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Triple P to Improve Behaviour in Children

Implementation Research of a Parenting Intervention to Improve Behaviour in Children in Primary Care

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01868919
Acronym
TriplePChile
Enrollment
87
Registered
2013-06-05
Start date
2011-11-30
Completion date
2013-05-31
Last updated
2013-06-05

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

Conditions

Child Behaviour, Family Research, Mental Health Wellness 1, Parenting

Keywords

Pilot Projects[Mesh], Parenting[Mesh], Child Behaviour[Mesh], Mental Health[Mesh], Family Practice[Mesh]

Brief summary

Joint research (quantitative and qualitative methodology) with quasi-experimental design, before-after without control group to evaluate the pilot implementation of Positive Parenting Program (Triple P) in the context of primary health care in Chile. The hypothesis is that the program is feasible and acceptable to the Chilean population.

Detailed description

General Purpose: ● Evaluate the pilot implementation of the Triple P program in the context of primary health care in Chile. Specific Objectives: 1. To assess the fidelity of implementation of the Triple P program 2. Analyze the perception of participants, providers and organization on determinants of program implementation. 3. Identify barriers and facilitators to plan future implementation of Triple P program in contexts similar to those in the study. 4. To estimate the magnitude of change in children's behavior, emotional difficulties and rearing practices of caregivers before and after participation.

Interventions

Level 3 or 4 of Triple P

Sponsors

Pontificia Universidad Catolica de Chile
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Parents or caregivers of children from 2 to 10 years old attending primary care clinic * Parents or caregivers must be worried about child behaviour or their parenting skills and be willing to get professional help

Exclusion criteria

* Children: Pervasive Developmental Disorder, severe intellectual disability or severe psychopathology * Caregivers: illiteracy, decompensated severe psychopathology or current psychotherapy

Design outcomes

Primary

MeasureTime frameDescription
Assess implementability of the program in primary care in terms of feasibility, acceptability and level of participationAfter one year of implementationInstrument: focus groups

Secondary

MeasureTime frameDescription
Percentage of change in intensity of behaviour in childrenAfter one year of implementationInstrument: Eyberg Child Behaviour Inventory
Fidelity of program implementationAfter one year of implementationSupervision meetings and video recordings

Countries

Chile

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026