[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"eating-habit\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:eating-habit":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,53,74,101],{"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":37,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100529981","effect-of-sleep-extension-on-ceramides-in-people-with-overweight-and-obesity-100529981",false,"NCT06180837","Effect of Sleep Extension on Ceramides in People with Overweight and Obesity","Biomarkers of Habitual Short Sleep and Related Cardiometabolic Risk","Inclusion Criteria:\n\n1. Age: 18-45 years old; equal numbers of men and women\n2. Body mass index (BMI): 27.5-34.9 kg\u002Fm2\n3. Sleep Habits: habitual self-reported average total sleep time (TST) \\\u003C6.5 hours per night for prior 6 months\n\nExclusion Criteria:\n\n1. Clinically diagnosed sleep disorder or major psychiatric illness\n2. Evidence of significant organ dysfunction or disease (e.g., heart disease, kidney disease)\n3. Clinically diagnosed diabetes or fasting plasma glucose ≥126 mg\u002FdL or HbA1c ≥6.5%\n4. Use of prescription drugs or substances known to influence sleep or glucose metabolism, or anticoagulant medications.\n5. Cancer that has been in remission less than 5 years\n6. Pregnant\u002Fnursing, experiencing menopause or post-menopausal\n7. Shift-work: current or history of within last year\n8. Weight change: \\>10% of body weight over prior six months\n9. Current enrollment in weight loss or physical activity program like the Diabetes Prevention Program\n10. Currently smoking\n11. Alcohol intake\\>14 drinks per week or \\>3 drinks per day",true,"ALL","18 Years","45 Years",{"count":21,"type":22},70,"ESTIMATED","INTERVENTIONAL",[25],"NA","The overall goal is to determine how a sleep extension intervention (increasing time in bed) in individuals who maintain less than 6.5 hours sleep per night affects their plasma ceramides and insulin sensitivity. Participants will undergo a randomized controlled trial, with sleep extension (intervention) and healthy lifestyle (control) groups. The sleep extension is designed to increase participant's time in bed by 2 hours per night. Alternatively, the control group will receive basic health information (e.g., physical activity, goal setting, and nutrition when eating out).",[28,29,30,31,32,33,34,35,36],"Lifestyle Factors","Overweight and Obesity","Insulin Sensitivity","Eating Habit","Sleep Hygiene","Type 2 Diabetes","Sleep","Sleep Deprivation","Insufficient Sleep Syndrome",[38,39],"sleep","insulin sensitivity","RECRUITING","2024-12-18",{"date":43,"type":44},"2024-12-20","ACTUAL",{"date":46,"type":44},"2024-02-12",{"date":48,"type":22},"2028-01",{"name":50,"class":51},"University of Utah","OTHER",1,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":59,"eligibilityCriteria":60,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":61,"targetDuration":4,"studyType":23,"phases":63,"briefSummary":64,"conditions":65,"keywords":4,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":68,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":52},"100511760","circadian-intervention-to-improve-cardiometabolic-health-100511760","NCT05943626","Circadian Intervention to Improve Cardiometabolic Health","Timing of Circadian Synchronizers: the TOCS Study","TOCS","Inclusion Criteria:\n\n1. Age: 18-45 years old; equal numbers of men and women\n2. Body mass index (BMI): 25.0-34.9 kg\u002Fm2,\n3. Sleep Habits: habitual self-reported average total sleep time (TST) \\\u003C6.5 hours per night for prior 6 months\n\nExclusion Criteria:\n\n1. Clinically diagnosed sleep disorder or major psychiatric illness\n2. Evidence of significant organ dysfunction or disease (e.g., diagnosed diabetes, cardiovascular disease, or kidney disease)\n3. Use of prescription drugs or substances known to influence sleep or glucose metabolism\n4. Shift-work: current or history of within last year\n5. Weight change: \\>10% of body weight over prior six months\n6. Experiencing menopause or post-menopausal\n7. Current enrollment in weight loss or physical activity program like the Diabetes Prevention Program\n8. Currently pregnant or planning to become pregnant, or currently lactating.\n9. Currently smoking\n10. Alcohol intake \\>3 drinks per day or \\>14 drinks per week",{"count":62,"type":22},20,[25],"The overall goal is to examine the efficacy of a circadian intervention in people with overweight and obesity and habitual short sleep duration (HSSD). Participants will undergo a randomized controlled trial, with circadian intervention and control (healthy lifestyle) groups. The circadian intervention is designed to reduce nighttime light exposure and after-dinner snack food intake. Alternatively, the control group will receive basic health information (e.g., physical activity, goal setting, and nutrition when eating out).",[66,33,34,67,28,29,30,31,32],"Cardiometabolic Syndrome","Time Restricted Feeding",{"date":43,"type":44},{"date":70,"type":44},"2023-06-13",{"date":72,"type":22},"2026-03",{"name":50,"class":51},{"id":75,"slug":76,"hasResults":11,"nctId":77,"briefTitle":78,"officialTitle":79,"acronym":80,"eligibilityCriteria":81,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":82,"targetDuration":4,"studyType":23,"phases":84,"briefSummary":85,"conditions":86,"keywords":4,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":91,"lastUpdatePostDateStruct":92,"startDateStruct":94,"completionDateStruct":96,"leadSponsor":98,"locationsCount":100},"100552580","adapting-food-culture-to-the-mediterranean-pattern-for-international-students-in-italy-100552580","NCT06474936","Adapting Food Culture to the Mediterranean Pattern for International Students in Italy","Nutritional Health Assistance for Adapting Food Culture to the Mediterranean Pattern for International Students at the University of Pavia (MeditEat)","MeditEat","Inclusion Criteria:\n\n* ≥ 18 years old\n* Able to understand English or Italian\n* Nationality diverse than Italian\n* Absence of major morbidities that interfere with food choices, such as diabetes, hypertension, renal dysfunction, etc.\n\nExclusion Criteria:\n\n* ≤18 years old;\n* Italian nationality;\n* Presence of major morbidities that interfere with food choices, such as diabetes, hypertension, renal dysfunction, etc.",{"count":83,"type":22},23,[25],"The goal of this clinical trial is to describe the adherence to the Mediterranean diet, the nutritional status, the level of physical activity, and possible eating disorders in international students attending the University of Pavia before and after a food education intervention. The main questions it aims to answer are:\n\nDoes the intervention of food education change the nutritional status of the international students of the University of Pavia? Does the intervention of food education change the level of physical activity of international students of the University of Pavia? Does the intervention of food education change the possible risk of eating disorders related to the possible change of diet from the country of origin of international students? Researchers will compare the measurements done at the first meeting to the measurements made at the last meeting (6 months) to see if the food educational intervention helped the students.\n\nParticipants will:\n\n* have the body composition analysed by anthropometric measurements (weight, height, electric bio impedance)\n* Receive personalized guidance and support from our team of experts for 6 months.\n\nVisit the clinic 3 times (beginning, 3 months, and by the end of 6 months) for check-ups and tests, and participate in online meetings the other 3 months (second, fourth, and fifth).\n\nAnswer online questionnaires and perform a 3-day food diary (beginning, 3 months, and by the end of 6 months).",[87,88,31,89,90],"Physical Inactivity","Eating Disorders","Diet, Healthy","Diet Habit","2024-06-19",{"date":93,"type":44},"2024-06-26",{"date":95,"type":44},"2024-05-01",{"date":97,"type":22},"2025-11-01",{"name":99,"class":51},"University of Pavia",2,{"id":102,"slug":103,"hasResults":11,"nctId":104,"briefTitle":105,"officialTitle":106,"acronym":107,"eligibilityCriteria":108,"healthyVolunteers":16,"sex":17,"minAge":109,"maxAge":110,"enrollmentInfo":111,"targetDuration":4,"studyType":23,"phases":113,"briefSummary":114,"conditions":115,"keywords":121,"overallStatus":126,"whyStopped":4,"lastUpdateSubmitDate":127,"lastUpdatePostDateStruct":128,"startDateStruct":130,"completionDateStruct":132,"leadSponsor":134,"locationsCount":52},"100544862","the-mind-gut-digital-pilot-intervention-study-100544862","NCT06374407","The MIND-GUT Digital Pilot Intervention Study","Exploring the Interplay Between Diet, Obesity, Mental Health, and the Gut Microbiome. The MIND-GUT Digital Pilot Intervention Study.","MINDGUT","Inclusion Criteria:\n\n* age 30- 50;\n* BMI ≥ 30 kg\u002Fm2;\n* stable physical activity;\n* one person per household;\n* commitment to full protocol.\n\nExclusion Criteria:\n\n* use of psychiatric medications (e.g., serotonin reuptake inhibitors);\n* use of weight loss medications (GLP-1 receptor agonists);\n* food allergies affecting adherence to the MIND diet;\n* diagnosis of eating disorders;\n* diagnosis of diabetes;\n* diagnosis of polycystic ovary syndrome;\n* sensory deficits (e.g., COVID-19-induced loss of taste\u002Fsmell);\n* antibiotic use during the latest 3 months;\n* participation in another study;\n* language understanding limitations (i.e., not able to understand either Swedish or English); - coeliac\u002Finflammatory bowel disease;\n* planned weight management program within three months;\n* pregnancy;\n* lactation;\n* menopause.","30 Years","50 Years",{"count":112,"type":22},126,[25],"This 12-week pilot study aims to evaluate the feasibility and effectiveness of a dietary intervention targeting diet, obesity, mental health, and the gut microbiome in promoting weight loss and enhancing mental health among obese men and women aged 30-50. Participants, excluding those with specific medical conditions, will be randomly assigned to either an intervention or control group using a meal planning smartphone app. Clinical assessments will include anthropometry, mental health questionnaires, dietary recalls, and stool sample collections. The study's endpoints include program retention, adherence, changes in body weight, mental health, and gut microbiome diversity. Statistical analyses will evaluate intervention effects and the potential mediating roles of the gut microbiome. This pilot study has implications for health policies, public healthcare, digital health companies, and the biotech and pharmacology industries. Future plans involve a large-scale intervention study in multiple countries with ongoing collaborations.",[116,117,118,119,31,120],"Obesity","Depressive Symptoms","Anxiety","Stress","Dysbiosis",[122,123,124,125],"mental health","obesity","mind gut diet","gut microbiome","NOT_YET_RECRUITING","2024-04-15",{"date":129,"type":44},"2024-04-18",{"date":131,"type":22},"2024-06",{"date":133,"type":22},"2026-12",{"name":135,"class":51},"University of Skövde"]