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A Targeted Prevention Approach to Reducing Child Emotional and Behaviour Problems

Making the Race Fair for Young Children at Risk: A Targeted Prevention Approach to Reducing Child Emotional and Behaviour Problems

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02800603
Enrollment
207
Registered
2016-06-15
Start date
2017-08-18
Completion date
2020-06-30
Last updated
2020-09-02

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

Conditions

Behavior Problems, Emotional Problems

Keywords

preschool mental health, emotional and behaviour problems

Brief summary

The purpose of the study is to evaluate the first Canadian implementation project of the Family Check up (FCU), an evidence-based prevention and early intervention model that engages families and communities in reducing the burden of childhood emotional and behaviour problems (EBP).

Detailed description

The aim of this study is to establish and evaluate the first Canadian implementation project of the FCU as an evidence-based prevention and early intervention model that engages families and communities in reducing the burden of childhood EBP. These objectives will be achieved in two foundational phases. During Phase 1, the clinical and systems infrastructure required to deliver, sustain and ultimately scale up the FCU will be built. During Phase 2, a 1:1 randomized controlled trial (RCT) will be conducted. The RCT will involve 280 participating caregiver-child dyads to examine the effects of the FCU as a targeted prevention intervention within the Canadian context, as delivered to caregivers and children aged 2-4 years at high risk of persistent childhood EBP. Phase 1: Training, and Implementation: The REACH Institute at Arizona State University has developed an efficient model for international implementation of the FCU. They will help implement the intervention within McMaster Children's Hospital (MCH), train MCH therapists as FCU consultants, and two trainers. All therapists will be credentialed as FCU consultants by REACH through a process of supervision, consultation and monitoring of therapeutic fidelity. Phase 2: Investigators will conduct a 1:1 randomized controlled trial of 280 children aged 2-4 years into either the FCU (n=140) or community control (CC, n=140). All 280 participants will undergo screening and a baseline FCU assessment before randomization. Once randomized, the FCU group will be provided with a feedback visit and up to 6 optional sessions of the Everyday Parenting (EDP) curriculum over 16 weeks. The CC group will receive general information about currently available community services in Hamilton. At 6 months, both groups will undergo light assessments. At 12 months both groups will repeat the baseline assessment, and the FCU group will have 1-2 FCU visits.

Interventions

BEHAVIORALFamily Check Up

The FCU is an ecologically sensitive, evidence-based, targeted intervention that aims to reduce child EBP. Features of the FCU: 1) Assessment-driven: a multi-method, multi-informant assessment in which the consultant reviews strengths and difficulties across domains of contextual risk, family functioning and child health. A tailored intervention plan is then created based on results 2) Motivational interviewing: Caregivers engage in self-assessment about motivation and barriers to addressing factors that may perpetuate risk. The consultant and caregiver work to establish a menu of services 3) The family may be offered up to 6 sessions of the Everyday Parenting curriculum. The FCU has demonstrated effectiveness and cultural sensitivity across multiple US settings.

Sponsors

Hamilton Health Sciences Corporation
CollaboratorOTHER
Arizona State University
CollaboratorOTHER
University of Calgary
CollaboratorOTHER
Simon Fraser University
CollaboratorOTHER
McMaster University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
2 Years to 4 Years
Healthy volunteers
No

Inclusion criteria

Screening eligibility criteria include: 1. Custodial caregivers of a child aged 2 years, 0 months to 4 years, 11 months. 2. Definition of at-risk for child EBP as measured by (a) OR (b): * Elevated child EBP as indexed by above-population mean total scores on Strengths and Difficulties Questionnaire (SDQ), plus one of the following family or contextual risk factors * Caregiver challenges: teen parent status, caregiver mental health problems (as indexed by K6 psychological distress scale), lone caregiver * Sociodemographic risk factors (as indexed by the 2014 Ontario Child Health Study (OCHS) demographics questionnaire): family income below low-income cut-off (LICO), caregiver with less than grade 12 education, caregiver on social assistance. * Families who score within norms on caregiver or sociodemographic risk AND child SDQ scores fall within the high range, indicating significant burden of EBP (and thus increased risk of persistent, severe problems over time). 3. Caregivers with sufficient knowledge of English needed for assessment measures 4. Caregivers capable of giving informed, written consent

Exclusion criteria

1. Children with suspected severe to profound developmental delay 2. Current enrolment in another clinical intervention trial 3. Caregiver or child with a serious medical condition that, based on Investigator judgment, might interfere with the conduct of the study, confound interpretation of the study results, or endanger their own well-being

Design outcomes

Primary

MeasureTime frameDescription
Primary Outcome- Change in Child Externalizing BehaviorsPrimary outcome will be measured at baseline, 6- and 12-months after enrollmentChange in Child Behavior Checklist (CBCL) scores

Secondary

MeasureTime frameDescription
Secondary Outcome - Change in Parental Mental HealthThis will be measured at baseline, 6- and 12-monthsThe Kessler-6 (K6) will be used to measure change in psychological distress over time
Secondary Outcome - Change in Parental StressThis will be measured at baseline and 12-monthsParenting Daily Hassles will be used to measure changes in parental stress over time
Secondary Outcome - Change in Positive Parenting PracticeThis will be measured at baseline and 12-monthsPositive parenting practice will be coded from videotaped parent-child interactions - outcome is change in positive parenting practice over time
Secondary Outcome - Change in Child ComplianceThis will be measured at baseline and 12-monthsThe Coder Impressions Inventory (COIMP) will be used to score the child's behaviour from videotaped interactions - outcome is change in behaviour over time

Other

MeasureTime frameDescription
Exploratory outcome - Change in Child Executive FunctioningThis will be measured at baseline and at 12 months.Child executive functioning will be assessed using observation of structured tasks
Exploratory outcome - Health Service UtilizationThis will be measured at baseline, 3-, 6-, 9- and 12- months.Service utilization questionnaire
Exploratory outcome - Change in Hair CortisolThis will be measured at baseline, 6-months and 12 months.Small amounts of hair will be collected from child and parents to assess hair cortisol
Exploratory outcome - Change in Behavioural Observations of ParentingThis will be measured at baseline, 6-months and 12 months.Behavioural Observations of Parenting will be assessed using videotapes of structured interaction between the child and parent
Exploratory outcome - Change in Parental Emotional RegulationExploratory outcomes will be measured at baseline and at 12 months.Difficulties in Emotion Regulation Scale (DERS)
Exploratory outcome - Change in Child Emotional RegulationThis will be measured at baseline and at 12 months.Child emotional regulation will be assessed using videotapes of the child performing structured tasks
Exploratory outcome -Parent Executive FunctioningThis will be measured at baseline.Parent executive functioning will be assessed using observation of structured tasks

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026