change in school readiness
Time Frame: Yearly, across 2 years: in Pre-Kindergarten and Kindergarten
Change in the total score of The Lollipop Test comprising 4 dimensions: 1) Identification of Colors and Shapes, and Copying Shapes, 2) Picture Description, Position, and Spatial Recognition, 3) Identification of Numbers, and Counting, and 4) Identification of Letters, and Writing.
Yearly, across 2 years: in Pre-Kindergarten and Kindergarten
Academic skills scores- Change in Number Knowledge abilities
Time Frame: Yearly, across 3 years: in Pre-Kindergarten, Kindergarten and Grade 1
Change in a score combining The Number Knowledge Test (NKT) and the Mathematics subtest of the Canadian Achievement Test (CAT).
Yearly, across 3 years: in Pre-Kindergarten, Kindergarten and Grade 1
Academic skills scores - Change in receptive vocabulary
Time Frame: Yearly, across 3 years: in Pre-Kindergarten, Kindergarten and Grade 1
Change in the total score of the Peabody Picture Vocabulary Test (PPVT) in French or English versions.
Yearly, across 3 years: in Pre-Kindergarten, Kindergarten and Grade 1
Academic skills scores - Change in Reading ability
Time Frame: Grade 1 only
The Kaufman Assessment Battery for Children (K-ABC) reading ability test score in French or English versions.
Grade 1 only
Academic skills scores - Change in academic performance.
Time Frame: Yearly, across 2 years: in Grades 1 and 2
Change in teacher reports on child academic achievement.
Yearly, across 2 years: in Grades 1 and 2
Change in Morning and evening salivary cortisol levels
Time Frame: Pre-Kindergarten to Grade 1 (Across a 16 months period from June in Year 1 to September in Year 2)
A subsample of 382 (out of 400 targeted) from cohorts 2 and 3 participated in a measurement burst design of 11 measurement days (2 samples/day), in June and August preceding entry into kindergarten (baseline), then twice one week apart at kindergarten entry in early September, then first Wednesday in each of November, February, and April. The following June, August, and early September measures were then repeated as the children moved towards entry to 1st grade.
Pre-Kindergarten to Grade 1 (Across a 16 months period from June in Year 1 to September in Year 2)

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Jean R. Séguin, Ph.D., CHU Ste-Justine Research Center and Université de Montréal
  • Principal Investigator: Sophie Parent, Ph.D., CHU Ste-Justine Research Center and Université de Montréal
  • Principal Investigator: Natalie Castellanos-Ryan, Ph.D., CHU Ste-Justine Research Center and Université de Montréal

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)

May 1, 2017

Primary Completion (Anticipated)

December 21, 2022

Study Completion (Anticipated)

December 21, 2022

Study Registration Dates

First Submitted

April 13, 2021

First Submitted That Met QC Criteria

May 4, 2021

First Posted (Actual)

May 5, 2021

Study Record Updates

Last Update Posted (Actual)

May 12, 2022

Last Update Submitted That Met QC Criteria

May 6, 2022

Last Verified

May 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • MP-21-2017-1461
  • PJT-148551 (Other Grant/Funding Number: Canadian Institutes for Health Research)
  • PJT-165824 (Other Grant/Funding Number: Canadian Institutes for Health Research)
  • CRI-88413 (Other Grant/Funding Number: Canadian Institutes for Health Research)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

The procedures by which de-identified data will be accessible are being clarified as rules and regulations are currently under study in this jurisdiction. In the meantime the investigators can be contacted for updates - see "More information"

IPD Sharing Time Frame

Partial data from earlier waves may be available upon request. The bulk of the data should be available by March 2023.

IPD Sharing Access Criteria

Data are under the jurisdiction of the Centre Hospitalier Universitaire (CHU) Ste-Justine Research Ethics Committee and subject to current provincial and national privacy laws guiding their ethical use in Québec, Canada. To submit a request, please visit the 3D-Cohort Study website or contact the principal investigator.

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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