Boosting Refugee Integration Through Psychological Intervention
Launched by UNIVERSITY OF ZURICH · Jan 9, 2025
Trial Information
Current as of November 11, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial, titled "Boosting Refugee Integration Through Psychological Intervention," is focused on helping refugees and asylum seekers who are experiencing psychological distress, including PTSD and other common mental health issues. Due to the many challenges they face, these individuals often struggle with their mental health and have limited access to the care they need. To tackle this issue, the trial is using a program called Problem Management Plus (PM+), which is a short and simple psychological intervention delivered by trained non-professionals. The trial aims to enhance the PM+ program by adding extra support sessions and reminders for practicing skills at home, while also assessing how well it works within public health services.
To be eligible for this study, participants must be refugees or asylum seekers aged 16 and older who live in selected Swiss municipalities where the program is available. They should also speak one of several languages, including German, English, or Arabic, and have moderate to high levels of psychological distress as indicated by a screening questionnaire. Those who have severe mental health issues or are at risk of suicide will not be included in the trial. Participants can expect to receive support through the PM+ program, which will help them manage their mental health in a practical way. This study is currently recruiting participants and aims to make a meaningful difference in the lives of refugees and asylum seekers facing mental health challenges.
Gender
ALL
Eligibility criteria
- The inclusion criteria for participating in the study are:
- • refugees and asylum seekers (RAS) aged 16 or older;
- • residing in one of the participating local sites (Swiss municipalities, namely, Gemeinden, and transitional asylum centers, namely, Durchgangszentren) where PM+ is offered and which gave their consent for participation in the RCT;
- • speaking at least one of the following 12 languages: German, English, French, Arabic, Farsi, Kurdish, Tigrinya, Turkish, Ukrainian, Russian, Tamil, and Pashto;
- • obtaining a score of 20 or higher on the Kessler Psychological Distress Scale (K10; Kessler et al., 2002), a brief clinically validated screening questionnaire that assesses general psychological distress in the past 30 days. A score equal to or higher than 20 is used as an indication of moderate to high levels of psychological distress.
- The exclusion criteria for participating in the study are:
- • significant cognitive or neurological impairment measured through specific tools developed by the WHO and integrated into the PM+ manual (impairment questionnaire);
- • acute medical conditions or severe mental disorders (e.g., psychotic or substance-abuse disorders) measured through specific tools developed by the WHO and integrated into the PM+ manual (impairment questionnaire);
- • acute risk of suicide as measured by the Suicidal Ideation Attribution Scale (SIDAS; van Spijker et al., 2014) and the Thoughts of Suicide Questionnaire (World Health Organization WHO, 2016).
About University Of Zurich
The University of Zurich, a leading institution in research and education, is dedicated to advancing medical knowledge and improving patient care through innovative clinical trials. With a robust framework for conducting high-quality research, the university collaborates with multidisciplinary teams of experts to explore cutting-edge therapeutic approaches and interventions. Its commitment to ethical standards and patient safety ensures that all clinical trials are conducted with the utmost integrity, aiming to contribute valuable insights to the medical community and enhance health outcomes globally.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Zurich, Switzerland
Patients applied
Trial Officials
Naser Morina, PD Dr.
Principal Investigator
Klinik für Konsiliarpsychiatrie und Psychosomatik
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported