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Clinical Trials/NCT01777724
NCT01777724
Terminated
Not Applicable

Evaluation of a Parenting and Stress Management Programme: An Exploratory Randomised Controlled Trial of Triple P-Positive Parenting Program and Stress Control

Medical Research Council1 site in 1 country14 target enrollmentJanuary 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Parenting
Sponsor
Medical Research Council
Enrollment
14
Locations
1
Primary Endpoint
Change in dysfunctional parenting practices as measured by the Parenting Scale
Status
Terminated
Last Updated
11 years ago

Overview

Brief Summary

The study will use a randomised controlled trial design to evaluate the effects of a combined intervention of Triple P-Positive Parenting Program Discussion Groups and Stress Control in comparison to a waitlist condition. The combined intervention will be evaluated with parents in Glasgow, United Kingdom, with a 3-8 year old child.

Registry
clinicaltrials.gov
Start Date
January 2013
End Date
February 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dr Marion Henderson

Senior Investigator Scientist

Medical Research Council

Eligibility Criteria

Inclusion Criteria

  • Has a child aged between 3 and 8 years old
  • Able to attend the group sessions held at Langside Halls, Shawlands in Glasgow, United Kingdom
  • Able to read a newspaper without assistance

Exclusion Criteria

  • Child has a diagnosis of a developmental or intellectual disability or other significant health impairment

Outcomes

Primary Outcomes

Change in dysfunctional parenting practices as measured by the Parenting Scale

Time Frame: Baseline, mid-intervention (approximately 4 weeks after baseline), post-intervention (approximately 12 weeks after baseline), 3-month follow-up (approximately 24 weeks after baseline)

Measures dysfunctional parenting practices: laxness, overreactivity, and verbosity

Change in symptoms of depression, anxiety and stress as measured by the Depression Anxiety Stress Scales 21

Time Frame: Baseline, mid-intervention (approximately 4 weeks after baseline), post-intervention (approximately 12 weeks after baseline), 3-month follow-up (approximately 24 weeks after baseline)

Secondary Outcomes

  • Change in positive mental wellbeing as measured by the Short Warwick-Edinburgh Mental Well-being Scale(Baseline, post-intervention (approximately 12 weeks after baseline), 3-month follow-up (approximately 24 weeks after baseline))
  • Change in parents' perceptions of their parenting self-efficacy as measured by the Child Adjustment and Parent Efficacy Scale-Parent Efficacy subscale(Baseline, post-intervention (approximately 12 weeks after baseline), 3-month follow-up (approximately 24 weeks after baseline))
  • Change in the frequency of disruptive child behaviours as measured by Eyberg Child Behavior Inventory-Intensity scale(Baseline, post-intervention (approximately 12 weeks after baseline), 3-month follow-up (approximately 24 weeks after baseline))
  • Change in parents' perceptions of their parenting experiences as measured by the Parenting Experience Survey(Baseline, post-intervention (approximately 12 weeks after baseline), 3-month follow-up (approximately 24 weeks after baseline))
  • Change in parents' perceptions of their family relationships as measured by the Parenting and Family Adjustment Scale-Family Relationships subscale(Baseline, post-intervention (approximately 12 weeks after baseline), 3-month follow-up (approximately 24 weeks after baseline))

Study Sites (1)

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