[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100626290":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":19,"centralContacts":20,"locations":26,"responsibleParty":39,"collaborators":19,"id":41,"slug":19,"hasResults":42,"nctId":43,"briefTitle":44,"officialTitle":44,"acronym":19,"eligibilityCriteria":45,"healthyVolunteers":46,"sex":47,"minAge":48,"maxAge":19,"enrollmentInfo":49,"targetDuration":19,"studyType":52,"phases":53,"briefSummary":55,"conditions":56,"keywords":19,"overallStatus":28,"whyStopped":19,"lastUpdateSubmitDate":59,"lastUpdatePostDateStruct":60,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":68},{"fullName":5,"class":6},"University of Minnesota","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Project REACH Intervention","EXPERIMENTAL","The primary interactions with participants of Project REACH will consist of syringe service program (SSP)-based recruitment and enrollment, provision of telehealth services at SSPs for the 6-month pilot duration, and exit interviews with a subset of participants and SSP study staff following the trial.",[13],"Other: Project REACH",[15],{"type":6,"name":16,"description":17,"armGroupLabels":18,"otherNames":19},"Project REACH","The primary interactions with participants of Project REACH will consist of SSP-based recruitment and enrollment, provision of telehealth services at SSPs for the 6-month pilot duration, and exit interviews with a subset of participants and SSP study staff following the trial.",[9],null,[21],{"name":22,"role":23,"phone":24,"phoneExt":19,"email":25},"Kumi Smith","CONTACT","612-301-3051","smi00831@umn.edu",[27],{"facility":5,"status":28,"city":29,"state":30,"zip":31,"country":32,"cosmosGeoPoint":33,"geoPoint":38,"contacts":19},"RECRUITING","Minneapolis","Minnesota","55455","United States",{"type":34,"coordinates":35},"Point",[36,37],-93.26384,44.97997,{"lat":37,"lon":36},{"type":40,"investigatorFullName":19,"investigatorTitle":19,"investigatorAffiliation":19,"oldNameTitle":19,"oldOrganization":19},"SPONSOR","100626290",false,"NCT07433712","Project REACH: A Comprehensive Telehealth Intervention at Syringe Service Programs to Engage People Who Use Drugs","People Who Use Drugs Inclusion Criteria:\n\n* 18 years of age or older\n* able to speak and understand English\n* have used an illicit substance at least once in the past year\n* have lived in the study area (in or near their city of their recruitment) for at least 6 months\n* have active health insurance by the start of the Project REACH trial date\n\nPeople Who Use Drugs Exclusion Criteria:\n\n* Unable or unwilling to provide informed consent\n\nStakeholder Inclusion Criteria:\n\n* 18 years of age or older\n* able to speak and understand English\n* currently employed or volunteering with the PCC or an SSP enrollment site for at least one year at the time of the interview OR hired as a study navigator at one of the four enrollment sites\n\nStakeholder Exclusion Criteria:\n\n* Unable or unwilling to provide informed consent",true,"ALL","18 Years",{"count":50,"type":51},121,"ESTIMATED","INTERVENTIONAL",[54],"NA","This trial will assess the feasibility, acceptability, and preliminary effectiveness of Project REACH (Remote Engagement \\& Access for Community Health), a telehealth intervention at syringe service programs (SSP) to improve access to HIV-related evidence-based interventions (EBI) for people who use drugs including those who inject them.",[57,58],"Substance Use","Drug Use","2026-05-18",{"date":61,"type":62},"2026-05-19","ACTUAL",{"date":64,"type":62},"2026-05-06",{"date":66,"type":51},"2028-05-01",{"name":5,"class":6},1]