[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"health-care-utilization\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:health-care-utilization":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,15,0,[8,43,67,94,117,147,172,211,233,257,280,319,344,377,416],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":21,"briefSummary":23,"conditions":24,"keywords":27,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100541185","comprehensive-connected-cancer-care-c4-intervention-evaluation-100541185",false,"NCT06326567","Comprehensive Connected Cancer Care (C4): Intervention Evaluation","Inclusion Criteria:\n\n* Patients with newly diagnosed or recurrent cancer who have not initiated treatment of any kind, including surgery, medical management, and\u002For radiation\n* Patients with one reported social determinants of health (SDOH) need OR patients at high-risk for SDOH needs based on demographic information (racial \\& ethnic minorities, medicaid\u002Funinsured populations).\n* Willingness to provide informed consent to participate\n\nExclusion Criteria:\n\n* Not able to understand and communicate in English\n* Unable and\u002For unwilling to access the internet on a phone, tablet, or computer","ALL","18 Years",{"count":18,"type":19},300,"ESTIMATED","INTERVENTIONAL",[22],"NA","The C4 program aims to provide a multi-level intervention program (Patient Level, Healthcare Team and Healthcare System Level) that improves the coordination of care with supportive\u002Fancillary care providers and community services through the use of patient navigation and a digital needs assessment and a closed-loop referral system and improves patient-centered communication and engagement in care through skills training for the healthcare team and provision of culturally appropriate patient educational tools and resources. The program components incorporate three areas that are critical to improving patient-centered care: coordination of care, patient-centered communication and engagement, and psychosocial care and other supportive services.",[25,26],"Cancer","Health Care Utilization",[28,29],"Community Programs","Health Equity","RECRUITING","2026-06-17",{"date":33,"type":34},"2026-06-22","ACTUAL",{"date":36,"type":34},"2024-02-01",{"date":38,"type":19},"2027-12",{"name":40,"class":41},"Timothy Mullett","OTHER",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":15,"minAge":50,"maxAge":51,"enrollmentInfo":52,"targetDuration":4,"studyType":54,"phases":4,"briefSummary":55,"conditions":56,"keywords":4,"overallStatus":57,"whyStopped":4,"lastUpdateSubmitDate":58,"lastUpdatePostDateStruct":59,"startDateStruct":61,"completionDateStruct":63,"leadSponsor":65,"locationsCount":4},"100627029","evaluation-of-barriers-and-unmet-needs-parental-satisfaction-and-measurement-of-utilization-of-dental-care-and-dental-services-100627029","NCT07443319","Evaluation of Barriers and Unmet Needs, Parental Satisfaction, and Measurement of Utilization of Dental Care and Dental Services","Evaluation of Barriers and Unmet Needs, Parental Satisfaction, and Measurement of Utilization of Dental Care and Dental Services Provided in Pediatric Dentistry Department in El Kasr El Einy. A Cross-Sectional Study: Part II","Inclusion Criteria:\n\n* Parents of children aged 2 to 12 years old.\n\nExclusion Criteria:\n\n* Parents refuse to sign the informed consent.","2 Years","12 Years",{"count":53,"type":19},1058,"OBSERVATIONAL","Evaluation of the barriers and unmet needs of using dental services for children and measure the extent of parents' satisfaction with the service provided to their children using database information for the health facility by cross sectional studies",[26],"NOT_YET_RECRUITING","2026-02-25",{"date":60,"type":34},"2026-03-02",{"date":62,"type":19},"2026-03",{"date":64,"type":19},"2026-09",{"name":66,"class":41},"Cairo University",{"id":68,"slug":69,"hasResults":11,"nctId":70,"briefTitle":71,"officialTitle":72,"acronym":4,"eligibilityCriteria":73,"healthyVolunteers":74,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":75,"targetDuration":4,"studyType":20,"phases":76,"briefSummary":77,"conditions":78,"keywords":79,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":84,"lastUpdatePostDateStruct":85,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":93},"100485744","ucsd-relink-connecting-adults-to-supportive-services-100485744","NCT05605054","UCSD RELINK: Connecting Adults To Supportive Services","An RCT Testing a Health Literacy Intervention to Reduce Disparities in Access to Care Among Minority Justice-Involved Adults","Inclusion Criteria:\n\n1. Provision of signed and dated informed consent form\n2. Stated willingness to comply with all study procedures and availability for the duration of the study\n3. Persons, aged 18 and over\n4. Resident of San Diego County\n5. Not incarcerated at time of enrollment\n6. Justice involved in the past 3 years (on parole, probation, court diverted)\n7. Understands English\n8. Access to a cell phone\n\nExclusion Criteria:\n\n1. Under the age of 18 years old\n2. Not a resident of San Diego County\n3. Incarcerated at enrollment\n4. Not justice-involved within the last 3 years (i.e., not on probation or parole or was court-diverted in the past 3 years)\n5. No access to a cell phone\n6. Cannot provide informed consent\n7. Does not understand English\n8. Previously enrolled in the pilot UCSD RELINK program\n9. Adults who have current or prior convictions related to sexual violence\u002Fabuse (Penal Code \\[PC\\] 290), lewd acts with a child (PC 288), child abduction (PC 280), or arson (PC 451)",true,{"count":18,"type":19},[22],"The goal of this randomized intervention study is to learn about effective health literacy teaching methods in Justice Involved Adults (JIA).\n\nResearchers will compare coach-guided health literacy or self-study design to see if there is a difference in the access and use of healthcare in this population.\n\nThe main questions it aims to answer are:\n\n* Will this improve access and use of heath services?\n* Will this improve health insurance coverage and long term use of health services?\n\nParticipants will:\n\n* Meet with a health coach and service navigator during 12 sessions or meet with service navigator and complete online training over 12 weeks.\n* Complete surveys at different time (6months, 1 year)",[26],[80,81,82,83],"Justice Involved Adults","Re-entry Population","Health Coaching","Service Navigation","2026-02-17",{"date":86,"type":34},"2026-02-20",{"date":88,"type":34},"2023-03-17",{"date":90,"type":19},"2027-03-31",{"name":92,"class":41},"Victoria D. Ojeda",2,{"id":95,"slug":96,"hasResults":11,"nctId":97,"briefTitle":98,"officialTitle":99,"acronym":4,"eligibilityCriteria":100,"healthyVolunteers":11,"sex":15,"minAge":101,"maxAge":4,"enrollmentInfo":102,"targetDuration":4,"studyType":20,"phases":104,"briefSummary":105,"conditions":106,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":108,"lastUpdatePostDateStruct":109,"startDateStruct":111,"completionDateStruct":113,"leadSponsor":115,"locationsCount":42},"100422279","acp-video-intervention-for-patients-with-life-limiting-illness-100422279","NCT04778761","ACP Video Intervention for Patients With Life-Limiting Illness","Randomized Trial of a Home-Advance Care Planning Video Intervention for Patients With Life-Limiting Illness","Inclusion Criteria:\n\n* Aged 21 or over\n* Have a one-year prognosis or less as determined by Clover Health's validated algorithm\n* Speak either English or one of the other 25 languages in which the video intervention is available\n\nExclusion Criteria:\n\n* Visually impaired beyond 20\u002F200 corrected\n* Acute psychiatric illness or other comorbid condition that impairs cognitive ability to participate in advance care planning discussion as determined by the primary House Call Provider.","21 Years",{"count":103,"type":19},500,[22],"The goal of this research is to increase patients' knowledge about advance care planning (ACP) discussions and hospice care for patients with serious illness receiving home-based care.",[26,107],"End Stage Disease","2026-01-15",{"date":110,"type":34},"2026-01-20",{"date":112,"type":34},"2021-04-01",{"date":114,"type":19},"2027-12-01",{"name":116,"class":41},"Massachusetts General Hospital",{"id":118,"slug":119,"hasResults":11,"nctId":120,"briefTitle":121,"officialTitle":122,"acronym":123,"eligibilityCriteria":124,"healthyVolunteers":74,"sex":125,"minAge":16,"maxAge":4,"enrollmentInfo":126,"targetDuration":4,"studyType":20,"phases":128,"briefSummary":129,"conditions":130,"keywords":131,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":138,"lastUpdatePostDateStruct":139,"startDateStruct":141,"completionDateStruct":143,"leadSponsor":145,"locationsCount":42},"100568537","evaluation-of-a-health-system-integrated-model-for-postpartum-education-and-support-in-rural-populations-100568537","NCT06682520","Evaluation of a Health System Integrated Model for Postpartum Education and Support in Rural Populations","Evaluation of a Health System Integrated Model for Postpartum Education and Support in Rural Populations - NEST-Rural","NEST-Rural","Inclusion Criteria:\n\n1. Women that deliver an infant(s) at The Birth Center at Atrium Health Wake Forest Baptist and currently reside in Davidson, Davie, Stokes, Wilkes or Yadkin County in North Carolina\n2. Women that delivered an infant(s) at home, were transported to Atrium Health Wake Forest Baptist and received postpartum care at The Birth Center and currently reside in Davidson, Davie, Stokes, Wilkes or Yadkin County in North Carolina\n3. Ages 18 years or older\n\nExclusion Criteria:\n\n1. Women that delivered an infant(s) and did not receive postpartum care at The Birth Center at Atrium Health Wake Forest Baptist.\n2. Women that currently reside outside of Davidson, Davie, Stokes, Wilkes or Yadkin County in North Carolina\n3. Under 18 years of age","FEMALE",{"count":127,"type":19},1300,[22],"This study was designed to evaluate the implementation of the Nurse Education and Support Team (NEST) Program for postpartum women who reside in 5 rural counties in North Carolina. Overarching Hypothesis: Mothers and infants residing in rural communities, randomized to the NEST-Rural care model over the 3-year course of the project will: 1. Receive more coordinated care for addressing social, mental and physical health needs. 2. Experience fewer postpartum hospital readmissions and decreased utilization of emergency departments (ED) for healthcare. 3. Experience higher adherence to American College of Obstetricians and Gynecologists (ACOG) and American Academy of Pediatrics (AAP) guidelines for preventive care, including recently updated ongoing postpartum care, serial well-child visits and vaccinations compared to those assigned to usual care. This group will be compared to those assigned to usual care,",[26],[132,133,134,135,136,137],"Remote blood pressure monitoring","Postpartum Nurse home visiting","Postpartum Health Care Services","Postpartum Hospital Program Service Model","Maternal Health","Newborn Health","2025-10-24",{"date":140,"type":34},"2025-10-28",{"date":142,"type":34},"2024-12-04",{"date":144,"type":19},"2029-12",{"name":146,"class":41},"Wake Forest University Health Sciences",{"id":148,"slug":149,"hasResults":11,"nctId":150,"briefTitle":151,"officialTitle":152,"acronym":153,"eligibilityCriteria":154,"healthyVolunteers":74,"sex":155,"minAge":156,"maxAge":4,"enrollmentInfo":157,"targetDuration":4,"studyType":20,"phases":159,"briefSummary":160,"conditions":161,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":163,"lastUpdatePostDateStruct":164,"startDateStruct":166,"completionDateStruct":168,"leadSponsor":170,"locationsCount":42},"100530388","universal-basic-income-and-structural-racism-in-the-us-south-hiv-care-100530388","NCT06186128","Universal Basic Income and Structural Racism in the US South: HIV Care","Universal Basic Income and Structural Racism in the US South: Differences in HIV Care Utilization Between Low-income African American Men Living With HIV","017744S","Inclusion Criteria:\n\n1. be at least 25 years old;\n2. self-report as having received from a medical professional a diagnosis for HIV;\n3. have an annual income up to 400% of the federal poverty threshold (the 2023 federal poverty threshold is defined as an annual income of less than $14,580 for single adults) in the 12-month period prior to study enrollment;\n4. be able to understand and speak English and to provide written and verbal informed consent;\n5. plan to remain in the central Arkansas area for the duration of the study period;\n6. be willing and able to provide weekly information about all activities related to seeking employment and to share financial and income-related information with the study team;\n7. self-identify as Black or African American;\n8. have been assigned the male gender at birth;\n9. be willing to provide medical releases to allow project staff to access healthcare records, and\n10. in need of HIV care services (defined as having a detectable viral load meaning \\>200 copies\u002FmL on most recent viral load test or not having attended a HIV medical care visit in the past 6 months, excluding any visits to the emergency department or rooms or urgent care clinics)\n\nExclusion Criteria:\n\n\\-","MALE","25 Years",{"count":158,"type":19},80,[22],"Universal Basic Income (UBI) is a promising strategy aimed at recalibrating economic systems that are grounded in structural racism. Black men have long been the target of oppressive and interconnected systems of finance and healthcare access, leading to a disproportionate burden of exposure to infectious disease with little healthcare support. Yet to our knowledge, no published UBI studies have ever been implemented exclusively with Black men living with HIV in the US. Motivated and inspired by the innovative health and social science being conducted in extremely resource-limited environments in other parts of the world, we recognize an urgent need to better understand the effect of cash transfers on HIV care among Black men in the US South. The proposed study will be based in Arkansas, which, like other Southern states, has a long history of institutional racism and extremely high rates of racial health disparities, poverty, and chronic disease. We will use a mixed methods research design to conduct an in-depth exploration of a UBI intervention to reduce the racial wage gap and promote the use of culturally relevant protective factors. The provision of a UBI is intended to increase receipt and retention of HIV care services and treatment for Black men through the influx of capital and subsequent increases in culturally-based protective factors such as personal agency and social connections. We hypothesize that providing UBI of $500 per month for 6 months will result in increased HIV care utilization among low-income Black men living with HIV. Secondarily, we hypothesize that the effect of UBI will also increase adherence to HIV medication, such that more UBI recipients will achieve and maintain viral suppression compared to individuals in the control condition.",[162,26],"HIV","2025-10-16",{"date":165,"type":34},"2025-10-20",{"date":167,"type":34},"2023-08-03",{"date":169,"type":19},"2026-12-31",{"name":171,"class":41},"University of Arkansas",{"id":173,"slug":174,"hasResults":11,"nctId":175,"briefTitle":176,"officialTitle":177,"acronym":178,"eligibilityCriteria":179,"healthyVolunteers":74,"sex":125,"minAge":16,"maxAge":4,"enrollmentInfo":180,"targetDuration":4,"studyType":20,"phases":182,"briefSummary":183,"conditions":184,"keywords":194,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":202,"lastUpdatePostDateStruct":203,"startDateStruct":205,"completionDateStruct":207,"leadSponsor":209,"locationsCount":42},"100592937","enhanced-mentor-mother-strategy-for-pregnant-and-postpartum-women-living-with-hiv-100592937","NCT06999928","Enhanced Mentor Mother Strategy for Pregnant and Postpartum Women Living With HIV","Pilot Implementation-Effectiveness Study of an Enhanced Mentor Mother Strategy","PIE-eMMs","Inclusion Criteria:\n\n* Pregnant and postpartum women living with HIV (and their infants born during the study)\n* ≥18 years of age\n* Enrolled in PMTCT services at BFSDH\n* Able to understand and provide informed consent in English or Kiswahili\n\nExclusion Criteria:\n\n* Women who are not pregnant or postpartum\n* \\\u003C18 years of age\n* Not enrolled in PMTCT services at BFSDH\n* Unable to understand and provide informed consent in English or Kiswahili\n* Cognitive impairment that would interfere with ability to participate in the study",{"count":181,"type":19},200,[22],"Mentor Mothers (MMs) are peer supporters who help pregnant and postpartum women living with HIV (WLHIV) as they receive prevention of mother-to-child transmission of HIV (PMTCT) services in resource-limited settings like Kenya. Differentiated service delivery (DSD) is a care model that tailors services based on clients' needs, helping to improve both the quality and efficiency of care.\n\nThis hybrid implementation-effectiveness study will test whether an enhanced MM strategy that uses DSD can be successfully carried out and improve health outcomes for mothers and infants. The study will take place at Burnt Forest Sub-District Hospital (BFSDH) in Kenya.\n\nResearchers will ask:\n\n* Can the enhanced MM strategy be delivered as planned and accepted by patients and staff?\n* Does the strategy improve clinical outcomes like keeping mothers in PMTCT care, achieving HIV viral suppression, completing infant HIV testing, and preventing HIV transmission to infants? Researchers will compare health outcomes before and after the strategy is introduced at BFSDH, and also compare outcomes at other similar clinics that continue with standard MM services.\n\nWomen who choose to participate will meet with a MM during their routine antenatal and postnatal clinic visits. They will be offered the enhanced MM support, but can choose to receive standard care if they prefer.",[185,186,187,188,189,190,26,191,192,193],"Hiv","Transmission Vertical","Viremia","Adherence, Treatment","Stigmatization","Socioeconomic Adversity","Health Care Acceptability","Peer Group","Mothers",[195,196,197,198,199,200,201],"prevention of mother-to-child transmission","retention","implementation","mentor mothers","differentiated service delivery","maternal-child health","Kenya","2025-07-14",{"date":204,"type":34},"2025-07-15",{"date":206,"type":34},"2025-07-10",{"date":208,"type":19},"2026-10-12",{"name":210,"class":41},"Indiana University",{"id":212,"slug":213,"hasResults":11,"nctId":214,"briefTitle":215,"officialTitle":216,"acronym":217,"eligibilityCriteria":218,"healthyVolunteers":74,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":219,"targetDuration":4,"studyType":54,"phases":4,"briefSummary":221,"conditions":222,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":224,"lastUpdatePostDateStruct":225,"startDateStruct":227,"completionDateStruct":229,"leadSponsor":231,"locationsCount":42},"100515267","structural-conditions-and-health-after-release-from-prison-100515267","NCT05989282","Structural Conditions and Health After Release From Prison","Healthcare Organizational Structural Conditions and the Health of People Recently Released From Prison","SCHARP","Inclusion Criteria:\n\n* Recenlty released from state prison into the Denver\u002FAurora Colorado metro area\n* Age 18 and older\n* Ability to understand study procedures in English or Spanish\n* No plans to leave the area for six months\n\nExclusion Criteria:\n\n* On \"current inmate\" status or still under correctional observation (i.e., under locked confinement part of the day or night)\n* Plans to leave area within six months\n* Unable to consent",{"count":220,"type":19},400,"People released from prison experience two times higher cardiovascular (CV) mortality than the general population, have a high prevalence of poor CV health and increased risk of CV events within 2 years of release. Access to high quality healthcare following release from prison is key to preventing poor health and CV outcomes. Our study team will investigate facilitators and barriers to health care access experienced by people released from prison.",[223,26],"Cardiovascular Diseases","2025-02-26",{"date":226,"type":34},"2025-02-28",{"date":228,"type":34},"2023-08-05",{"date":230,"type":19},"2028-06-30",{"name":232,"class":41},"Kaiser Permanente",{"id":234,"slug":235,"hasResults":11,"nctId":236,"briefTitle":237,"officialTitle":238,"acronym":4,"eligibilityCriteria":239,"healthyVolunteers":74,"sex":15,"minAge":16,"maxAge":240,"enrollmentInfo":241,"targetDuration":4,"studyType":20,"phases":243,"briefSummary":244,"conditions":245,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":248,"lastUpdatePostDateStruct":249,"startDateStruct":251,"completionDateStruct":253,"leadSponsor":255,"locationsCount":42},"100474213","one-4-all-initiative-100474213","NCT05454969","One-4-ALL Initiative","Transforming Healthcare in Post-Pandemic Recovery: Innovation in Process & Technology to Increase Patient Throughput While Reducing Clinician Burden and Addressing Health Disparities (One-4-ALL Initiative)","Inclusion Criteria:\n\n* All guardians of patients and the providers (surgeons, doctors, nurses, etc) that serve these patients.\n\nExclusion Criteria:\n\n* None.","99 Years",{"count":242,"type":19},100,[22],"This study aims to improve health outcomes of individuals and populations, enhance the patient experience, reduce the per capita cost of care, and ensure the well-being of our healthcare providers (quadruple aim). These goals are increasingly difficult to achieve, given the challenges of changes to workflow, staffing shortages, and increased costs brought on by the COVID-19 pandemic. Further, the pandemic brought to light the critical need to transform healthcare access for our racially and culturally minoritized and low-income families that have long been victims of health disparities, specifically with poorer health outcomes.",[246,247,26],"Literacy","Burden, Caregiver","2024-09-27",{"date":250,"type":34},"2024-10-01",{"date":252,"type":34},"2023-09-01",{"date":254,"type":19},"2025-12-30",{"name":256,"class":41},"University of Colorado, Denver",{"id":258,"slug":259,"hasResults":11,"nctId":260,"briefTitle":261,"officialTitle":262,"acronym":4,"eligibilityCriteria":263,"healthyVolunteers":11,"sex":125,"minAge":16,"maxAge":4,"enrollmentInfo":264,"targetDuration":4,"studyType":20,"phases":266,"briefSummary":267,"conditions":268,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":270,"lastUpdatePostDateStruct":271,"startDateStruct":273,"completionDateStruct":275,"leadSponsor":277,"locationsCount":42},"100562545","the-effect-of-patient-discharge-from-the-maternal-and-fetal-medicine-unit-with-receiving-a-discharge-letter-later-using-the-apollo-app-on-discharge-data-safety-and-patient-satisfaction-100562545","NCT06604559","The Effect of Patient Discharge From the Maternal and Fetal Medicine Unit With Receiving a Discharge Letter Later Using the Apollo App on Discharge Data, Safety and Patient Satisfaction","The Effect of Patient Discharge From the Maternal and Fetal Medicine Unit With Receiving a Discharge Letter Later Using the Apollo App on Discharge Data, Safety and Patient Satisfaction - a Prospective Randomized Controlled Trial","Inclusion Criteria:\n\n* Women who are admitted to the maternal and fetal medicine unit with the intention to be discharged before delivery\n* 18 years old and older\n* Consent to participate\n* Owner of a smart phone\n* Consent to download the Apollo app\n\nExclusion Criteria:\n\n* Delivery during her admission\n* Doesn't own a smart phone\n* Refusal to download to Apollo app\n* Refusal to participate",{"count":265,"type":19},140,[22],"Women admitted to the maternal and fetal medicine unit are often discharged after a short hospital stay. The routine work in the department is prioritized such that the discharge letter are written. In the last year the Apollo mobile application (app) was introduced. It contains general information on the medical center and the maternal and fetal unit department as well as the medical records, laboratory results and summary and discharge letters. The Apollo app is used in the maternal and fetal unit in the discharge process so the patient can receive the discharge letter in the app and does not need to wait until the discharge letter is written.\n\nIt is not known whether this process is more effective than the regular discharge process and patients' satisfaction was not assessed previously.\n\nIn the present study we will compare discharge data, satisfaction and safety of discharging using the Apollo app versus the routine process.",[269,26],"Patient Satisfaction","2024-09-17",{"date":272,"type":34},"2024-09-19",{"date":274,"type":19},"2024-11-30",{"date":276,"type":19},"2025-09-05",{"name":278,"class":279},"The Baruch Padeh Medical Center, Poriya","OTHER_GOV",{"id":281,"slug":282,"hasResults":11,"nctId":283,"briefTitle":284,"officialTitle":284,"acronym":285,"eligibilityCriteria":286,"healthyVolunteers":74,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":287,"targetDuration":289,"studyType":54,"phases":4,"briefSummary":290,"conditions":291,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":310,"lastUpdatePostDateStruct":311,"startDateStruct":313,"completionDateStruct":314,"leadSponsor":316,"locationsCount":42},"100553518","virtual-peri-menopause-registry-of-australia-100553518","NCT06487130","Virtual perI-\u002FMenopause Registry of AusTrALia","VITAL","Inclusion Criteria:\n\n* Any Australian over 18 years of age.\n\nExclusion Criteria:\n\n* None.",{"count":288,"type":19},10000,"50 Years","13 million (50.7%) Australians are born with ovaries, 14% (\\~3 million) are currently aged 40-59 yrs, \\& all such who live to midlife will experience menopause, defined as \\>12 months without a period. Peri-menopause (peri), typically occurs 5 yrs before menopause as hormone levels decrease. As with oestrogen, peri symptoms can affect every bodily system; e.g. depression\u002Fanxiety, diminished mental function, irregular periods, hot flushes, sleep problems, vaginal atrophy \\& urinary urgency. These symptoms are linked with lower quality of life \\& significantly higher work impairment; a third experiencing symptoms so severe as to impede daily life \\& increase risk of suicide. Lifetime increased risks of diabetes, heart disease, osteoporosis \\& dementia are also associated with menopause, yet it remains disconcertingly poorly studied.\n\nThe investigators propose to create a world-first, cutting-edge, consumer-driven, Virtual peri-\u002Fmenopause registry of AusTrALia (VITAL). The unique design will enable consumers to determine VITAL's questions, encourage secure revelation of private data e.g. vaginal \\& mental health symptoms, \\& to direct priorities for research, education, \\& health service improvements. VITAL will thus deliver optimal assessments of incidence, prevalence \\& impact.\n\nThe participating consumers, researchers, clinical specialists, policy makers, \\& modern virtual data infrastructure enable this unique \\& innovative registry design, future translation to improved community health, \\& promote awareness \\& collaborative synergies. Leveraging the investigators' critical range of expertise \\& ongoing feedback opportunities for both participants \\& stakeholder partnerships, the investigators will create a ground-breaking platform that:\n\n* empowers the consumer voice and priorities,\n* enables peri-\u002Fmenopause research to extend beyond existing niche focuses,\n* evidences the true impact of peri-\u002Fmenopause across the nation,\n* evolves healthcare services and outcomes, \\&\n* educates community, clinicians, \\& policy-makers. After Australian registry establishment, the investigators will expand VITAL to mirror it in other nations while still protecting individual's data the right way, but so all can learn \\& apply the best aspects of care from across the world.",[292,293,294,295,296,26,297,298,299,300,301,302,303,304,223,305,306,307,308,309],"Menopause","Perimenopausal Disorder","Postmenopausal Symptoms","Health Knowledge, Attitudes, Practice","Healthy Aging","Health Care Seeking Behavior","Mental Health Impairment","Mental Deterioration","Mental Health Issue","Osteoporosis, Postmenopausal","Diabetes Mellitus Risk","Diabetes Mellitus, Type 2","Dementia","Menopause Related Conditions","Hot Flashes","Hot Flushes Aggravated","Economic Burden","Social Stigma","2024-07-02",{"date":312,"type":34},"2024-07-05",{"date":167,"type":34},{"date":315,"type":19},"2073-08",{"name":317,"class":318},"Bespoke Clinical Research","INDUSTRY",{"id":320,"slug":321,"hasResults":11,"nctId":322,"briefTitle":323,"officialTitle":323,"acronym":324,"eligibilityCriteria":325,"healthyVolunteers":74,"sex":125,"minAge":326,"maxAge":16,"enrollmentInfo":327,"targetDuration":4,"studyType":20,"phases":329,"briefSummary":330,"conditions":331,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":335,"lastUpdatePostDateStruct":336,"startDateStruct":338,"completionDateStruct":340,"leadSponsor":342,"locationsCount":42},"100519442","evaluation-of-the-safespace-app-intervention-100519442","NCT06043596","Evaluation of the SafeSpace App Intervention","SafeSpace","Inclusion Criteria:\n\n* Participants must be assigned female or intersex at birth\n* Participants must be youth in the U.S. (14-18 years old)\n* Participants must have daily access to an iPhone\n\nExclusion Criteria:\n\n\\- Participants must not be currently pregnant or currently trying to become pregnant\n\nOther Criteria:\n\n\\- The study's priority\u002Fpreference population is for Black and\u002For Latine youth, LGBTQ+ youth, youth from geographic areas with high teen birth rates, and youth living in rural areas.","14 Years",{"count":328,"type":19},1000,[22],"The goal of this study is to evaluate the impact of SafeSpace Sexual Health App, an innovative sexual health promotion program focused on reducing sexual risk factors and promoting sexual and reproductive health and wellbeing among young people assigned female or intersex at birth, particularly Black and\u002For Latine youth, LGBTQ+ youth, youth in states with high teen birth rates and youth who live in rural communities. This study utilizes a two-arm randomized control trial design to measure impacts of receiving the SafeSpace Sexual Health program compared to receiving a similar-length control app program, SafeSpace General Health that focuses on general health.\n\nThe investigators will ask participants to:\n\n* Keep the SafeSpace app downloaded to their device and visit the app regularly over the course of 10 weeks.\n* Provide contact information.\n* Receive and open app push notifications for 10 weeks (up to 3 per week).\n* Complete 3 online surveys over a year: baseline, short-term follow-up (10 weeks after baseline), and long-term follow up (9 months after short-term follow-up).\n* Receive occasional text messages from the study team.",[332,26,333,334],"Health Behavior","Unprotected Sex","Sexually Transmitted Infections","2023-11-17",{"date":337,"type":34},"2023-11-21",{"date":339,"type":34},"2023-06-12",{"date":341,"type":19},"2026-09-29",{"name":343,"class":41},"Child Trends",{"id":345,"slug":346,"hasResults":11,"nctId":347,"briefTitle":348,"officialTitle":349,"acronym":350,"eligibilityCriteria":351,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":352,"enrollmentInfo":353,"targetDuration":4,"studyType":20,"phases":355,"briefSummary":356,"conditions":357,"keywords":365,"overallStatus":57,"whyStopped":4,"lastUpdateSubmitDate":368,"lastUpdatePostDateStruct":369,"startDateStruct":371,"completionDateStruct":373,"leadSponsor":375,"locationsCount":4},"100516284","relief-pathway-in-patients-with-upper-abdominal-pain-100516284","NCT06002516","RELIEF-pathway in Patients With Upper Abdominal Pain","The RELIEF-pathway in Patients With Upper Abdominal Pain; an Open-label Multicenter Randomized Controlled Trial","RELIEF","Inclusion Criteria:\n\n* Patients between 18 and 70 years old.\n* First referral due to upper abdominal pain (UAP) and symptoms due to Functional dyspepsia (ICPC code 87.02), Irritable Bowel syndrome (ICPC 93.0) or uncomplicated symptomatic cholecystolithiasis (ICPC 98.03).\n* Proficient in reading and understanding of the Dutch language.\n* Referred to the outpatient clinic of gastroenterology or surgery.\n* Providing informed consent.\n\nExclusion Criteria:\n\n* If the following alarm symptoms are reported in the referral letter by the GP: weight loss, persistent vomiting, dysphagia, jaundice, hematemesis, melena, haematochezia, or anaemia.\n* Any other direct or indirect signs of cancer or upper GI tract bleeding.\n* Patients with a first or second-degree relative with a history of upper GI tract malignant neoplasm.\n* Patients with a history of complicated cholecystolithiasis.\n* A history of or current malignancy (except SCC or BCC of the skin).\n* Pregnancy;\n* Expected short life span of less than 12 months.\n* Known cirrhosis of the liver\n* Current schizophrenia, memory deficiency, or any other disorder that predispose them to unreliable questionnaire responses;\n* Mentally incompetent;","70 Years",{"count":354,"type":19},471,[22],"Upper abdominal pain (UAP) is a common symptom and frequently the reason to visit the hospital. The prevalence of epigastric pain in the Dutch population is estimated to be as high as 37%. Moreover, Dutch hospitals yearly record \\>100.000 diagnoses related to UAP. In most patients, UAP can be attributed to symptomatic (functional) dyspepsia (FD), Irritable Bowel Syndrome (IBS) or uncomplicated gallstone disease (cholecystolithiasis), with a prevalence in the general population of 20-30%, 20%, and 6-9%, respectively. However, these conditions may have overlapping symptom patterns and generally affect similar populations. which contributes to ineffective (diagnostic) interventions. Patients are generally not aware of the similarity of symptoms and the poor outcome of some treatments.\n\nEducation positively influences patients' self-management and health judgment. In a recent open-label, multicentre trial the effectiveness of web-based patients' education is applied to reduce overuse of upper gastrointestinal endoscopies in patients with dyspepsia. This study illustrated that an web-based education tool safely reduced 40% in upper gastrointestinal endoscopies. Lifestyle interventions (such as change of diet and\u002For physical activity) are widely incorporated in treatment programs for cardio-vascular diseases including diabetes mellitus and obesity. An web-based education tool on upper abdominal pain and other complaints combined with a lifestyle interventions for patients may be an effective treatment option for this large group of patients.\n\nThis study investigates the potential of an individualized web-based education tool as intervention for patients with functional dyspepsia, irritable bowel syndrome and uncomplicated symptomatic cholecystolithiasis with the possibility to visit the Prevention and Lifestyle clinic (RELIEF pathway). The RELIEF pathway aims to reduce unnecessary health care utilization and, secondly, to maintain and improve quality of life by educating patients on lifestyle improvement.",[358,359,360,361,26,362,363,364],"Abdominal Pain","Gallstone; Colic","Dyspepsia","Irritable Bowel Syndrome","Patient Reported Outcomes","Upper Abdominal Pain","Decision Aid",[366,367],"Abdominal pain","Health care utilization","2023-08-15",{"date":370,"type":34},"2023-08-21",{"date":372,"type":19},"2024-05-01",{"date":374,"type":19},"2027-05-01",{"name":376,"class":41},"Radboud University Medical Center",{"id":378,"slug":379,"hasResults":11,"nctId":380,"briefTitle":381,"officialTitle":382,"acronym":4,"eligibilityCriteria":383,"healthyVolunteers":74,"sex":125,"minAge":326,"maxAge":384,"enrollmentInfo":385,"targetDuration":4,"studyType":20,"phases":387,"briefSummary":388,"conditions":389,"keywords":397,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":407,"lastUpdatePostDateStruct":408,"startDateStruct":410,"completionDateStruct":412,"leadSponsor":414,"locationsCount":42},"100427378","fresh-rx-nhs-2020-100427378","NCT04845230","Fresh RX: NHS 2020","Fresh RX: Nourishing Healthy Starts Clinical Study","Inclusion Criteria:\n\n* Female\n* Pregnant\n* Less than 24 weeks gestation\n* Screening positive to a USDA two-item food insecurity screener (described below)\n* Receiving care through a Missouri Medicaid managed care organization\n* English speaking\n* Age 14-55\n* Missouri resident residing in the following zip codes: 63031, 63033, 63042, 63074, 63114, 63121, 63130, 63132, 63133, 63135, 63136, 63137, 63138, 63140\n\nExclusion Criteria:\n\n* Male\n* Non-pregnant\n* Pregnant, but more than 24 weeks gestation\n* Does not screen positive to a USDA two-item food insecurity screener (described below)\n* Does not receive care through the Home State Health managed care organization\n* Non-English speaking\n* Aged less than 14 or more than 55\n* Does not reside in the following zip codes: 63031, 63033, 63042, 63074, 63114, 63121, 63130, 63132, 63133, 63135, 63136, 63137, 63138, 63140","55 Years",{"count":386,"type":19},750,[22],"This study is an evaluation of the Fresh Rx: Nourishing Healthy Starts program administered by Operation Food Search, a St. Louis-based nonprofit organization. The program provides food and nutrition supports to food insecure pregnant women in conjunction with integrative care services in order to improve health and birth outcomes for both the mother and the child. The purpose of this study is to test the efficacy of this approach through a field experiment, and to assess the extent to which these services can provide cost savings to the healthcare system.",[390,391,392,26,393,394,395,396],"Premature Birth","Birth Weight","Post Partum Depression","Nutrition Deficiency Due to Insufficient Food","Housing Problems","Fetal Complications","Food Deprivation",[398,399,400,401,402,403,404,405,406],"food insecurity","pregnancy","maternal health","neonatal health","birth outcomes","poverty","health care utilization","field experiment","integrative care","2022-11-27",{"date":409,"type":34},"2022-11-29",{"date":411,"type":34},"2021-08-09",{"date":413,"type":19},"2026-09-15",{"name":415,"class":41},"Washington University School of Medicine",{"id":417,"slug":418,"hasResults":11,"nctId":419,"briefTitle":420,"officialTitle":421,"acronym":422,"eligibilityCriteria":423,"healthyVolunteers":11,"sex":15,"minAge":384,"maxAge":424,"enrollmentInfo":425,"targetDuration":4,"studyType":20,"phases":426,"briefSummary":427,"conditions":428,"keywords":4,"overallStatus":57,"whyStopped":4,"lastUpdateSubmitDate":433,"lastUpdatePostDateStruct":434,"startDateStruct":436,"completionDateStruct":438,"leadSponsor":440,"locationsCount":442},"100385501","urinary-proteomics-combined-with-home-blood-pressure-telemonitoring-for-health-care-reform-100385501","NCT04299529","Urinary Proteomics Combined With Home Blood Pressure Telemonitoring for Health Care Reform","Urinary Proteomics Combined With Home Blood Pressure Telemonitoring for Health Care Reform: a Randomised Controlled Trial","UPRIGHT-HTM","Inclusion Criteria:\n\n* Patients must have at least three additional guideline-defined risk factors, preferably including hypertension, type 2 diabetes mellitus (T2DM), or both;\n* Patients should be willing patients to engage for the duration of the study in home blood pressure telemonitoring (1 reading per day);\n* Patients must have an email address and internet access via smartphone, tablet, or laptop or desktop computer;\n* Patients should comply with the study protocol during the run-in phase.\n\nExclusion Criteria:\n\n* Type 1 diabetes mellitus;\n* Absence of a practicable echocardiographic window;\n* Previous or concurrent severe cardiovascular or non-cardiovascular disease;\n* Cancer within 5 years of enrolment;\n* Suspected substance abuse;\n* Psychiatric illness;\n* Use of nephrotoxic drugs;\n* Particpation in another clinical study.","75 Years",{"count":328,"type":19},[22],"UPRIGHT-HTM will compare risk stratification, treatment efficiency and health economic outcomes of a diagnostic approach based on home blood pressure telemonitoring combined with urinary proteomic profiling with home blood pressure telemonitoring alone",[429,430,26,431,432],"Protein Deregulation","Blood Pressure","Cost Effectiveness","Patient Empowerment","2020-03-05",{"date":435,"type":34},"2020-03-06",{"date":437,"type":19},"2020-04-01",{"date":439,"type":19},"2026-07-31",{"name":441,"class":41},"KU Leuven",12]