[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"diet-habits\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:diet-habits":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,7,0,[8,51,80,107,136,166,199],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":30,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":50},"100644544","lifestyle-advice-in-cvd-100644544",false,"NCT07672054","Lifestyle Advice in CVD","Perspectives and Experience of Patients From Minority Ethic Communities on Advice Provided About Diet and Lifestyle Advice in Management of Their Cardiovascular Disease","Inclusion Criteria:\n\n* Patients over the age of 18 years with a personal history of minority ethnicity (non-white) and a diagnosis of cardiovascular disease\n\nExclusion Criteria:\n\n* Patients with a personal history of white ethnicity Patients without a history of cardiovascular disease","ALL","18 Years",{"count":19,"type":20},15,"ESTIMATED","OBSERVATIONAL","Individuals living in the UK who are from ethnic minority communities have a higher risk of heart disease and strokes than white individuals. This risk arises from the social determinants of health. These include lifestyle factors such as diet, physical activity and smoking. Improving these lifestyle factors in individuals is an essential part of reducing the chances of heart attacks and stroke. Patients may have diets and lifestyles arising from their cultural and religious backgrounds but receive advice which is not aligned to their own customs and experiences. Receiving advice which is not relevant to their own types of diet and lifestyle customs may create difficulties for patients in managing their heart and circulation health. Moreover, the dissonance between advice given and patient-specific relevance may lead to poorer adherence to the recommendations made to manage their condition. This can lead to poorer health outcomes for these patients. In addition, they may be advised to adopt diets and behaviours which are not appropriate to their cultures and may be also difficult to put into practice. This is important because lifestyle advice aligned to a patient's existing diet, behaviours and cultural beliefs leads to improved control of these health conditions. Learning to provide dietary and lifestyle advice relevant to individual patients needs is an important skill for the clinicians caring for them.",[24,25,26,27,28,29],"Cardio Vascular Disease","Dietary Change","Dietary Behaviors","Diet Habits","Experience","Ethnicity",[31,32,29,33,34,35,36,37],"Diet","Cardiovascular disease","Behavioural change","Modification","Healthcare experience","Healthcare access","Medical education","NOT_YET_RECRUITING","2026-06-22",{"date":41,"type":42},"2026-06-26","ACTUAL",{"date":44,"type":20},"2026-07-06",{"date":46,"type":20},"2027-01-31",{"name":48,"class":49},"University of Nottingham","OTHER",1,{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":56,"acronym":4,"eligibilityCriteria":57,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":58,"targetDuration":4,"studyType":60,"phases":61,"briefSummary":63,"conditions":64,"keywords":68,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":78,"locationsCount":50},"100634527","regular-diet-after-colorectal-surgery-100634527","NCT07540845","Regular Diet After Colorectal Surgery","Impact of Postoperative Regular Diet on Colorectal Outcomes and Patient Quality of Life","Inclusion Criteria:\n\n* Male or female ≥ 18 years of age\n* Scheduled to undergo colorectal resection\n\nExclusion Criteria:\n\n* Patients with bowel obstructions\n* Patients below the age of 18",{"count":59,"type":20},10,"INTERVENTIONAL",[62],"NA","The goal of this pilot study is to assess the safety and feasibility of regular diet after surgical removal of the colon. The study will enroll patients preoperatively, prior to colon surgery, and will follow participants for up to 30 days. The study hypothesizes that simplifying nutritional recommendations is safe and may improve quality of life.",[65,27,66,67],"Colorectal","Surgery","Post-operative Care",[69,70],"diet after surgery","nutrition counseling","RECRUITING","2026-05-20",{"date":74,"type":42},"2026-05-22",{"date":76,"type":42},"2026-05-13",{"date":46,"type":20},{"name":79,"class":49},"Weill Medical College of Cornell University",{"id":81,"slug":82,"hasResults":11,"nctId":83,"briefTitle":84,"officialTitle":84,"acronym":4,"eligibilityCriteria":85,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":86,"enrollmentInfo":87,"targetDuration":4,"studyType":60,"phases":89,"briefSummary":91,"conditions":92,"keywords":95,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":98,"lastUpdatePostDateStruct":99,"startDateStruct":101,"completionDateStruct":103,"leadSponsor":105,"locationsCount":50},"100629657","phase-1-effects-of-high-fiber-diet-on-gut-microbiota-metabolism-and-immune-microenvironment-in-solid-tumor-patients-a-clinical-study-100629657","NCT07477522","Effects of High-Fiber Diet on Gut Microbiota, Metabolism, and Immune Microenvironment in Solid Tumor Patients: A Clinical Study","Inclusion Criteria:\n\n* (1) Sign a written informed consent form before any study - related procedures are carried out.\n\n  (2) Males or females, aged 18 - 80 years old. (3) Diagnosed with solid tumors by pathological tissue biopsy. (4) According to the RECIST v1.1 (Response Evaluation Criteria in Solid Tumors Version 1.1) criteria, there is at least 1 measurable lesion (lesions previously treated with local therapies such as radiotherapy cannot be regarded as measurable lesions).\n\n  (5) ECOG (Eastern Cooperative Oncology Group Performance Status) score of 0 - 1.\n\n  (6) NRS - 2002 (Nutritional Risk Screening 2002) score \\\u003C 3. (7) BMI (Body Mass Index) ≥ 18.5 (can be adjusted appropriately according to the actual situation).\n\n  (8) Patients who can eat orally or through a feeding tube and can tolerate enteral nutrition.\n\n  (9) Sufficient organ function, and the subjects need to meet the following laboratory indicators: In the absence of granulocyte - colony - stimulating factor use in the past 14 days, the absolute neutrophil count ≥ 1.5×10⁹\u002FL.\n\nPlatelets ≥ 75×10⁹\u002FL. In the absence of blood transfusion or erythropoietin use in the past 7 days, hemoglobin ≥ 8 g\u002FdL.\n\nSerum albumin ≥ 3.0 g\u002FdL. Total bilirubin ≤ 1.5× the upper limit of normal (ULN). Aspartate Aminotransferase (AST) and Alanine Aminotransferase (ALT) ≤ 2.5×ULN. In case of liver metastasis, ALT and\u002For AST ≤ 5×ULN, and total bilirubin ≤ 3×ULN. In case of liver or bone metastasis, Alkaline Phosphatase (AKP) ≤ 5×ULN.\n\nCreatinine clearance rate ≥ 50 mL\u002Fmin (calculated according to the Cockcroft - Gault formula) or serum creatinine ≤ 1.5×ULN.\n\nInternational Normalized Ratio (INR) ≤ 1.5×ULN, Prothrombin Time (PT) and Activated Partial Thromboplastin Time (APTT) ≤ 1.5×ULN.\n\nUrine protein \\\u003C 2+ (if urine protein ≥ 2+, a 24 - hour urine protein quantification can be performed, and subjects with a 24 - hour urine protein quantification \\\u003C 2.0 g can be enrolled).\n\n(10) Women of child - bearing potential must agree to avoid sexual intercourse (heterosexual intercourse) or use a reliable and effective contraceptive method from the signing of the informed consent form until at least 6 months after the last administration of the study drug. In addition, the serum HCG (Human Chorionic Gonadotropin) test must be negative within 3 days before the start of the study treatment, and the subject must be non - lactating. A female patient is considered to be of child - bearing potential if she is post - menopausal but has not reached the post - menopausal state (non - menstrual period ≥ 12 consecutive months, and no other causes are found except menopause) and has not undergone sterilization surgery (such as hysterectomy, bilateral tubal ligation, or bilateral oophorectomy).\n\n(11) If there is a risk of pregnancy, all subjects (regardless of male or female) need to use a contraceptive method with an annual failure rate of less than 1% throughout the treatment period until 120 days after the last administration of the study drug (or 180 days after the last administration of the chemotherapy drug)\n\nExclusion Criteria:\n\n* (1) Patients with cognitive impairment or mental illness who are unable to understand the study content.\n\n  (2) Patients with central nervous system or meningeal metastases. (3) Patients with clinically symptomatic moderate or severe ascites (that is, those who require therapeutic paracentesis within 2 weeks before the start of study treatment; patients with only a small amount of ascites shown on imaging and no clinical symptoms can be enrolled).\n\n  (4) Patients with uncontrolled or moderate to severe pleural effusion and pericardial effusion.\n\n  (5) Patients with severe diarrhea, intractable vomiting, severe malabsorption syndrome, paralytic and mechanical intestinal obstruction; tracheoesophageal fistula, gastrointestinal perforation or gastrointestinal fistula, or abdominal abscess; patients with extra - gastrointestinal bleeding with a CTCAE (Common Terminology Criteria for Adverse Events) grade 3 or above within 6 months before the start of study treatment or grade 2 or above within 3 months (such as abnormal vaginal bleeding, hematemesis).\n\n  (6) Patients known to be allergic to the active ingredients or excipients of the study drug.\n\n  (7) Patients with poorly controlled diabetes. (8) Patients with poorly controlled hypertension (systolic blood pressure ≥ 140 mmHg and\u002For diastolic blood pressure ≥ 90 mmHg under routine antihypertensive treatment), with a history of hypertensive crisis or hypertensive encephalopathy.\n\n  (9) Patients with severe cardiovascular and cerebrovascular diseases, including cerebrovascular accident (CVA), transient ischemic attack (TIA), myocardial infarction, and major vascular diseases within 6 months before enrollment (including but not limited to aortic aneurysms requiring surgical repair or recent arterial thrombosis); patients with poorly controlled clinical symptoms or heart diseases, such as unstable angina pectoris, NYHA (New York Heart Association) heart failure grade II or above, left ventricular ejection fraction \\\u003C 50% on color Doppler echocardiography, or severe arrhythmias that cannot be controlled by drug treatment.\n\n  (10) Pregnant or lactating women. (11) Other situations considered by the investigator as inappropriate for enrollment.","75 Years",{"count":88,"type":20},25,[90],"PHASE1","Cancer remains a major global public-health challenge and a central focus of medical research. According to the International Agency for Research on Cancer (IARC, 2020), 19.29 million new malignant tumors and 9.96 million cancer deaths occurred worldwide, \\>90 % being solid cancers. Lung cancer alone accounted for 2.2 million new cases and 1.8 million deaths; \\>75 % of patients were already at an advanced stage at diagnosis. Current options for late-stage solid tumors are limited: surgery is often impossible because of metastasis; cytotoxic chemotherapy produces dose-limiting toxicities (grade Ⅲ-Ⅳ myelosuppression 15-40 %, mucositis 50-80 %); radiotherapy risks pneumonitis (5-15 %) or enteritis (5-20 %) when tumors abut vital organs; targeted agents succumb to acquired resistance after a median 9-13 months; and immune-checkpoint inhibitors achieve \\\u003C40 % objective response with 7-15 % grade 3-4 immune-related adverse events.\n\nDietary intervention is therefore emerging as a promising adjunct. Dietary fibre protects against cardiovascular and metabolic diseases, yet intake is universally low. WHO and the Chinese Nutrition Society recommend 25-30 g total fibre per day (≈15-21 g insoluble), whereas Chinese adults consume only \\~11 g insoluble fibre. High-fibre diets reshape gut microbiota, augment short-chain fatty acid (SCFA) production, strengthen intestinal barrier function, activate CD8⁺ T cells and dampen regulatory T cells, thereby enhancing anti-tumour immunity. A melanoma cohort showed improved progression-free survival under immunotherapy when fibre intake was high. Similar microbiota-immune axes may operate in colorectal and other solid cancers, but clinical data are scarce.\n\nWe therefore propose a study to examine whether a high-insoluble-fibre diet (\\>21 g\u002Fday) modulates gut-microbiota composition, metabolite profiles and peripheral-blood immune subsets in solid-tumour patients, and to evaluate consequent effects on treatment response and quality of life. The findings will clarify whether fibre-driven microbiota-immune crosstalk can be harnessed as a personalised nutritional strategy to improve cancer outcomes.",[93,27,94],"Colorectal Cancer (Diagnosis)","High-fibre Diet",[96,97],"high-fibre diet","Colorectal Cancer","2026-03-12",{"date":100,"type":42},"2026-03-17",{"date":102,"type":42},"2025-10-31",{"date":104,"type":20},"2026-06-30",{"name":106,"class":49},"West China Hospital",{"id":108,"slug":109,"hasResults":11,"nctId":110,"briefTitle":111,"officialTitle":112,"acronym":113,"eligibilityCriteria":114,"healthyVolunteers":115,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":116,"targetDuration":4,"studyType":60,"phases":118,"briefSummary":119,"conditions":120,"keywords":122,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":127,"lastUpdatePostDateStruct":128,"startDateStruct":130,"completionDateStruct":132,"leadSponsor":134,"locationsCount":50},"100609832","dietary-fiber-and-time-restricted-eating-100609832","NCT07219706","Dietary Fiber and Time Restricted Eating","Examining the Independent and Combined Effects of Dietary Fiber and Time Restricted Eating on Indicators of Cancer Risk: the Fiber and Time Restricted Eating (F.I.T.) Study","FIBER+TRE","Inclusion Criteria:\n\n* ≥18 age\n* Body mass index ≥30 kg\u002Fm2\n* Dietary fiber intake ≤15 g\u002Fday\n* Compatible cell phone for use of ecological momentary assessment app\n\nExclusion Criteria:\n\n* Self-reported diagnosis that precludes fiber intake (e.g., inflammatory bowel disease)\n* Food allergies or intolerances that limit ability to engage with the intervention\n* Positive screen on the SCOFF eating disorder screener39\n* Current self-reported use of GLP-1 receptor agonists\n* Currently pregnant or breastfeeding, or planning to become pregnant",true,{"count":117,"type":20},90,[62],"This study is seeking to examine combinations of two different dietary interventions on cancer risk.",[27,121],"Cancer Prevention",[31,123,124,125,126],"Weight loss","Fasting","Time restricted eating","Time restricted feeding","2026-03-11",{"date":129,"type":42},"2026-03-13",{"date":131,"type":20},"2026-12-10",{"date":133,"type":20},"2027-06-30",{"name":135,"class":49},"University of Oklahoma",{"id":137,"slug":138,"hasResults":11,"nctId":139,"briefTitle":140,"officialTitle":141,"acronym":142,"eligibilityCriteria":143,"healthyVolunteers":115,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":144,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":146,"conditions":147,"keywords":151,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":158,"lastUpdatePostDateStruct":159,"startDateStruct":160,"completionDateStruct":162,"leadSponsor":164,"locationsCount":50},"100628688","body-composition-and-lifestyles-in-athletes-with-disabilities-100628688","NCT07464899","Body Composition and Lifestyles in Athletes With Disabilities","Anthropometric, Dietary, Exercise, and Supplementation Profile in Athletes With Disabilities (PADES)","PADES","Inclusion Criteria:\n\n* Acceptation of informed consent\n* Have a federation license and at least two years of experience practicing the sport in which they will be classified.\n* Follow a training program with a minimum frequency of three days per week.\n* Have maintained training continuity for at least one month without absences.\n* Any type of disability.\n\nExclusion Criteria:\n\n* No attendance to the evaluations\n* Reporting less than 80% of assistance to physical activity sessions reported by trainer",{"count":145,"type":20},300,"Disability involves limitations that affect mobility and the ability to perform daily activities and achieve competitive goals. It is expected that disability has a significant impact on body composition, including reductions in lean mass and bone mineral content, and increases in fat mass and its distribution. Additionally, the assessment of food and dietary supplement intake among athletes with disabilities remains poorly described, despite its relevance in both sports and health contexts due to the potential benefits of individualized nutritional strategies.\n\nThis research project, entitled Anthropometric, Dietary, Exercise, and Supplementation Profile in Athletes with Disabilities (PADES), aims to describe the anthropometric characteristics, physical exercise practices, and food and supplement intake in Spanish athletes with disabilities. The study seeks to address the current lack of standardized anthropometric data and the limited information on dietary and supplementation patterns in this population, which hinders a comprehensive understanding of the physiological, nutritional, and biomechanical aspects essential for their health and athletic performance. A cross-sectional, descriptive-correlational study will be conducted in Spanish athletes with disabilities recruited through the Spanish Federation of Sports for People with Physical Disabilities (FEDDF), the Spanish Federation of Sports for the Blind (FEDC), and the Spanish Federation of Sports for the Deaf (FEDS).",[27,148,149,150],"Body Composition","Athlete Assessment","Sport Nutrition",[152,153,154,155,156,157],"sport nutrition","questionnaries","athletes","dietary-nutritional assessment","body composition","disability","2026-03-09",{"date":127,"type":42},{"date":161,"type":42},"2024-02-01",{"date":163,"type":20},"2030-04-30",{"name":165,"class":49},"University of Alicante",{"id":167,"slug":168,"hasResults":11,"nctId":169,"briefTitle":170,"officialTitle":171,"acronym":4,"eligibilityCriteria":172,"healthyVolunteers":115,"sex":16,"minAge":173,"maxAge":174,"enrollmentInfo":175,"targetDuration":4,"studyType":60,"phases":177,"briefSummary":178,"conditions":179,"keywords":185,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":190,"lastUpdatePostDateStruct":191,"startDateStruct":193,"completionDateStruct":195,"leadSponsor":197,"locationsCount":4},"100622884","school-meals-in-denmark-100622884","NCT07389421","School Meals in Denmark","School Meals in Denmark: Evaluation of a National School Meal Pilot Program on Children's Health, Learning and Well-being - a Natural Experiment","Inclusion Criteria:\n\n* All children attending 3rd, 4th or 7th grade in the recruited schools\n\nExclusion Criteria:\n\n* No exclusion criteria will be applied","9 Years","14 Years",{"count":176,"type":20},3200,[62],"This study looks at how a national school meal program affects the health, well-being, and learning of Danish schoolchildren aged 10 to 15 years.\n\nThe study is part of the Danish National School Meal Pilot Program (2025-2028), which provides free school meals at selected public schools. Some school classes receive free school meals, while other classes do not and are used for comparison.\n\nChildren are followed for about 1.5 years. Information is collected before and after the program using simple health measurements, questionnaires about well-being, and age-appropriate cognitive tests.\n\nThe study also uses information from Danish national registers to better understand the children's background and to study longer-term outcomes related to health, education, and social conditions. In addition, the study examines whether school meal programs are cost-effective by comparing their costs with potential benefits for children and society.\n\nThe goal of the study is to find out whether free school meals can improve children's health, well-being, and learning, and help reduce social differences.",[180,181,182,27,183,184],"Childhood Obesity","Childhood Obesity Pevention","Well-being\u002FQuality of Life","Cognitive Abilities","Healthy",[186,187,188,189],"physical health","well-being","learning","diet","2026-01-28",{"date":192,"type":42},"2026-02-05",{"date":194,"type":20},"2026-02-11",{"date":196,"type":20},"2029-12-31",{"name":198,"class":49},"University of Copenhagen",{"id":200,"slug":201,"hasResults":11,"nctId":202,"briefTitle":203,"officialTitle":204,"acronym":4,"eligibilityCriteria":205,"healthyVolunteers":115,"sex":16,"minAge":17,"maxAge":206,"enrollmentInfo":207,"targetDuration":4,"studyType":60,"phases":209,"briefSummary":210,"conditions":211,"keywords":214,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":215,"lastUpdatePostDateStruct":216,"startDateStruct":218,"completionDateStruct":220,"leadSponsor":222,"locationsCount":50},"100480142","effectiveness-of-an-app-for-mobile-phones-e-12hr-to-increase-adherence-to-mediterranean-diet-in-university-students-100480142","NCT05532137","Effectiveness of an App for Mobile Phones (e-12HR) to Increase Adherence to Mediterranean Diet in University Students","Effectiveness of a Personalized Intervention Program for the Promotion of the Mediterranean Diet, Based on a Mobile Phone Application (e12HR), in Students of the University of Seville","Inclusion Criteria:\n\n* Both genders.\n* Over the age of 18.\n* Be a student at the Faculties of Medicine or Pharmacy (University of Seville).\n* Possess a mobile telephone with Internet access and iOS or Android operating system.\n\nExclusion Criteria:\n\n\\- Chronic pathologies, food intolerances or pregnancy (situations that could require specialized dietary recommendations).","65 Years",{"count":208,"type":20},322,[62],"This is a controlled, randomized and multicentric clinical trial aimed at university students and performed at the Faculties of Medicine and Pharmacy at the University of Seville (Spain). Its objective is to evaluate the effect of an intervention based on the use of an information and communication technology (ICT) tool, specifically an application for mobile telephones (called e-12HR), in the improvement of adherence to the Mediterranean diet.",[212,27,213],"Mediterranean Diet","Healthy Eating Index",[212,27,213],"2024-12-18",{"date":217,"type":42},"2024-12-24",{"date":219,"type":42},"2022-04-04",{"date":221,"type":20},"2025-12-16",{"name":223,"class":49},"Luis María Béjar Prado"]