Trial of a Parenting Discussion Group in Panama, Central America

Parenting Practices Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01771068
• Other study ID #: PTY12
• Status: Completed
• Phase: N/A
• First received: January 11, 2013
• Last updated: January 17, 2013
• Start date: April 2012
• Est. completion date: December 2012

Study information

• Verified date: January 2013
• Source: University of Manchester
• Contact: n/a
• Is FDA regulated: No
• Health authority: United Kingdom: Research Ethics Committee
• Study type: Interventional

Clinical Trial Summary

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).

Description:

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 108
• Est. completion date: December 2012
• Est. primary completion date: December 2012
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 80 Years

Eligibility

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

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Child Behavioural and Emotional Difficulties
• Parenting Practices

Intervention

Behavioral:
• Triple P Positive Parenting Program Discussion Group "Dealing with Disobedience"

Locations

Country	Name	City	State
Panama	Ministry of Education, District of Panama	Panama

Sponsors (2)

Lead Sponsor	Collaborator
University of Manchester	National Secretariat of Science, Technology and Innovation in Panama (SENACYT)

Country where clinical trial is conducted

Panama, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Eyberg Child Behaviour Inventory (ECBI)		baseline, 2 weeks post intervention, 3 months and 6 months	No
Secondary	Change in Depression Anxiety Stress Scale 21 (DASS 21)		baseline, 2 weeks post intervention, 3 months and 6 months	No
Secondary	Change in Parenting Scale (PS)		baseline, 2 weeks post intervention, 3 months and 6 months	No
Secondary	Change in Parenting Task Checklist (PTC)		baseline, 2 weeks post intervention, 3 months and 6 months	No