[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100593631":3},{"organization":4,"armGroups":7,"interventions":18,"overallOfficials":23,"centralContacts":31,"locations":37,"responsibleParty":53,"collaborators":56,"id":60,"slug":61,"hasResults":62,"nctId":63,"briefTitle":64,"officialTitle":64,"acronym":65,"eligibilityCriteria":66,"healthyVolunteers":67,"sex":68,"minAge":69,"maxAge":69,"enrollmentInfo":70,"targetDuration":17,"studyType":73,"phases":74,"briefSummary":76,"conditions":77,"keywords":81,"overallStatus":40,"whyStopped":17,"lastUpdateSubmitDate":89,"lastUpdatePostDateStruct":90,"startDateStruct":93,"completionDateStruct":95,"leadSponsor":97,"locationsCount":98},{"fullName":5,"class":6},"American University of Beirut Medical Center","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Group receiving SEEK intervention","EXPERIMENTAL","Participants randomly assigned to the experimental group will be further randomly assigned to 16 subgroups of no more than 12 participants per groups to receive the SEEK integrated intervention package on sexual reproductive health, family planning, and wellbeing.",[13],"Other: The Self-Efficacy and Knowledge Trial",{"label":15,"type":16,"description":17,"interventionNames":17},"Control group not receiving SEEK intervention","NO_INTERVENTION",null,[19],{"type":6,"name":20,"description":21,"armGroupLabels":22,"otherNames":17},"The Self-Efficacy and Knowledge Trial","The intervention is composed on 8 sessions given over a period of 8 weeks covering topics of emotional regulation, communication, problem management, decision making, self-efficacy and others in relation to sexual reproductive health, family planning, and wellbeing. The intervention package will be delivered by trained non-specialists with at least 12 years of formal education. The package will be administered once a week for a duration of 90 minutes.",[9],[24,28],{"name":25,"affiliation":26,"role":27},"Shadi Saleh, PhD","Global Health Institute American University of Beirut","PRINCIPAL_INVESTIGATOR",{"name":29,"affiliation":30,"role":27},"Lale Say, MD","World Health Organization",[32],{"name":33,"role":34,"phone":35,"phoneExt":17,"email":36},"Shadi Saleh, PhD, MPH","CONTACT","+961 3 047 578","ss117@aub.edu.lb",[38],{"facility":39,"status":40,"city":41,"state":17,"zip":42,"country":43,"countryCode":44,"cosmosGeoPoint":45,"geoPoint":50,"contacts":51},"American University of Beirut","RECRUITING","Beirut","00000","Lebanon","LB",{"type":46,"coordinates":47},"Point",[48,49],35.50157,33.89332,{"lat":49,"lon":48},[52],{"name":25,"role":34,"phone":35,"phoneExt":17,"email":36},{"type":27,"investigatorFullName":54,"investigatorTitle":55,"investigatorAffiliation":5,"oldNameTitle":17,"oldOrganization":17},"Shadi Saleh","Professor and Founding Director of the Global Health Institute",[57,58],{"name":30,"class":6},{"name":59,"class":6},"Elrha","100593631","self-efficacy-and-knowledge-seek-trial-to-improve-sexual-reproductive-health-and-well-being-for-syrian-refugee-women-and-girls-in-lebanon-100593631",false,"NCT07008950","Self-efficacy and Knowledge (SEEK) Trial to Improve Sexual Reproductive Health and Well-being for Syrian Refugee Women and Girls in Lebanon","SEEK","Inclusion Criteria:\n\n\\-\n\nThe target population of the study are Syrian adolescent girls and young women refugees (age 15-24 years) residing in Beqaa governorate in Lebanon. Participants will be included in the study if they meet the following inclusion criteria:\n\n1. are currently married and between the ages of 15 - 24 years,\n2. completed an average stay in Lebanon for a minimum of 6 months,\n3. are willing to take part in the study as indicated by them signing an informed consent (for young women 18 years of age or older) or through a legal guardian consent form and written assent for adolescents' girls between 15 and 17,\n4. have none of the exclusion criteria listed below upon screening.\n\nExclusion Criteria:\n\nParticipants will be excluded from the study if they meet any of the following criteria:\n\n1. are currently pregnant and\u002For lactating,\n2. have reported chronic health problems interfering with the ability to follow the intervention protocol,\n3. have high levels of anxiety and\u002For depression as well as suicidal ideations and\u002For attempts upon screening and\u002For a current diagnosis of a severe mental illness, or undergoing mental health treatment.\n\n   \\-",true,"FEMALE","15 Years",{"count":71,"type":72},485,"ESTIMATED","INTERVENTIONAL",[75],"NA","This community-based randomized controlled trial (RCT) aims to evaluate a low-resource\u002Flow-intensity integrated sexual reproductive health (SRH) and wellbeing intervention package. It will be delivered in Primary Healthcare Centres (PHCs) in a rural area in Lebanon to Syrian refugee women and girls aged 15-24.",[78,79,80],"Mental Health Care","Sexual Health Quality of Life","Family Planning Services",[82,83,84,85,86,43,87,88],"sexual health","reproductive health","psychosocial support","wellbeing","RCT","Refugees","Girls and young women","2025-06-05",{"date":91,"type":92},"2025-06-06","ACTUAL",{"date":94,"type":92},"2024-01-01",{"date":96,"type":72},"2025-06-30",{"name":5,"class":6},1]