University Hospital Zurich
Zurich, Canton of Zurich, 8006, Switzerland
NCT Number: NCT03830008
The current refugee crisis across the Middle East and Europe has large effects on individual refugees' psychological well-being, as well as on the healthcare systems of countries hosting refugees. For example, in Switzerland patients sometimes have to wait up to 12 months for the specific psychological treatment due to a lack of specialists. To address this problem the WHO has developed Problem Management Plus (PM+), a brief (five sessions), low-intensity psychological intervention, delivered by paraprofessionals, that addresses common mental disorders in people in communities affected by adversity. The feasibility of PM+ has never been examined in Switzerland before, this is the aim of the current pilot study.
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Not applicable
Zurich, Canton of Zurich, 8006, Switzerland
Recent crises in the Middle East, most notably in Syria, have resulted in an unprecedented increase in the worldwide number of refugees and asylum seekers. Switzerland (CH) is strongly affected by this crisis too. Eight percent of asylum requests in 2016 were made by people from Syria (2015: 12 %). More than 7'000 asylum seekers from Syria entered CH over the last two years. Due to the ongoing war in this region, it is unlikely that this kind of migration and flight will stop. Notably, 50% of the refugee population are children and adolescents.
Refugees have typically been exposed to multiple stressors related to war and displacement including loss of family members, destruction of homes and livelihoods and human rights violations such as sexual violence or torture. They have often undertaken a risky and stressful flight leaving their homes for an unknown future. Accordingly, studies consistently show that refugees are at considerable risk of developing common mental disorders, including depression, anxiety, posttraumatic stress disorder (PTSD) and related somatic health symptoms. Recent WHO projections suggest that approximately 15-20% of Syrian refugees will develop some type of mental health problem and therefore represent an enormous public mental health challenge.
According to the UNHCR, 86% of all displaced persons remain in conflict or neighboring countries where appropriate health care is mostly not available. But also Western health systems are often unable to appropriately cover the needs of this particularly vulnerable population regarding prevention and treatment of mental health problems. As a response to this situation, the WHO developed the low-intensity Problem Management Plus (PM+) programs, a new generation of shorter, less expensive and trans-diagnostic (i.e., not specifically aimed at treating a certain mental disorder) programs to reduce common mental health symptoms and improve psychosocial functioning. PM+ is based on the WHO treatment guidelines for conditions related to stress. PM+ is a 5-sessions intervention aimed at reducing symptoms of depression, anxiety, PTSD, and related conditions, is delivered by trained non-specialized workers or lay people, and is available in individual and group delivery formats for both children and adults. It comprises evidence-based techniques of (a) problem solving, (b) stress management, (c) behavioral activation, and (d) accessing social support. PM+ has been successfully implemented in Kenya and Pakistan.
The STRENGTHS (Syrian REfuGees MeNTal HealTH Care Systems) study aims at evaluating the effectiveness and implementation of PM+ with Syrian refugees in different settings in low- and high-resource countries. The study consortium includes international experts in the domains of trauma and public mental health as well as representatives of WHO and UNHCR. The Zürich study site has been consigned to examine PM+ with adult refugees in an individual treatment setting in Switzerland. At the same time, similar studies in other countries will be undertaken. Despite the objective of these studies to implement and evaluate the effectiveness of PM+ in refugees, each research institution acts independently. Moreover, the other studies will be completed in different treatment settings - i.e., in children and adolescents (Lebanon), in groups (Turkey and Netherlands), and internet-delivered PM+ (Germany and Egypt).
To date, the feasibility of PM+ has not been investigated in a highly industrialized country, such as Switzerland.
In the present study, the investigators will evaluate the feasibility of PM+ in Syrian refugees in Switzerland.
This research entails single-blind randomized controlled trial.
The amendment was secured by December 2018. Trainers, assessors, supervisors and helpers are already identified, recruited an trained.
After the approval, the first participants will be identified, invited to screening and if they fulfill the criteria they will be invited to participate in the pilot study. The pilot study will end by the end of 2019. After the pilot study the results will be evaluated, analyzed and integrated in the planning of the definitive randomized controlled trial (RCT) (next study, not the part of current registration).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
PM+ is a new, brief, psychological intervention program based on CBT techniques that are empirically supported and formally recommended by the WHO. The full protocol was developed by the WHO and the University of New South Wales, Australia. The manual involves the following empirically supported elements: problem solving plus stress management, behavioural activation, facing fears, and accessing social support. These elements have been recommended in recent WHO guidelines.
Time frame: baseline assessment (before PM+)
measured by the Hopkins Symptom Checklist (HSCL-25)
Time frame: post-assessment baseline (after PM+/ETAU)
measured by the Hopkins Symptom Checklist (HSCL-25)
Time frame: 3-months follow-up (after PM+/ETAU)
measured by the Hopkins Symptom Checklist (HSCL-25)
Time frame: baseline assessment (before PM+)
measured using the PTSD Checklist for Diagnostic and Statistical Manual of Mental Disorders (DSM-5) (PCL-5)
Time frame: post-assessment baseline (after PM+/ETAU)
measured using the PTSD Checklist for Diagnostic and Statistical Manual of Mental Disorders (DSM-5) (PCL-5)
Time frame: 3-months follow-up (after PM+/ETAU)
measured using the PTSD Checklist for Diagnostic and Statistical Manual of Mental Disorders (DSM-5) (PCL-5)
Time frame: screening (before PM+)
assessed by the WHODAS 2.0 (WHO Disability Assessment Schedule 2.0)
Time frame: post-assessment baseline (after PM+/ETAU)
assessed by the WHODAS 2.0 (WHO Disability Assessment Schedule 2.0)
Time frame: 3-months follow-up (after PM+/ETAU)
assessed by the WHODAS 2.0 (WHO Disability Assessment Schedule 2.0)
Time frame: screening (before PM+)
Monitoring of the dropouts by number of patients
Time frame: baseline assessment (before PM+)
Monitoring of the dropouts by number of patients
Time frame: post-assessment baseline (after PM+/ETAU)
Monitoring of the dropouts by number of patients
Time frame: 3-months follow-up (after PM+/ETAU)
Monitoring of the dropouts by number of patients
Time frame: screening (before PM+)
Monitoring of wrong understanding or wrong translation (by number of patients and the scope of the feedback)
Time frame: baseline assessment (before PM+)
Monitoring of wrong understanding or wrong translation (by number of patients and the scope of the feedback)
Time frame: post-assessment baseline (after PM+/ETAU)
Monitoring of wrong understanding or wrong translation (by number of patients and the scope of the feedback)
Time frame: 3-months follow-up (after PM+/ETAU)
Monitoring of wrong understanding or wrong translation (by number of patients and the scope of the feedback)
Time frame: baseline assessment (before PM+)
patient-generated outcome measure by the Psychological Outcomes Profiles (PSYCHLOPS) scale [PSYCHLOPS has questions on Problems, Function and Wellbeing. Participants are asked to describe their main Problem or Problems and how this affects them (Function). Responses to all questions are scored [likert-scale 0 to 5 from "severely affected" to "not at all affected"); it is a highly sensitive measure of change during the course of psychotherapeutic interventions.]
Time frame: post-assessment baseline (after PM+/ETAU)
patient-generated outcome measure by the Psychological Outcomes Profiles (PSYCHLOPS) scale [PSYCHLOPS has questions on Problems, Function and Wellbeing. Participants are asked to describe their main Problem or Problems and how this affects them (Function). Responses to all questions are scored [likert-scale 0 to 5 from "severely affected" to "not at all affected"); it is a highly sensitive measure of change during the course of psychotherapeutic interventions.]
Time frame: 3-months follow-up (after PM+/ETAU)
patient-generated outcome measure by the Psychological Outcomes Profiles (PSYCHLOPS) scale [PSYCHLOPS has questions on Problems, Function and Wellbeing. Participants are asked to describe their main Problem or Problems and how this affects them (Function). Responses to all questions are scored [likert-scale 0 to 5 from "severely affected" to "not at all affected"); it is a highly sensitive measure of change during the course of psychotherapeutic interventions.]
Time frame: baseline assessment (before PM+)
will be assessed using a version of the Post-Migration Living Difficulties Checklist (PMLDC)
Time frame: post-assessment baseline (after PM+/ETAU)
will be assessed using a version of the Post-Migration Living Difficulties Checklist (PMLDC)
Time frame: 3-months follow-up (after PM+/ETAU)
will be assessed using a version of the Post-Migration Living Difficulties Checklist (PMLDC)
Time frame: baseline
assessed using the Traumatic Events (TE) - a combination of two standardized questionnaires, namely the Life Events Checklist (LEC) (Weathers et al., 2013) and the Harvard Trauma Questionnaire (HTQ) (Mollica et al., 1992). HTQ consists of 3 sections with 48 questions. LEC consists of 17 question. Single questions from HTQ (Section 1) and LEC are summarized to the sequence of 27 questions (about experienced trauma or adversities with yes/no answer format). The number of positive answers is the outcome value.
Time frame: baseline assessment (before PM+)
The set of question regarding previous contact with the mental health care services and the previous experiences regarding the utilization of any forms of mental support
Time frame: baseline assessment (before PM+)
accessed using the Client Service Receipt Inventory (CSRI) as the basis for calculating the costs of care for mental health cost-effectiveness research
Time frame: post-assessment baseline (after PM+/ETAU)
accessed using the Client Service Receipt Inventory (CSRI) as the basis for calculating the costs of care for mental health cost-effectiveness research
Time frame: 3-months follow-up (after PM+/ETAU)
accessed using the Client Service Receipt Inventory (CSRI) as the basis for calculating the costs of care for mental health cost-effectiveness research
University of Zurich
Other
Acronym: STRENGTHS_CH
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT04574466
Anxiety, Anxiety Disorders
Zurich, Switzerland
View Trial DetailsNCT03002896
Anxiety, Anxiety Disorders
Aurora, Colorado, United States
View Trial DetailsNCT01084694
Anxiety, Anxiety Disorders
Atlanta, Georgia, United States
View Trial DetailsNCT02518308
Anxiety, Anxiety Disorders
Madison, Wisconsin, United States
View Trial Details