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Promoting Healthy Families: A Canadian Evaluation (PHF)

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McMaster University

Status

Completed

Conditions

Parenting
Child Behavior Problem

Treatments

Behavioral: Triple P
Behavioral: Circle of Security Parenting

Study type

Interventional

Funder types

Other

Identifiers

NCT04702191
10583 (Registry Identifier)

Details and patient eligibility

About

Interventions that promote safe, stable, and nurturing relationships between caregivers and children are key to improving healthy family relationships, reducing child socioemotional and behaviour problems, and preventing child maltreatment. Although a broad range of parenting programs are currently implemented in communities across Ontario, most programs are inadequately evaluated, or else not evaluated at all. Using a three-armed randomized controlled trial, the aim of the current study is to evaluate the effectiveness of two parenting programs, the Triple P - Positive Parenting Program (group - level 4) and the Circle of Security Parenting Program (group) compared to treatment as usual in Ontario, Canada.

Full description

The overall goal of the evaluation is to provide robust evidence about the implementation and effectiveness of two parenting programs, the Triple P and Circle of Security Parenting (COSP), in the province of Ontario, on parenting practices and functioning, and child emotional behaviour problems outcomes, and secondary outcomes including selected child maltreatment-related outcomes. These objectives will be achieved in two phases. The investigators will conduct a multi-site, three-arm randomized controlled trial of 600 participating caregivers and their children to compare Triple P (level 4 group) and COSP to treatment as usual (TAU) with respect to improving positive practices and child outcomes. Participants will be randomly assigned to one of the three conditions using stratified (by site) block randomization. All participants will undergo screening and a baseline assessment before randomization. Once randomized, the Triple P and COSP caregivers will receive 8-week session. The TAU group will receive a different program, or short therapy sessions depending on the organization. Caregivers will complete follow-up assessments at post-treatment, 6- and 12-months.

Enrollment

502 patients

Sex

All

Ages

2 to 6 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Caregivers of children are eligible for inclusion if:

  • Custodial caregiver of child is aged 2 to 6 years at time of screening.

  • Families with sufficient knowledge of English needed for assessment measures.

  • Caregivers capable of giving informed, written consent.

  • Definition of 'at-risk' as measured by one of the following criteria as outlined below:

    • Elevated child emotional behavioural problems as indexed by above- population mean total scores on the Strengths and Difficulties Questionnaire (SDQ); OR
    • One of the following family or contextual risk factor
    • Parental challenge - parental mental health problems, as indexed by score on K6 distress scale ≥ 13; adolescent parent status (less than 20 years of age); single parent status; OR Sociodemographic risk factor - parent with less than grade 12 education; parent on social assistance;
    • Expressed difficulties with parenting: Do you often feel like your child is difficult to take care of?

Exclusion criteria

• Children with suspected severe to profound developmental delay.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

502 participants in 3 patient groups

Triple P (Positive Parenting Program)
Experimental group
Description:
Triple P - level 4 group: All 600 participants will undergo screening and a baseline assessment before randomization. Once randomized, the Triple P group (n=200) will be provided with 8-week group/individual sessions.
Treatment:
Behavioral: Triple P
Circle of Security Parenting
Experimental group
Description:
Circle of Security - Parenting (COS-P): Once randomized to the COSP group (n=200), caregivers will be provided with an 8-week group session.
Treatment:
Behavioral: Circle of Security Parenting
Treatment As Usual
No Intervention group
Description:
Treatment as usual: Caregivers randomized to this arm (n=200) will receive either a different program, or brief services depending on the organization.

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Andrea Gonzalez, PhD

Data sourced from clinicaltrials.gov

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