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FMBI With War-affected Families

University of Minnesota (UMN) logo

University of Minnesota (UMN)

Status

Completed

Conditions

War-Related Trauma
Family Mindfulness-based Intervention in War-affected Families
Intergenerational Trauma

Treatments

Behavioral: Learning to BREATHE
Behavioral: After Deployment Adaptive Parenting Tools (ADAPT)

Study type

Interventional

Funder types

Other

Identifiers

NCT05241314
STUDY00011195

Details and patient eligibility

About

This study has two central research questions: 1) Is implementing a family mindfulness-based intervention with war-affected immigrant families through community based participatory research methods feasible?; and 2) Does the intervention demonstrate preliminary improvements in the social and behavioral health of war-affected caregivers and youth by addressing patterns of behavior that potentiate intergenerational trauma? The objective in the proposed study is to use Community Based Participatory Research strategies to test the feasibility and acceptability of a mindfulness-based intervention for Karen refugee families living post-resettlement in the United States. A key focus in this phase of the pilot will be intervention adaptation and establishing fidelity monitoring and quality improvement procedures through which the PI and community health worker interventionists are trained and evaluated in the delivery of the intervention.

Full description

Intergenerational trauma is a major public health problem impacting war-affected families. The investigators' specific research contribution will test the feasibility of a 7-week family mindfulness-based intervention addressing key mechanisms central to the health of war-affected families. The significance of this contribution is tied to the conceptual understanding that caregivers uniquely influence the ways in which their children process trauma, experience stressful events, and thrive socially, behaviorally and physically. The responses of youth, in turn, affect the well-being of their parents. Left unaddressed, intergenerational trauma will continue to negatively impact the health and life course of immigrant youth and families. Collectively, this contributes to: higher burden of unaddressed mental and physical health disturbances in caregivers and youth; disruptions in family systems and community structures that negatively impact educational achievement and other indicators of youth adjustment; and increased exposure to familial and community violence. If a mindfulness-based intervention delivered directly to war-affected families in their homes can demonstrate improvements in the behavioral and social health effects of war trauma experienced by caregivers and their youth, then this study has the potential to offer a novel, effective approach to disrupting the generational impacts of war on war-affected families. The study will engage mothers, fathers, and youth to address intergenerational trauma fully. The investigators will establish plans for collaborative dissemination with WellShare International in phase I of the Clinical Translational Research Service pilot award, including academic dissemination (presentation and publication) as well as dissemination of results among key stakeholders and community members.

Enrollment

25 patients

Sex

All

Ages

11+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adult inclusion criteria:

    • Above the age of 18
    • Karen refugees resettled to the United States greater than one year prior to enrollment
    • Caregiving responsibility for at least one child between the ages of 11 and 18
    • Reported primary or secondary torture or war trauma exposure, based on assessments conducted during UMN IRB STUDY00000729
    • Participation in UMN IRB STUDY00000729 and having agreed to be contacted for future research
  • Youth inclusion criteria:

    • Ages 11 to 18
    • Living in the home with the primary caregivers
    • Considered a dependent of the primary caregivers (still in high school or transitioning from school to workforce, not married and/or raising their own children - will take individual youth circumstances into consideration individually to make a determination of dependence)

Exclusion criteria

  • Self-reported or study team observed severe or unstable mental or physical illness such as acute psychosis, presence or risk of safety concerns, and/or a physical disability or illness, which prevents the potential participant from engaging in the study activities. Youth will be excluded if screening is positive for PTSD. Caregivers will not be excluded if mental health screening is positive for PTSD/severe depression.
  • Nonbiological caregiving relationships with child
  • If one member of the family declines to participate in the initial enrollment, the family will be excluded. If the randomly selected index youth declines to participate, we will open enrollment to other youth in the family that meet the inclusion criteria.

Trial design

Primary purpose

Health Services Research

Allocation

Non-Randomized

Interventional model

Sequential Assignment

Masking

None (Open label)

25 participants in 2 patient groups

Phase 2 Youth
Experimental group
Description:
One randomly selected index youth per participating Karen family. Community health worker interventionists (CHWI) will deliver 7 weeks of home-based intervention with optional post-intervention focus groups to examine the feasibility of the community-based participatory research approach and intervention delivery by CHWIs.
Treatment:
Behavioral: Learning to BREATHE
Phase 2 Caregivers/Adults
Experimental group
Description:
Maternal and paternal caregivers (if present) of participating Karen family. Community health worker interventionists (CHWI) will deliver 7 weeks of home-based intervention with optional post-intervention focus groups to examine the feasibility of the community-based participatory research approach and intervention delivery by CHWIs.
Treatment:
Behavioral: After Deployment Adaptive Parenting Tools (ADAPT)

Trial documents
2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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