[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"nutrition-poor\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:nutrition-poor":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,7,0,[8,43,88,118,142,176,201],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":4},"100508541","phase-4-effect-of-iodine-containing-multiple-micronutrient-during-lactation-on-infant-neurodevelopment-100508541",false,"NCT05901766","Effect of Iodine-containing Multiple Micronutrient During Lactation on Infant Neurodevelopment","Effect of Maternal Supplementation With an Iodine-containing Multiple Micronutrient During Lactation on Infant Iodine Status, Thyroid Function and Neurodevelopment","To be eligible, women will be required to meet the following inclusion criteria:\n\n* Maternal age 18 years or above, singleton pregnancy,\n* data available on Last Menstrual Period (LMP) or early ultrasound,\n* Intention to exclusively feed breastmilk for 4 to 6 months,\n* Intention to stay in the study catchment area for at least 6 months,\n* Willingness to take a daily supplement of MMS for 6 months\n\nExclusion criteria include:\n\n* Severe maternal morbidity (postpartum eclampsia, postpartum hemorrhage),\n* Maternal condition leading to inability for infant to directly\u002Fexclusively breastfeed (maternal mastectomy, or other breast surgery),\n* Breast cancer,\n* Tuberculosis",true,"FEMALE","18 Years",{"count":20,"type":21},600,"ESTIMATED","INTERVENTIONAL",[24],"PHASE4","The goal of this clinical trial is to learn about the effects of iodine-containing multiple micronutrient supplements provided to breastfeeding mothers who live in settings with mild iodine deficiency.\n\nThe main questions it aims to answer are:\n\n1. What are the effects of iodine-containing multiple micronutrient supplements provided to breastfeeding mothers on infant development, as measured by electroencephalography\u002Fvisual evoked potentials?\n2. What are the effects of iodine-containing multiple micronutrient supplements on breast milk concentrations of iodine, and infant iodine and thyroid status?\n3. How do iodine and iron interact with each other to affect thyroid function in the mother during lactation?\n\nParticipants will be randomized to receive a daily multiple micronutrient tablet containing iodine (UNIMAPP) for 6 months postpartum, or routine postnatal care per Ethiopia Ministry of Health. Mothers will provide a breast milk sample and blood at 3 and 6 months postpartum. Infants will provide a urine sample and drop of blood, and have a neurodevelopmental assessment at 3 and 6 months.\n\nResearchers will compare the groups that received the iodine-containing micronutrient supplement with the group that received routine care and see if there were any benefits on infant development and iodine and thyroid status in the mother and baby.",[27,28,29,30],"Iodine Deficiency","Nutrition Poor","Development, Infant","Breastfeeding","NOT_YET_RECRUITING","2026-05-21",{"date":34,"type":35},"2026-05-26","ACTUAL",{"date":37,"type":21},"2026-05-01",{"date":39,"type":21},"2028-03-31",{"name":41,"class":42},"Brown University","OTHER",{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":50,"minAge":18,"maxAge":51,"enrollmentInfo":52,"targetDuration":4,"studyType":22,"phases":54,"briefSummary":56,"conditions":57,"keywords":71,"overallStatus":77,"whyStopped":4,"lastUpdateSubmitDate":78,"lastUpdatePostDateStruct":79,"startDateStruct":81,"completionDateStruct":83,"leadSponsor":85,"locationsCount":87},"100596191","the-florida-ascent-study-100596191","NCT07042243","The Florida ASCENT Study","The Florida Partnership for Adding Social Context to Address Cancer Survivorship Outcomes (Florida ASCENT)","Patient Eligibility Inclusion Criteria:\n\n1. ≥18 years old.\n2. Pathologically confirmed diagnosis of colorectal, prostate, lung, breast, gynecologic, hematologic, or skin (including melanoma) cancer within the past 12 months.\n3. Self-reported ability to read and speak English.\n4. Able to provide informed consent.\n5. Participant must not be considered a \"vulnerable population\" (pregnant women, neonates, children etc.)\n\nPatient Eligibility Exclusion Criteria:\n\n1. ≤18 years old.\n2. Participant do not have a pathologically confirmed diagnosis of colorectal, prostate, lung, breast, gynecologic, hematologic, or skin (including melanoma) cancer within the past 12 months.\n3. Participant does not live within the state of Florida.\n\n3\\) Does not self-reported ability to read and speak English or Spanish. 4) Not able to provide informed consent. 5) Participant is considered a \"vulnerable population\" (pregnant women, neonates, children etc.)\n\nProvider Eligibility Inclusion Criteria\n\n1. ≥18 years old.\n2. Currently works as a physician, physician assistant, patient navigator and\u002For health system\u002Fadministrative leader in UF and UM affiliated clinics.\n3. Self-reported ability to read and speak English or Spanish.\n4. Able to provide informed consent.\n5. Participant must not be considered a \"vulnerable population\" (pregnant women, neonates, children etc.)\n\nProvider Eligibility Exclusion Criteria\n\n1. ≤ 18 years old.\n2. Does not currently works as a physician, physician assistant, patient navigator and\u002For health system\u002Fadministrative leader in UF and UM affiliated clinics.\n3. Does not self-report having the ability to read and speak English.\n4. Not able to provide informed consent.\n5. Participant is considered a \"vulnerable population\" (pregnant women, neonates, children etc.)","ALL","100 Years",{"count":53,"type":21},100,[55],"NA","The goal of this clinical trial is to adapt, implement, and evaluate MyCarePulse and ASCENT patient navigator to overcome barriers to care among patients with cancer.\n\nThe main hypotheses it aims to test are:\n\n* At the patient level, the intervention will result in higher levels of food security, self- efficacy for dietary behaviors, and higher diet quality than standard care.\n* At the provider level, the intervention will be feasible, acceptable, appropriate, and able to enhance individualized care for patient wellness.\n\nResearchers will compare cancer patients receiving the MyCarePulse and ASCENT patient navigator intervention to those receiving standard care, to see if the intervention improves food security, self-efficacy, and diet quality.\n\nPhase 1\n\nPatient Participants will:\n\n* Complete the ASCENT Questionnaire, which is comprised of the following:\n\n  * U.S. Food Security Survey Module (U.S. FSSM)\n  * Patient-Reported Outcomes Measurement Information System (PROMIS-29)\n  * Automated Self-Administered 24-Hour (ASA24®) Dietary Assessment Tool\n* Be assessed using the Veggie Meter instrument\n* Participate in two semi-structured interviews\n\nProvider Participants will:\n\n•Participate in one semi-structured interview\n\nPhase 2\n\nPatient Participants will:\n\n* Participate in ASCENT patient navigator screenings and consultations\n* Complete the ASCENT Questionnaire, which comprises the U.S. FSSM, PROMIS-29, and ASA24®",[58,59,60,61,62,63,64,65,66,67,68,69,28,70],"Cancer","Food Deprivation","Food Habits","Food Selection","Colorectal Cancer","Prostate Cancer","Lung Cancer","Breast Cancer","Gynecologic Cancer","Hematologic Cancer","Skin Cancer","Melanoma","Nutritional Deficiency",[72,58,73,74,75,76],"Food Insecurity","Food Access","Community-Informed Research","Nutritional Needs","Mixed-Methods","RECRUITING","2026-02-19",{"date":80,"type":35},"2026-02-20",{"date":82,"type":35},"2025-12-05",{"date":84,"type":21},"2027-08",{"name":86,"class":42},"University of Florida",1,{"id":89,"slug":90,"hasResults":11,"nctId":91,"briefTitle":92,"officialTitle":93,"acronym":4,"eligibilityCriteria":94,"healthyVolunteers":11,"sex":50,"minAge":18,"maxAge":4,"enrollmentInfo":95,"targetDuration":4,"studyType":22,"phases":97,"briefSummary":98,"conditions":99,"keywords":103,"overallStatus":77,"whyStopped":4,"lastUpdateSubmitDate":108,"lastUpdatePostDateStruct":109,"startDateStruct":111,"completionDateStruct":113,"leadSponsor":115,"locationsCount":87},"100537392","nutrition-care-in-patients-living-with-chronic-pain-100537392","NCT06277232","Nutrition Care in Patients Living With Chronic Pain","Developing Nutrition Care Integrated Into Pain Rehabilitation: a Feasibility and Non-Randomized, Controlled Quasi-Experimental Study","Inclusion Criteria:\n\n* Self reported Body Mass Index (BMI)\\>=25;\n* Written consent to participate and attend to the pain rehabilitation program due to disabling chronic pain (on sick leave or experiencing major interference in daily life due to chronic pain)\n* Agreement not to participate in other parallel treatments for weight reduction\n* Not currently using medications of weight reduction\n* Available to get access to internet via own mobile\u002Fcellphone.\n\nExclusion Criteria:\n\n* Health conditions such as pregnancy, active metabolic disease, rheumatoid arthritis, and serious psychiatric disease (investigator's judgement, eg, psychosis or suicidal ideation);\n* Coagulation disorders with predisposition to bleeding, medication with anticoagulants (low- dose aspirin is permitted);\n* hypersensitivity to anaesthetic\n* Difficulties in understanding the Swedish language.",{"count":96,"type":21},200,[55],"The investigators' purpose is to develop and test the feasibility, usability, and satisfaction of the Diet4painrelief app as a platform for implementing nutrition care in a specialist pain rehabilitation clinic. The Diet4painrelief will consist of two components: a) a screening tool for nutrition status b) an individually tailored behavior change program aiming to improve the dietary habits and behaviors of patients living with chronic pain.\n\nPart I: Included 20 patients with complex chronic pain to examine the feasibility and outcomes of evidence-based Interdisciplinary Pain Rehabilitation Program (IPRP) integrated with nutrition care. The Diet4painrelief includes a screening tool to assess basic nutritional status as well as their intake of key unhealthy and healthy foods and drinks (through three 24hour-dietary recordings or food diary). Thereafter, the patients receive a personalized behavior change program for dietary optimization. The investigators will design and adapt 6 modules in the digital platform (Diet4painrelief app) based on the International Association for the Study of Pain (IASP) recommendations (6 aspects about 'nutrition and pain') and Sweden's food culture. Clinical outcomes using patient-reported data on socio-demographics, pain aspects, psychometric data, physical disability, and quality of life will be measured at three occasions: first appointment (Pre-IPRP), immediately after completing the rehabilitation program (Post-IPRP), and at a 12-month follow-up (FU-IPRP). Blood samples will be taken to identify biomarkers at the same occasions that provide objective information on metabolic and nutritional abnormalities and further to evaluate the effect of the dietary intervention on changing of pain rehabilitation outcomes.\n\nPart II: Included 192 patients with complex chronic pain. Half of the participants receive IPRP and nutrition care (described above) and the other half receive standard IPRP.",[28,100,101,102],"Overweight and Obesity","Mobile Phone Use","Pain, Chronic",[104,105,106,107],"Chronic pain","Nutrition care","Pain rehabilitation","eHealth","2026-02-13",{"date":110,"type":35},"2026-02-18",{"date":112,"type":35},"2024-08-01",{"date":114,"type":21},"2028-12-31",{"name":116,"class":117},"Linkoeping University","OTHER_GOV",{"id":119,"slug":120,"hasResults":11,"nctId":121,"briefTitle":122,"officialTitle":123,"acronym":4,"eligibilityCriteria":124,"healthyVolunteers":11,"sex":50,"minAge":18,"maxAge":4,"enrollmentInfo":125,"targetDuration":4,"studyType":22,"phases":127,"briefSummary":128,"conditions":129,"keywords":131,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":133,"lastUpdatePostDateStruct":134,"startDateStruct":136,"completionDateStruct":138,"leadSponsor":140,"locationsCount":87},"100502685","development-and-testing-of-nutritional-algorithms-nacho-100502685","NCT05825469","Development and Testing of Nutritional Algorithms (NACHO)","Development and Usability Testing of Nutrition Algorithms for Cancer Health Outcomes (NACHO) and Quality of Life During Cancer Treatment","Inclusion Criteria for Dietitians\u002FOncology clinicians - Have worked with at least 3 patients at the study site who had nutritional challenges\n\nInclusion Criteria for Patient and Family Advisory Council (PFAC) participants\n\n* Current member of adult PFAC\n* \\> 18 years old\n\nInclusion Criteria for Patient participants\n\n* \\> 18 years old\n* Able to speak and read English\n* Completed primary treatment (aim 2b) or actively undergoing treatment (aim 2b and aim 3, exploratory)\n* Access to a device (e.g., computer, tablet, smartphone) through which they can receive and engage with a REDCap link\n\nExclusion Criteria for Patient Participants\n\n• Provider does not recommend",{"count":126,"type":21},130,[55],"The goal of this research study is to develop a nutrition algorithm to optimize nutritional status and improve quality of life during for participants who are completing or have completed cancer treatment.\n\nThe name of the intervention used in this research study is:\n\nNutrition Algorithm for Cancer Health Outcomes (NACHO) (a technology-based platform that houses the algorithms for the person-centered nutrition program)",[28,70,130],"Quality of Life",[132,70,130],"Poor Nutrition","2026-02-03",{"date":135,"type":35},"2026-02-06",{"date":137,"type":21},"2026-09-01",{"date":139,"type":21},"2027-03-31",{"name":141,"class":42},"Dana-Farber Cancer Institute",{"id":143,"slug":144,"hasResults":11,"nctId":145,"briefTitle":146,"officialTitle":147,"acronym":4,"eligibilityCriteria":148,"healthyVolunteers":16,"sex":50,"minAge":4,"maxAge":149,"enrollmentInfo":150,"targetDuration":4,"studyType":22,"phases":151,"briefSummary":152,"conditions":153,"keywords":158,"overallStatus":77,"whyStopped":4,"lastUpdateSubmitDate":167,"lastUpdatePostDateStruct":168,"startDateStruct":170,"completionDateStruct":172,"leadSponsor":174,"locationsCount":87},"100563342","addressing-food-insecurity-plant-based-food-prescription-program-100563342","NCT06614920","Addressing Food Insecurity: Plant-Based Food Prescription Program","Addressing Food-Insecurity: Plant-Based Food Prescription Program to Improve Health Food Access","Inclusion Criteria:\n\n* Participants will be all ages 0-99 (all arms)\n* Families living under the federal poverty line AND who have food insecurity (all arms except Arm 2 which can include families with income above the federal poverty line who do not have food insecurity).\n* Families cared for in either the Pediatric Mobile Clinic, Pediatric, Family Medicine, Internal Medicine or Med-Peds primary care clinics in the UHealth\u002FJackson Health System\u002FDade County Street Response.\n\nExclusion Criteria:\n\n* Families who are not under the federal poverty line AND are not food insecure (all arms except Arm 2, which will include participants of all socioeconomic statuses and regardless of food security status, with no exclusion criteria in this category).\n* Families who are not actively receiving outpatient primary care (all arms).","99 Years",{"count":53,"type":21},[55],"Reduce food insecurity by improving plant-based health food consumption, access, health and nutrition literacy and the health of the food-insecure families we serve.",[154,155,28,72,156,157],"Health Literacy","Nutrition, Healthy","Food Insecurity Among Children","Low Income Population",[159,160,161,162,163,164,165,166],"Plant-based food prescription program","Plant-based","Food prescription","Food insecurity","Poverty","Nutrition education","Plant-based nutrition literacy","Plant-based nutrition education","2026-02-01",{"date":169,"type":35},"2026-02-04",{"date":171,"type":35},"2025-01-09",{"date":173,"type":21},"2028-03",{"name":175,"class":42},"University of Miami",{"id":177,"slug":178,"hasResults":11,"nctId":179,"briefTitle":180,"officialTitle":181,"acronym":182,"eligibilityCriteria":183,"healthyVolunteers":16,"sex":50,"minAge":184,"maxAge":185,"enrollmentInfo":186,"targetDuration":4,"studyType":22,"phases":188,"briefSummary":189,"conditions":190,"keywords":4,"overallStatus":77,"whyStopped":4,"lastUpdateSubmitDate":192,"lastUpdatePostDateStruct":193,"startDateStruct":195,"completionDateStruct":197,"leadSponsor":199,"locationsCount":87},"100525029","nutrition-and-obesity-in-under-represented-populations-food-insecurity-research-to-advance-science-and-improve-health-100525029","NCT06116422","Nutrition and Obesity in Under-Represented Populations: Food Insecurity Research to Advance Science and Improve Health","Nutrition and Obesity in Under-Represented Populations: Food Insecurity Research to Advance Science and Improve Health: A Multi-disciplinary Approach for Study and Mitigation of Food Insecurity and Obesity","NOURISH","Inclusion:\n\n* Aged 9-12 months and their primary caregiver \"parent\".\n* Medicaid and WIC-eligible (proxy for \"at risk for food insecurity\")\n* World Health Organization BMI ≥ 85%ile at current or most recent encounter (early-onset obesity) OR ≥ 20 pounds at 9 months old.\n* Caregiver speaks either English or Spanish as their primary language.\n* Infant was born as a singleton infant.\n\nExclusion:\n\n* Diagnosed with monogenic obesity.\n* Plans to move from the area in the next 12 months.\n* Parent is currently pregnant.","12 Months","24 Months",{"count":187,"type":21},228,[55],"Food insecurity is associated with obesity in children, and childhood obesity leads to long term health consequences. While existing research shows that food benefit programs reduce food insecurity, little is known about the mediating factors between food benefit programs and child health. The purpose of this study is to understand if the resolution of food insecurity in young children with early onset obesity can improve body mass index (BMI) over one year, and if so, by what mechanisms. The investigators will conduct a randomized comparative effectiveness study among infants (n=228) aged 12 months at risk for food insecurity and deliver two different food security interventions. Both will provide families with $50\u002Fweek for one year of study enrollment. The first group will receive this as an unrestricted cash benefit (\"cash benefit group\") and the second group will receive this as a benefit in the form of weekly grocery purchases with the support of a trained nutrition expert to guide healthy grocery purchasing (\"grocery benefit group\"). The investigators will also construct a contemporary comparison cohort of infants meeting the inclusion\u002Fexclusion criteria from the electronic health record, using propensity score matching to allow comparisons between both intervention groups and usual care. The primary endpoint is difference in BMI at 12 months post-enrollment (24 months of age). Secondary outcomes include measures of nutrition, food security, electronic health record data related to general child health, and other factors related to parental stress and unmet social needs. Patients will have the opportunity to participate in post-study interviews to report on intervention satisfaction, and facilitators and barriers of infant feeding. Data analysis will be conducted by a trained statistician (Duke Biostatistics, Epidemiology, and Research Design; BERD) and will employ a two-means test for a repeated-measures design. The benefits to participants outweigh the minimal risks of loss of privacy, and confidential information will be managed carefully to minimize this risk.",[191,72,155,28],"Pediatric Obesity","2026-01-14",{"date":194,"type":35},"2026-01-16",{"date":196,"type":35},"2024-05-30",{"date":198,"type":21},"2027-12-31",{"name":200,"class":42},"Duke University",{"id":202,"slug":203,"hasResults":11,"nctId":204,"briefTitle":205,"officialTitle":205,"acronym":4,"eligibilityCriteria":206,"healthyVolunteers":11,"sex":50,"minAge":18,"maxAge":4,"enrollmentInfo":207,"targetDuration":4,"studyType":22,"phases":209,"briefSummary":210,"conditions":211,"keywords":213,"overallStatus":77,"whyStopped":4,"lastUpdateSubmitDate":217,"lastUpdatePostDateStruct":218,"startDateStruct":220,"completionDateStruct":222,"leadSponsor":224,"locationsCount":87},"100475554","linking-education-produce-provision-and-community-referrals-to-improve-diabetes-care-link-100475554","NCT05472441","Linking Education, Produce Provision, and Community Referrals to Improve Diabetes Care (LINK)","Inclusion Criteria:\n\n* Type 2 Diabetes based on American Diabetes Association Criteria\n* Hemoglobin A1c ≥ 7.5%\n* Screen Positive on 2-item Food Security Screener\n\nExclusion Criteria:\n\n* Unwilling to Attest to Release of Information to Mid-Ohio Food Collective",{"count":208,"type":21},568,[55],"This is a pragmatic randomized controlled trial (pRCT) that aims to test the effect of produce provision, diabetes education, and community referrals on hemoglobin A1c levels in individuals with type 2 diabetes experiencing food insecurity.",[212,28,59],"Diabetes Mellitus, Type 2",[72,214,215,216],"Social Determinants of Health","Non-medical, health related social needs","Diabetes Self-Management Education and Support","2025-08-06",{"date":219,"type":35},"2025-08-11",{"date":221,"type":35},"2023-02-06",{"date":223,"type":21},"2026-10-01",{"name":225,"class":42},"Ohio State University"]