[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100642173":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":12,"centralContacts":12,"locations":12,"responsibleParty":25,"collaborators":29,"id":33,"slug":12,"hasResults":34,"nctId":35,"briefTitle":36,"officialTitle":37,"acronym":38,"eligibilityCriteria":39,"healthyVolunteers":34,"sex":40,"minAge":41,"maxAge":12,"enrollmentInfo":42,"targetDuration":12,"studyType":45,"phases":46,"briefSummary":48,"conditions":49,"keywords":54,"overallStatus":57,"whyStopped":12,"lastUpdateSubmitDate":58,"lastUpdatePostDateStruct":59,"startDateStruct":62,"completionDateStruct":64,"leadSponsor":66,"locationsCount":12},{"fullName":5,"class":6},"Stanford University","OTHER",[8,13],{"label":9,"type":10,"description":11,"interventionNames":12},"Usual Care","NO_INTERVENTION","This arm is the control group. They will receive usual care from their regular provider and care team with no change in their care plans as a result of the intervention. Outcomes will be assessed at each of the following times: baseline, 3-months, and 6-months post-enrollment.",null,{"label":14,"type":15,"description":16,"interventionNames":17},"EMBRACE plus usual care","EXPERIMENTAL","Participants assigned to the intervention will receive education provided by a trained RA who will meet with participants by phone for 30 minutes once a month for 6 months to: 1) discuss shared decision-making and 2) encourage to engage in SDM with their clinicians. Outcomes will be assessed at each of the following times: baseline, 3-months, and 6-months.",[18],"Behavioral: Research Assistant Support",[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":12},"BEHAVIORAL","Research Assistant Support","For those in the experimental group, a Research Assistant will provide health education and support as described in the Intervention arm.",[14],{"type":26,"investigatorFullName":27,"investigatorTitle":28,"investigatorAffiliation":5,"oldNameTitle":12,"oldOrganization":12},"PRINCIPAL_INVESTIGATOR","Manali Indravadan Patel","Principal Investigator",[30],{"name":31,"class":32},"Gilead Sciences","INDUSTRY","100642173",false,"NCT07652359","Empowering Monterey Bay Residents for Activated, Collaborative, and Equitable Care","EMBRACE - Empowering Monterey Bay Residents for Activated, Collaborative, and Equitable Care","EMBRACE","Inclusion Criteria:\n\n* Participants must be receiving clinical care by a primary care physician in the Monterey area\n* Participants must be 18 years or older.\n* Participants must speak either English or Spanish.\n* Participants must be able to consent verbally in English or Spanish to all study procedures.\n* Participants must self-identify as a racial\u002Fethnic minorities OR identify as having low-income status\n\nExclusion Criteria:\n\n\\- Patients unable to respond to survey questions in either English or Spanish.","ALL","18 Years",{"count":43,"type":44},138,"ESTIMATED","INTERVENTIONAL",[47],"NA","The purpose of the EMBRACE Study is to evaluate whether a facilitated intervention improves shared decision-making (SDM) and patient activation among low-income and minority individuals more than usual care only. The ultimate goal is to enhance SDM and patient activation in care.",[50,51,52,53],"Shared Decision-Making","Quality of Life","Advanced Illness","Terminal Illness",[55,56],"Goals of care","Advanced care planning","NOT_YET_RECRUITING","2026-06-10",{"date":60,"type":61},"2026-06-17","ACTUAL",{"date":63,"type":44},"2026-10-01",{"date":65,"type":44},"2030-01-01",{"name":5,"class":6}]