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Completed

NCT Number: NCT01868919

Triple P to Improve Behaviour in Children

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.

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Key information

Conditions

Parenting Child Behaviour Family Research Mental Health Wellness 1

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Pontificia Universidad Católica de Chile

Santiago, Santiago Metropolitan, Chile

About this study

General Purpose:

● Evaluate the pilot implementation of the Triple P program in the context of primary health care in Chile.

Specific Objectives:

  • To assess the fidelity of implementation of the Triple P program
  • Analyze the perception of participants, providers and organization on determinants of program implementation.
  • Identify barriers and facilitators to plan future implementation of Triple P program in contexts similar to those in the study.
  • To estimate the magnitude of change in children's behavior, emotional difficulties and rearing practices of caregivers before and after participation.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Positive Parenting Program

Behavioral

Level 3 or 4 of Triple P

Other names: Triple P

Primary outcomes

  1. Assess implementability of the program in primary care in terms of feasibility, acceptability and level of participation

    Time frame: After one year of implementation

    Instrument: focus groups

Secondary outcomes

  1. Percentage of change in intensity of behaviour in children

    Time frame: After one year of implementation

    Instrument: Eyberg Child Behaviour Inventory

  2. Fidelity of program implementation

    Time frame: After one year of implementation

    Supervision meetings and video recordings

Sponsors and collaborators

Lead sponsor

Pontificia Universidad Catolica de Chile

Other

Registry information

Official study title

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

Acronym: TriplePChile

Important dates

Study start
2011
Primary completion
2013
Study completion
2013
First posted
Jun 5, 2013
Registry last updated
Jun 5, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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