NCT01868919

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
87

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Nov 2011

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 1, 2011

Completed
1.2 years until next milestone

First Submitted

Initial submission to the registry

January 19, 2013

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2013

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2013

Completed
1 month until next milestone

First Posted

Study publicly available on registry

June 5, 2013

Completed
Last Updated

June 5, 2013

Status Verified

May 1, 2013

Enrollment Period

1.5 years

First QC Date

January 19, 2013

Last Update Submit

May 30, 2013

Conditions

Keywords

"Pilot Projects"[Mesh]"Parenting"[Mesh]"Child Behaviour"[Mesh]"Mental Health"[Mesh]"Family Practice"[Mesh]

Outcome Measures

Primary Outcomes (1)

  • 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

Secondary Outcomes (2)

  • Percentage of change in intensity of behaviour in children

    After one year of implementation

  • Fidelity of program implementation

    After one year of implementation

Study Arms (1)

Positive Parenting Program

EXPERIMENTAL

Level 3 or 4 of Triple P

Behavioral: Positive Parenting Program

Interventions

Level 3 or 4 of Triple P

Also known as: Triple P
Positive Parenting Program

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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

You may not qualify if:

  • Children: Pervasive Developmental Disorder, severe intellectual disability or severe psychopathology
  • Caregivers: illiteracy, decompensated severe psychopathology or current psychotherapy

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Pontificia Universidad Católica de Chile

Santiago, Santiago Metropolitan, Chile

Location

Related Links

MeSH Terms

Interventions

(tris(diphenylphosphinomethyl)phenylborate)(p-tolylnitrido)iron(I)

Study Officials

  • Gladys Moreno, Dra.

    Pontificia Universidad Catolica de Chile

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 19, 2013

First Posted

June 5, 2013

Study Start

November 1, 2011

Primary Completion

May 1, 2013

Study Completion

May 1, 2013

Last Updated

June 5, 2013

Record last verified: 2013-05

Locations