[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100579846":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":21,"centralContacts":25,"locations":35,"responsibleParty":54,"collaborators":56,"id":60,"slug":61,"hasResults":62,"nctId":63,"briefTitle":64,"officialTitle":65,"acronym":66,"eligibilityCriteria":67,"healthyVolunteers":68,"sex":69,"minAge":70,"maxAge":71,"enrollmentInfo":72,"targetDuration":20,"studyType":75,"phases":76,"briefSummary":78,"conditions":79,"keywords":81,"overallStatus":38,"whyStopped":20,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":88,"startDateStruct":91,"completionDateStruct":93,"leadSponsor":95,"locationsCount":96},{"fullName":5,"class":6},"McMaster University","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Implementation of syphilis\u002FHIV point-of-care testing","EXPERIMENTAL","The syphilis\u002FHIV point-of-care test will be offered to all prenatal clients with at least 1 risk factor for syphilis, and to the sexual partners of syphilis-positive participants",[13],"Diagnostic Test: Rapid Syphilis\u002FHIV point-of-care test",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"DIAGNOSTIC_TEST","Rapid Syphilis\u002FHIV point-of-care test","The INSTI Multiplex HIV\u002FSyphilis Duo Antibody Test is a rapid immunoassay that can detect HIV and syphilis antibodies in the blood using finger-prick blood samples. The test is Health Canada-approved.",[9],null,[22],{"name":23,"affiliation":5,"role":24},"Laura K Erdman, MD PhD FRCPC","PRINCIPAL_INVESTIGATOR",[26,32],{"name":27,"role":28,"phone":29,"phoneExt":30,"email":31},"Njideka Sanya","CONTACT","+1-905-521-2100","77577","sanyan@mcmaster.ca",{"name":33,"role":28,"phone":29,"phoneExt":30,"email":34},"Stacey Clark","clarksta@mcmaster.ca",[36],{"facility":37,"status":38,"city":39,"state":40,"zip":20,"country":41,"countryCode":42,"cosmosGeoPoint":43,"geoPoint":48,"contacts":49},"Maternity Centre of Hamilton","RECRUITING","Hamilton","Ontario","Canada","CA",{"type":44,"coordinates":45},"Point",[46,47],-79.84963,43.25011,{"lat":47,"lon":46},[50],{"name":51,"role":28,"phone":52,"phoneExt":20,"email":53},"Suzanne Turner","+1-905-547-1110","turnes19@mcmaster.ca",{"type":55,"investigatorFullName":20,"investigatorTitle":20,"investigatorAffiliation":20,"oldNameTitle":20,"oldOrganization":20},"SPONSOR",[57],{"name":58,"class":59},"Canadian Institutes of Health Research (CIHR)","OTHER_GOV","100579846","the-feasibility-of-implementing-syphilis-point-of-care-testing-into-a-prenatal-clinic-for-people-facing-barriers-to-care-100579846",false,"NCT06829602","The Feasibility of Implementing Syphilis Point-of-care Testing Into a Prenatal Clinic for People Facing Barriers to Care","PREnatal Syphilis Point-of-care ScreenING in an Urban Low-barrier Clinic: A Prospective Single Arm Feasibility Trial","PRESSING","1. Pregnant people\n\n   Inclusion Criteria:\n   * Pregnant clients with at least one risk factor for syphilis infection:\n\n     1. Substance use or accessed addiction services in the past 1 year\n     2. Unstable housing in the past 1 year\n     3. Multiple sexual partners in the past 1 year\n     4. History of a sexually transmitted or blood-borne infection (STBBI)\n     5. Late to prenatal care (initial prenatal visit \\>20 weeks)\n   * Eligible for syphilis screening at that clinic visit, as per Public Health guidelines\n\n   Exclusion Criteria:\n   * Previous syphilis diagnosis\n   * Not competent to consent to study participation\n2. Sexual partners\n\nInclusion Criteria:\n\n* Sexual partners of pregnant clients who are newly diagnosed with syphilis\n* Physically present in the clinic\n\nExclusion Criteria:\n\n* Previous syphilis diagnosis\n* Not competent to consent to study participation",true,"ALL","13 Years","49 Years",{"count":73,"type":74},77,"ESTIMATED","INTERVENTIONAL",[77],"NA","The goal of this clinical trial is to learn if a finger-prick blood test for rapid diagnosis of syphilis infection can be implemented in a low-barrier prenatal clinic for people at risk of syphilis in pregnancy. The test gives results in 5 minutes and also tests for HIV.\n\nThe main questions the study aims to answer are:\n\n* How often do pregnant people at risk of syphilis agree to the rapid test?\n* How well do healthcare providers perform the rapid test?\n* Does the rapid test speed up diagnosis and treatment of syphilis in pregnant people and their sexual partners?\n\nParticipants will:\n\n* Give feedback about why they did or did not want to take the rapid test, and what their experience was taking the test; and\n* Share information about their health, pregnancy, and syphilis treatment (if applicable).",[80],"Syphilis",[82,83,84,85,86],"syphilis","pregnancy","access to care","acceptability","point-of-care test","2025-07-03",{"date":89,"type":90},"2025-07-06","ACTUAL",{"date":92,"type":90},"2025-06-25",{"date":94,"type":74},"2026-05",{"name":5,"class":6},1]