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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01868919
Other study ID # TRIPLEP.PUC.CHILE
Secondary ID
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


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
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