Triple P to Improve Behaviour in Children
- Conditions
- ParentingChild BehaviourMental Health Wellness 1Family 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
- 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
- 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
Group Intervention Description Positive Parenting Program Positive Parenting Program Level 3 or 4 of Triple P
- Primary Outcome Measures
Name Time Method Assess implementability of the program in primary care in terms of feasibility, acceptability and level of participation After one year of implementation Instrument: focus groups
- Secondary Outcome Measures
Name Time Method Percentage of change in intensity of behaviour in children After one year of implementation Instrument: Eyberg Child Behaviour Inventory
Fidelity of program implementation After one year of implementation Supervision meetings and video recordings
Trial Locations
- Locations (1)
Pontificia Universidad Católica de Chile
🇨🇱Santiago, Chile