[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"gestational-weight-gain\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:gestational-weight-gain":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,9,0,[8,45,77,109,134,161,188,222,246],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100578685","delivering-hope-helping-women-optimize-prenatal-equity-100578685",false,"NCT06814509","Delivering HOPE (Helping Women Optimize Prenatal Equity)","Inclusion Criteria:\n\n* Aged 16-44 years\n* ≤18 weeks pregnant\n* Speak English, Spanish, or Marshallese\n* Valid email address",true,"FEMALE","16 Years","44 Years",{"count":20,"type":21},1440,"ESTIMATED","INTERVENTIONAL",[24],"NA","The overarching research question is: \"Does the provision of healthy food (Delivering HOPE) during pregnancy reduce the proportion of women who experience excessive gestational weight gain compared with enhanced standard of care (ESoC)?\" To answer this question, the investigators will conduct a large multi-site randomized controlled trial with 1,440 women. Women will be randomized to either the Delivering HOPE arm or the ESoC arm, with approximately 720 participants per arm. Participants randomized to the ESoC arm will receive the standard clinical protocol for nutritional and gestational weight gain counseling recommended for all pregnant women, WIC and SNAP enrollment assistance, referrals to safety net food organizations.Those randomized to the Delivering HOPE arm will be provided the same nutritional and gestational weight gain counseling, WIC and SNAP assistance, and food referrals, as well as a total of $1000\u002F$2000\u002F$3000 (depending on household size) during pregnancy to be used specifically for the purchase of healthy foods recommended in the nutritional counseling. Data for the primary outcome (pre-pregnancy weight and weight at delivery) will be collected from birth records.",[27,28,29,30,31],"Gestational Weight Gain","Diet, Healthy","Gestational Hypertension","Gestational Diabetes","Pregnancy Complications","RECRUITING","2026-06-25",{"date":35,"type":36},"2026-06-26","ACTUAL",{"date":38,"type":36},"2025-06-24",{"date":40,"type":21},"2029-12-31",{"name":42,"class":43},"University of Arkansas","OTHER",8,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":16,"minAge":53,"maxAge":54,"enrollmentInfo":55,"targetDuration":4,"studyType":57,"phases":4,"briefSummary":58,"conditions":59,"keywords":62,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":76},"100618055","effect-of-gestational-weight-gain-on-spinal-anesthesia-in-elective-cesarean-delivery-100618055","NCT07326644","Effect of Gestational Weight Gain on Spinal Anesthesia in Elective Cesarean Delivery","Effect of Gestational Weight Gain on Regional Anesthesia in Cesarean Patients","GWG-CESA","Inclusion Criteria:\n\n* Pregnant women aged 18-45 years\n\n  * Single pregnancy\n  * Planned elective cesarean section\n  * Spinal anesthesia (regional anesthesia technique)\n  * Pre-pregnancy weight information available (maternal health record, e-Nabız or file record)\n  * Recorded pre-delivery weight information\n  * Gestational weight gain (GWG) calculable according to the IOM 2009 classification\n  * ASA I-II pregnant women\n  * Voluntary participation in the study and informed consent\n\nExclusion Criteria:\n\n* Pregnant women with preeclampsia, severe preeclampsia, eclampsia, or HELLP syndrome\n\n  * Pregnant women with a history of gestational diabetes or pregestational diabetes\n  * Multiple pregnancy (twins, triplets, etc.)\n  * Preterm pregnancy (\\\u003C37 weeks)\n  * Failure of spinal anesthesia or need for conversion to general anesthesia\n  * Lack of pre-pregnancy weight information or weight gain data during pregnancy\n  * Pregnancies with fetal anomalies\n  * Morbid obesity (BMI ≥ 45 kg\u002Fm²)","18 Years","45 Years",{"count":56,"type":21},200,"OBSERVATIONAL","This prospective, observational, non-interventional study aims to evaluate the effect of gestational weight gain on regional anesthesia characteristics in pregnant women undergoing elective cesarean delivery. No additional intervention, medication, or procedure beyond routine clinical care will be performed. Participants will be classified according to gestational weight gain categories based on the Institute of Medicine (IOM) 2009 guidelines, and spinal anesthesia block characteristics, hemodynamic responses, and perioperative outcomes will be assessed.",[27,60,61],"Regional Anesthesia","Cesarean Delivery",[63,64,65,66],"Gestational weight gain","Spinal anesthesia","Cesarean delivery","Hemodynamic response","2026-04-20",{"date":69,"type":36},"2026-04-23",{"date":71,"type":36},"2025-12-05",{"date":73,"type":21},"2026-05-10",{"name":75,"class":43},"Elazıg Fethi Sekin Sehir Hastanesi",1,{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":83,"eligibilityCriteria":84,"healthyVolunteers":15,"sex":16,"minAge":85,"maxAge":86,"enrollmentInfo":87,"targetDuration":4,"studyType":22,"phases":89,"briefSummary":90,"conditions":91,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":99,"lastUpdatePostDateStruct":100,"startDateStruct":102,"completionDateStruct":104,"leadSponsor":106,"locationsCount":108},"100448470","effects-of-the-mediterranean-diet-during-pregnancy-on-the-onset-of-allergies-in-the-offspring-100448470","NCT05119868","Effects of the Mediterranean Diet During Pregnancy on the Onset of Allergies in the Offspring","Effects of the Mediterranean Diet During Pregnancy on the Onset of Allergies in the Offspring: a Multi-center Randomised-controlled Trial (the PREMEDI Project)","PREMEDI","Inclusion Criteria:\n\n\\- healthy women (aged 20-35 years), at first trimester of pregnancy, of at risk for atopy baby\n\nExclusion Criteria:\n\n* concomitant presence of infections;\n* concomitant presence of malignancies;\n* concomitant presence of major gastrointestinal malformations;\n* concomitant presence of immunodeficiencies;\n* concomitant presence of autoimmune diseases;\n* concomitant presence of chronic inflammatory bowel diseases;\n* concomitant presence of functional gastrointestinal disorders;\n* concomitant presence of celiac disease;\n* history of abdominal surgery with gastrointestinal resection;\n* concomitant presence of neuropsychiatric disorders;\n* concomitant presence of central nervous system disorders;\n* vegan diet;\n* twin pregnancy;\n* concomitant presence of genetic disorders;\n* concomitant presence of metabolic disorders.","20 Years","35 Years",{"count":88,"type":21},276,[24],"Allergy prevalence is increasing steadily with some describing as the \"epidemic of the twenty-first century\". Maternal diet during pregnancy has been linked to offspring allergy risk, so it represents a potential target for allergy prevention. The Mediterranean Diet (MD) is considered one of the healthiest dietary models which exerts regulatory effects on immune system, due to the synergistic and interactive combinations of nutrients. We aim to study the effects of MD in pregnancy on the onset of allergic diseases at 2 years of age in the offspring.",[92,93,94,27,95,96,97,98],"Allergies","Obesity","Gestational Complications","Perinatal Condition","Birth Weight","Chronic Diseases in Children","Breast Feeding","2026-02-11",{"date":101,"type":36},"2026-02-12",{"date":103,"type":36},"2021-11-02",{"date":105,"type":21},"2026-03-10",{"name":107,"class":43},"Federico II University",2,{"id":110,"slug":111,"hasResults":11,"nctId":112,"briefTitle":113,"officialTitle":114,"acronym":115,"eligibilityCriteria":116,"healthyVolunteers":15,"sex":16,"minAge":53,"maxAge":54,"enrollmentInfo":117,"targetDuration":4,"studyType":22,"phases":119,"briefSummary":120,"conditions":121,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":125,"lastUpdatePostDateStruct":126,"startDateStruct":128,"completionDateStruct":130,"leadSponsor":132,"locationsCount":76},"100501310","healthy-mom-zone-gestational-weight-gain-management-intervention-20-100501310","NCT05807594","Healthy Mom Zone Gestational Weight Gain Management Intervention 2.0","Efficacy of a Novel Digital Platform to Scale-Up a Personalized Prenatal Weight Gain Intervention Using Control Systems Methodology","HMZ Two","Inclusion Criteria:\n\n* Pregnant women\n* ≥ 8 and \\\u003C 18 weeks gestation at time of screening. This range of gestational age is chosen to: a) reduce chances of false pregnancy or miscarriage under 8 weeks gestation and b) recruit women in the 1st trimester for greatest impact of the intervention on gestational weight gain. In the feasibility and initial impact study, the investigators had less than 10% (n=3) miscarriages prior to randomization using these criteria\n* Singleton gestation\n* Not currently heavily smoking (\\>20 cigarettes\u002Fday)\n* Any parity (i.e., first-time pregnancy, second pregnancy, etc.)\n* Any race\u002Fethnicity\n* Ages 18-45 years\n* Body mass index (BMI) range 20.0 to 45.0. If BMI is over 40, consultation with woman's health care provider will be made to determine eligibility and ensure she does not have any contraindications to physical activity or other concerns with intervention participation.\n* Haven't exceeded 25% or more of their total GWG (based on BMI and IOM guidelines) from pre-pregnancy to date of enrollment.\n* Participant has physician consent to confirm subject participation\n* Able to read, understand, and speak English\n* Access to a computer\u002Fphone\n* Willingness and ability to complete study materials and intervention sessions electronically (e.g., email, Facetime, Zoom), at home (e.g., Zoom sessions delivered synchronous and asynchronous) or if requested by the participant, on-site at Penn State University Park or Hershey campuses.\n* No current use of weight loss medications\n* No current participation in another interventional study or program that influences weight control\n* No planned bariatric surgery during this current pregnancy\n* No absolute contraindications to exercise in pregnancy and relative contraindications with provider consent (see below)\n\nExclusion Criteria:\n\n* Not pregnant women\n* Men (unable to become pregnant)\n* Multiple gestation\n* \\\u003C 8 weeks gestation or \\> 18 weeks gestation at time of pre-intervention assessment\n* Currently smoking \\> 20 cigarettes\u002Fday\n* Outside of the age range of 18-45 years\n* Outside of the BMI range of 20.0-45.0\n* Exceeded 25% of their total GWG (based on BMI and IOM guidelines) from pre-pregnancy to date of enrollment\n* Not able to read and\u002For understand English\n* Unable to access materials by computer or phone (even with data plan assistance if necessary)\n* Current use of weight loss medications\n* Current participation in another interventional study or program that influences weight control\n* Planned bariatric surgery during this current pregnancy\n* Contraindications to aerobic exercise in pregnancy:\n\nAbsolute contraindications to exercise:\n\n* Hemodynamically significant heart disease\n* Restrictive lung disease (pulmonary fibrosis, sarcoidosis, pleural effusion, neuromuscular disease). This DOES NOT include ASTHMA\n* Incompetent cervix\u002Fcerclage\n* Severe anemia\n* Multiple gestation at risk for premature labor\n* Persistent 2nd or 3rd trimester bleeding\n* Placenta previa after 26 weeks gestation\n* Premature labor during the current pregnancy\n* Ruptured membranes\n* Poorly controlled chronic hypertension\n* Preeclampsia diagnosis during current pregnancy\n* Poorly controlled Type 1 diabetes\n\nRelative contraindications to exercise (if permission is not given by provider):\n\n* Unevaluated maternal cardiac arrhythmia\n* Chronic bronchitis\n* Extreme morbid obesity (BMI \\> 40.0; needs provider consent to participate)\n* Extreme underweight (BMI \\\u003C 12.0)\n* History of extremely sedentary lifestyle\n* Current eating disorder(s) diagnosis\n* Severe food allergies and\u002For dietary restrictions that may preclude study participation.\n* Intrauterine growth restriction in current pregnancy\n* Poorly controlled respiratory disorder (severe asthma) that precludes study participation\n* Orthopedic limitations\n* Poorly controlled seizure disorder\n* Poorly controlled thyroid disease\n* Uncontrolled sleep disorder (insomnia, sleep-disordered breathing)",{"count":118,"type":21},144,[24],"The goal of this clinical trial is to see if the enhanced HMZ 2.0 intervention with new control system\u002Fdigital platform to regulate gestational weight gain (GWG) and impact maternal-infant outcomes while collecting implementation data works and can be given to other pregnant women in various settings. The question this study aims to answer are:\n\n1. Does the new intervention manage GWG?\n2. Does the new intervention have any influence on sleep and eating behaviors and infant outcomes.\n3. Does the new platform and other data collected help inform how well the research and information can be used in health care settings?\n\n144 pregnant women with overweight\u002Fobesity will be randomized to either the HMZ 2.0 intervention or attention control groups from \\~8-36 weeks gestation. All participants will be asked to:\n\n1. Weight themselves and wear an activity monitor each day over the study.\n2. Complete online surveys at either a weekly or monthly level about their thoughts, attitudes, and behaviors on GWG, physical activity, eating behaviors, sleep, their anxiety, depression, and stress.\n3. Attend weekly sessions with a registered dietician.\n\nThe weekly sessions will differ based on intervention group. The HMZ 2.0 intervention group will receive education, create and follow goal-setting and action plans, self-monitor their behaviors, and receive feature evidence and fetal growth facts. Education, goals, and self-monitoring will focus on GWG, physical activity, eating behaviors, sleep, self-regulating behaviors and emotions, and preparing for labor\u002Fdelivery and postpartum.\n\nThe attention control group will receive weekly sessions on preparing for labor\u002Fdelivery and benefits of behavioral pain management strategies (e.g., mindfulness-based relaxation, imagery, music, massage, deep-breathing) to help with pain after childbirth without medicine.",[27,122,123,124],"Overweight and Obesity","Pregnancy","Energy Balance","2026-01-14",{"date":127,"type":36},"2026-01-16",{"date":129,"type":36},"2023-11-27",{"date":131,"type":21},"2028-01-31",{"name":133,"class":43},"Penn State University",{"id":135,"slug":136,"hasResults":11,"nctId":137,"briefTitle":138,"officialTitle":139,"acronym":4,"eligibilityCriteria":140,"healthyVolunteers":15,"sex":141,"minAge":142,"maxAge":143,"enrollmentInfo":144,"targetDuration":4,"studyType":22,"phases":146,"briefSummary":147,"conditions":148,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":152,"lastUpdatePostDateStruct":153,"startDateStruct":155,"completionDateStruct":157,"leadSponsor":159,"locationsCount":76},"100498776","lipo-teen-the-lifestyle-in-pregnancy-and-offspring-teenagers-100498776","NCT05774652","LiPO Teen (the Lifestyle in Pregnancy and Offspring Teenagers","LiPO Teen (the Lifestyle in Pregnancy and Offspring Teenagers): Identification of Modifiable Risk Factors for Childhood Obesity - a Follow-up of a Randomized Controlled Trial","Inclusion Criteria:\n\n* Mothers in the initial LiP study selected at the baseline study in 2007-2010\n* Teenagers of mothers in the initial LiP study\n\nExclusion Criteria:\n\n• None","ALL","13 Years","65 Years",{"count":145,"type":21},301,[24],"The study is a follow-up of a Randomized Controlled Trial (RCT) performed in 2007-10 - the \"Lifestyle in Pregnancy\" LiP study.\n\nThe LiP study included 360 pregnant women with BMI ≥30 kg\u002Fm2 from Odense University Hospital and Aarhus University Hospital. The women were randomized to intervention with low-calorie diet and physical activity from gestational age 10-14 in pregnancy and until delivery - or to a standard care control group. The objective of the LiPO-Teen project is to perform a clinical follow-up study of the eligible 301 mothers who completed the trial until delivery with a liveborn child, and their 14 year-old offspring. The overall ambition is to understand whether lifestyle intervention in pregnancy prevents obesity and its complications across generations, with a specific focus on modifiable factors.",[93,149,150,27,151],"Life Style, Healthy","Follow-up","Body Weight","2025-11-16",{"date":154,"type":36},"2025-11-19",{"date":156,"type":36},"2023-10-26",{"date":158,"type":21},"2026-03-01",{"name":160,"class":43},"Odense University Hospital",{"id":162,"slug":163,"hasResults":11,"nctId":164,"briefTitle":165,"officialTitle":165,"acronym":4,"eligibilityCriteria":166,"healthyVolunteers":11,"sex":16,"minAge":53,"maxAge":4,"enrollmentInfo":167,"targetDuration":4,"studyType":22,"phases":169,"briefSummary":170,"conditions":171,"keywords":174,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":179,"lastUpdatePostDateStruct":180,"startDateStruct":182,"completionDateStruct":184,"leadSponsor":186,"locationsCount":76},"100602529","cessation-of-dual-use-of-cigarettes-and-e-cigarettes-during-pregnancy-100602529","NCT07124702","Cessation of Dual Use of Cigarettes and E-cigarettes During Pregnancy","Inclusion Criteria:\n\n* Less than 21 weeks pregnant to ensure adequate time for intervention;\n* 18 years or older;\n* Actively using both cigarettes and electronic cigarettes (e-cigarettes);\n* Willing to receive cessation information;\n* Able to read, understand, and speak English;\n* Having a low household income defined as ≤185% of the federal poverty level.\n\nExclusion Criteria:\n\n* Teen pregnancy (\\\u003C18 y);\n* Unstable housing;\n* Uncontrolled mental health disorders;\n* Non-English speakers.",{"count":168,"type":21},45,[24],"We propose a randomized controlled trial to develop and evaluate a cessation program with two different strategies for dual users during pregnancy. We plan to enroll 45 pregnant mothers (≤20 gestational weeks) with low household incomes from the Western NY region. To be eligible, they must be currently dual using CCs and nicotine-containing ECs. These mothers will be randomized into one of three groups: 1) simultaneous cessation intervention group (N=15), 2) stepwise cessation intervention group (N=15), and 3) control group (N=15). We hypothesize that nicotine abstinence rates at 8 weeks after randomization will be higher in the intervention groups than in the control group.",[172,27,173],"Dual Use of Cigarettes and E-cigarettes","Birth-weight-for-gestational-age z Score",[175,176,177,123,178],"Randomized Controlled Trial","Tobacco use","Electronic cigarette","Intervention","2025-11-11",{"date":181,"type":36},"2025-11-13",{"date":183,"type":36},"2025-10-01",{"date":185,"type":21},"2027-03-31",{"name":187,"class":43},"State University of New York at Buffalo",{"id":189,"slug":190,"hasResults":11,"nctId":191,"briefTitle":192,"officialTitle":193,"acronym":4,"eligibilityCriteria":194,"healthyVolunteers":15,"sex":16,"minAge":195,"maxAge":196,"enrollmentInfo":197,"targetDuration":4,"studyType":22,"phases":199,"briefSummary":200,"conditions":201,"keywords":205,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":213,"lastUpdatePostDateStruct":214,"startDateStruct":216,"completionDateStruct":218,"leadSponsor":220,"locationsCount":108},"100504101","teen-mom-study-feasibility-trial-100504101","NCT05843903","Teen Mom Study Feasibility Trial","Teen Mom Study Feasibility Trial: A Multicomponent Digital Health Intervention to Improve Cardiometabolic Health in Pregnant Black Adolescents","Inclusion criteria:\n\n* 15- to 19-years\n* Black or African American\n* \\\u003C20 weeks' gestation\n* Enrolled in WIC\n* Residing in 1 of 8 Mississippi Delta Counties\n* English speaking\n* Own or have personal use of a mobile smart phone\n* Singleton pregnancy\n* Plan to carry the fetus to term and keep the infant after birth\n* No history of chronic medical conditions in the past year that could influence weight loss or gain\n\nExclusion Criteria:\n\n* Restrictions on physical activity or exercise","15 Years","19 Years",{"count":198,"type":21},20,[24],"The proposed multicomponent digital health intervention has the potential to significantly impact the trajectory of maternal health in a rural, pregnant, Black adolescent population with the highest risks for cardiometabolic diseases worldwide. The proposed implementation strategy leverages mobile technologies which are ubiquitous across the socioeconomic gradient and proposes to train young adult WIC moms to deliver peer health coaching in a telehealth setting to address social barriers and support behavior change in pregnant, Black adolescent WIC clients in the Mississippi Delta - a rural region where the population is more than two-thirds percent Black and the teen birth rate is the highest in the United States. This is a scalable and sustainable approach to enhance WIC services and improve WIC's impact on population health and cardiometabolic health disparities in Black women.",[202,203,27,204],"Physical Activity","Sedentary Behavior","Social Determinants of Health",[206,207,208,209,210,211,212],"implementation science","pragmatic clinical trial","telemedicine","health disparity, minority and vulnerable populations","behavior and behavior mechanisms","adolescent pregnancy","black maternal health","2025-05-13",{"date":215,"type":36},"2025-05-15",{"date":217,"type":36},"2025-04-07",{"date":219,"type":21},"2026-06-01",{"name":221,"class":43},"University of Mississippi Medical Center",{"id":223,"slug":224,"hasResults":11,"nctId":225,"briefTitle":226,"officialTitle":227,"acronym":4,"eligibilityCriteria":228,"healthyVolunteers":11,"sex":16,"minAge":195,"maxAge":196,"enrollmentInfo":229,"targetDuration":4,"studyType":22,"phases":230,"briefSummary":231,"conditions":232,"keywords":234,"overallStatus":237,"whyStopped":4,"lastUpdateSubmitDate":238,"lastUpdatePostDateStruct":239,"startDateStruct":241,"completionDateStruct":243,"leadSponsor":245,"locationsCount":4},"100532754","teen-mom-study-a-confirmatory-pragmatic-cluster-rct-100532754","NCT06216925","Teen Mom Study: A Confirmatory Pragmatic Cluster RCT","Teen Mom Study: A Confirmatory Pragmatic Cluster Randomized Controlled Trial","Inclusion Criteria:\n\n* Less than 16 weeks pregnant\n* Black or African-American\n* Between 15 and 19 years of age (inclusive)\n* Enrolled in WIC\n* Residing in 1 of 12 counties constituting the Mississippi Delta region\n* Singleton pregnancy\n* Planning to carry the fetus to term\n* English speaking\n* Possession of a mobile device\n\nExclusion Criteria:\n\n* Individuals with physical activity restrictions",{"count":118,"type":21},[24],"The goal of this clinical trial is to test the effectiveness of #BabyLetsMove - a 24-week mobile Health and peer health coaching intervention paired with the Special Supplemental Nutrition Program for Women, Infants, and Children (WIC) - to increase physical activity and reduce sedentary behavior in pregnant, Black teens in the Mississippi Delta. The main questions it aims to answer are:\n\n* Does #BabyLetsMove increase objective moderate-to-vigorous physical activity and decrease sedentary behavior from ≤16 to 26- and 36-gestational weeks compared to usual WIC care alone?\n* Does # BabyLetsMove decrease the rate of gestational weight gain and mean arterial pressure from ≤16 to 26- and 36-gestational weeks compared to usual WIC care alone?\n* Is #BabyLetsMove a feasible and acceptable intervention according to the RE-AIM framework?\n* Using the Practical, Robust Implementation and Sustainability Model and the Consolidated Framework for Implementation Research, what are the barriers to organizational uptake and how can strategies be improved for future testing?\n\nParticipants will be given three empirically supported behavior goals including (1) watching ≤2 hours of TV or other screen time per day, and (2) walking ≥10,000 steps per day - or - (3) engaging in ≥20 minutes of organized exercise per day.\n\nResearchers will compare the #BabyLetsMove groups to the WIC care only groups to see if the #BabyLetsMove intervention improves traditional WIC care for bettering health outcomes ( amongst pregnant, Black teens in the Mississippi Delta.",[203,202,27,233],"Arterial Pressure",[123,235,236],"Adolescent","Mobile Health","NOT_YET_RECRUITING","2025-04-23",{"date":240,"type":36},"2025-04-27",{"date":242,"type":21},"2025-08-01",{"date":244,"type":21},"2026-06-30",{"name":221,"class":43},{"id":247,"slug":248,"hasResults":11,"nctId":249,"briefTitle":250,"officialTitle":250,"acronym":4,"eligibilityCriteria":251,"healthyVolunteers":15,"sex":141,"minAge":252,"maxAge":253,"enrollmentInfo":254,"targetDuration":4,"studyType":22,"phases":256,"briefSummary":257,"conditions":258,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":262,"lastUpdatePostDateStruct":263,"startDateStruct":265,"completionDateStruct":267,"leadSponsor":269,"locationsCount":76},"100463187","nutri-cap-nutrition-for-children-adolescent-girls-and-pregnant-women-in-slums-of-dhaka-city-100463187","NCT05311436","Nutri-CAP: Nutrition for Children, Adolescent Girls, and Pregnant Women in Slums of Dhaka City","Inclusion Criteria:\n\n* Pregnant women:\n\n  * Age 18-39 years\n  * Before 16 weeks of gestation\n  * BMI 15-24.99 kg\u002Fm2 measured on enrolment\n  * Have the plan to stay in the study area till delivery\n  * Willing to participate in the study\n  * Not enrolled in any nutrition project\u002Fprogramme currently\n\nAdolescent girls:\n\n* Aged 11-19 years\n* Willing to participate in the study\n* Not involved in any nutrition project\u002Fprogramme\n* Will stay in the study area for the next 2 years\n\nChildren:\n\n* Aged 0-24 months\n* Youngest child of the household\n* Caregivers have the plan to stay in the study area at least up to two years of age\n* Not enrolled in any nutrition project\u002Fprogramme currently\n\nExclusion Criteria:\n\n* Pregnant women:\n\n  * Subject not willing to provide consent\n  * Subject has the plan to migrate outside of the study area during the study period\n  * Subject has a plan to go elsewhere ( village\u002F parents' house) for delivery\n  * Any reported\u002Fdiagnosed chronic diseases (such as hypertension, heart disease, chronic obstructive pulmonary disease, chronic kidney disease, chronic liver disease, pancreatic diseases, diabetes mellitus, thyroid dysfunction, immunological diseases, malignancy, or any other diseases which could impede compliance with the study protocol)\n  * Extremely obese\n  * Subject involved in any nutrition programme\u002F intervention currently\n\nAdolescent girls:\n\n* Subject not willing to give assent\u002Fconsent\n* Subject has the plan to migrate outside the study area during the study period\n* Subject involved in any nutrition programme\u002Fintervention currently\n\nChildren:\n\n* Caregiver\u002Fguardian not willing to provide consent\n* Have the plan to migrate outside of the study area during the study period\n* Child with any congenital anomaly\n* Subject involved in any nutrition programme\u002Fintervention currently","1 Day","39 Years",{"count":255,"type":21},3278,[24],"The objective of the research project is to establish an evidence-based sustainable nutrition service delivery platform for optimizing pregnancy weight gain, increasing dietary diversity of adolescent girls, and ensuring proper physical growth of under 2 children.\n\nHypothesis\n\n1. Pregnant Women: Intensive nutrition and WASH counseling, iron-folate, calcium supplementation during pregnancy, can improve gestational weight gain and improve hemoglobin status in pregnant women in a slum of Dhaka city\n2. Adolescent girl: Iron and zinc supplementation and nutrition counseling on dietary diversity could improve nutritional status and dietary diversity score in adolescent girls of slums in Dhaka\n3. Children \\\u003C2 years: Counselling on IYCF, growth monitoring, and promotion, ensuring six-monthly vitamin A supplementation, counseling on WASH, treatment of acute malnutrition, and daily 1 egg supplementation for 3 months for severely stunted children can improve the nutritional status of children\n4. Counselling to improve Water, Sanitation and Hygiene (WASH) practice: WASH intervention can improve EED biomarkers",[27,259,260,261],"Diet, Food, and Nutrition","Undernutrition","Health Behavior","2024-10-27",{"date":264,"type":36},"2024-10-30",{"date":266,"type":36},"2022-04-01",{"date":268,"type":21},"2024-12-31",{"name":270,"class":43},"International Centre for Diarrhoeal Disease Research, Bangladesh"]