[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100626290":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":19,"centralContacts":20,"locations":26,"responsibleParty":40,"collaborators":19,"id":42,"slug":19,"hasResults":43,"nctId":44,"briefTitle":45,"officialTitle":45,"acronym":19,"eligibilityCriteria":46,"healthyVolunteers":47,"sex":48,"minAge":49,"maxAge":19,"enrollmentInfo":50,"targetDuration":19,"studyType":53,"phases":54,"briefSummary":56,"conditions":57,"keywords":19,"overallStatus":28,"whyStopped":19,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":69},{"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,"countryCode":33,"cosmosGeoPoint":34,"geoPoint":39,"contacts":19},"RECRUITING","Minneapolis","Minnesota","55455","United States","US",{"type":35,"coordinates":36},"Point",[37,38],-93.26384,44.97997,{"lat":38,"lon":37},{"type":41,"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":51,"type":52},121,"ESTIMATED","INTERVENTIONAL",[55],"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.",[58,59],"Substance Use","Drug Use","2026-05-18",{"date":62,"type":63},"2026-05-19","ACTUAL",{"date":65,"type":63},"2026-05-06",{"date":67,"type":52},"2028-05-01",{"name":5,"class":6},1]