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Completed

NCT Number: NCT01771068

Trial of a Parenting Discussion Group in Panama, Central America

The present study aims to examine the effectiveness of a parenting intervention, the Triple P Positive Parenting Program Level 3 discussion groups "dealing with disobedience". Triple P is a system of interventions to support families and was developed at the University of Queensland in Australia in the 1980's. As few studies have tested the effectiveness of parenting programs in developing countries, the present study took place in a developing country, Panama.

In a recent study carried out in Australia, this same intervention was found effective in reducing child behaviour problems and the use of dysfunctional parenting (Morawska, Haslam, Milne & Sanders, 2011).

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Ministry of Education, District of Panama

Panama City, Provincia de Panamá, Panama

About this study

This is a randomized controlled trial (RCT) with two groups (waiting list versus Triple P discussion groups) and measurements at pre-intervention, post intervention, three and six months follow up.

The intervention trialed was a 2-hour, one-session discussion group on child noncompliance. Groups were composed by a maximum of 10 parents and were facilitated by the principal researcher, who is an accredited practitioner. The groups were interactive and discussion based, and a power point presentation with embedded-video clips were used to aid the facilitator. The key points that were covered in the discussion group included reasons for disobedience, parenting traps, encouraging good behaviour, and managing disobedience. Parents also received a workbook that included the content covered in the discussion group and 2 follow up telephone calls to check how they were doing after.

Participants were randomly assigned to a treatment group (Triple P discussion groups) or to a waiting list group. A statistician independent from the research team generated a random list of numbers. Randomization was stratified based on the level of child behavioural difficulties (high or low) measured at baseline. In order to ensure allocation concealment, sequentially-numbered, opaque, sealed envelopes (SNOSE) were opened after participants agreed to take part in the study and completed a baseline assessment. After randomization, those assigned to the waiting list group were assessed at time 1 (baseline) and then 4 weeks, 3 months and 6 months after the first assessment. Those assigned to the treatment group were assessed at time 1 (baseline), 2 weeks, 3 months and 6 months after the intervention. Assessments were carried out by a research assistant who was blind to group allocation.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participants must be Panamanian
  • must have at least one child between 3 and 12 years old
  • must report some level of difficulty in dealing with their child behaviour.

Exclusion criteria

  • no report of difficulty in dealing with child behaviour
  • illiteracy

Treatment and study plan

Triple P Positive Parenting Program Discussion Group "Dealing with Disobedience"

Behavioral

Primary outcomes

  1. Change in Eyberg Child Behaviour Inventory (ECBI)

    Time frame: baseline, 2 weeks post intervention, 3 months and 6 months

Secondary outcomes

  1. Change in Depression Anxiety Stress Scale 21 (DASS 21)

    Time frame: baseline, 2 weeks post intervention, 3 months and 6 months

  2. Change in Parenting Scale (PS)

    Time frame: baseline, 2 weeks post intervention, 3 months and 6 months

  3. Change in Parenting Task Checklist (PTC)

    Time frame: baseline, 2 weeks post intervention, 3 months and 6 months

Sponsors and collaborators

Lead sponsor

University of Manchester

Other

Collaborators

  • National Secretariat of Science, Technology and Innovation in Panama (SENACYT)

Registry information

Important dates

Study start
2012
Primary completion
2012
Study completion
2012
First posted
Jan 18, 2013
Registry last updated
Jan 18, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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