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Trial record 34 of 120 for:    Recruiting, Not yet recruiting, Available Studies | "Parenting"

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

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ClinicalTrials.gov Identifier: NCT03045159
Recruitment Status : Recruiting
First Posted : February 7, 2017
Last Update Posted : February 7, 2017
Sponsor:
Collaborators:
The University of Texas Health Science Center at San Antonio
RAND
Information provided by (Responsible Party):
Boston University

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
Deployment Behavioral: Strong Families Strong Forces Behavioral: Strong Parents Not Applicable

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 Type : Interventional  (Clinical Trial)
Estimated 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 : March 2016
Estimated Primary Completion Date : March 2019
Estimated Study Completion Date : March 2019

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Parenting

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




Primary Outcome Measures :
  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 Outcome Measures :
  1. Coparenting Scale [ Time Frame: Change from baseline to 24 months ]
    Assesses parents' perception of their own coparenting behavior.



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03045159


Contacts
Contact: Kathering Dondanville, PsyD (254) 288-1474
Contact: Trenton James, MAJ (254) 288-2147

Locations
United States, Texas
STRONG STAR Research Consortium Recruiting
Fort Hood, Texas, United States, 76544
Contact: Katherine Dondanville, PsyD    254-288-1474      
Contact: Trenton James    (254) 288-2147      
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

Responsible Party: Boston University
ClinicalTrials.gov Identifier: NCT03045159     History of Changes
Other Study ID Numbers: W81XWH-14-2-0123
First Posted: February 7, 2017    Key Record Dates
Last Update Posted: February 7, 2017
Last Verified: March 2016
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided

Keywords provided by Boston University:
deployment cycle
military family
prevention
stress
military child
parenting
coparenting