Evaluating a Shortened Version of the Incredible Years (IY) Basic Programme in a Non-clinical Community Sample
1 other identifier
interventional
189
0 countries
N/A
Brief Summary
Aim of study: To evaluate the effects of the shortened version of the Incredible Years (IY) Basic programme, the study which the parents were recruited to. A randomising experimental control between-group design was used with pre- and post-intervention measurements, and a one-year, four-year and ten-year follow-up. Children and families were randomized to either the shortened basic version (n = 89), or the control group (n = 97).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jan 2004
Longer than P75 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2004
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2015
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2016
CompletedFirst Submitted
Initial submission to the registry
July 20, 2016
CompletedFirst Posted
Study publicly available on registry
August 1, 2016
CompletedAugust 1, 2016
July 1, 2016
11.9 years
July 20, 2016
July 29, 2016
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Longitudinal change in ECBI scores
Eyberg Child Behavior Inventory (Robinson et al., 1980). The ECBI provides a list of 36 problem behaviours commonly reported by parents of children with disruptive behaviour problems. The inventory assesses behaviour on two dimensions: the frequency of the behaviour and its identification as a problem. The frequency ratings range from 1 (never) to 7 (always), and are summed to yield an overall problem behaviour Intensity score (Cronbach's alpha 1⁄4 0.82) ranging from 36 to 252.
baseline, 6-8 weeks after intervention, one-year follow up, four-year follow up, ten-year follow up
Secondary Outcomes (4)
Reasons for participation and help seeking behaviour
Four-year follow up
Longitudinal change in PROC scores
baseline, 6-8 weeks after intervention, one-year follow up, four-year follow up, ten-year follow up
Longitudinal change in PSI scores
baseline, 6-8 weeks after intervention, one-year follow up, four-year follow up, ten-year follow up
Longitudinal change in PPI scores
baseline, 6-8 weeks after intervention, one-year follow up, four-year follow up, ten-year follow up
Study Arms (2)
Brief Incredible Years parent training
EXPERIMENTALParent training
No parent training
NO INTERVENTIONNo parent training
Interventions
The IY parent training programme (3-8 years) developed by Webster-Stratton at the Parenting Clinic, University of Washington, is a manualised and video-based training programme for parents of young children with conduct problems (Webster-Stratton and Reid, 2003a). Parents assigned to the short IY Basic (S-IY) condition were divided into groups of 10-12 parents. The S-IY was led by two experienced group leaders and parents met weekly for two-hour sessions at a public health care center in the community. The group leaders led discussions regarding central aspects of parenting on the basis of the video vignettes, role play and homework.
Eligibility Criteria
You may qualify if:
- No diagnosable behavior problems in child
You may not qualify if:
- Diagnosable behavior problems in child
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Related Publications (2)
Reedtz C, Klest SK, Aalo NM, Rasmussen ID, Vitterso J. Results From an RCT on Brief Parent Training: Long Term Effects on Parental Quality of Life. Front Psychol. 2019 Feb 18;10:260. doi: 10.3389/fpsyg.2019.00260. eCollection 2019.
PMID: 30833915DERIVEDReedtz C, Klest S. Improved parenting maintained four years following a brief parent training intervention in a non-clinical sample. BMC Psychol. 2016 Aug 24;4(1):43. doi: 10.1186/s40359-016-0150-3.
PMID: 27553950DERIVED
Study Officials
- PRINCIPAL INVESTIGATOR
Charlotte Reedtz, Dr. Philos
Arctic University of Norway
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate professor, Dr. Philos
Study Record Dates
First Submitted
July 20, 2016
First Posted
August 1, 2016
Study Start
January 1, 2004
Primary Completion
December 1, 2015
Study Completion
June 1, 2016
Last Updated
August 1, 2016
Record last verified: 2016-07