[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"common-mental-health-problems\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:common-mental-health-problems":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,47,91],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":30,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100575764","boosting-refugee-integration-through-psychological-intervention-100575764",false,"NCT06776523","Boosting Refugee Integration Through Psychological Intervention","BRIGHT","The inclusion criteria for participating in the study are:\n\n* refugees and asylum seekers (RAS) aged 16 or older;\n* 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;\n* speaking at least one of the following 12 languages: German, English, French, Arabic, Farsi, Kurdish, Tigrinya, Turkish, Ukrainian, Russian, Tamil, and Pashto;\n* 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.\n\nThe exclusion criteria for participating in the study are:\n\n* significant cognitive or neurological impairment measured through specific tools developed by the WHO and integrated into the PM+ manual (impairment questionnaire);\n* 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);\n* 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).","ALL","16 Years",{"count":19,"type":20},1200,"ESTIMATED","INTERVENTIONAL",[23],"NA","Refugees and asylum seekers (RAS) face numerous stressors and adversities which put them at risk for developing mental health problems. However, access to adequate mental health care in host countries is limited. To address this problem, the World Health Organization (WHO) introduced Problem Management Plus (PM+), a short, low-intensity psychological intervention administered by non-professionals, aiming to alleviate common mental disorders among crisis-affected communities.\n\nThe present study aims at expanding the existing PM+ intervention by providing additional booster sessions and homework reminders while evaluating its effectiveness and implementation in the public health system.",[26,27,28,29],"Psychological Distress","PTSD","Trauma","Common Mental Health Problems",[31,26,32,33],"Problem Management Plus","Mental Health Care","Refugees","RECRUITING","2026-04-21",{"date":37,"type":38},"2026-04-27","ACTUAL",{"date":40,"type":38},"2025-01-16",{"date":42,"type":20},"2027-09",{"name":44,"class":45},"University of Zurich","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":16,"minAge":55,"maxAge":56,"enrollmentInfo":57,"targetDuration":4,"studyType":21,"phases":59,"briefSummary":60,"conditions":61,"keywords":73,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":82,"lastUpdatePostDateStruct":83,"startDateStruct":85,"completionDateStruct":87,"leadSponsor":89,"locationsCount":46},"100579744","culturally-adapted-i-cbt-for-farsidari-speaking-migrants-100579744","NCT06828276","Culturally Adapted i-CBT for Farsi\u002FDari Speaking Migrants","Culturally and Language-Adapted i-CBT for Common Mental Health Problems: A Randomized Controlled Study With Farsi\u002FDari-Speaking Migrants","i-CBT","Inclusion Criteria:\n\n* Between the ages of 15 and 29.\n* A score above the cut-off 1.75 on HSCL-25\n* Has a refugee or migrant background\n* Has a good and stable internet connection\n* Has access to a computer, tablet or smartphone\n* Is fluent in reading and writing Arabic\n* Has the ability to dedicate time to take part in the intervention for 6-10 weeks.\n\nExclusion Criteria:\n\n* Is suffering from a severe mental illness, such as psychosis or severe depression.\n* Is suffering from substance abuse\n* Is undergoing a psychological treatment\n* Has a high risk of suicide","15 Years","29 Years",{"count":58,"type":20},128,[23],"The aim of this randomized controlled trial (RCT) is to investigate the effectiveness of a culturally adapted internet-based cognitive behavioral therapy (i-CBT) intervention in reducing symptoms of common mental health issues among Farsi\u002FDari-speaking youth migrants and refugees. Investigator hypothesizes that there will be a significant decrease in psychological symptoms after participants receive the intervention compared to a control group.",[62,63,64,65,66,67,68,69,70,71,29,72],"Depressive Symptoms","Anxiety Symptoms","Grief","Psychological Trauma","Insomnia","Resilience","Stress","Psychological Well Being","Marital Relationship","Wellbeing","Rumination",[74,75,76,77,78,79,80,67,81],"Refugee","Cognitive behavioral therapy","Psychological problems","Persian speaking","Psychological well-being","Youth","Mental problems","Asylum seeker","2025-12-05",{"date":84,"type":38},"2025-12-12",{"date":86,"type":38},"2025-03-25",{"date":88,"type":20},"2026-12-31",{"name":90,"class":45},"Karolinska Institutet",{"id":92,"slug":93,"hasResults":11,"nctId":94,"briefTitle":95,"officialTitle":96,"acronym":97,"eligibilityCriteria":98,"healthyVolunteers":11,"sex":16,"minAge":99,"maxAge":4,"enrollmentInfo":100,"targetDuration":4,"studyType":21,"phases":102,"briefSummary":103,"conditions":104,"keywords":107,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":120,"lastUpdatePostDateStruct":121,"startDateStruct":123,"completionDateStruct":125,"leadSponsor":127,"locationsCount":130},"100571632","trial-of-an-online-group-psychotherapy-intervention-for-common-mental-health-disorders-100571632","NCT06722781","Trial of an Online Group Psychotherapy Intervention for Common Mental Health Disorders","UpLift-X Trial 1: A Cluster Factorial Randomised Controlled Trial of Digitally-enabled Group Psychotherapy for Common Mental Disorders","UpLift-X","Inclusion Criteria:\n\n* 17 years old and over\n* Literate and fluent in the English language, which would enable group interactions and learning via online materials\n* With access to an internet-connected device (e.g., computer, phone) and confidential space\n* Referred to NHS-TT services\n* Assessed by a qualified psychological professional and deemed to be eligible for high intensity CBT (this includes low risk of harm to self or others)\n* Currently on waiting list for high intensity CBT and not accessing any other psychological interventions. This includes patients accessing pharmacotherapy but who are additionally seeking psychological treatment\n* Presenting symptoms of one or more internalizing disorders (major depressive disorder, generalised anxiety disorder, panic disorder, agoraphobia, specific phobias, somatoform disorder, obsessive-compulsive and related disorders, body dysmorphic disorder, post-traumatic stress and related disorders)\n\nExclusion Criteria:\n\n* 16 years old and under\n* Not able to speak or read English fluently, which would require more individualised support with interpreters\n* No access to internet-connected device or confidential space to engage with digital intervention\n* Not involved with NHS-TT services\n* Assessed by a qualified psychological professional and not deemed to be eligible for high intensity CBT on the basis of mental health condition and\u002For risk assessment (e.g., acute risk of suicide at the time of assessment)\n* Already accessing a high intensity psychotherapy or other forms of psychological treatment (e.g., private therapy, counselling)\n* Presenting with symptoms of eating disorders, substance use disorders, psychotic disorders, personality disorders, bipolar disorders identified at the time of initial assessment.","17 Years",{"count":101,"type":20},660,[23],"The goal of this clinical trial is to understand how to deliver online group therapy for adults with common mental health problems in a personalised way. This study will test a new online group therapy program for various common mental health problems like anxiety and depression. The therapy is based on an approach called the Unified Protocol, which includes eight modules teaching different coping skills. The therapy will be delivered via a video call and a website, which will also have helpful videos and information about coping skills.\n\nAims:\n\n1. Does changing the order of the therapy modules affect how well treatment works or how many patients drop-out of treatment?\n2. Do some modules work better for different patients based on their individual features and if patients receive the therapy module that is most likely to be helpful for them first, does it mean they have a better chance of feeling better by the end of treatment?\n3. Does online group therapy work as well to treat common mental health problems as standard care (individual cognitive behavioural therapy \\[CBT\\])?\n\nHypotheses:\n\n1. Changing the order of therapy modules will not change how well therapy works or how many people drop-out.\n2. Patients with specific profiles (based on their individual characteristics) will benefit more from some treatment modules and will see greater improvements in their symptoms if they received their best therapy module before other modules\n3. There will be no differences in overall treatment outcome or dropout rates when comparing online group therapy vs. individual CBT\n\nResearchers will compare whether delivering the modules in different orders, with five different versions of the treatment, to see if changing the order of therapy modules affects how well it works or drop-out rates. Researchers will test how best to match patients to the most helpful parts of treatment for them. The group therapy outcomes and costs will also be compared to data from patients who have had individual CBT to see how the intervention compares to standard care.\n\nParticipants will:\n\n* Complete online symptom questionnaires before treatment starts and before each therapy session\n* Attend 12 weekly group therapy sessions delivered by a video call on a website (called Uplift-X).\n* Access online resources like videos and practice exercises to use between therapy sessions.\n* Complete the online symptom questionnaires again at the end of treatment and 6 months later.",[29,105,106],"Anxiety","Depression Disorders",[108,109,110,111,112,113,114,115,116,117,118,119],"Psychological interventions","Internalizing disorders","High intensity CBT","Common mental health problems","Unified Protocol","Digitally-enabled therapy","Group therapy","Digital Health Technology","NHS Talking Therapies","Personalised treatment","Pragmatic clinical trial","Transdiagnostic","2025-07-07",{"date":122,"type":38},"2025-07-10",{"date":124,"type":38},"2025-04-30",{"date":126,"type":20},"2026-09-30",{"name":128,"class":129},"Rotherham Doncaster and South Humber NHS Foundation Trust","OTHER_GOV",2]