[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"University of California, Riverside\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":154},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,42,67,91,113,132],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100638277","phase-2-a1cantus-vs-placebo-100638277",false,"NCT07585630","A1Cantus vs. Placebo","Double-Blind Randomized Controlled Trial of A1Cantus Drink vs. Placebo for Reduction of Ha1c","Inclusion Criteria:\n\n* Adults 21 years of age or older and not older than 75 recruited from UCR Health\n* Clinical diagnosis of type II DM with Ha1c \\>= 8 but less than or equal to 10\n* Stable medications for at least 6 months\n* Speak Spanish and\u002For English\n* Sign an informed consent form\n* No other members in their household are participating in the study\n\nExclusion Criteria:\n\n* Patients \\\u003C21 years of age, who do not have type II DM, whose Ha1c is less than 8 or \\> 10,\n* Have major complications of diabetes, including CKD, diabetic retinopathy, ADVD risk \\> 5, or history of CVD\u002Fstroke\n* Do not speak and understand either English or Spanish well\n* Allergic to cinnamon\n* Severe diseases, such as cancer\n* Compromised immune system\n* Eating disorders\n* BMI of 40 or higher\n* Already have a family member participating in the study\n* Substance use disorder",true,"ALL","21 Years","75 Years",{"count":21,"type":22},50,"ESTIMATED","INTERVENTIONAL",[25],"PHASE2","The investigators will conduct a randomized controlled 2-arm parallel trial of A1c Drink vs. Placebo over a 3-month period and compare changes in Ha1c from baseline to 3 months. Investigator and study personnel, as well as participants, will be blinded to drink assignments.",[28],"Type 2 Diabetes","NOT_YET_RECRUITING","2026-05-13",{"date":32,"type":33},"2026-05-18","ACTUAL",{"date":35,"type":22},"2026-06-15",{"date":37,"type":22},"2028-06-01",{"name":39,"class":40},"University of California, Riverside","OTHER",1,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":46,"acronym":4,"eligibilityCriteria":47,"healthyVolunteers":11,"sex":17,"minAge":48,"maxAge":49,"enrollmentInfo":50,"targetDuration":4,"studyType":23,"phases":52,"briefSummary":54,"conditions":55,"keywords":4,"overallStatus":58,"whyStopped":4,"lastUpdateSubmitDate":59,"lastUpdatePostDateStruct":60,"startDateStruct":62,"completionDateStruct":64,"leadSponsor":66,"locationsCount":41},"100622709","community-health-worker-navigation-to-support-mental-health-100622709","NCT07387146","Community Health Worker Navigation to Support Mental Health","Inclusion Criteria:\n\n* Are 18 years of age or older\n\n  * Speak either English or Spanish\n  * Report moderate or higher perceived stress, defined as scoring 14 or above on the Perceived Stress Scale (PSS)\n\nExclusion Criteria:\n\n* Score below 14 on the Perceived Stress Scale (PSS), indicating low perceived stress and ineligibility for enrollment.\n\nEndorse suicidal ideation on PHQ-9 item 9 (any score \\> 0) and score at moderate to high risk on the Columbia Suicide Severity Rating Scale (C-SSRS) as assessed by the study psychiatrist\u002FPI.\n\nReport verbal or written suicidal ideation to any study team member. Exhibit any indication of suicidality or threats of harm to others reported or observed by research staff.\n\nScore 16 or higher on the AUDIT, indicating severe alcohol use. Score 6 or higher on the DAST-10, indicating severe drug use. Arrive at screening intoxicated, impairing informed consent capacity or ability to participate.\n\nPresent to the screening or interview space with any of the following concerning clinical signs:\n\n* Marked emotional dysregulation such that engagement is not feasible\n* Significant physical dishevelment suggesting acute impairment\n* Apparent intoxication from alcohol or other substances\n* Possible hallucinations or other signs of psychosis\n* Any indication that psychological status may compromise safe participation Are unable to complete the screening process due to any of the above concerns (screening will be halted and the participant will be referred for appropriate support).","18 Years","120 Years",{"count":51,"type":22},80,[53],"NA","This pilot study tests the feasibility and preliminary impact of a protocolized promotora-led navigation intervention to improve behavioral health access among Latinx and Native American underserved adults. The study is embedded within a community cultural center, leveraging a trusted and culturally grounded environment for recruitment and intervention delivery. Participants will be randomized 1:1 to receive either the promotora navigation intervention or a treatment-as-usual (TAU) condition consisting of cultural resources and promotora-supported wait-list control. The TAU group will continue to receive any usual care during the study period and will be offered the protocolized navigation intervention after completing follow-up assessments. Primary outcomes include feasibility, acceptability, and preliminary changes in behavioral health access, stress reduction, self-efficacy, and wellbeing.",[56,57],"Stress","Service Utilization","RECRUITING","2026-04-28",{"date":61,"type":33},"2026-05-04",{"date":63,"type":33},"2026-04-16",{"date":65,"type":22},"2028-09-19",{"name":39,"class":40},{"id":68,"slug":69,"hasResults":11,"nctId":70,"briefTitle":71,"officialTitle":72,"acronym":4,"eligibilityCriteria":73,"healthyVolunteers":11,"sex":17,"minAge":74,"maxAge":75,"enrollmentInfo":76,"targetDuration":4,"studyType":23,"phases":78,"briefSummary":79,"conditions":80,"keywords":4,"overallStatus":58,"whyStopped":4,"lastUpdateSubmitDate":82,"lastUpdatePostDateStruct":83,"startDateStruct":85,"completionDateStruct":87,"leadSponsor":89,"locationsCount":90},"100551152","digital-health-intervention-for-children-with-adhd-100551152","NCT06456372","Digital Health Intervention for Children With ADHD","Digital Health Intervention for Children With ADHD: Improving Mental Health Intervention, Patient Experiences, and Outcomes","Inclusion Criteria:\n\n1. DSM-5TR diagnosis of ADHD through prior medical or psychological evaluations at the time of admission to the program,\n2. ability to complete questionnaires and use an app in English,\n3. reported IQ of at least 80 in order to ensure that the participant has the cognitive skills needed to use the app, and\n4. parent\u002Fguardian available to consent and provide feedback in English.\n\nExclusion Criteria:\n\n* Failure to meet any of the inclusion criteria","8 Years","12 Years",{"count":77,"type":22},60,[53],"To conduct an RCT to evaluate the efficacy of the system, we will recruit 60 children (ages 8-12) with ADHD who will be randomized to either immediate (n=30) or delayed (n=30) treatment (i.e., a wait-list control group). Among those randomized to immediate treatment, half will be assigned to DHI (delivered via a smartwatch and smartphone application) and half will be assigned to an active control treatment as usual (TAU) group who will receive the smartwatch with no assigned activities, applications, or interventions on the devices. The intervention period will last 16 weeks; after a participant has been in the delayed treatment group for 16 weeks and has completed the post-waiting period assessment, he or she will be assigned to either the intervention or active control group. Thus, 30 participants will complete the intervention and 30 will complete the active control, with half of the total sample also completing a wait-list period.",[81],"ADHD","2026-01-26",{"date":84,"type":33},"2026-01-28",{"date":86,"type":33},"2025-02-22",{"date":88,"type":22},"2027-09-29",{"name":39,"class":40},2,{"id":92,"slug":93,"hasResults":11,"nctId":94,"briefTitle":95,"officialTitle":95,"acronym":4,"eligibilityCriteria":96,"healthyVolunteers":16,"sex":17,"minAge":97,"maxAge":98,"enrollmentInfo":99,"targetDuration":4,"studyType":23,"phases":101,"briefSummary":102,"conditions":103,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":82,"lastUpdatePostDateStruct":107,"startDateStruct":108,"completionDateStruct":110,"leadSponsor":112,"locationsCount":4},"100525511","by-youth-for-youth-digital-supported-peer-navigation-for-addressing-child-mental-health-care-100525511","NCT06122688","By Youth, For Youth: Digital Supported Peer Navigation for Addressing Child Mental Health Care","Inclusion Criteria:\n\n* Youth 13-22 enrolled in high school or participating primary care clinics, and their caregivers.\n\nExclusion Criteria:\n\n* Those not meeting inclusion criteria","13 Years","99 Years",{"count":100,"type":22},8360,[53],"Despite significant progress in research, practice, and policy over the past few decades, many children and youth continue to experience poor mental health outcomes. With their unrivaled ability to reach youth, school-based services and primary care are ideal hubs to provide mental health, healthcare, social services, and prevention to youth and families who otherwise face barriers to care. Using Participatory Design and Community Partnered Participatory Research (CPPR) for app development, mobile technology is designed to optimize access to wellness resources. The proposed intervention is a model of care using technology and navigators for connecting youth ages 13-22 to mental health care and supports. The app is co-created with the community and supported by culturally responsive individuals called family and youth navigators, in schools and primary care clinics. Outcomes are measured using the cascade of care model.",[104,105,106],"Anxiety","Depression","Mental Health Issue",{"date":84,"type":33},{"date":109,"type":22},"2026-07-01",{"date":111,"type":22},"2029-06-30",{"name":39,"class":40},{"id":114,"slug":115,"hasResults":11,"nctId":116,"briefTitle":117,"officialTitle":117,"acronym":4,"eligibilityCriteria":118,"healthyVolunteers":11,"sex":17,"minAge":48,"maxAge":4,"enrollmentInfo":119,"targetDuration":4,"studyType":23,"phases":120,"briefSummary":121,"conditions":122,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":124,"lastUpdatePostDateStruct":125,"startDateStruct":127,"completionDateStruct":129,"leadSponsor":131,"locationsCount":4},"100556887","comparing-two-linkage-to-care-models-for-latinx-immigrant-patients--a-pilot-comparative-clinical-effectiveness-trial-100556887","NCT06530953","Comparing Two Linkage-to-Care Models for Latinx Immigrant Patients : A Pilot Comparative Clinical Effectiveness Trial","Inclusion Criteria:\n\n* 1\\) live in the Coachella Valley, 2) 18 or older, 3) household income less than or equal to or below 200% of federal poverty guidelines, 4) do not currently have health insurance, and 5) have access to a telephone.\n\nExclusion Criteria:\n\n* Do not speak English, Spanish or Purépecha (an indigenous dialect spoken among the Purépecha of Mexico).",{"count":21,"type":22},[53],"The goal of this randomized clinical comparative effectiveness trail is to compare the effects of patient navigator models on follow-up care in Latinx and Indigenous Mexican immigrant patient populations. The main question\\[s\\] it aims to answer \\[is\u002Fare\\]:\n\n* Participants randomized to PN-CHW compared to the PN-CS model will be more likely to follow through with follow-up care referrals\n* Trust will be a driving factor as to why PN-CHW will be a more effective intervention for the patient population.\n\nResearchers will compare patients in a patient navigator community health worker (PN-CHW) intervention to those in a patient navigator clinical staff (PN-CS) intervention to see which model of linkage to care is more effective for follow-up care in the patient population.\n\nParticipants will be asked to:\n\n* Complete a baseline survey about healthcare access\n* Receive calls and text messages from either a CHW or clinical staff\n* Complete a follow up survey",[123],"Chronic Disease","2024-07-28",{"date":126,"type":33},"2024-07-31",{"date":128,"type":22},"2024-09-01",{"date":130,"type":22},"2025-12-31",{"name":39,"class":40},{"id":133,"slug":134,"hasResults":11,"nctId":135,"briefTitle":136,"officialTitle":136,"acronym":4,"eligibilityCriteria":137,"healthyVolunteers":16,"sex":17,"minAge":48,"maxAge":138,"enrollmentInfo":139,"targetDuration":4,"studyType":23,"phases":141,"briefSummary":142,"conditions":143,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":146,"lastUpdatePostDateStruct":147,"startDateStruct":149,"completionDateStruct":151,"leadSponsor":153,"locationsCount":41},"100542042","preventing-alcohol-use-disorders-and-alcohol-related-harms-in-pacific-islander-young-adults-100542042","NCT06337721","Preventing Alcohol Use Disorders and Alcohol-Related Harms in Pacific Islander Young Adults","Inclusion Criteria:\n\n1. Of full or part self-reported Pacific Islander heritage;\n2. Fluent (oral and reading) in English\n3. For young adult participants: 18 - 30 years of age\n4. Current drinking (1+ drink in past 30 days)\n5. High AUD risk (AUDIT-C score # 4 for men, # 3 for women)\n6. Not currently in alcohol treatment (medication, therapeutic).\n\nExclusion Criteria:\n\n1. Do not meet inclusion criteria\n2. Are unwilling to participate\n3. Fail to provide or retracts consent\n4. Reside outside the target Pacific Islander communities","30 Years",{"count":140,"type":22},240,[53],"This study will: (1) refine and finalize the SPEAR intervention manual for preventing alcohol use disorders (AUD) and associated harms for Pacific Islander young adults; and (2) test SPEAR for efficacy by conducting a pretest-posttest randomized controlled trial (RCT).",[144,145],"Alcohol Use Disorder","Alcohol; Harmful Use","2024-03-22",{"date":148,"type":33},"2024-03-29",{"date":150,"type":22},"2024-09",{"date":152,"type":22},"2028-08",{"name":39,"class":40},""]