[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"functioning-psychosocial\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:functioning-psychosocial":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,52],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":33,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":40,"lastUpdatePostDateStruct":41,"startDateStruct":44,"completionDateStruct":46,"leadSponsor":48,"locationsCount":51},"100489612","ifd-survive-functional-efficacy-and-biological-correlates-reconcile-study-100489612",false,"NCT05655390","iFD-SuRvivE funCtiONal effiCacy and bIologicaL corrElates (RECONCILE Study)","The SURVIVE 2 Project: An Extended Cohort Study to Investigate Suicidal Behavior in Spain and the Efficacy of Secondary Prevention Strategies: iFD-SuRvivE funCtiONal effiCacy and bIologicaL corrElates (RECONCILE Study)","RECONCILE","Inclusion Criteria:\n\n* Age over 18 years old\n* Having attempted suicide\n* Provide written informed consent\n* No claustrophobia\u002Fmetallic objects\u002Fimplants\n\nExclusion Criteria:\n\n* Intelligence quotient below 70 and impaired functioning\n* Any medical condition that could affect neuropsychological performance (such as neurological diseases) or a history of head trauma with loss of consciousness\n* Participation in any structured psychological intervention within the past 6 months\n* Patients who received electroconvulsive therapy within the past 6 months\n* Inability to give inform consent",true,"ALL","18 Years",{"count":21,"type":22},120,"ESTIMATED","INTERVENTIONAL",[25],"NA","The goal of this clinical trial is to assess the effectiveness of an original intervention 'Functional Recovery in Depression and Suicide Risk Prevention Based on Emotion Regulation and Values: A Group Program' (from the original Spanish version: Programa Grupal De Recuperación Funcional En Depresión Y Prevención De Riesgo Suicida Basado En Regulación Emocional Y Valores) in depressed patients who have recently attempted suicide by improving their psychosocial functioning and therefore enhancing their ability to perform activities of daily living. As secondary objectives, the effectiveness of the intervention will be evaluated by determining cognitive performance (particularly decision-making, inhibition, and attention), quality of life, clinical status, and their relationship with neuroimaging correlates. Main target neuroimaging areas include the orbitofrontal cortex and dorsal prefrontal cortex.",[28,29,30,31,32],"Suicide, Attempted","Functioning, Psychosocial","Cognition","Neuroimaging","Quality of Lifte",[34,35,36,37,38],"suicide","cognition","neuroimaging","psychosocial functioning","quality of life","RECRUITING","2026-05-08",{"date":42,"type":43},"2026-05-12","ACTUAL",{"date":45,"type":43},"2025-09-16",{"date":47,"type":22},"2027-10",{"name":49,"class":50},"Iria Grande","OTHER",4,{"id":53,"slug":54,"hasResults":11,"nctId":55,"briefTitle":56,"officialTitle":57,"acronym":58,"eligibilityCriteria":59,"healthyVolunteers":17,"sex":18,"minAge":60,"maxAge":4,"enrollmentInfo":61,"targetDuration":4,"studyType":23,"phases":63,"briefSummary":64,"conditions":65,"keywords":69,"overallStatus":77,"whyStopped":4,"lastUpdateSubmitDate":78,"lastUpdatePostDateStruct":79,"startDateStruct":81,"completionDateStruct":83,"leadSponsor":85,"locationsCount":5},"100627383","combining-mental-health-and-parenting-interventions-to-improve-child-wellbeing-among-refugee-families-in-tanzania-100627383","NCT07447921","Combining Mental Health and Parenting Interventions to Improve Child Wellbeing Among Refugee Families in Tanzania","Combining Mental Health and Violence Prevention Interventions to Enhance Child Wellbeing Under Adversity - Study Protocol for a Three-arm, Cluster-randomized, Superiority Trial With Primary Caregivers in Nyarugusu Refugee Camp, Tanzania (WEMA Trial)","WEMA","Inclusion Criteria:\n\n* Families residing in Nyarugusu Refugee Camp, Tanzania\n* Congolese refugee origin (for cultural and linguistic homogeneity)\n* Two primary caregivers (one male, one female) aged 18 years or older, caring for at least two children aged 7-10 years\n* Ability to speak and understand Kiswahili\n* Willingness to provide informed consent (and child assent)\n* No plans to leave the camp within the next 12 months\n\nExclusion Criteria:\n\n* Caregivers currently enrolled in other mental health or parenting programs\n* Caregivers displaying imminent suicide risk, psychosis, or severe cognitive impairment that would impede participation\n* Children with known developmental disabilities reported by caregivers","7 Years",{"count":62,"type":22},1296,[25],"The goal of this clinical trial is to learn whether improving caregivers' mental health and parenting practices can enhance child wellbeing among Congolese refugee families living in the Nyarugusu Refugee Camp, Tanzania. The WEMA trial (\"Wellbeing through combined Evidence-based tools for Mental health and Attuned parenting\") is a three-arm, family-level cluster-randomized, controlled superiority trial involving 324 families (approximately 648 children aged 7-10 years and their two primary caregivers). Participants and intervention facilitators will know which program a family receives, but outcome assessors (enumerators) will not know group assignment.\n\nThe main questions it aims to answer are:\n\n* Does Self-Help Plus (SH+), a World Health Organization (WHO) group stress-management program, improve children's emotional and behavioral functioning at 12 months post-intervention, compared with usual care?\n* Does adding Interaction Competencies with Children for Parents (ICC-P), a participatory parenting program, after SH+ further improve children's emotional and behavioral functioning at 12 months post-intervention, compared with SH+ alone?\n\nResearchers will compare (1) Usual Care, (2) SH+, and (3) SH+ followed by ICC-P to see whether SH+ improves outcomes versus usual care, and whether SH+ followed by ICC-P provides additional benefits beyond SH+ alone.\n\nParticipants will:\n\n* Be assigned by chance by family clusters to one of three groups: Usual Care, SH+, or SH+ followed by ICC-P.\n* Receive either (a) information about available psychosocial and mental health services (Usual Care), (b) SH+ (five group sessions delivered by trained non-specialists), or (c) SH+ followed by ICC-P (a four-day participatory parenting training to strengthen positive parenting and reduce harsh discipline).\n* Complete study assessments at baseline, 3 months, and 12 months post-intervention.\n\nThe primary outcome is children's emotional and behavioral functioning, measured using the Pediatric Symptom Checklist-17 (PSC-17) at 12 months post-intervention. Secondary outcomes include children's wellbeing and quality of life, as well as caregivers' mental health, well-being, and parenting practices. Additional exploratory outcomes will also be assessed, including measures collected from caregivers and behavioral tasks with children.\n\nThe trial is implemented by Uppsala University in collaboration with the Dar es Salaam University College of Education (DUCE) and partners, with funding from the Swedish Research Council (grant no. 2022-02476).",[66,67,29,68],"Mental Health","Socio-emotional Well-being","Parenting Behavior",[70,71,72,73,74,75,76],"Mental health","Child development","Parenting","Refugees","Self-Help Plus","Interaction Competencies with Children - for Parents","Tanzania","NOT_YET_RECRUITING","2026-02-25",{"date":80,"type":43},"2026-03-04",{"date":82,"type":22},"2026-03-15",{"date":84,"type":22},"2027-07",{"name":86,"class":50},"Uppsala University"]