Triple P to Improve Behaviour in Children

Parenting Clinical Trial

— TriplePChile  

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01868919
• Other study ID #: TRIPLEP.PUC.CHILE
• Status: Completed
• Phase: N/A
• First received: January 19, 2013
• Last updated: May 30, 2013
• Start date: November 2011
• Est. completion date: May 2013

Study information

• Verified date: May 2013
• Source: Pontificia Universidad Catolica de Chile
• Contact: n/a
• Is FDA regulated: No
• Health authority: Chile: Institutional Review Board
• Study type: Interventional

Clinical Trial 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.

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 information / eligibility

• Status: Completed
• Enrollment: 87
• Est. completion date: May 2013
• Est. primary completion date: May 2013
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years and older

Eligibility

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

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Health Services Research

Related Conditions & MeSH terms

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

Intervention

Behavioral:
• Positive Parenting Program
Level 3 or 4 of Triple P

Locations

Country	Name	City	State
Chile	Pontificia Universidad Católica de Chile	Santiago

Sponsors (1)

Lead Sponsor	Collaborator
Pontificia Universidad Catolica de Chile

Country where clinical trial is conducted

Chile, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Assess implementability of the program in primary care in terms of feasibility, acceptability and level of participation	Instrument: focus groups	After one year of implementation	No
Secondary	Percentage of change in intensity of behaviour in children	Instrument: Eyberg Child Behaviour Inventory	After one year of implementation	No
Secondary	Fidelity of program implementation	Supervision meetings and video recordings	After one year of implementation	No

External Links

•   Triple P Chilean website
•   Triple P Official Website
•   Triple P Provider Network