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

Sponsor
St. Justine's Hospital (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT04873518
Collaborator
Canadian Institutes of Health Research (CIHR) (Other), Université de Sherbrooke (Other), CHU de Quebec-Universite Laval (Other), Université de Montréal (Other), Laval University (Other)
939
3
67.7
313
4.6

Study Details

Study Description

Brief Summary

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.

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 Design

Study Type:
Observational
Actual Enrollment :
939 participants
Observational Model:
Family-Based
Time Perspective:
Prospective
Official Title:
3D-Transition Study: Challenges and Resources of Children and Their Families During the Transition From Preschool to School, in a Pregnancy Cohort
Actual Study Start Date :
May 1, 2017
Anticipated Primary Completion Date :
Dec 21, 2022
Anticipated Study Completion Date :
Dec 21, 2022

Arms and Interventions

Arm Intervention/Treatment
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

Outcome Measures

Primary Outcome Measures

  1. Mental health: Change in child mental health represented by one latent symptom score of the overarching category: externalizing symptoms. [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).

  2. Mental health: Change in child mental health represented by one latent symptom score of the overarching category: internalizing symptoms. [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).

  3. Neurodevelopment - Change in executive function [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: Dimensional Change Card Sort (DCCS) measuring degree of cognitive flexibility Random Object Span Task (ROST), a child version of the Self-Ordered Pointing (SOP) test measuring degree of working memory. Wechsler's Digit Span subtest measuring degree of working memory.

  4. Neurodevelopment - Change in visuo-spatial ability [Yearly, across 3 years: in Pre-Kindergarten, Kindergarten and Grade 1]

    Change in visuo-spatial ability based on the Wechsler's Block Design subtest.

  5. Neurodevelopment - Change in visuo-motor integration [Yearly, across 2 years: in Pre-Kindergarten and in Kindergarten]

    Change on the Beery Visuo-Motor integration subtest.

  6. Neurodevelopment - Change in social cognition [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.

  7. Neurodevelopment - Change in emotional development [Yearly, across 3 years: in Pre-Kindergarten, Kindergarten and Grade 1]

    Change on the Pons and Harris (2000) Test of Emotion Comprehension (TEC) score.

  8. Academic skills scores - Change in school readiness [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.

  9. Academic skills scores- Change in Number Knowledge abilities [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).

  10. Academic skills scores - Change in receptive vocabulary [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.

  11. Academic skills scores - Change in Reading ability [Grade 1 only]

    The Kaufman Assessment Battery for Children (K-ABC) reading ability test score in French or English versions.

  12. Academic skills scores - Change in academic performance. [Yearly, across 2 years: in Grades 1 and 2]

    Change in teacher reports on child academic achievement.

  13. Change in Morning and evening salivary cortisol levels [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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
4 Years to 10 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHU Ste-Justine Research Center Montréal Quebec Canada H3T 1C5
2 CHU de Quebec-Universite Laval Québec Quebec Canada G1V 4G2
3 Université de Sherbrooke Sherbrooke Quebec Canada J1H 5N4

Sponsors and Collaborators

  • St. Justine's Hospital
  • Canadian Institutes of Health Research (CIHR)
  • Université de Sherbrooke
  • CHU de Quebec-Universite Laval
  • Université de Montréal
  • Laval University

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

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Jean Séguin, Researcher, St. Justine's Hospital
ClinicalTrials.gov Identifier:
NCT04873518
Other Study ID Numbers:
  • MP-21-2017-1461
  • PJT-148551
  • PJT-165824
  • CRI-88413
First Posted:
May 5, 2021
Last Update Posted:
May 12, 2022
Last Verified:
May 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Jean Séguin, Researcher, St. Justine's Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 12, 2022