CClinicalTrials.gg
Status unknownNCT04873310TriplePChileUpdated Nov 1, 2021

Behavior Problems Prevention Using the Online Triple P Parenting Program

An interventional study of Triple P online with professional support and Triple P online without professional support in Parenting, sponsored by Universidad de los Andes, Chile. Status unknown at 1 site in Chile. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2021-11-01.

Sponsored by Universidad de los Andes, Chile · Not applicable, Interventional, and Prevention

The sponsor has not verified this record recently (last verified Oct 2021), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
1,920
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The Triple P program is a comprehensive system of parenting and family support of multilevel preventive intervention, developed for families with members up to 16 years of age, whose objective is to improve parenting skills and prevent or modify dysfunctional parenting practices, thus reducing Family risk factors that affect both child abuse, behavioral problems and emotional problems.

Read the detailed description

Based on the importance that evidence-based parental interventions have acquired and the need from the health field to provide innovative alternatives that facilitate access to this type of services, parental support programs given through the web emerge. There is evidence that supports the idea that parenting programs taught through the web have an influence on reducing disruptive behaviors in children.

Triple P Online (TPOL) is an adaptation of the Positive Parenting Program, Triple P, a program that has been empirically tested. This adaptation is a parental intervention through the web with self-directed modality, which is based on Level 4 of the Triple P parental program and is configured in 8 interactive sessions with online modules. The topics covered are: 1) What is Positive Parenting, 2) Reinforcing the behavior we want, 3) Teaching new skills, 4) Managing negative behaviors, 5) Managing disobedience, 6) Preventing problems through planning, 7) Making fun outings, 8) Raising confident and competent children.

The main results observed in the implementation of the online Triple P program are (Sanders et al, 2012): reduction of problem child behavior, dysfunctional parenting styles, increasing parents' confidence in their parenting role, and reduction of parental anger.

02

Conditions studied

  • Parenting

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Keywords

  • program
  • parental competence
  • behavior problems
  • emotional problems
03

In context

Problem Behavior

517 studies on the registry are indexed under Problem Behavior; 92 are open to participants now.

This study's planned enrollment of 1,920 is above the median of 90 across 391 interventional studies indexed under Problem Behavior.

Browse Problem Behavior studies →

Lead sponsor

Universidad de los Andes, Chile is the lead sponsor of 44 studies on the registry; 13 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Belong to one of the three socio-economic levels according to SIMCE classification (High, Medium and Low).
  • Attend to a primary school of the Municipality of Lo Barnechea, Santiago, Chile.
  • Previous participation in the instruments validations stages.
  • Identification in The Strengths and Difficulties Questionnaire (SDQ) with behavior problems above the 80th percentile.
  • Have Internet access.

Exclusion criteria

Exclusion Criteria:

  • Attend to a school that is developing or implementing a manualized program for parents associated with the prevention of behavioral problems
  • Participating in a similar study.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
1,920 participants (estimated)

Study arms

  • Experimental
    Triple P online with professional support

    In the online version with professional support, the psychologist in charge will have the role of monitoring the autonomous work of the participants during the 8 sessions, as well as answering questions and doubts that the participants may have regarding the program and its implementation.

    Other: Triple P online with professional support

  • Experimental
    Triple P online without professional support

    In the version without professional support, the role of the psychologist in charge will be to keep the platform updated so that the person who self-administers the intervention does not have technical problems associated with the platform.

    Other: Triple P online without professional support

  • No intervention
    Control group

    Control group without any intervention.

Interventions

  • OtherTriple P online with professional support

    The psychologist in charge will have the role of monitoring the autonomous work of the participants during the 8 sessions. The psychologist in charge will also verify that the participants are able to complete the online modules week by week, that they understand the contents taught in the module and that they are practicing the tasks and exercises assigned in each of the modules; in addition to generating an action plan in case the participants are not adhering week by week to the self-administration of the program. The follow-up and contact with the families will be carried out by phone and through a weekly email-type messaging system, implemented within the same platform on which the program material is found

  • OtherTriple P online without professional support

    The role of the psychologist in charge will be to keep the platform updated so that the person who self-administers the intervention does not have technical problems associated with the platform.

06

What researchers measure

Primary outcomes

  1. Acceptability of the program by parents/main caregivers using the Acceptability Scale (AS)

    A questionnaire exploring the acceptability of the program will be answered by parents/main caregivers of students attending Grade 1 to Grade 4, Primary school, who will participate in the intervention. This questionnaire asks about the parents´opinions about the content of the intervention, strategies used, materials, and performance of the health professional helping in the intervention.The latter is only applicable for parents participating in "Group Triple-p online with professional support". The questionnaire also asks about satisfaction and the helpfulness of the program to improve parenting management. For each statement, the answers can go from 1=Strongly disagree to 5=Strongly agree. A high score means higher acceptably and satisfacción with the program. This is a questionnaire created by the research team.

    Time frame: Inmediately Post-intervention

  2. Feasibility of the program using the Feasibility Inventory (FI)

    A register will be used to determine the number of schools initially contacted and the number of schools that accepted to participate; number of parents/main caregivers contacted and that consented and assented to participate in the study at baseline and at follow-up; the number of sessions completed by parents in the platform, the number of telephone contacts delivered by the health professionals, the number of meeting over the phone conducted with parents. This Feasibility Inventory (FI) was created by the research team. This registry will not produce a score, rather it will provide indicators to achievements for several areas of the implementation of the program.

    Time frame: 6 months

Secondary outcomes

  1. Parenting Scale (PS)

    This 30-item questionnaire measures three dysfunctional discipline styles: Laxness (permissive discipline), Over-reactivity (authoritarian discipline, anger, meanness and irritability) and Verbosity (long reprimands or reliance on talking). The scale has good test-retest reliability (r = .83, .82, and .79, respectively) and has been found to discriminate between parents of clinic and nonclinic children; and to correlate with observational measures of dysfunctional discipline. Each item is answered in a scale of 7 points, according to what are the typical behavior parent perform under each scenario. A total score is computed, ranging from 30 to 210. A high score means parents are choosing more effective strategies to deal with different scenarios.

    Time frame: One month

  2. Parenting Task Checklist (PTC)

    This checklist assesses parents' confidence in successfully dealing with 14 difficult child behaviors like whining and temper tantrums (Behavior Self-efficacy), and in dealing with difficult behavior in 14 different settings such as shopping and having visitors (Setting Self-efficacy).

    Time frame: One month

  3. Alabama Parenting Questionnaire (APQ)

    The APQ measures five dimensions of parenting that are relevant to the etiology and treatment of child externalizing problems: (1) positive involvement with children, (2) supervision and monitoring, (3) use of positive discipline techniques, (4) consistency in the use of such discipline and (5) use of corporal punishment. The project will use the dimensions (1), (3), and (4)., and it will not use the dimension of "(2) supervision and monitoring" because it is not relevant for the target population; and "(5) use of corporal punishment" because it is not the focus of the intervention. The parent form will be used. This questionnaire has 22 items. Each statement is answered from 1= Never to 4 = Often. The score ranges from 22 to 44. a High scores means better parenting skills.

    Time frame: One month

  4. The Strengths and Difficulties Questionnaire (SDQ)

    The 25-item SDQ measures perceptions of prosocial and difficult behaviors in children aged 3-16 years. It has good test-retest reliability (r = .85) and has been found to discriminate well between low-risk and high-risk samples. Five scale scores are computed: Emotional Symptoms, Conduct Problems, Inattention/Hyperactivity, Peer Problems, and Prosocial Behavior. The first four sub-scales are included into one scleras of "Total Difficulties". Each item is answered from 0=Not true to 2=Certainly true. The score of each sub-scale ranges from 0 to 10. In the case of the Total Difficulties scale, Emotional symptoms sub-scale, Conduct Problems sub-scale, Inattention/Hyperactivity sub-scale, and Peer Problems sub-scale, a high score means more symptoms. In the cae of the Prosocial Behavior scale, a high score means stronger prosocial skills.

    Time frame: 2 months

07

Study locations

1 of 1 sites recruiting
  • Universidad de los Andes
    Santiago, Las Condes 7620001, Chile
    Recruiting
08

References and documents

Publications

  • Sanders MR, Baker S, Turner KM. A randomized controlled trial evaluating the efficacy of Triple P Online with parents of children with early-onset conduct problems. Behav Res Ther. 2012 Nov;50(11):675-84. doi: 10.1016/j.brat.2012.07.004. Epub 2012 Aug 18. PubMed 22982082 ↗
  • Arnold DS, O'Leary SG, Wolff LS, Acker MM. The Parenting Scale: A measure of dysfunctional parenting in discipline situations. Psychological Assessment. 1993; 5(2), 137-144. https://doi.org/10.1037/1040-3590.5.2.137
  • Goodman R, Scott S. Comparing the Strengths and Difficulties Questionnaire and the Child Behavior Checklist: is small beautiful? J Abnorm Child Psychol. 1999 Feb;27(1):17-24. doi: 10.1023/a:1022658222914. PubMed 10197403 ↗
  • Sanders MR, Woolley ML. The relationship between maternal self-efficacy and parenting practices: implications for parent training. Child Care Health Dev. 2005 Jan;31(1):65-73. doi: 10.1111/j.1365-2214.2005.00487.x. PubMed 15658967 ↗

Individual participant data

Plan to share: Undecided — Investigators plan to deposit the data collected in this study in the "UK Data Service". Data sharing will never compromise participant privacy, neither schools nor students.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 1, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04873310
Lead sponsor
Universidad de los Andes, Chile
Collaborators
Municipalidad de Lo Barnechea, Chile
Responsible party
Jorge Gaete (Associate Professor, Universidad de los Andes, Chile) — Principal investigator
First posted
May 5, 2021
Start date
Apr 6, 2021
Primary completion
Dec 30, 2022 (estimated)
Completion
Dec 30, 2022 (estimated)
Last update
Nov 1, 2021

Study contacts

Jorge Gaete, Phd
Contact
jgaete@uandes.cl
+56940245650
Saray Ramirez
Contact
saramirez1@miuandes.cl
+56988191548

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in Oct 2021. You cannot join it, but the record below documents what was studied.

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