[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"nutrition-status\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:nutrition-status":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,50,80,103,127],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":16,"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},"100630591","indigenous-nutritional-supplements-for-pregnancy-to-improve-resilience-in-environmental-heat-100630591",false,"NCT07489664","Indigenous Nutritional Supplements for Pregnancy to Improve Resilience in Environmental Heat","INSPIRE","Inclusion Criteria:\n\n1. Women aged 18-45 years belonging to a low to middle socioeconomic status, residing in Mithi, Districts in Sindh.\n2. Planning to conceive within the study time frame and expect to become pregnant within four months of starting nutritional intervention.\n3. Women who confirm their pregnancy during the first trimester i.e., before 8 weeks of gestational age.\n\nExclusion Criteria:\n\n1. Women using long-lasting contraceptives such as IUDs, implants, and injectable methods like Depo-Provera.\n2. Women with a history of multiple miscarriage or stillbirths.\n3. Women with known chronic diseases, such as cardiovascular disorders, hepatic disorders, renal disorders, and infectious diseases.\n4. Women suffering from severe malnutrition (WHO: Underweight i.e., having BMI \\\u003C 16 Kg\u002Fm2 or obese having BMI ≥ 30 Kg\u002Fm2).\n5. Women having severe anemia (WHO: Severe anemia i.e., Hb \\\u003C 7g\u002FdL).\n6. Women currently enrolled in BISP supplementation programs or taking any supplements other than iron and folic acid (IFA) will be excluded from the study.\n7. Those who do not become pregnant within three months of supplementation during pre-conception.",true,"FEMALE","18 Years","45 Years",{"count":21,"type":22},292,"ESTIMATED","INTERVENTIONAL",[25],"NA","The purpose of this study is to learn whether a simple, traditional, and balanced meal made from local foods, eaten once a day during pregnancy, can help women in rural Pakistan stay healthier in hot weather and give birth to healthier babies. Climate change has made heat a serious challenge for pregnant women, especially in areas with limited resources. This study will explore whether an indigenous meal that is culturally acceptable and easy to prepare can improve resilience to heat stress and support better outcomes for both mothers and newborns.\n\nThe study will focus on two main questions:\n\n* Can this daily balanced meal reduce the harmful effects of heat stress during pregnancy?\n* Does it improve newborn health, especially birth weight?\n\nResearchers will compare women who eat the balanced local meal every day with women who continue their usual meals. They will check changes in women's health, levels of key vitamins and nutrients, and their babies' birth outcomes.\n\nDuring the study, participants will:\n\n* Either eat the balanced local meal daily or continue their usual meals.\n* Share information on their health, diet, and heat exposure.\n* Provide small samples, such as blood and stool, to study nutrient levels and gut health.\n* Have their newborns' health and growth measured at birth.",[28,29,30,31],"Heat Stress","Pregnancy","Women of Reproductive Age","Nutrition Status",[33,34,35,36],"Local Food-Based Diet to Improve Birth Outcomes and Heat Resilience in Pregnant Women","maternal depression","placental transcriptomics","microbiome","NOT_YET_RECRUITING","2026-03-19",{"date":40,"type":41},"2026-03-24","ACTUAL",{"date":43,"type":22},"2026-03",{"date":45,"type":22},"2028-12",{"name":47,"class":48},"Aga Khan University","OTHER",1,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":4,"eligibilityCriteria":56,"healthyVolunteers":11,"sex":57,"minAge":58,"maxAge":59,"enrollmentInfo":60,"targetDuration":62,"studyType":63,"phases":4,"briefSummary":64,"conditions":65,"keywords":66,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":49},"100613088","the-impact-of-preoperative-nutrition-intervention-on-muscle-mass-preserve-in-older-adults-undergoing-elective-surgery-100613088","NCT07262034","The Impact of Preoperative Nutrition Intervention on Muscle Mass Preserve in Older Adults Undergoing Elective Surgery","The Impact of Preoperative Nutritional Intervention on Muscle Mass Preserve in Older Adult Undergoing Elective Surgery: A Prospective Cohort Study (SiPAP Trail) Study","Inclusion Criteria:\n\n1. Patients aged 60 years to 90 years\n2. Schedules for elective major surgery and formally enrollment in the Enhanced Recovery After Surgery (ERAS) program at Siriraj Hospital. (At Siriraj Hospital, patients scheduled for pre-specific elective major surgeries are enrolled into the ERAS program as individual hospital protocols for each ERAS module. All patients are informed about the ERAS program by their surgical team.)\n3. Referred to the SiPAP center for prehabilitation based on established ERAS hospital preoperative protocol.\n4. Able to provide written informed consent and willing to undergo all research assessments at both time points.\n\nExclusion Criteria:\n\n1. Presence of conditions that interfere with bioelectrical impedance analysis (BIA), including an implanted pacemaker or other non-removable electronic medical devices.\n2. Use of medications or supplements known to acutely or chronically affect muscle mass (e.g. corticosteroids, hormonal therapies) during the study period.\n3. Diagnosed neuromuscular disorders that affect baseline muscle mass and strength\n4. Undergo emergency surgery\n5. A planned interval of less than 14 days between the initial SiPAP visit and hospital admission for surgery.\n6. Alcohol consumption or strenuous exercise within the 12 hours preceding the scheduled BIA measurement.\n7. Incomplete data on muscle mass or nutritional assessment at either time point.","ALL","60 Years","90 Years",{"count":61,"type":22},62,"3 Months","OBSERVATIONAL","Sarcopenia-the progressive loss of muscle mass and strength-is a major clinical issue, especially in surgical patients with malignancy. It's strongly linked to poor postoperative outcomes like increased complications, longer hospital stays, and higher mortality. Surgical stress (trauma, fasting, immobilization) significantly worsens this muscle catabolism.\n\nConsequently, early identification and targeted preoperative intervention are essential. Preoperative nutrition, part of a prehabilitation program, is a key strategy known to attenuate muscle loss and improve recovery. The Skeletal Muscle Index (SMI) is an objective metric used for risk stratification.\n\nThe Siriraj Integrated Preoperative and Prehabilitation Center (SiPAP) uses a multidisciplinary model with nutritional counseling, but lacks routine sarcopenia screening or objective SMI measurement. Therefore, the impact of their specific nutritional interventions on preserving muscle mass remains unevaluated.\n\nHypothesis: The structured, individualized preoperative nutritional intervention delivered by SiPAP to intraabdominal oncology patients will result in a net preservation or positive change in the Skeletal Muscle Index (SMI) over the preoperative period.",[31],[67,68,69,70],"Preoperative","Sarcopenia","Body Composition Analyzer (BIA)","Skeletal Muscle Index (SMI)","2026-03-04",{"date":73,"type":41},"2026-03-06",{"date":75,"type":22},"2026-04-01",{"date":77,"type":22},"2028-12-01",{"name":79,"class":48},"Siriraj Hospital",{"id":81,"slug":82,"hasResults":11,"nctId":83,"briefTitle":84,"officialTitle":85,"acronym":4,"eligibilityCriteria":86,"healthyVolunteers":11,"sex":57,"minAge":18,"maxAge":4,"enrollmentInfo":87,"targetDuration":4,"studyType":63,"phases":4,"briefSummary":89,"conditions":90,"keywords":91,"overallStatus":94,"whyStopped":4,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":98,"completionDateStruct":100,"leadSponsor":102,"locationsCount":49},"100602618","malnutrition-prevalence-and-nutritional-change-after-preoperative-nutrition-counseling-100602618","NCT07125859","Malnutrition Prevalence and Nutritional Change After Preoperative Nutrition Counseling","Prevalence of Preoperative Malnutrition and Changes in Nutritional Status Following Preoperative Nutrition Education in Surgical Patients Attending a Preoperative Clinic","Inclusion Criteria:\n\n1. Adults aged ≥18 years.\n2. Enrolled in the Enhanced Recovery After Surgery (ERAS) program.\n3. Referred to the SiPAP program for prehabilitation prior to elective surgery.\n4. screened for malnutrition risk using the Society of Parenteral and Enteral Nutrition of Thailand (SPENT) screening tool.\n5. Complete clinical records available for analysis.\n\nExclusion Criteria: Have incomplete nutritional records.",{"count":88,"type":22},600,"Preoperative nutrition risk or Malnutrition is a prevalent up to 65% of surgical patients, leading to significant negative outcomes such as increased complications, poor wound healing, and higher healthcare costs. Preoperative nutrition status is a modifiable risk factor that can be optimized to improve surgical outcomes. Preoperative malnutrition screening creates an opportunity to identify and optimize the nutritional status of at-risk patients before surgery. This study is initiated to determine the prevalence of malnutrition among surgical patients enrolled in an Enhanced recovery after surgery (ERAS) program, using the SPENT and modified Nutrition Alert Form (NAF) during their visit to the preoperative clinic and evaluate the impact of preoperative nutrition education on body weight and nutrition status prior to surgery.",[31],[67,92,93],"Malnutrition","Nutrition education","RECRUITING","2026-02-25",{"date":97,"type":41},"2026-02-27",{"date":99,"type":41},"2025-07-15",{"date":101,"type":22},"2026-07-01",{"name":79,"class":48},{"id":104,"slug":105,"hasResults":11,"nctId":106,"briefTitle":107,"officialTitle":107,"acronym":4,"eligibilityCriteria":108,"healthyVolunteers":11,"sex":57,"minAge":18,"maxAge":109,"enrollmentInfo":110,"targetDuration":4,"studyType":23,"phases":112,"briefSummary":113,"conditions":114,"keywords":4,"overallStatus":94,"whyStopped":4,"lastUpdateSubmitDate":118,"lastUpdatePostDateStruct":119,"startDateStruct":120,"completionDateStruct":122,"leadSponsor":124,"locationsCount":49},"100626613","a-randomized-triple-blind-placebo-controlled-study-to-evaluate-the-effects-of-a-supplement-on-nutrient-gaps-and-gut-health-among-individuals-utilizing-glp-1-ras-100626613","NCT07437911","A Randomized, Triple-blind, Placebo-controlled Study to Evaluate the Effects of a Supplement on Nutrient Gaps and Gut Health Among Individuals Utilizing GLP-1 RAs","Inclusion Criteria:\n\n* Be male or female\n* Be aged 18-59.\n* Has a BMI between 20-31.9.\n* Anyone currently taking GLP-1 medication at their maintenance dose (week 8+), and without any plans to alter their dosage. This includes: Semaglutide (Ozempic®, Wegovy®, Rybelsus®), Liraglutide (Saxenda®, Victoza®), Dulaglutide (Trulicity®), Exenatide (Byetta®, Bydureon®), Lixisenatide (Adlyxin®)\n* Anyone willing to follow the study protocol, including immediately prior to the all blood tests, duplicating their diet for 72 hours (3 days), refraining from caffeine and exercise for 24 hours, and fasting for 10 hours.\n* Anyone willing to maintain their current diet, sleep pattern, and activity levels for the duration of the trial.\n* Anyone willing to avoid introducing any other supplements, medications, or herbal remedies for the duration of this trial.\n* Anyone who is generally healthy - does not live with any diagnosed uncontrolled chronic disease.\n* Has access to a consistent weighing scale for the duration of the study.\n* Resides in the United States.\n\nExclusion Criteria:\n\n* Anyone with a diagnosis of Type I or Type II diabetes.\n* Anyone with a diagnosis of any metabolic health condition, such as hypertension and dyslipidemia.\n* Anyone who has taken any multivitamin\u002Fmultimineral supplements within the past 3 months.\n* Anyone who has taken a probiotic supplement within the past month.\n* Anyone who has regularly consumed (5 days\u002Fweek or more) products that target healthy aging, anti-aging, longevity, gut health, energy, or ingestive behaviour (such as cravings), including resveratrol, quercetin, pterostilbene, coQ10, grapefruit, nicotinamide riboside, prebiotic fiber, green tea, niacin (vitamin B3) within the past 2 months.\n* Anyone who has received an antibiotic, antifungal, antiparasitic, or antiviral treatment within the past 90 days.\n* Anyone who has a known history of severe digestive disorders or metabolic conditions that impact nutrient absorption or metabolism, including acid reflux, Irritable Bowel Syndrome (IBS), Irritable Bowel Disease (IBD), Crohn's disease, a history of colon resection, gastroparesis, Inborn errors of metabolism (such as PKU), or gastrointestinal tract surgeries.\n* Anyone with any known allergies or hypersensitivities to any supplement product ingredients.\n* Anyone with any chronic health conditions that could impact participation in this study, such as asthma, gout, fibromyalgia, chronic inflammatory conditions (such as Crohn's, Lupus, HIV\u002FAIDS), thyroid conditions, cancer (within the past 5 years), mental health disorders, history of serious illness in the last three months, history of substance abuse, or planned surgery during the study period.\n* Anyone currently pregnant, trying to conceive, or breastfeeding.\n* Anyone who has undergone a change in hormone therapy (including oral contraceptives) within the past 4 weeks, or is unwilling to maintain their current hormone therapy\u002Foral contraceptive use throughout the course of the study.\n* Anyone who consumes more than 2 standard alcoholic drinks per day or more than 10 drinks per week, or has within the past 6 months.\n* Anyone who is currently a smoker or has been a smoker within the past month.\n* Anyone who follows a specific exclusion diet, including vegan, vegetarian, carnivore, paleo, atkins, or ketogenic.","59 Years",{"count":111,"type":22},120,[25],"This study is a triple-blind, placebo-controlled, randomized controlled trial of 120 adults that will evaluate the impact of a novel nutritional supplement on improving nutrient gaps and changing nutrient status and the gut microbiome among glucagon-like peptide-1 receptor agonist (GLP-1 RA) users.",[115,31,116,117],"Nutrition Intake","Gastrointestinal Microbiome","GLP-1","2026-02-24",{"date":97,"type":41},{"date":121,"type":22},"2026-02",{"date":123,"type":22},"2026-08",{"name":125,"class":126},"Athletic Greens International","INDUSTRY",{"id":128,"slug":129,"hasResults":11,"nctId":130,"briefTitle":131,"officialTitle":131,"acronym":132,"eligibilityCriteria":133,"healthyVolunteers":16,"sex":57,"minAge":134,"maxAge":135,"enrollmentInfo":136,"targetDuration":4,"studyType":23,"phases":138,"briefSummary":139,"conditions":140,"keywords":145,"overallStatus":94,"whyStopped":4,"lastUpdateSubmitDate":147,"lastUpdatePostDateStruct":148,"startDateStruct":150,"completionDateStruct":152,"leadSponsor":154,"locationsCount":49},"100593835","integrated-childhood-activity-and-nutrition-ican-study-100593835","NCT07011602","INTEGRATED CHILDHOOD ACTIVITY AND NUTRITION (ICAN) STUDY","ICAN","Inclusion Criteria:\n\n* Parental\u002Fguardian consent\n* Child assent\n* Child participant is between the chronological age of 6-11 years.\n* Child participant is considered economically or educationally disadvantaged (e.g., eligible for Supplemental Nutritional Assistance Program \\[SNAP\\] and\u002For qualifies for free-and-reduced lunch.\n* Child participant must have 20\u002F20 or corrected 20\u002F20 vision.\n* Child participant absent of cognitive or neurological disorder (e.g., autism spectrum disorder)\n\nExclusion Criteria:\n\n* Parental\u002Fguardian does not provide consent\n* Child non-assent\n* Child participant chronological age when enrolling into the iCANS program falls below 6 or above 11 years of age\n* Child participant is not eligible for SNAP or does not qualify for free-and-reduced lunch.\n* Child participant does not have 20\u002F20 or corrected 20\u002F20 vision.\n* Presence of cognitive or neurological disorder (e.g., autism spectrum disorder)","6 Years","11 Years",{"count":137,"type":22},100,[25],"This study is a multi-functional integrated research and education project to prevent losses in academic achievement, cognitive function, and behavioral health among at-risk youth. The study tests the effects of a 8-week nutrition and physical activity-based program (Integrated Childhood Activity and Nutrition \\[ICAN\\]) to prevent summer learning loss. Outcomes include standardized academic achievement as well as executive function among 6-10-year-olds affected by poverty. The nutrition component of the intervention involves daily consumption of a snack containing the carotenoid lutein, typically found in high quantities in green leafy vegetables. The physical activity components will involve group games or activities.",[141,142,143,144,31],"Achievement","Weight Change","Cognition","Fitness",[146],"brain, exercise, carotenoids, body composition","2025-06-05",{"date":149,"type":41},"2025-06-09",{"date":151,"type":41},"2025-06-04",{"date":153,"type":22},"2027-07-31",{"name":155,"class":48},"University of Illinois at Urbana-Champaign"]