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

Sponsor
Boston University (Other)
Overall Status
Unknown status
CT.gov ID
NCT03045159
Collaborator
The University of Texas Health Science Center at San Antonio (Other), RAND (Other)
300
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2
36
8.3

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Strong Families Strong Forces
  • Behavioral: Strong Parents
N/A

Detailed Description

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
300 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Masking Description:
outcomes assessor blinded to study condition
Primary Purpose:
Prevention
Official Title:
Supporting Military Families With Young Children Throughout the Deployment Lifecycle
Study Start Date :
Mar 1, 2016
Anticipated Primary Completion Date :
Mar 1, 2019
Anticipated Study Completion Date :
Mar 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Strong Families

parenting program

Behavioral: Strong Families Strong Forces
Parenting program

Active Comparator: Strong Parents

self-care program

Behavioral: Strong Parents
self-care program

Outcome Measures

Primary Outcome Measures

  1. Parenting Stress Index (PSI) [Change from baseline to 24 months]

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

Secondary Outcome Measures

  1. Coparenting Scale [Change from baseline to 24 months]

    Assesses parents' perception of their own coparenting behavior.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 STRONG STAR Research Consortium Fort Hood Texas United States 76544

Sponsors and Collaborators

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

Investigators

  • Principal Investigator: Ellen DeVoe, Ph. D. LICSW, Boston University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Boston University
ClinicalTrials.gov Identifier:
NCT03045159
Other Study ID Numbers:
  • W81XWH-14-2-0123
First Posted:
Feb 7, 2017
Last Update Posted:
Feb 7, 2017
Last Verified:
Mar 1, 2016
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Keywords provided by Boston University

Study Results

No Results Posted as of Feb 7, 2017