[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100622133":3},{"organization":4,"armGroups":7,"interventions":18,"overallOfficials":10,"centralContacts":23,"locations":29,"responsibleParty":67,"collaborators":71,"id":77,"slug":78,"hasResults":79,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":83,"eligibilityCriteria":84,"healthyVolunteers":79,"sex":85,"minAge":86,"maxAge":10,"enrollmentInfo":87,"targetDuration":10,"studyType":90,"phases":10,"briefSummary":91,"conditions":92,"keywords":10,"overallStatus":94,"whyStopped":10,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"locationsCount":104},{"fullName":5,"class":6},"Norton Healthcare","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"LEN LAI PrEP",null,"Those receiving or initiating LEN LAI PrEP",[13],"Other: Interview and survey to evaluate patient reported outcomes between the two medications.",{"label":15,"type":10,"description":16,"interventionNames":17},"CAP LAI PrEP","Those receiving or initiating CAB LAI PrEP",[13],[19],{"type":6,"name":20,"description":21,"armGroupLabels":22,"otherNames":10},"Interview and survey to evaluate patient reported outcomes between the two medications.","No intervention, the two cohorts will receive the same surveys and interviews.",[15,9],[24],{"name":25,"role":26,"phone":27,"phoneExt":10,"email":28},"NIDI Research Clinic","CONTACT","502-861-4646","SystemNIDI@nortonhealthcare.org",[30,44,57],{"facility":5,"status":10,"city":31,"state":32,"zip":33,"country":34,"countryCode":35,"cosmosGeoPoint":36,"geoPoint":41,"contacts":42},"Louisville","Kentucky","40202","United States","US",{"type":37,"coordinates":38},"Point",[39,40],-85.75941,38.25424,{"lat":40,"lon":39},[43],{"name":25,"role":26,"phone":10,"phoneExt":10,"email":10},{"facility":45,"status":10,"city":31,"state":32,"zip":33,"country":34,"countryCode":35,"cosmosGeoPoint":46,"geoPoint":48,"contacts":49},"University of Louisville, School of Public Health and Information Sciences",{"type":37,"coordinates":47},[39,40],{"lat":40,"lon":39},[50,54],{"name":51,"role":26,"phone":52,"phoneExt":10,"email":53},"Elana Nance","502-852-0418","e.nance@louisville.edu",{"name":55,"role":56,"phone":10,"phoneExt":10,"email":10},"Jelani Kerr, MSPH, PhD","SUB_INVESTIGATOR",{"facility":58,"status":10,"city":31,"state":32,"zip":59,"country":34,"countryCode":35,"cosmosGeoPoint":60,"geoPoint":62,"contacts":63},"University of Louisville, Kent School of Social Work","40292",{"type":37,"coordinates":61},[39,40],{"lat":40,"lon":39},[64,65],{"name":51,"role":26,"phone":52,"phoneExt":10,"email":53},{"name":66,"role":56,"phone":10,"phoneExt":10,"email":10},"Lesley Harris, MSW, PhD",{"type":68,"investigatorFullName":69,"investigatorTitle":70,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"SPONSOR_INVESTIGATOR","Anupama Raghuram MD","Chief Research Scientist",[72,75],{"name":73,"class":74},"Gilead Sciences","INDUSTRY",{"name":76,"class":6},"University of Louisville","100622133","long-acting-injectable-hiv-prep-pros-100622133",false,"NCT07379658","Long-Acting Injectable HIV PrEP PROs","Improving HIV Prevention Outcomes: Insights on Long-Acting Injectable (LAI) HIV Pre-Exposure Prophylaxis (PrEP) Patient-Reported Medication Preferences, Adherence, and Clinical Outcomes (IMPACT) in a Southern US State","IMPACT","Inclusion Criteria:\n\n1. Adults aged 18 and older\n2. Deemed eligible for HIV PrEP per healthcare provider\n3. Receiving or initiating LAI PrEP, defined as:\n\n   1. Current use of CAB or LEN LAI PrEP at study entry\n   2. Initiation of either CAB or LEN LAI PrEP within 30 days of study enrollment\n4. Receiving PrEP services in Louisville, KY\n5. Able to provide informed consent and complete study assessments\n\nExclusion Criteria:\n\n1. HIV diagnosis prior to enrollment\n2. Currently on oral PrEP with no plans to switch to LAI PrEP\n3. Hypersensitivities to LEN or CAB\n4. Pregnant or planning to become pregnant\n5. PI discretion","ALL","18 Years",{"count":88,"type":89},128,"ESTIMATED","OBSERVATIONAL","The goal of this observational study is to learn about the real world effectiveness, patient satisfaction and clinical outcomes of LAI PrEP with lenacapavir (LEN) versus cabotegravir (CAB) through surveys and interviews.\n\nParticipants receiving or initiating LAI PrEP part of their regular medical care will complete surveys and interviews at three study visits over the course of 12 months.",[93],"HIV Pre-exposure Prophylaxis","NOT_YET_RECRUITING","2026-01-23",{"date":97,"type":98},"2026-01-30","ACTUAL",{"date":100,"type":89},"2026-01-15",{"date":102,"type":89},"2028-01",{"name":69,"class":6},3]