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Recruiting NCT06261463

Hybrid Type 1 Randomized Pilot Trial of a Peer-led Family and Social Strengthening Group Intervention for Refugee Families

No phase Interventional Depression Anxiety PTSD Family Dynamics

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: CAFES2.
Who it may be relevant to
Registry conditions: Depression, Anxiety, PTSD, Family Dynamics. Basic parameters: 12 years — 55 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Leveraging Implementation Science and Design Methods to Sustain Community-based Mental Health Services for Refugees

Overview

The proposed study draws on prior research to evaluate the feasibility, acceptability and explore preliminary effectiveness of Coffee and Family Education and Support, Version (CAFES2) using a pilot randomized type 1 hybrid effectiveness-implementation design. CAFES2 is a peer-led family and social strengthening multiple family group intervention that is designed to respond to multi-level needs of refugee families. Results of the trial will contribute to the emerging evidence base on family-based mental health interventions for refugee and newcomer communities. The trial will also generate new insights regarding implementation strategies needed to promote successful delivery of services by peer providers and the unique role of human-centered design practices for adaptation of mental health and psychosocial interventions.

Detailed description

In partnership with refugee service organizations in Chicago, the investigator explored the problems, strengths, and help-seeking preferences of refugee families. Qualitative findings indicated ongoing problems coping with stress, trauma and loss, strain and tension in family relationships and limited social support networks. Participants identified a need for family-focused, group-based services led by individuals with similar life experiences. Based on these findings, the investigators identified an evidence-based multiple-family group model, Coffee and Family Education and Support (CAFES) as a foundational model that could be adapted to meet the needs of refugee families. Drawing on this formative work and strong community partnerships, further research is needed to adapt CAFES to a new population, to reflect multi-level needs of families and for use by refugee peer facilitators in community-based organizations. Research is also needed to assess feasibility, acceptability and fidelity of model implementation, attentive to barriers and facilitators specific to peer-led mental health services and community settings.

The investigators will use a hybrid type 1 randomized pilot trial design to achieve the following specific research aims:

Aim 1: To adapt the multiple family CAFES model for delivery by peers in community organizations using an implementation science adaptation framework and participatory human-centered design methods to develop an intervention that addresses the complex needs of refugee families.

Aim 2: To pilot the adapted CAFES2 model with refugee families from Arabic-speaking countries in the Middle East to examine feasibility, acceptability and provider fidelity when implemented by refugee peers in two community-based organizations in Chicago. (n=74, 37 intervention, 37 control) Aim 3: To explore the impact of the adapted CAFES2 model compared to enhanced control on outcomes of adult and child mental health and family and community support and explore variables expected to mediate the intervention's impact.

Interventions

  • Behavioral CAFES2
    The adapted CAFES2 model includes an initial home visit and six multiple family group sessions delivered by peer providers. Families include at least one caregiver and one youth 12 years or older. Key model components include: 1) interfamilial discussion of stressors affecting families and family relationships, 2) psychoeducation on the effects of war and forced displacement on individuals, families and social relationships; 3) emotion regulation and self management strategies; 4) identification

Primary outcome measures

  • Changes in feasibility of the intervention via the Feasibility of Intervention Measure [Time frame: immediate post-intervention]
  • Changes in acceptability of the intervention via the Acceptability of Intervention Mesure [Time frame: immediate post-intervention.]
  • Changes in PTSD symptoms via the PTSD Checklist (adult, exploratory) [Time frame: baseline, immediate post-intervention and 6-week follow up]
  • Changes in adult depression and anxiety via the Hopkins Symptom Checklist (HSCL, adult, exploratory) [Time frame: baseline, immediate post-intervention and 6-week follow up]
  • Changes in youth depression and anxiety via the Arab Mental Health Scale (youth, exploratory) [Time frame: baseline, immediate post-intervention and 6-week follow up]
  • Changes in PTSD in children and youth via the Child Revised Impacted of Events Scale (CRIES, youth, exploratory) [Time frame: baseline, immediate post-intervention and 6-week follow up]
  • Changes in post-migration stress in youth and adults via the Refugee Post-Migration Stress Scale [Time frame: baseline, immediate post-intervention and 6-week follow up]
Secondary outcome measures (5)
  • Changes in social support via the Medical Outcomes Study (MOS) Social Support Survey [Time frame: baseline, immediate post-intervention and 6-week follow up]
  • Changes in social interaction via the Duke Social Support Index, social interaction subscale [Time frame: baseline, immediate post-intervention and 6-week follow up]
  • Changes in family support via the Multidimensional Scale of Perceived Social Support (MSPSS, Family Support Sub-scale) [Time frame: baseline, immediate post-intervention and 6-week follow up]
  • Quality of the parent-child relationship via the Dimensions of Parenting Scale (sub-scale, warmth and responsiveness of parent-child relationship) [Time frame: baseline, immediate post-intervention and 6-week follow up]
  • Degree of family strengths and difficulties via the SCORE-15 (family strengths, family difficulties sub-scales [Time frame: baseline, immediate post-intervention and 6-week follow up]

Eligibility criteria

To participate in the study, the families must meet the following criteria:

  • Country of origin: Iraq, Syria, Lebanon, Jordan, Palestine or Yemen
  • refugee family living in Chicago < three years
  • Contains at least one adult caregiver (18-55) and at least one of their children (age 12 and older) living in one household
  • One family member with > 3 on the GHQ-12
  • able to give written informed consent.

Exclusion criteria for refugee families:

  • Not from one of the following Arabic-speaking countries in the Middle East: Iraq, Syria, Jordan, Lebanon, Palestine, Yemen
  • men and women who do not have least one child aged 12 years and older living in one household
  • arrived in the U.S as a refugee greater than 3 years ago
  • persons with developmental disabilities which would preclude their participation in the adapted CAFES intervention
  • persons with severe mental health (e.g., suicidality psychotic disorder), active substance use or current in family crisis (e.g., domestic violence, divorce proceedings).

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Prevention

Study locations

United States · 1 center
  • University of Illinios Chicago — Chicago

Identifiers

NCT: NCT06261463 · 2023-0326 · K01MH128524-01A1

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗