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Evaluation of a Parenting and Stress Management Programmme

Not Applicable
Terminated
Conditions
Parenting
Parent Mental Health
Child Behaviour Problems
Interventions
Behavioral: Combination of Triple P Discussion Groups and Stress Control
Registration Number
NCT01777724
Lead Sponsor
Medical Research Council
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
14
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
InterventionCombination of Triple P Discussion Groups and Stress ControlThe intervention is a combination of Triple P Discussion Groups and Stress Control
Primary Outcome Measures
NameTimeMethod
Change in dysfunctional parenting practices as measured by the Parenting ScaleBaseline, 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 21Baseline, mid-intervention (approximately 4 weeks after baseline), post-intervention (approximately 12 weeks after baseline), 3-month follow-up (approximately 24 weeks after baseline)
Secondary Outcome Measures
NameTimeMethod
Change in positive mental wellbeing as measured by the Short Warwick-Edinburgh Mental Well-being ScaleBaseline, 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 subscaleBaseline, 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 scaleBaseline, post-intervention (approximately 12 weeks after baseline), 3-month follow-up (approximately 24 weeks after baseline)

Measures parents' perceptions of their child's disruptive behaviour

Change in parents' perceptions of their parenting experiences as measured by the Parenting Experience SurveyBaseline, 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 subscaleBaseline, post-intervention (approximately 12 weeks after baseline), 3-month follow-up (approximately 24 weeks after baseline)

Trial Locations

Locations (1)

Medical Research Council Social and Public Health Sciences Unit

🇬🇧

Glasgow, United Kingdom

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