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CompletedNCT01955551Updated Dec 2, 2015

Motivational Interviewing to Increase Parent Engagement in Preventive Parenting Programming

A Phase 2 interventional study of Motivational Interviewing and Anticipatory Guidance on Child Development in Behavior Problems and Parent-Child Relations, sponsored by University of Michigan. Completed at 1 site in United States. Open to participants aged 2 Years and older. Per ClinicalTrials.gov, last updated 2015-12-02.

Sponsored by University of Michigan · Phase 2, Interventional, and Prevention

Phase
Phase 2
Study type
Interventional
Enrollment
112
Allocation
Randomized
Ages
2 Years and older
Sex
All
01

Study summary

Evidence-based programs aimed at enhancing parenting skills are effective, and pediatricians identify many parents who could benefit from such programs. Low-income children have high rates of behavior problems and their family system and environmental exposures often lead to cumulative and daunting levels of risk for poor functional outcomes; their parents are highly likely to benefit from parenting supports. However, low-income families are the most likely to drop out of parenting interventions, meaning the families and children with the greatest need receive the least support. Fewer than 25% of low-income families recruited to parenting programs will participate in even one session, and only about half of these parents will participate in more than half of the sessions offered. The aims of this trial are:

Aim 1: To test the hypothesis that the provision of motivational interviewing (MI), as compared to an attention control (AC) condition, will increase the engagement of low-income parents of preschoolers in an evidence-based parenting skills group (the Incredible Years Series (IYS)). For this study, the outcome of engagement is operationally defined as intention to attend IYS sessions, attendance, and satisfaction with the IYS program.

Aim 2: To test the hypothesis that the effect of MI on engagement in IYS will be impacted by the following moderators: parenting self-efficacy, child behavior problems, and maternal depression.

The investigators hypothesize that the effect of MI on engagement will be greater among parents with lower parenting self-efficacy and parents of children with more behavior problems, but less among parents with more maternal depressive symptoms.

The investigators will use a stratified, randomized controlled trial (RCT) design to evaluate the impact of MI on parent engagement in a well-validated preventive parenting skills intervention, the Incredible Years Series (IYS).

02

Conditions studied

  • Behavior Problems
  • Parent-Child Relations

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03

In context

Mental Disorders

2,148 studies on the registry are indexed under Mental Disorders; 425 are open to participants now.

This study's enrollment of 112 is above the median of 96 across 1,607 interventional studies indexed under Mental Disorders.

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Lead sponsor

University of Michigan is the lead sponsor of 1,503 studies on the registry; 189 are open to participants now.

Of its 167 completed or terminated interventional studies of FDA-regulated products, 132 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
2 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • all children enrolled in the Head Start agencies involved in this study, who were randomized to the study arm involving the Incredible Years Series

Exclusion criteria

Exclusion Criteria:

  • child is a foster child
  • parent or child cannot communicate in English
05

Study design

Phase
Phase 2
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
112 participants (actual)

Study arms

  • Experimental
    Motiv. Interviewing

    In the MI (motivational interviewing) study arm, participants will receive MI phone calls designed to evoke change talk and to prompt the participant to identify goals in regards to child behavior or parenting. The caller will engage in problem solving with the participants.

    Behavioral: Motivational Interviewing

  • Active comparator
    Anticipatory Guidance

    In the Anticipatory Guidance on Child Development study arm, the participants will receive two phone calls with no MI content. The content of these phone calls is derived from an alignment of the Teaching Strategies GOLD® standards with the Head Start Development and Early Learning Framework. , This content is entirely scripted and pre-specified.

    Behavioral: Anticipatory Guidance on Child Development

Interventions

  • BehavioralMotivational Interviewing

    In the Motivational Interviewing study arm, participants will receive MI phone calls designed to evoke change talk and to prompt the participant to identify goals in regards to child behavior or parenting. The caller will engage in problem solving with the participants.

  • BehavioralAnticipatory Guidance on Child Development

    In the Anticipatory Guidance on Child Development study arm, the participants will receive two phone calls with no MI content. The content of these phone calls is derived from an alignment of the Teaching Strategies GOLD® standards with the Head Start Development and Early Learning Framework. , This content is entirely scripted and pre-specified.

06

What researchers measure

Primary outcomes

  1. Participant intention to attend IYS sessions

    Time frame: 1 week

Secondary outcomes

  1. Attendance at initial IYS session

    Time frame: 1 month

  2. Number of IYS sessions attended

    Time frame: 9 months

  3. Satisfaction with the IYS program, as measured by a 46-item IYS questionnaire

    Time frame: 9 months

07

Study locations

1 site
  • University of Michigan
    Ann Arbor, Michigan 48109-5406, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 2, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01955551
Responsible party
Julie Lumeng (Associate Professor of Pediatrics, University of Michigan) — Principal investigator
First posted
Oct 7, 2013
Start date
Sep 2013
Primary completion
Jun 2015
Completion
Jun 2015
Last update
Dec 2, 2015

Study contacts

Julie C Lumeng
principal investigator · University of Michigan

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2015. You cannot join it, but the record below documents what was studied.

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