[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"disease-management\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:disease-management":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,50,74],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":32,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100505073","delivering-food-resources--kitchen-skills-forks-to-adults-with-food-insecurity-and-hypertension-100505073",false,"NCT05856591","Delivering Food Resources & Kitchen Skills (FoRKS) to Adults With Food Insecurity and Hypertension","Delivering Food Resources & Kitchen Skills (FoRKS) to Adults With Food Insecurity and Hypertension: An RCT","FoRKS","Inclusion Criteria:\n\n1. Fluent in English\n2. Marion County resident\n3. 35-75 years\n4. Systolic BP of ≥120 in prior 12 months\n5. Ability to see and read street signs (self report)\n6. Stable housing with independent access to kitchen, including functional stove or hotplate, oven, refrigerator, and freezer (self report)\n7. Activity independence per functional activities questionnaire (FAQ; \\\u003C3 responses of \"Require Assistance\" and 0 responses of \"Dependent\")\n8. Food insecurity per first two items of USDA 18-item survey with ≥ 1 response of \"Often true\" or \"Sometimes true\" \\[1) Within the past 12 months, you worried that your food would run out before you got the money to buy more; 2) Within the past 12 months, the food you bought just didn't last and you didn't have money to get more.\\] OR currently listed as food insecure in Eskenazi EMR; OR currently receiving SNAP benefits.\n9. normal cognition per six-item screener (SIS; score of ≥ 5)\n10. Mean systolic BP of ≥120 from 3 standard BP measurements taken by research staff following standardized wait periods.\n\nExclusion Criteria:\n\n1. lives in nursing home\n2. diagnosis of dementia or Alzheimer disease or mild cognitive impairment; Parkinson disease; brain tumor\u002Finfection\u002Fsurgery (within the last 10 years with residual symptoms and\u002For functional loss\u002Fdeficit, such as impaired learning, memory, or communication); psychosis, schizophrenia, or bipolar disorder\n3. ICD 10 code I11\u002Fhypertensive heart disease, ICD 10 code I12\u002Fhypertensive CKD, ICD 10 code I13\u002Fhypertensive heart disease and CKD, ICD 10 code I15, or ICD 10 code I16\n4. alcohol consumption ≥ 8 drinks per week for women, or ≥15 drinks per week for men\n5. drug use\u002Fabuse (excluding marijuana) per EMR\n6. moving out of area during study timeline\n7. scheduling conflicts with intervention schedule\n8. unwilling to use a touchscreen\n9. unwilling to be on video conferencing\n10. low communicative ability, functional status, or other disorders (examiner rated) that would interfere with interventions and assessments\n11. unable to provide informed consent","ALL","35 Years","75 Years",{"count":21,"type":22},200,"ESTIMATED","INTERVENTIONAL",[25],"NA","The goal of this clinical trial is to determine the impact of a home-delivered foods and kitchen skills program on health and nutrition in adults with high blood pressure and food insecurity.\n\nResearchers will compare Food Resources \\& Kitchen Skills (FoRKS) and Enhanced Usual Care (EUC) to evaluate the effects on mean systolic blood pressure (SPB), HbA1c, food security and nutrition.\n\nParticipants will complete 24-hr blood pressure monitoring, standard blood pressure measurements, weight, finger stick for A1c point-of-care testing, and questionnaires.",[28,29,30,31],"Food Insecurity","Hypertension","Nutrition","Disease Management",[33,34,35,36],"randomized controlled trial","kitchen skills","diet","social determinants of health","RECRUITING","2026-02-03",{"date":40,"type":41},"2026-02-05","ACTUAL",{"date":43,"type":41},"2023-04-17",{"date":45,"type":22},"2027-07-30",{"name":47,"class":48},"Indiana University","OTHER",1,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":54,"acronym":4,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":17,"minAge":56,"maxAge":4,"enrollmentInfo":57,"targetDuration":4,"studyType":59,"phases":4,"briefSummary":60,"conditions":61,"keywords":4,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":49},"100592484","feasibility-study-of-a-relapse-investigation-questionnaire-administered-by-an-ms-care-coordinator-nurse-in-patients-with-multiple-sclerosis-100592484","NCT06994026","Feasibility Study of a Relapse Investigation Questionnaire Administered by an MS Care Coordinator Nurse in Patients With Multiple Sclerosis","Inclusion Criteria:\n\n* Patients followed by Dr. Manchon for Relapsing-Remitting Multiple Sclerosis or active Secondary Progressive Multiple Sclerosis\n* Adult patients (aged 18 or older)\n* Patients who have provided informed consent for participation in the local task-sharing protocol\n\nExclusion Criteria:\n\n* Pregnant women\n* Minors (under 18 years old)\n* Patients with known renal failure\n* Patients who have not provided or are unable to provide consent for the local task-sharing protocol","18 Years",{"count":58,"type":22},10,"OBSERVATIONAL","This study aims to evaluate a questionnaire used by a specialized nurse to help manage relapses in people with multiple sclerosis (MS). The questionnaire is completed during a phone call when the patient reports new or worsening symptoms. It helps the nurse decide whether further tests or treatments are needed, based on a protocol developed with a neurologist. The goal is to improve how quickly and effectively patients receive care during a relapse. The study will include 10 adult patients with active forms of MS over a two-month period.",[62,31,63],"Multiple Sclerosis","Feasibility Studies","NOT_YET_RECRUITING","2025-05-20",{"date":67,"type":41},"2025-05-29",{"date":69,"type":22},"2025-06-15",{"date":71,"type":22},"2025-08-15",{"name":73,"class":48},"Centre Hospitalier de Gonesse",{"id":75,"slug":76,"hasResults":11,"nctId":77,"briefTitle":78,"officialTitle":79,"acronym":4,"eligibilityCriteria":80,"healthyVolunteers":81,"sex":17,"minAge":82,"maxAge":4,"enrollmentInfo":83,"targetDuration":4,"studyType":23,"phases":85,"briefSummary":86,"conditions":87,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":91,"lastUpdatePostDateStruct":92,"startDateStruct":94,"completionDateStruct":96,"leadSponsor":98,"locationsCount":49},"100539923","evaluation-of-the-chronic-disease-co-care-pilot-scheme-100539923","NCT06310148","Evaluation of the Chronic Disease Co-Care Pilot Scheme","An Evaluation of the Effectiveness and Cost-effectiveness of the Chronic Disease Co-Care (CDCC) Pilot Scheme: a Commissioned Study","Inclusion Criteria of interventional group:\n\n* Hong Kong residents\n* Aged ≥45 years\n* Registered as a member of DHC\u002FDHC Express\n* Provided informed consent on sharing their data in the electronic Health Record Sharing System\n* Provided consent to join the CDCC Pilot Scheme Terms and Conditions.\n\nExclusion Criteria of interventional group:\n\n* With known history of DM or HT\n\nInclusion Criteria of comparison group:\n\n* Hong Kong residents\n* Aged ≥45 years\n* Provided informed consent for the study.\n\nExclusion Criteria of comparison group:\n\n* Without known history of DM or HT",true,"45 Years",{"count":84,"type":22},3772,[25],"The Chronic Disease Co-Care (CDCC) Pilot Scheme is initiated for early screening and management of people with hypertension (HT), pre-diabetes mellitus (pre-DM) and diabetes mellitus (DM) in Hong Kong. This study will evaluate the quality of care, feasibility, acceptability, effectiveness and cost-effectiveness of the Scheme.\n\nThis is a 12-month cohort study among the District Health Centre (DHC) or DHC Express, healthcare providers, CDCC participants and a comparison group of 1,886 non-participants. All the person-in charge, 2 family doctors and 1 of each allied health provider from each DHC\u002FDHC Express will be administered with the questionnaires on quality of care and costing. All CDCC participants will be included in subject characteristics, among which a convenience sample of 548 will complete a telephone survey on experience, enablement and satisfaction of the CDCC Pilot Scheme. The health outcomes of 1,886 CDCC participants and 1,886 non-participants will be compared for evaluation of effectiveness and cost-effectiveness.\n\nParticipant characteristics, enablement, compliance to the standards of care, and costing of CDCC Pilot Scheme will be summarized using descriptive statistics. Differences in the proportion of patients meeting treatment targeted for HT, pre-DM and DM after 12 months will be compared by chi-squared test and logistic regressions. The incremental cost-effectiveness ratio will be evaluated by comparing with the World Health Organization (WHO) threshold. This study will inform future healthcare planning and policy for manpower and resource allocation.",[88,29,89,31,90],"Diabetes Mellitus, Type 2","Chronic Disease","Primary Healthcare","2024-03-20",{"date":93,"type":41},"2024-03-22",{"date":95,"type":41},"2024-01-18",{"date":97,"type":22},"2026-12-31",{"name":99,"class":48},"The University of Hong Kong"]