SMART Optimization of a Parenting Program for Active-duty Families
Completed · Not applicable
Conditions studied: Parenting
In brief
The overarching goal of the "SMART Optimization of a Parenting Program for Active-Duty Families" study is to advance the "development, adaptation, efficiency or optimization, and testing of a prevention intervention by using a sequential, multiple assignment, randomized trial/SMART to test multiple components of an empirically-supported parent training prevention intervention - After Deployment Adaptive Parenting Tools (ADAPT) for active-duty families negotiating multiple deployments and high deployment OPTEMPO (an army program that provides critical responses).
Key facts
- Study ID
- NCT05509348
- Run by
- University of Minnesota
- People needed
- 423
- Starts
- 2017-07-01
- Expected to finish
- 2022-09-29
- Last updated by the study team
- 2022-12-01
Who can join
Age: 18 and older, up to 100. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- families in which one parent has returned from deployment
- families with at least one child age 5 to 12 in their custody and living with parent(s) in the home
- must agree to randomization
- must indicate willingness to interact with study materials and complete assessment batteries
You may not qualify if…
- families with children younger than 5 or older than 12
- families in which at least one parent has an active psychosis
- families with an open child protection case for abuse or neglect in the family
- families in which there is a child with a serious mental health diagnosis (i.e., autism, child psychosis)
- youth who have a documented pervasive developmental disability or mental retardation
- families who participated in the focus group
- those with less than a 5th grade comprehension level in English
Where it is running
- Fort Campbell — Fort Campbell North, Kentucky, United States
- Fort Bragg — Fort Bragg, North Carolina, United States
- Fort Myer — Arlington, Virginia, United States
- Fort Belvoir — Fort Belvoir, Virginia, United States
Full record on ClinicalTrials.gov
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