Skip to main content
OpenTrials
Completed

NCT Number: NCT03045159

Strong Families Strong Forces: Supporting Active Duty Families With Very Young Children

The purpose of this research is to evaluate the efficacy of the Strong Families Strong Forces Parenting Program compared to a parental self-care (Strong Parents) condition in a sample of 150 Active Duty Families with children ages birth to 5 years.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

STRONG STAR Research Consortium

Fort Hood, Texas, 76544, United States

About this study

The overall aim of this research is to adapt and evaluate the efficacy of a parenting program compared to a parental self-care program for Active Duty families. A sample of 150 Active Duty families with young children who have a parent scheduled to deploy in the next six months will be recruited to participate. Families will be assigned either to receive the Strong Families Strong Forces Parenting Program, designed to reduce the impact of deployment separation on parenting stress and co-parenting, or to the Strong Parents Self-Care program, designed to support parents to focus on the importance of self-care throughout the deployment cycle. Investigators will compare the two groups on parenting stress, quality of parent-child relationships, parenting/co-parenting, and family and child well-being.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Cohabitating couple with at least one child age birth to 5 years old in which one parent is active duty and is scheduled to deploy within the next 6 months
  • Anticipated deployment time must be at least six months and excludes separations due to the Service Member attending a school
  • Anticipate that non-deploying parent will remain in the area during the deployment
  • Both parents are willing to consent to study participation
  • DEERS -eligible
  • 18 years or older
  • English-speaking
  • The parent remaining at home to care for the children anticipates remaining within 30 miles of Fort Hood to be seen in home, otherwise will need to be seen in office
  • Anticipate that both parents will remain in the area for at least three months after redeployment to complete intervention and follow-up assessment

Exclusion criteria

  • Any family member with a significant medical or psychiatric condition requiring a higher level of care than can be provided by the study/comparison protocols
  • Active psychosis or mania

Treatment and study plan

Strong Families Strong Forces

Behavioral

Parenting program

Strong Parents

Behavioral

self-care program

Primary outcomes

  1. Parenting Stress Index (PSI)

    Time frame: Change from baseline to 24 months

    Assesses parenting stress in three domains: parental distress, parent-child dysfunctional interaction, and difficult child.

Secondary outcomes

  1. Coparenting Scale

    Time frame: Change from baseline to 24 months

    Assesses parents' perception of their own coparenting behavior.

Sponsors and collaborators

Lead sponsor

Boston University Charles River Campus

Other

Collaborators

  • RAND
  • The University of Texas Health Science Center at San Antonio

Registry information

Official study title

Supporting Military Families With Young Children Throughout the Deployment Lifecycle

Important dates

Study start
2016
Primary completion
2019
Study completion
2019
First posted
Feb 7, 2017
Registry last updated
Jul 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.