[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"glucose-variability\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:glucose-variability":35},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,55],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":37,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":43,"lastUpdatePostDateStruct":44,"startDateStruct":47,"completionDateStruct":49,"leadSponsor":51,"locationsCount":54},"100595769","enjoying-affordable-and-tasty-food-together-100595769",false,"NCT07036757","Enjoying Affordable and Tasty Food Together","PROJECT EATT: Enjoying Affordable and Tasty Food Together","PROJECT EATT","Inclusion Criteria:\n\n* Adults aged 40 years and older.\n* Household income at or less than the 200% the federal poverty level (household size 1: $30,120, household size 2: $40,880, household size 3: $51,640, household size 4: $62,400, and household size 5: $73,160)\n* Willing to provide informed consent and complete the study requirements, including attending study visits and completing questionnaires.\n* Access to a refrigerator or other means to safely store perishable food, as the meal kits require refrigeration.\n* BMI \\> 30 kg\u002Fm2 and self-report having at least one of the following: elevated blood pressure or hypertension, elevated glucose, prediabetes or diabetes.\n* Reside in the Greater Lowell area or surrounding regions to ensure feasibility of meal kit delivery and data collection.\n\nExclusion Criteria:\n\n* Less than 40 years old\n* Does not have BMI \\>30 kg\u002Fm2, elevated blood pressure or hypertension, or elevated glucose, prediabetes or diabetes\n* Not able to provide consent (adults lacking capacity)\n* Follow a medically restricted diet or have allergies to wheat, soy, or dairy\n* Plans to move from the Greater Lowell area within the next 12 months\n* Live outside the Greater Lowell area because this will impact meal kit delivery\n* Individuals without a working refrigerator in your household\n* Have a serious medical condition requiring a doctor's care including cancer, chronic kidney disease and\u002For celiac disease\n* Currently part of a study on diabetes, cardiovascular disease, nutrition or weight-loss\n* Currently taking any weight loss medication like Ozempic, or medication for diabetes, dyslipidemia or hypertension\n* Currently using a continuous glucose monitor","ALL","40 Years",{"count":20,"type":21},120,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this pilot study is to examine the feasibility of a novel meal kit and nutrition education intervention among adults aged 40 years and older, who are lower income, and to evaluate the preliminary impact of the meal kit and nutrition education intervention on food insecurity, dietary quality, mental health, quality of life and cardiovascular risk factors compared with general nutrition education materials in this population.\n\nThe main questions are:\n\nWhat is the acceptability and satisfaction with the meal kits and nutrition education intervention?\n\nWhat are the participation rates in the nutrition education program and the evaluation of the intervention?\n\nWhat is the impact of the intervention on food insecurity, dietary quality and cooking and food preparation self-efficacy compared with general nutrition education materials?\n\nWhat is the impact of the intervention of psychosocial health, quality of life and cardiometabolic outcomes compared with general nutrition education materials?",[27,28,29,30,31,32,33,34,35,36],"Food Insecurity","Dietary Quality","Quality of Life","Cooking Self-efficacy","Perceived Stress","Anxiety","Depressive Symptomatology","Anthropometrics: Height and Weight","Glucose Variability","Blood Pressure",[38,39,40,41,29],"Nutrition Education","Cardiometabolic outcomes","Meal Kits","Stress and Mental Health","RECRUITING","2026-04-28",{"date":45,"type":46},"2026-05-05","ACTUAL",{"date":48,"type":46},"2026-02-01",{"date":50,"type":21},"2026-10-30",{"name":52,"class":53},"University of Massachusetts, Lowell","OTHER",1,{"id":56,"slug":57,"hasResults":11,"nctId":58,"briefTitle":59,"officialTitle":59,"acronym":4,"eligibilityCriteria":60,"healthyVolunteers":61,"sex":17,"minAge":62,"maxAge":63,"enrollmentInfo":64,"targetDuration":4,"studyType":22,"phases":66,"briefSummary":67,"conditions":68,"keywords":72,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":80,"completionDateStruct":82,"leadSponsor":84,"locationsCount":54},"100609082","inter--and-intraindividual-variability-of-the-acute-glucose-response-to-exercise-in-healthy-adults-and-people-living-with-type-1-diabetes-a-cross-over-replicate-trial-100609082","NCT07209930","Inter- and Intraindividual Variability of the Acute Glucose Response to Exercise in Healthy Adults and People Living With Type 1 Diabetes: A Cross-over Replicate Trial","Inclusion Criteria:\n\n(Healthy and T1D phases):\n\n* age between 18 and 60 years old;\n* being healthy individuals;\n* engagement in physical activity at least once a week; (T1D phase):\n* diagnosis of T1D for \\>18 months;\n* hypoglycaemia self awareness.\n\nExclusion Criteria:\n\n(Healthy and T1D phases)\n\n* presence of cardiovascular disease or contraindications to exercise;\n* infectious or inflammatory conditions;\n* chronic renal or liver disease;\n* pregnancy;\n* gestational diabetes;\n* diagnosed eating disorders;\n* any physical or mental condition preventing participation; (Healthy phase)\n* diabetes mellitus (type 1 or type 2); (T1D phase)\n* inability to self-manage diabetes.",true,"18 Years","60 Years",{"count":65,"type":21},24,[24],"The goal of this clinical trial is to investigate if blood glucose responses are similar between and within individuals in response to standardized exercise in adults with and without Type 1 diabetes. The main questions it aims to answer are:\n\nWhat is the reproducibility of acute glycaemic responses to exercise within and between subjects in adults living with Type 1 Diabetes and in healthy adults? What is the agreement between glucose levels obtained by continuous glucose monitor (CGM) and blood glucose monitor?\n\nParticipants will cycle on a cycle ergometer or rest after consuming a standardized breakfast, while glucose levels are monitored by CGM and capillary blood sampling.",[69,70,35,71],"Exercise","Healthy Participants","Type 1 Diabetes (T1D)",[73,74,75,76],"reproducibility","exercise","Type 1 diabetes","glucose","2025-09-29",{"date":79,"type":46},"2025-10-07",{"date":81,"type":46},"2025-01-28",{"date":83,"type":21},"2026-07-31",{"name":85,"class":53},"University College Dublin"]