Comparing Web, Group, and Telehealth Formats of a Military Parenting Program
1 other identifier
interventional
244
1 country
1
Brief Summary
The overarching goal of this study is to advance research on family-based prevention of negative child outcomes for reintegrating Operation Enduring Freedom/Operation Iraqi Freedom personnel by evaluating different formats of a parenting program, After Deployment, Adaptive Parenting Tools (ADAPT). The ADAPT program is based upon the Parent Management Training-Oregon Model/PMTO, but adapted for military deployed families. The PI will examine which of three delivery formats of ADAPT is most effective at reducing youth risk behaviors associated with negative childhood outcomes by improving parenting, child, and parent adjustment. There is a clear intent to benefit all subjects in this study (except surveyed teachers), including children.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jun 2014
Longer than P75 for not_applicable
1 active site
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
June 1, 2014
CompletedFirst Submitted
Initial submission to the registry
May 4, 2015
CompletedFirst Posted
Study publicly available on registry
November 28, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 30, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
August 30, 2020
CompletedMarch 19, 2026
March 1, 2026
6 years
May 4, 2015
March 16, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Change in parenting practices and parent/child interactions
Observed parenting is coded using FIT (Family Interaction Task) and self-report of parenting using the APQ (Alabama parenting Questionnaire),
Change from Baseline, 6 months, 12 months, 24 months
Secondary Outcomes (3)
Change in child adjustment and substance use
Change from Baseline, 6 months, 12 months, 24 months
Change in parenting stress and support
Change from Baseline, 6 months, 12 months, 24 months
Participant report of satisfaction with intervention
Change from Baseline, 6 months, 12 months, 24 months
Study Arms (3)
ADAPT Self Directed web
OTHERADAPT Self Directed Web. In the self-directed web-only ADAPT condition, participants have access to the full ADAPT website (10 modules, online discussion forum)
ADAPT individualized web-facilitated
OTHERThis condition comprises access to the full ADAPT web program with augmentation of individual facilitator web support (i.e. the facilitator connects via Google Hangout). Facilitators meet with families at a mutually convenient time weekly (10-14 weeks, approximately 3 sessions per month).
Group-based ADAPT
OTHERGroups will meet weekly for 120 minutes, at a time convenient to participants (usually early evening). Groups cover core ADAPT/PMTO topics
Interventions
In the self-directed web-only ADAPT condition, participants have access to the full ADAPT website (10 modules, online discussion forum
This condition comprises access to the full ADAPT web program as described above, with augmentation of individual facilitator web support (i.e. the facilitator connects via Google Hangout). Facilitators meet with families at a mutually convenient time weekly (10-14 weeks, approximately 3 sessions per month).
Groups will meet weekly for 120 minutes, at a time convenient to participants (usually early evening). Groups cover core ADAPT/PMTO topics:
Eligibility Criteria
You may qualify if:
- one parent has returned from deployment to OIF or OEF
- at least one child ages 5-12 in their custody and living with parent(s) in the home
- high speed internet access at home We will include both single-and two-parent families, as well as families where care is shared between non-partnered adults (e.g. grandparent and mother)
You may not qualify if:
- active psychosis
- an open child protection case for abuse or neglect in the family
- a serious child mental health diagnosis
- families who piloted material or participated in or are currently participating in the original ADAPT RCT.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Institute for Translational Research in Children's Mental Health
Minneapolis, Minnesota, 55415, United States
Study Officials
- PRINCIPAL INVESTIGATOR
Abigail Gewirtz, PhD
Institute for Translational Research in Children's Mental Health University of Minnesota
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 4, 2015
First Posted
November 28, 2016
Study Start
June 1, 2014
Primary Completion
May 30, 2020
Study Completion
August 30, 2020
Last Updated
March 19, 2026
Record last verified: 2026-03