Peer-led family support intervention for refugee families

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This pilot trial evaluates the feasibility and preliminary effectiveness of the Coffee and Family Education and Support (CAFES2) intervention, which is designed for refugee families facing mental health challenges. The intervention is peer-led and focuses on strengthening family dynamics and social support through group sessions. The study aims to adapt the CAFES model to meet the unique needs of refugee families in Chicago, utilizing community partnerships and human-centered design methods. By assessing the implementation strategies and barriers, the trial seeks to enhance the delivery of mental health services in community settings.

Why it matters

Who can join: the full rules

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

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

Exclusion criteria for refugee families:

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

Where it's running

• University of Illinios Chicago
  Chicago, Illinois, United States Recruiting

Study contacts

• Principal investigator: Mary Bunn, PhD — University of Illinois Chicago
• Study coordinator: Mary Bunn, PhD
• Email: mbunn@uic.edu
• Phone: (312) 355-2136

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

• Family guidance program for families with children who have neurodevelopmental disorders

  This study tests a family guidance program to see if it helps families with children who have neurodevelopmental disorders by providing tailored support and information.

  Recruiting Tampere University · Helsinki · NCT06322511

• Evaluating the H.O.O.V.E.S. Healing Intensives Program for Veterans

  This study is testing if the H.O.O.V.E.S. Healing Intensives Program can help veterans with anxiety, PTSD, and depression feel better over time.

  Recruiting VA Salt Lake City Health Care System · Salt Lake City, Utah · NCT06300255

• Mindful Smartphone Use: A Mindfulness-Based Program for Teens with Sleep and Mood Challenges

  This study tests Mindwire, a mindfulness-based program, to see if it helps teens with problematic phone use who also have depression or anxiety.

  Recruiting Brown University · Providence, Rhode Island · NCT07892807

• Tele-based wellbeing centres for women's mental health in Bangladesh

  A randomized trial tests whether tele-counselling for depression and anxiety in Bangladeshi women is as effective as in-person counselling.

  Recruiting at 2 sites International Centre for Diarrhoeal Disease Research, Bangladesh · Chāndpur, Matlab Dakshin and 1 other locations · NCT07890896

• HBOT to see if it helps cognition and well‑being in first responders with prior brain injury

  This study tests whether 40 hyperbaric oxygen therapy sessions can improve thinking skills and post-concussion symptoms in current or former first responders with a history of brain injury.

  Recruiting Phase 2 Summit Hyperbarics and Wellness · Boise, Idaho · NCT07852728

• Focused ultrasound for mood and anxiety disorders

  This study tests whether repeated low-intensity focused ultrasound using the ATTN201 device can help people with subsyndromal to moderate depression, anxiety, or OCD.

  Recruiting Attune Neurosciences Inc · San Francisco, California and 1 other locations · NCT07851038

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.