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Triple P to Improve Behaviour in Children

Not Applicable
Completed
Conditions
Parenting
Child Behaviour
Mental Health Wellness 1
Family Research
Interventions
Behavioral: Positive Parenting Program
Registration Number
NCT01868919
Lead Sponsor
Pontificia Universidad Catolica de Chile
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.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
87
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Positive Parenting ProgramPositive Parenting ProgramLevel 3 or 4 of Triple P
Primary Outcome Measures
NameTimeMethod
Assess implementability of the program in primary care in terms of feasibility, acceptability and level of participationAfter one year of implementation

Instrument: focus groups

Secondary Outcome Measures
NameTimeMethod
Percentage of change in intensity of behaviour in childrenAfter one year of implementation

Instrument: Eyberg Child Behaviour Inventory

Fidelity of program implementationAfter one year of implementation

Supervision meetings and video recordings

Trial Locations

Locations (1)

Pontificia Universidad Católica de Chile

🇨🇱

Santiago, Chile

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