[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"breast-feeding\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:breast-feeding":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,24,0,[8,48,74,102,134,165,193,225,249,277,309,336,382,412,438,463,483,506,533,560,585,610,641,663],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":24,"conditions":25,"keywords":29,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100524377","developmental-impacts-of-microplastics-exposure-in-early-life-100524377",false,"NCT06107933","Developmental Impacts of Microplastics Exposure in Early Life","Developmental Impacts of MicroPLastics Exposure in Early Life","DIMPLE","Inclusion Criteria:\n\n* All gender expressions\n* Mothers at 1 or 3 months postpartum (± 2 weeks)\n* Intent to exclusively breastfeed for ≥ 6 months\n* Nulliparous and singleton births\n* Receiving only breast milk from the mother, with no formula supplementation\n\nExclusion Criteria:\n\n* Physical, mental, or cognitive disability that prevents participation; current incarceration\n* Chronic conditions in mother and\u002For infant (e.g., heart disease, cancer, autoimmune disease, diabetes, intestinal bowel syndrome\u002Fdisease), conditions diagnosed for the first time during pregnancy (e.g. gestational diabetes), neurological conditions in mother and\u002For infant (e.g. epilepsy, seizures), psychological conditions in mother and\u002For infant (e.g. bipolar disorder), or neurological\u002Fpsychological conditions diagnosed in mother during or immediately after pregnancy (e.g. postpartum depression)\n* Previously diagnosed with any major illness (e.g., intrauterine growth restriction, birth asphyxia, cancer) or eating disorder or previous gastric band surgery\n* Maternal antibiotic use during pregnancy or the postpartum period. Infant antibiotic use at any time during life or taking medications that could affect plastic exposure or the microbiome, such as medications administered via a plastic syringe.\n* Use of any breast pump except the Silicon Breast Pump for the 14 days prior to the clinical visit.\n* PHQ9 score greater than or equal to 10 indicating clinically relevant symptoms of moderate or worse depression\n* Infants who are intersex\n* Smoking, drug use (including marijuana use), or alcohol abuse",true,"FEMALE","18 Years",{"count":21,"type":22},40,"ESTIMATED","OBSERVATIONAL","The goal of this observational study is to characterize and evaluate micro- and nano-plastic (MNP) exposures among mothers and infants in mother-infant dyads 1 or 3 months postpartum living in Baltimore, Maryland. The main questions it aims to answer are:\n\n* What MNPs are present in breastmilk and maternal blood samples and in their infants stool sample?\n* Are there associations between amount of maternal MNPs in breast milk and mass of MNP particles in infant stool?\n* Which environmental and lifestyle factors are most predictive of maternal MNP burden?\n* Is infant exposure to MNPs associated with birth weight and postnatal growth trajectories?\n\nParticipants will:\n\n* Complete several questionnaires assessing medical histories, lifestyle factors, environmental exposures, eating behaviors, etc.\n* Provide biological specimens including: maternal blood, stool, and breastmilk; infant stool\n* Clinical visit to have anthropometric measures documented including maternal height and weight, infant weight, length, and skin-fold thickness",[26,27,28],"Infant Development","Breast Feeding","Environmental Exposure",[30,31,32,33,34],"microplastic","breastmilk","infant microplastic exposure","gut microbiome","fecal metabolome","RECRUITING","2026-06-05",{"date":38,"type":39},"2026-06-09","ACTUAL",{"date":41,"type":39},"2023-10-01",{"date":43,"type":22},"2027-01-01",{"name":45,"class":46},"Johns Hopkins Bloomberg School of Public Health","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":52,"acronym":4,"eligibilityCriteria":53,"healthyVolunteers":17,"sex":18,"minAge":54,"maxAge":55,"enrollmentInfo":56,"targetDuration":4,"studyType":58,"phases":59,"briefSummary":61,"conditions":62,"keywords":4,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":47},"100640598","reliance-moringa-in-lactation-and-early-childhood-100640598","NCT07605091","RELIANCE: Moringa in Lactation and Early Childhood","Inclusion Criteria:\n\n* Mothers: Inclusion criteria - \\>18 years of age, s\u002Fp delivery of a healthy infant, and planning breast feeding.\n* Infants: must be born at term (=37-42 weeks), singleton birth, breastfeeding, age 7-21 days at enrollment\n\nExclusion Criteria:\n\n* Mothers - women reporting regular consumption of moringa in the last month (\\>1 time weekly), unable to consume moringa or unable to complete study activities within the first two weeks.\n* Mothers - Women with a contraindication to Moringa use (blood thinners, levothyroxine, antihypertensive treatments, insulin dependency).\n* Infants - significant congenital disease, are unable to feed orally.","7 Days","99 Years",{"count":57,"type":22},100,"INTERVENTIONAL",[60],"NA","This study will assess the impact of maternal moringa supplementation to mothers of breastfeeding infants on milk output, milk composition, exclusive breastfeeding duration, and maternal and child health. This will be accomplish by conducting a randomized, controlled dietary intervention study enrolling breastfeeding mothers and their newborn infants. Mothers will be randomized to receive either 10g dried moringa leaf powder in carrier vs. carrier alone, consumed daily for four months, with follow-up for 2 years.\n\nWomen must be \\>18 years of age, ≤ 30 days postpartum and exclusively breastfeeding at the time of enrollment. Infants must be at least 37 weeks of gestational age, be healthy and are able to feed orally and consume human milk.\n\nAfter randomization and enrollment, breast milk samples will be obtained at baseline, 2, 4, and 6 months. Serum from mothers will be collected at recruitment, 2, 6,and 9 months; infant serum will be collected by capillary sample at recruitment and approximately at 4, 6, 12, 18, and 24 months. Infant hemoglobin and infant feeding weights (test weights) will be collected on sequential days at recruitment, 4, and 6 months.\n\n24-hour dietary recall: the foods and drinks consumed by mothers in the 24 hours prior to each milk sample.\n\nOther assessments will include perceptions of breastfeeding, assess complementary feeding practices. Review will be conducted of maternal and infant infections, diagnoses, and hospitalizations at the time of visit or since the last visit.",[27,63],"Lactation","NOT_YET_RECRUITING","2026-05-19",{"date":67,"type":39},"2026-05-22",{"date":69,"type":22},"2026-11",{"date":71,"type":22},"2030-06",{"name":73,"class":46},"Philip Kern",{"id":75,"slug":76,"hasResults":11,"nctId":77,"briefTitle":78,"officialTitle":78,"acronym":79,"eligibilityCriteria":80,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":81,"targetDuration":4,"studyType":58,"phases":83,"briefSummary":84,"conditions":85,"keywords":88,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":93,"lastUpdatePostDateStruct":94,"startDateStruct":96,"completionDateStruct":98,"leadSponsor":100,"locationsCount":47},"100577343","breastfeeding-education-support-tool-100577343","NCT06797063","Breastfeeding Education Support Tool","BEST4Baby","Inclusion Criteria:\n\n* at least 18 years of age,\n* pregnant and 20-27 weeks of gestation at study enrollment,\n* singleton pregnancy,\n* no major antepartum complications,\n* living in a research site,\n* planning to deliver in the cluster area,\n* capable of giving informed consent,\n* willing to be visited by a PC and research personnel for up to 12 months post-delivery.\n\nExclusion Criteria:\n\ncomorbidities impacting breastfeeding,\n\n\\- severe psychological illness that could interfere with consent and study participation. Following a live birth, participants will remain eligible to continue in the study unless the mother or infant experiences: illness or clinical complications warranting prolonged hospitalization, stillbirth, low birth weight (\\\u003C 2500 g), congenital abnormality, or neonatal death.",{"count":82,"type":22},336,[60],"The proposed project seeks to evaluate the effectiveness and implementation of the Breastfeeding Education Support Tool for Baby (BEST4Baby) intervention, an mHealth-supported community-based peer counselor breastfeeding intervention for mothers in India. Given that rates of optimal infant feeding practices have remained stagnant over the past two decades in India, and that India is the most populous country and icontributes one-fifth of all global live births, this project could have major global health implications if the intervention is found to improve maternal breastfeeding practices and infant clinical outcomes. The project will also provide evidence needed to adopt BEST4Baby nationally and in other low resource communities.",[86,26,87,27],"Breastfeeding, Exclusive","Infant Growth",[89,90,91,92],"breastfeeding","India","infant feeding","peer counselors","2026-05-04",{"date":95,"type":39},"2026-05-05",{"date":97,"type":22},"2026-09-01",{"date":99,"type":22},"2029-09-01",{"name":101,"class":46},"Thomas Jefferson University",{"id":103,"slug":104,"hasResults":11,"nctId":105,"briefTitle":106,"officialTitle":107,"acronym":4,"eligibilityCriteria":108,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":109,"enrollmentInfo":110,"targetDuration":4,"studyType":58,"phases":112,"briefSummary":113,"conditions":114,"keywords":118,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":125,"lastUpdatePostDateStruct":126,"startDateStruct":128,"completionDateStruct":130,"leadSponsor":132,"locationsCount":47},"100629720","hybrid-breastfeeding-education-in-late-pregnancy-effects-on-antenatal-attachment-and-breastfeeding-100629720","NCT07478341","Hybrid Breastfeeding Education in Late Pregnancy: Effects on Antenatal Attachment and Breastfeeding","The Effect of Individualized Hybrid Breastfeeding Education in Late Pregnancy on Antenatal Attachment and Breastfeeding Behaviors in Primiparous Women","Inclusion Criteria:\n\nAged 18-35 years,\n\nAt 36 weeks of gestation or later,\n\nExperiencing their first pregnancy (primiparous),\n\nHaving a singleton pregnancy,\n\nAble to read and write in Turkish and capable of communication,\n\nHaving access to a smartphone or the internet,\n\nFree from any physical or mental health problems that would prevent participation in the education,\n\nWilling to voluntarily participate in the study and provide written informed consent.\n\nExclusion Criteria:\n\nPresence of chronic physical illness or pregnancy complications (e.g., preeclampsia, gestational diabetes),\n\nMultiple pregnancy,\n\nGestation earlier than 36 weeks,\n\nInability to actively participate in the education due to communication barriers or cognitive impairment,\n\nLack of access to a smartphone or the internet,\n\nFailure to attend any stage of the educational program or voluntary withdrawal from the study,\n\nRefusal to participate in the study or failure to sign the informed consent form.","35 Years",{"count":111,"type":22},64,[60],"This randomized controlled study aims to examine the effect of individualized hybrid breastfeeding education provided during late pregnancy on antenatal attachment and breastfeeding behaviors among first-time mothers. Participants will be randomly assigned to either the intervention or control group. Women in the intervention group will receive individualized hybrid breastfeeding education beginning at the 36th week of pregnancy. The program includes a face-to-face individual breastfeeding education session at 36 weeks of pregnancy and a reinforcement and practice session at 38 weeks. Participants will also have access to personalized digital educational materials, short educational videos, and online consultation support. In the postpartum period, participants will receive an online support session during the first week after birth and a follow-up session through online communication or telephone at the sixth postpartum week. The control group will receive routine hospital education during pregnancy. After completion of the study, the same educational materials will be provided to the control group in accordance with ethical principles. Data will be collected using the Demographic Information Form, Breastfeeding Behavior Evaluation Form, Antenatal Attachment Inventory, and Breastfeeding Self-Efficacy Scale. Written informed consent will be obtained from all participants prior to enrollment.",[27,115,116,117],"Exclusive Breast Feeding","Maternal-Fetal Attachment","Primiparity",[119,120,121,122,123,124],"Breastfeeding Education","Hybrid Education","Primiparous Women","Antenatal Attachment","Breastfeeding Self-Efficacy","Mother-Infant Bonding","2026-03-13",{"date":127,"type":39},"2026-03-17",{"date":129,"type":39},"2025-12-30",{"date":131,"type":22},"2026-08-01",{"name":133,"class":46},"Emel GÜÇLÜ CİHAN",{"id":135,"slug":136,"hasResults":11,"nctId":137,"briefTitle":138,"officialTitle":139,"acronym":140,"eligibilityCriteria":141,"healthyVolunteers":17,"sex":18,"minAge":142,"maxAge":109,"enrollmentInfo":143,"targetDuration":4,"studyType":58,"phases":145,"briefSummary":146,"conditions":147,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":155,"lastUpdatePostDateStruct":156,"startDateStruct":158,"completionDateStruct":160,"leadSponsor":162,"locationsCount":164},"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",{"count":144,"type":22},276,[60],"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.",[148,149,150,151,152,153,154,27],"Allergies","Obesity","Gestational Complications","Gestational Weight Gain","Perinatal Condition","Birth Weight","Chronic Diseases in Children","2026-02-11",{"date":157,"type":39},"2026-02-12",{"date":159,"type":39},"2021-11-02",{"date":161,"type":22},"2026-03-10",{"name":163,"class":46},"Federico II University",2,{"id":166,"slug":167,"hasResults":11,"nctId":168,"briefTitle":169,"officialTitle":170,"acronym":171,"eligibilityCriteria":172,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":173,"targetDuration":4,"studyType":58,"phases":175,"briefSummary":176,"conditions":177,"keywords":178,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":184,"lastUpdatePostDateStruct":185,"startDateStruct":187,"completionDateStruct":189,"leadSponsor":191,"locationsCount":47},"100561368","cannabidiol-into-breastmilk-100561368","NCT06589258","Cannabidiol Into Breastmilk","Study of the Passage of (CBD) Into Breast Milk and Its Biological Impact on Breast-fed Children","CBD-ALLT","Inclusion Criteria:\n\n* Women over 18\n* Breastfeeding CBD user\n* Having given written informed consent\n\nExclusion Criteria:\n\n* Women who do not understand French well\n* Women with a psychiatric or dual pathology that prevents proper participation in the study,\n* Women under protective supervision (guardianship\u002Fcuratorship),\n* Women under court protection,\n* Women not affiliated to a social security scheme",{"count":174,"type":22},60,[60],"Really few data published to date on the passage of CBD into breast milk. The investigators known that 17.5 percent of the French human being between 18 and 34 years old consume CBD and among this, nearly half are women. None official French data to say how many French breastfeeding mothers consume CBD. CBD is a legal, psychoactive but not psychoaddictive substance. CBD's pharmacokinetic and pharmacodynamics make us fear that CBD could easily go through mother's milk. No published data available on possible effect in breast-fed child, not even on possible biological passage in breast-fed child. The aim of his study is to evaluate the passage of CBD in blood and milk at different moments of the breastfeeding (mothers) and its possible found in the infants'urine.",[27],[179,180,181,182,183],"cannabidiol","Breast milk","Breast-feeding","Breast-feed children","PK POP","2026-01-29",{"date":186,"type":39},"2026-01-30",{"date":188,"type":39},"2025-10-06",{"date":190,"type":22},"2028-10",{"name":192,"class":46},"Centre Hospitalier Régional d'Orléans",{"id":194,"slug":195,"hasResults":11,"nctId":196,"briefTitle":197,"officialTitle":197,"acronym":4,"eligibilityCriteria":198,"healthyVolunteers":17,"sex":199,"minAge":200,"maxAge":201,"enrollmentInfo":202,"targetDuration":4,"studyType":58,"phases":204,"briefSummary":205,"conditions":206,"keywords":211,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":216,"lastUpdatePostDateStruct":217,"startDateStruct":219,"completionDateStruct":221,"leadSponsor":223,"locationsCount":47},"100615671","mobile-prenatal-education-for-expectant-fathers-and-its-effects-on-bonding-stress-breastfeeding-and-marital-satisfaction-100615671","NCT07295639","Mobile Prenatal Education for Expectant Fathers and Its Effects on Bonding, Stress, Breastfeeding and Marital Satisfaction","Inclusion Criteria:\n\n* Age between 19 and 65 years\n* First-time father\n* Has become a father within the last month\n* Has a healthy newborn without congenital anomalies or chronic illnesses\n* Does not have a premature or low-birth-weight baby\n* Has not become a father through adoption\n* Owns a mobile phone capable of accessing the mobile-based application\n* Has an Android or iOS operating system\n* Has not received any infant care training within the last 6 months\n* Has no physical or mental disability that would prevent viewing, hearing, or understanding the research questions or educational content\n* Voluntarily agrees to participate in the research\n\nExclusion Criteria:\n\n* Declines to participate in the research\n* Does not own a smartphone\n* Cannot use mobile applications\n* Has a physical or mental condition that prevents completing the questionnaires\n* Has a baby with congenital anomalies or chronic medical conditions\n* Has a premature or low-birth-weight baby\n* Has received infant care training within the last 6 months\n* Has adopted a child\n* Is outside the 19-65 age range","MALE","19 Years","65 Years",{"count":203,"type":22},80,[60],"The aim of this interventional clinical trial is to assess whether a mobile-based antenatal education programme for expectant fathers has a positive effect on father-infant bonding, stress levels, and breastfeeding attitudes.\n\nThe study aims to answer the following main questions:\n\nDoes participation in a mobile-based prenatal education programme strengthen fathers' emotional bonds with their babies? Does the education reduce fathers' stress levels during the prenatal and postnatal periods? Does it increase the father's knowledge and supportive attitude towards breastfeeding? Researchers will compare whether there are measurable differences in attachment, stress, and breastfeeding attitudes between the intervention group (fathers receiving mobile-based education) and the control group (fathers receiving standard routine information).\n\nParticipants: Will complete pre- and post-intervention questionnaires assessing attachment, stress, and breastfeeding attitudes.\n\nThe intervention group will have access to a six-module mobile application covering topics such as infant care, nutrition, sleep routines, health and safety, emotional development, and daily care practices.\n\nThe study will be conducted with fathers aged 19-65 who became fathers within the last month and voluntarily agreed to participate.",[207,27,208,209,210],"Breastfeeding Attitudes","Paternal Behavior","Health Education","Parent-Child Relations",[212,213,214,215],"father-infant bonding","paternal stress","breastfeeding attitudes","mobile-based education","2025-12-16",{"date":218,"type":39},"2025-12-19",{"date":220,"type":22},"2026-01",{"date":222,"type":22},"2026-10",{"name":224,"class":46},"Gaziantep Islam Science and Technology University",{"id":226,"slug":227,"hasResults":11,"nctId":228,"briefTitle":229,"officialTitle":229,"acronym":230,"eligibilityCriteria":231,"healthyVolunteers":11,"sex":232,"minAge":233,"maxAge":234,"enrollmentInfo":235,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":237,"conditions":238,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":240,"lastUpdatePostDateStruct":241,"startDateStruct":243,"completionDateStruct":245,"leadSponsor":247,"locationsCount":47},"100569260","at-the-breast-vs-expressed-human-milk-genesis-of-infant-nutrition-begin-100569260","NCT06691932","At-the-Breast vs. Expressed Human Milk: Genesis of Infant Nutrition (BEGIN)","BEGIN","Inclusion Criteria:\n\n* Lactating mothers between 20-40 years old at enrollment\n\n  o 120 mother\u002Finfant dyads who primarily feed HM ATB (average \\>75% of feeds,\n* pumping no more than one time per day)\n\n  o 120 mother\u002Finfant dyads who predominantly feed expressed HM (average \\>75% of feeds)\n* All races and ethnicities may enroll\n* Singleton infant delivered after 37 weeks\n* Infant between the ages of 0-1 months at the time of enrollment.\n* No serious health complications in mother or infant\n\nExclusion Criteria:\n\n* Non-English-speaking subjects as study personnel only speak English\n* Lactating moms who will be feeding both ATB and expressed HM (over 25% of the time in either feeding mode)\n* Infant supplementation with formula ≥10 oz before sample collections begin, and\u002For no more than 16 oz during active participation\u002F sample collections.","ALL","0 Days","40 Years",{"count":236,"type":22},240,"The purpose of this study is to define human milk (HM) as an ecosystem which investigators will then combine into temporal models of milk dynamics to accurately describe HM chronobiology. This study addresses 4 crucial public health gaps: 1) how breast milk changes over time and over the day, 2) how milk dynamics are related to infant sleep patterns, 3) how milk dynamics are related to infant microbiome dynamics, and 4) how all these relationships differ between infants fed directly at-the-breast vs pumped milk. These fundamental insights have been unknown until now, so that families who feed pumped breast milk are completely underserved. These results are critical to optimizing infant feeding and health outcomes for all infants receiving breast milk.",[27,239],"Exclusive Breastfeeding","2025-12-05",{"date":242,"type":39},"2025-12-11",{"date":244,"type":39},"2024-11-12",{"date":246,"type":22},"2029-11-01",{"name":248,"class":46},"University of Rochester",{"id":250,"slug":251,"hasResults":11,"nctId":252,"briefTitle":253,"officialTitle":254,"acronym":4,"eligibilityCriteria":255,"healthyVolunteers":17,"sex":18,"minAge":4,"maxAge":4,"enrollmentInfo":256,"targetDuration":4,"studyType":58,"phases":258,"briefSummary":259,"conditions":260,"keywords":262,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":268,"lastUpdatePostDateStruct":269,"startDateStruct":271,"completionDateStruct":273,"leadSponsor":275,"locationsCount":47},"100614572","effect-of-hypnobreastfeeding-education-in-high-risk-pregnant-women-100614572","NCT07281339","Effect of Hypnobreastfeeding Education in High-Risk Pregnant Women","The Effect of Hypnobreastfeeding Education Given to High-Risk Pregnant Women on Anxiety Levels, Infant Feeding Intention, Postpartum Perception of Insufficient Milk, and Breastfeeding Adaptation","Inclusion Criteria:\n\n* High-risk primiparous pregnant women\n* Those with 28-34 weeks of pregnancy\n* Those who volunteered to participate in the study\n* Those who can read and write Turkish\n\nExclusion Criteria:\n\n* Those with communication disabilities\n* Those with psychiatric and mental illnesses\n* Those who have an obstacle to breastfeeding\n* Those who have previously attended a birth preparation class\n* Those who receive breastfeeding-related training and consultancy\n* Those who gave birth prematurely\n* Those with anomalies in their babies",{"count":257,"type":22},68,[60],"It is thought that hypnobreastfeeding training given to high-risk pregnant women will reduce anxiety levels, increase lactation, encourage breastfeeding, reduce the perception of insufficient milk, and facilitate adaptation to the postpartum breastfeeding process. According to the results of the power analysis, at least 68 high-risk pregnant women, 34 experimental and 34 control, should be included in the study. Data will be collected with the \"Pregnancy Information Form\", \"Anxiety Assessment Scale\", \" Infant Feeding Intention Instrument\", \"Postpartum Information Form\", \"Perception of Insufficient Milk Questionnaire\" and \"Breastfeeding Adaptation Scale\". In the research, hypnobreastfeeding training will be applied by the researcher to the high-risk pregnant women in the experimental group.",[261,27],"High-risk Pregnancy",[263,264,265,266,267],"Hypnobreastfeeding","Anxiety","Infant Feeding Intention","Perception of Insufficient Milk","Breastfeeding Adaptation","2025-12-01",{"date":270,"type":39},"2025-12-15",{"date":272,"type":39},"2025-10-15",{"date":274,"type":22},"2026-06-30",{"name":276,"class":46},"Amasya University",{"id":278,"slug":279,"hasResults":11,"nctId":280,"briefTitle":281,"officialTitle":282,"acronym":4,"eligibilityCriteria":283,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":284,"enrollmentInfo":285,"targetDuration":4,"studyType":58,"phases":286,"briefSummary":287,"conditions":288,"keywords":291,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":300,"lastUpdatePostDateStruct":301,"startDateStruct":303,"completionDateStruct":305,"leadSponsor":307,"locationsCount":47},"100607938","trauma-informed-obstetric-care-for-perinatal-health-a-pilot-study-100607938","NCT07195058","Trauma-informed Obstetric Care for Perinatal Health: a Pilot Study","Trauma-informed Obstetric Care for Perinatal Health in Women With Histories of Childhood Abuse: a Pilot Randomized Clinical Trial","Inclusion Criteria:\n\n* Women who are \\\u003C19 weeks pregnant\n* Nulliparous (no previous live births)\n* 18 or more years of age\n* Carrying a single fetus\n* Can speak Spanish\n\nExclusion Criteria:\n\n* Any current psychiatric diagnosis or treatment\n* Medical complications (hypertension, cardiac disease, diabetes, chronic disease, autoimmune disease) before pregnancy","45 Years",{"count":174,"type":22},[60],"The study will test trauma-informed obstetric care training and supervision for obstetric clinicians in relation to prenatal mental health and attachment formation (early predictors of child development) in women presenting for prenatal care in a public hospital in Buenos Aires, Argentina.",[289,27,290],"Mother to Child Transmission","Trauma",[292,293,294,295,296,297,298,299],"Adverse childhood experiences (ACE)","Edinburgh Postnatal Depression Scale (EPDS)","Perceived Stress Scale (PSS)","Maternal antenatal attachment scale (MAAS)","Social Support Questionnaire (SSQ)","Prenatal Distress Questionnaire (NuPDQ)","Iowa Infant Feeding scale (IIFAS)","Trauma Informed Care","2025-09-19",{"date":302,"type":39},"2025-09-26",{"date":304,"type":39},"2025-05-23",{"date":306,"type":22},"2027-01",{"name":308,"class":46},"Columbia University",{"id":310,"slug":311,"hasResults":11,"nctId":312,"briefTitle":313,"officialTitle":314,"acronym":315,"eligibilityCriteria":316,"healthyVolunteers":17,"sex":232,"minAge":4,"maxAge":4,"enrollmentInfo":317,"targetDuration":4,"studyType":58,"phases":319,"briefSummary":320,"conditions":321,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":327,"lastUpdatePostDateStruct":328,"startDateStruct":330,"completionDateStruct":332,"leadSponsor":334,"locationsCount":47},"100530635","positive-feeding-of-the-preterm-infant-100530635","NCT06189352","Positive Feeding of the Preterm Infant","Positive Feeding of the Preterm Infant - a Feasibility Study of a Developmental Supportive Feeding Strategy in the NICU","PoP","Inclusion Criteria:\n\n* gestational age of 28 weeks\n* post menstrual age of 28 weeks after transition from regional hospital\n\nExclusion Criteria:\n\n* diagnoses or malformations that makes eating difficult\n* triplets or more\n* parents not speaking\u002Funderstanding Norwegian or English\n* parents with challenges or special needs for follow up",{"count":318,"type":22},15,[60],"The goal of this feasibility study is to assess the feasibility to implement a feeding strategy for preterm infants.\n\nThe main questions it aims to answer are:\n\n* Is it feasible to implement the PoP-intervention in a level 3a category Neonatal intensive care unit?\n* Is the PoP-intervention acceptable for parents of preterm infants and health care personnel working in Neonatal intensive care unit?\n\nParents of preterm infants and health care personnel will be asked to follow a protocol of a feeding strategy based on the preterm infants development and cues throughout the NICU-stay.",[322,27,323,324,325,326],"Preterm Infant","Bottle Feeding","Enteral Feeding","Cue Based Feeding","Develomentally Supportive Care","2025-08-05",{"date":329,"type":39},"2025-08-11",{"date":331,"type":39},"2024-10-14",{"date":333,"type":22},"2026-05",{"name":335,"class":46},"Oslo Metropolitan University",{"id":337,"slug":338,"hasResults":11,"nctId":339,"briefTitle":340,"officialTitle":341,"acronym":342,"eligibilityCriteria":343,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":344,"enrollmentInfo":345,"targetDuration":4,"studyType":58,"phases":347,"briefSummary":348,"conditions":349,"keywords":366,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":373,"lastUpdatePostDateStruct":374,"startDateStruct":376,"completionDateStruct":378,"leadSponsor":380,"locationsCount":47},"100598934","comparing-integrative-midwife-led-vs-fragmented-inpatient-postpartum-care-impact-on-satisfaction-and-transition-to-motherhood-100598934","NCT07077941","Comparing Integrative Midwife-led vs. Fragmented Inpatient Postpartum Care: Impact on Satisfaction and Transition to Motherhood","Supporting Mothers With Integrative Care by Midwives for Lifelong Empowerment (SMILE): A Randomized Controlled Trial Comparing Midwife-led Integrative and Fragmented Standard Inpatient Postpartum Care Models on Maternal Satisfaction and Transition to Motherhood","SMILE","Inclusion Criteria:\n\n* Women aged 18 to 50 years at the time of delivery\n* Classified as \"low-risk\" by the obstetric team in the delivery room\n* Gestational age at birth between 36+0 and 42+0 weeks\n* Singleton birth (only one child born)\n* Intent to breastfeed\n* Consent to participate in the study\n\nExclusion Criteria:\n\n* Women younger than 18 or older than 50 at the time of delivery\n* Classified as \"high-risk\" by the obstetric team\n* Multiple birth (e.g., twins, triplets)\n* No intention or ability to breastfeed the newborn","50 Years",{"count":346,"type":22},784,[60],"The goal of this clinical trial is to compare two different forms of postnatal care to find out which is most beneficial for mothers and their children after birth and with which they are most satisfied. One is a nurse-led, seperate model of care and the other is a midwife-led, integrative model of care. Participants are healthy women between the ages of 18 and 50. They gave birth between 36+0 and 42+0 weeks of pregnancy and had a child. The type of birth is not an inclusion or exclusion criteria. Our hypotheses are: i) that maternal satisfaction with care in a midwife-led, integrative care model is higher than in separate maternal and infant care; ii) that a positive postpartum experience leads to earlier and increased maternity competence; iii) that a higher breastfeeding rate at the time of the survey in the fourth month can be achieved through integrative care. Participants will be randomly assigned, after birth of their child, to either the group cared for by a nurse or the group cared for by a midwife.",[350,351,352,27,353,354,355,63,356,357,358,359,360,361,362,363,364,365],"Maternal Health Services","Infant, Newborn","Postnatal Care","Maternal-Child Relations","Postpartum Depression (PPD)","Mental Health","Breast Feeding, Exclusive","Patient Satisfaction and Experience With Integrative Therapies","Neonatal Jaundice","Maternal Behavior","Body Weight Decreased","Breast Feeding of Healthy Full Term Infants","Lactation Mastitis","Lactation Disorder - Postpartum Condition or Complication","Lactation Disorder With Baby Delivered","Lactation; Insufficient, Partial",[367,368,369,370,371,89,372],"Postnatal care","inpatient","maternity competence","satisfaction","integrative care","maternal behavior","2025-07-12",{"date":375,"type":39},"2025-07-22",{"date":377,"type":22},"2025-10-01",{"date":379,"type":22},"2026-12-31",{"name":381,"class":46},"Medical University of Vienna",{"id":383,"slug":384,"hasResults":11,"nctId":385,"briefTitle":386,"officialTitle":387,"acronym":388,"eligibilityCriteria":389,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":390,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":392,"conditions":393,"keywords":395,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":403,"lastUpdatePostDateStruct":404,"startDateStruct":406,"completionDateStruct":408,"leadSponsor":410,"locationsCount":47},"100519381","umbrellact-study-clinical-lactation-study-on-the-exposure-to-medicines-via-human-milk-100519381","NCT06042803","UmbrelLACT Study: Clinical Lactation Study on the Exposure to Medicines Via Human Milk","Clinical Lactation Study on the Exposure to Medicines Via Human Milk: an Umbrella Study Protocol","UmbrelLACT","Inclusion Criteria:\n\n* For breastfeeding women\n\n  * Maternal age: ≥ 18 year\n  * Currently exclusively or partially breastfeeding (\u002Fexpressing milk) at the time of milk sampling\n  * Using medicines for any indication, with at least 5 half-lives of the medicine taken\n  * Willing to express and collect human milk\n  * Signed informed consent to participate and for processing their personal data\n* For infants\n\n  * Gestational age at birth: ≥24 weeks\n  * Parental signed informed consent to participate and for processing their personal data\n\nExclusion Criteria:\n\n* Maternal age \\\u003C18 years\n* Mother of twins\n* Not meeting the inclusion criteria",{"count":391,"type":22},30,"The goal of this observational study is to determine the concentration of medicines in human milk during maternal medicine intake. The main questions it aims to answer are:\n\n* What is the concentration of maternal medicines in human milk?\n* What is the (estimated) intake and exposure in the breastfed infant?\n\nParticipants will be asked to\n\n* fill out a questionnaire regarding medical data of the mother and child\n* track medication intake for 3 days\n* collect milk samples during 24 hours\n* optionally, donate 2 blood samples of the mother and give consent to one blood sample of the child\n* fill out a questionnaire regarding the general health of the child.",[27,394],"Human Milk",[396,397,398,89,399,400,401,402],"Infant exposure","Physiologically-based pharmacokinetic models","Neonatology","Pharmacology","Medicines","Drug transfer","Medication intake","2025-02-24",{"date":405,"type":39},"2025-02-27",{"date":407,"type":39},"2023-02-01",{"date":409,"type":22},"2027-02",{"name":411,"class":46},"Universitaire Ziekenhuizen KU Leuven",{"id":413,"slug":414,"hasResults":11,"nctId":415,"briefTitle":416,"officialTitle":417,"acronym":4,"eligibilityCriteria":418,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":419,"targetDuration":4,"studyType":58,"phases":421,"briefSummary":422,"conditions":423,"keywords":424,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":429,"lastUpdatePostDateStruct":430,"startDateStruct":432,"completionDateStruct":434,"leadSponsor":436,"locationsCount":4},"100575681","evaluation-of-the-effectiveness-of-a-breastfeeding-education-program-based-on-planned-behavior-theory-100575681","NCT06775444","Evaluation of the Effectiveness of a Breastfeeding Education Program Based on Planned Behavior Theory","The Effect Of The Theory Of Planned Behavior Based Breastfeeding Education Program Given To Pregnant Women On Breastfeedıng Adaptation, Motivation, Self-Efficacy And The Tendency To Early Weaning.","Inclusion Criteria:\n\n* Those who are over 18 years old\n* Pregnant women in their last trimester (pregnant women who are 27 weeks or more)\n* Those who receive breastfeeding training at the Pregnancy School\n* Speak and understand Turkish\n* Do not have a risky pregnancy diagnosis\n* Do not have multiple pregnancies\n* Do not have a psychiatric or neurological disease that will affect their cognitive functions\n* Have the WhatsApp application on their phone\n* Volunteer to participate in the research\n* Want to breastfeed their baby\n* Have given birth at \\>37 weeks of pregnancy\n* Have a baby weighing at least 2500 grams\n* Have a single healthy baby in the postpartum period\n* Mothers who do not have breast problems that prevent breastfeeding, do not use medication that passes into breast milk, or have any disease (such as active tuberculosis, HIV) were determined as follows.\n\nExclusion Criteria:\n\n* Those who could not continue the study for any reason\n* Those who did not participate in all final tests\n* Those who did not participate in all training\n* Those who could not be reached more than 5 times in each planned telephone\u002Fface-to-face meeting.\n* Those whose babies were hospitalized in neonatal intensive care after birth (except for babies hospitalized for more than 24 hours - due to neonatal jaundice)",{"count":420,"type":22},88,[60],"The aim of the research is to examine the effect of a breastfeeding training program based on the theory of planned behavior on Pregnant Womens' Breastfeeding Adaptation, Motivation, Self-Efficacy And The Tendency To Early Weaning.",[27],[425,426,427,428,267],"Theory Of Planned Behavior","Breastfeeding","Self Efficacy","Motivation","2025-01-09",{"date":431,"type":39},"2025-01-15",{"date":433,"type":22},"2025-01",{"date":435,"type":22},"2026-03",{"name":437,"class":46},"Ankara University",{"id":439,"slug":440,"hasResults":11,"nctId":441,"briefTitle":442,"officialTitle":443,"acronym":4,"eligibilityCriteria":444,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":109,"enrollmentInfo":445,"targetDuration":4,"studyType":58,"phases":447,"briefSummary":448,"conditions":449,"keywords":450,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":454,"lastUpdatePostDateStruct":455,"startDateStruct":457,"completionDateStruct":459,"leadSponsor":461,"locationsCount":47},"100571576","integrated-sensory-supported-virtual-reality-and-gamified-digital-breastfeeding-education-100571576","NCT06722053","Integrated Sensory Supported Virtual Reality and Gamified Digital Breastfeeding Education","Effects of Integrative Sensory-Supported Virtual Reality and Gamified Digital Breastfeeding Education on Mothers' Breastfeeding Success, Self-Efficacy and Adaptation","Inclusion Criteria:\n\n* literate,\n* healthy (no systemic\u002Fchronic disease, diagnosed psychiatric or neurological disease, no risky pregnancies, etc.)\n* primiparous pregnant women with singleton pregnancies,\n* planning to breastfeed,\n* having an internet-connected smart phone\u002Ftablet\u002Fcomputer and being able to use it actively,\n* competent enough to play games and having no problems with their hands, no breast problems that would make breastfeeding difficult (indentation, missing nipple, sore nipple, etc.),\n* no vision, hearing or communication problems,\n* pregnant women who are not allergic to lemon or lemon oil\n\nExclusion Criteria:\n\n* the occurrence of a situation that prevents sucking\n* the baby is not healthy",{"count":446,"type":22},105,[60],"Breastfeeding is the most ideal form of nutrition that concerns the health of mother and baby. The World Health Organization (WHO) recommends that breastfeeding should be started within the first hour after birth. Although breastfeeding has many benefits, research shows that breastfeeding rates are not at the desired level. Breastfeeding self-efficacy, success and adaptation become important to increase breastfeeding rates. In order to provide these components related to breastfeeding, breastfeeding education must be given starting from prenatal period. Education methods have taken different forms in line with the developing technology and the needs of the generation. WHO states that information and communication technology is an opportunity to support breastfeeding. Virtual reality and online learning applications also positively affect learning. New teaching methods, which are increasingly used today, make learning easier and can be used easily in virtual environments. Providing learning by doing in a realistic environment is important for successful breastfeeding and gaining breastfeeding skills and competence. In order to gain breastfeeding skills, the mother can experience breastfeeding during pregnancy using virtual reality technology. While breastfeeding skills are gained through virtual reality, information about breastfeeding can be provided through gamified digital training. With the game, the student actively participates in education. Active participation of the student in gamification ensures that knowledge becomes permanent. It is thought that the effect of the integrative sense can be used to facilitate postpartum remembering of these trainings.",[27],[451,452,453],"breasfeeding","virtual reality","gamification","2024-12-07",{"date":456,"type":39},"2024-12-12",{"date":458,"type":22},"2024-12-01",{"date":460,"type":22},"2026-11-01",{"name":462,"class":46},"ipek turhan",{"id":464,"slug":465,"hasResults":11,"nctId":466,"briefTitle":467,"officialTitle":468,"acronym":4,"eligibilityCriteria":469,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":234,"enrollmentInfo":470,"targetDuration":4,"studyType":58,"phases":472,"briefSummary":473,"conditions":474,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":454,"lastUpdatePostDateStruct":477,"startDateStruct":478,"completionDateStruct":479,"leadSponsor":481,"locationsCount":47},"100563828","the-effect-of-musc-on-labor-pan-anxety-and-breastfeedng-success-100563828","NCT06621238","The Effect of Musıc on Labor Paın, Anxıety and Breastfeedıng Success","Effect of Musıc Lıstened to Prımarıparous Women Who Have Delıvered by Cesarean Sectıon on Paın, Status Anxıety and Breastfeedıng Success","Inclusion Criteria:\n\n* Caesarean section\n* Live birth\n\nExclusion Criteria:\n\n* Risky pregnancy\n* Twin pregnancy\n* Newborn with cleft palate, cleft lip",{"count":471,"type":22},140,[60],"The aim of this study is to examine the effects of music played to primiparous women who had a cesarean section on pain, state anxiety and breastfeeding success.",[475,264,27,476],"Labor Pain","Post Operative Pain",{"date":456,"type":39},{"date":454,"type":39},{"date":480,"type":22},"2025-04-15",{"name":482,"class":46},"Ataturk University",{"id":484,"slug":485,"hasResults":11,"nctId":486,"briefTitle":487,"officialTitle":488,"acronym":4,"eligibilityCriteria":489,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":284,"enrollmentInfo":490,"targetDuration":4,"studyType":58,"phases":491,"briefSummary":492,"conditions":493,"keywords":495,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":497,"lastUpdatePostDateStruct":498,"startDateStruct":500,"completionDateStruct":502,"leadSponsor":504,"locationsCount":47},"100557322","the-effect-of-oketani-breast-massage-on-breastfeeding-100557322","NCT06536608","The Effect of Oketani Breast Massage on Breastfeeding","The Effect of Oketani Breast Massage on Breastfeeding Success, Breastfeeding Self-Efficacy and Satisfaction in Primiparous Mothers: A Randomized Controlled Trial","Inclusion Criteria:\n\n* To volunteer to participate in the study,\n* To be over 18 years of age,\n* To be able to read and write,\n* To be able to read and understand Turkish,\n* To have no hearing, speech or visual impairments,\n* To have received breastfeeding training at a pregnancy school,\n* To be healthy in the 36th week of primiparous pregnancy.\n\nExclusion Criteria:\n\n* Obstacles to communication include having a visual, hearing or perception disorder,\n* Not being able to read or write,\n* Having a psychiatric illness,\n* Being multiparous and having a vaginal birth,\n* Having a risky pregnancy.",{"count":174,"type":22},[60],"This study aims to determine the effects of Oketani breast massage on breastfeeding success, breastfeeding self-efficacy and satisfaction of primiparous mothers.",[27,494],"Massage",[27,496,494],"Nursing","2024-11-26",{"date":499,"type":39},"2024-11-27",{"date":501,"type":39},"2024-11-04",{"date":503,"type":22},"2025-05-20",{"name":505,"class":46},"Saglik Bilimleri Universitesi",{"id":507,"slug":508,"hasResults":11,"nctId":509,"briefTitle":510,"officialTitle":511,"acronym":4,"eligibilityCriteria":512,"healthyVolunteers":17,"sex":232,"minAge":513,"maxAge":514,"enrollmentInfo":515,"targetDuration":4,"studyType":58,"phases":516,"briefSummary":517,"conditions":518,"keywords":521,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":526,"lastUpdatePostDateStruct":527,"startDateStruct":528,"completionDateStruct":530,"leadSponsor":531,"locationsCount":47},"100570351","effect-of-intranasal-breast-milk-administration-in-preterm-infants-100570351","NCT06706115","Effect of Intranasal Breast Milk Administration in Preterm Infants",": Effect of Intranasal Breast Milk Administration on Cerebral Oxygenation, Vital Signs and Transition Time to Full Oral Feeding in Preterm Babies: Randomized Controlled Study","Inclusion Criteria:\n\n* Birth weight \\>1000 gr,\n* APGAR score \\>7 at 5 minutes after birth,\n* Availability of breast milk,\n* No medical diagnosis affecting cerebral oxygenation (intraventricular hemorrhage, cardiovascular and neurological disorders, anemia),\n* No congenital anomalies or chromosomal abnormalities,\n* No congenital anomaly (such as cleft palate) affecting nasal patency.\n\nExclusion Criteria:\n\n* Being able to feed orally in all feedings\n* Being fed entirely on formula milk,\n* Administration of medication via the nasal route,\n* Being intubated or receiving continuous positive air pressure (CPAP) support,\n* Maternal substance abuse, alcohol abuse, HIV infection, untreated active tuberculosis, chemotherapy or radiotherapy treatment,\n* The mother has mastitis, breast trauma, abscesses or is taking any medication that passes into the milk,\n* The mother does not want to express milk.","28 Weeks","37 Weeks",{"count":21,"type":22},[60],"The aim of the study was to investigate the effect of intranasal breast milk administration on cerebral oxygenation level, vital signs and time to full oral feeding in preterm infants.",[519,520,27],"Newborn; Vitality","Nursing Caries",[180,522,523,524,525],"Newborn Nursing","Oral Nutrition","Physiological parameters","Preterm infant","2024-11-22",{"date":497,"type":39},{"date":529,"type":39},"2024-06-30",{"date":129,"type":22},{"name":532,"class":46},"Selcuk University",{"id":534,"slug":535,"hasResults":11,"nctId":536,"briefTitle":537,"officialTitle":537,"acronym":538,"eligibilityCriteria":539,"healthyVolunteers":11,"sex":232,"minAge":540,"maxAge":4,"enrollmentInfo":541,"targetDuration":4,"studyType":58,"phases":543,"briefSummary":544,"conditions":545,"keywords":550,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":552,"lastUpdatePostDateStruct":553,"startDateStruct":554,"completionDateStruct":556,"leadSponsor":558,"locationsCount":47},"100567801","impact-of-standardized-skin-to-skin-care-on-clinical-outcomes-in-infants-born--32-weeks-a-multicenter-study-100567801","NCT06672913","Impact of Standardized Skin-to-Skin Care on Clinical Outcomes in Infants Born ≤ 32 Weeks: A Multicenter Study","TR-SSCinNICU","Inclusion Criteria:\n\n* Infants born at gestational age ≤ 32 weeks\n\nExclusion Criteria:\n\n* Death before NICU discharge\n* Abdominal wall defects","1 Day",{"count":542,"type":22},120,[60],"This study is a multi-center, prospective pre-post clinical study conducted under the leadership of the Turkish Neonatal Society. It aims to investigate the effects of a standardized skin-to-skin care in NICU, initiated early and applied regularly, on recieving exclusive mothers' milk at discharge and clinical outcomes for preterm infants born ≤ 32 weeks of gestation.\n\n1. Primary Objective: To evaluate the rate of receiving exclusive mothers' milk at discharge for infants born ≤ 32 weeks of gestation who have received skin-to-skin care in accordance with the study protocol.\n2. Secondary Objective: To evaluate the rates of neonatal sepsis, intraventricular hemorrhage, and necrotizing enterocolitis (stage 2 and above) as well as the length of hospital stay for infants born at or below 32 weeks of gestation who have received skin-to-skin care in accordance with the study protocol.",[546,547,27,548,549],"Premature","Skin to Skin Contact","Necrotizing Enterocolitis","Retinopathy of Prematurity",[546,551,27,548,549],"Skin to skin contact","2024-11-01",{"date":501,"type":39},{"date":555,"type":39},"2024-09-01",{"date":557,"type":22},"2025-06-01",{"name":559,"class":46},"Baskent University Ankara Hospital",{"id":561,"slug":562,"hasResults":11,"nctId":563,"briefTitle":564,"officialTitle":565,"acronym":496,"eligibilityCriteria":566,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":567,"targetDuration":4,"studyType":58,"phases":568,"briefSummary":569,"conditions":570,"keywords":572,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":576,"lastUpdatePostDateStruct":577,"startDateStruct":579,"completionDateStruct":581,"leadSponsor":583,"locationsCount":47},"100508505","development-of-my-breastfeeding-guide-mobile-nursing-application-100508505","NCT05901298","Development of 'My Breastfeeding Guide' Mobile Nursing Application","Development of 'My Breastfeeding Guide' Mobile Nursing Application and Its Effect on Breastfeeding Process, Self-Efficacy, Infant Nutrition and Attachment","Inclusion Criteria:\n\n* Women aged 18 and over,\n* Women who are in the last trimester of pregnancy (32nd gestational week and above),\n* Women with singleton pregnancy,\n* Women who do not have any health problems that may prevent breastfeeding,\n* Women with smartphones with Android and iOS operating systems,\n* Women who can access the Internet,\n* There will be women who do not have literacy problems, mental disabilities and communication problems.\n\nExclusion Criteria:\n\n* Women under 18 years of age,\n* Women who are under the last trimester of pregnancy (32nd week of pregnancy),\n* Women who do not speak Turkish,\n* Women who own a smartphone with an operating system other than Android and iOS.",{"count":420,"type":22},[60],"The research was planned to develop the \"My Breastfeeding Guide\" mobile nursing application, which was developed based on Dennis' Breastfeeding Self-Efficacy Theory and Pender's Health Promotion Model, and to determine its effect on the postpartum breastfeeding process, breastfeeding self-efficacy, infant feeding and attachment. The research is in randomized controlled experimental and longitudinal (prospective) design. The research will be carried out with pregnant women who applied to Famagusta State Hospital Obstetrics and Gynecology Polyclinic and a pregnant polyclinic of a private hospital in Famagusta. Pregnant women who applied to Famagusta State Hospital Gynecology and Obstetrics Polyclinic and private hospital's pregnancy polyclinic and met the inclusion criteria of the study will constitute the population of the research. The research will be designed in two groups as the mobile nursing practice group (intervention) and standard care group (control) developed based on Dennis's Breastfeeding Self-Efficacy Theory and Pender's Health Promotion Model. By calculating the sample size in the research, 44 people in the intervention group and 44 people in the control group will reach a total of 88 people. Pregnant Identification Form, Maternal Information Form, Breastfeeding Self-Efficacy Short Form Scale (Postnatal Form), Antenatal Self-Efficacy Short Form Scale, Infant Nutrition Attitude Scale, Breastfeeding Rating Scale, Maternal Attachment Scale and Breastfeeding Self-assessment Form will be used to collect data. Statistical analyzes of the data obtained from the research will be made using the Statistical Package for the Social Science (SPSS) 20.0 package program. While evaluating the research data, frequency, percentage, mean, standard deviation, median, variance analysis from descriptive statistical methods will be used. For homogeneity test between intervention and control groups, the Chi-square test for categorical variables, Mann Whitney test for numerical variables, and sociodemographic variables (age, education status, employment status of himself and his spouse, income level, etc.) and whether the groups are similar in terms of some characteristics. U test will be used. The conformity of the scale scores to the normal distribution will be evaluated with the Shapiro-Wilk test. The results will be evaluated at the 95% confidence level, and the significance at the p\\\u003C0.05 level.",[427,27,571],"Attachment",[426,573,574,575],"Nurse","Mobile application","Self-efficiency","2024-09-11",{"date":578,"type":39},"2024-09-19",{"date":580,"type":39},"2023-12-15",{"date":582,"type":22},"2024-12-15",{"name":584,"class":46},"Eastern Mediterranean University",{"id":586,"slug":587,"hasResults":11,"nctId":588,"briefTitle":589,"officialTitle":590,"acronym":4,"eligibilityCriteria":591,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":592,"targetDuration":4,"studyType":58,"phases":594,"briefSummary":595,"conditions":596,"keywords":597,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":601,"lastUpdatePostDateStruct":602,"startDateStruct":604,"completionDateStruct":606,"leadSponsor":608,"locationsCount":47},"100556298","the-effect-of-nature-images-accompanied-by-music-on-breastfeeding-breastfeeding-satisfaction-and-maternal-attachment-100556298","NCT06523283","The Effect of Nature Images Accompanied by Music on Breastfeeding, Breastfeeding Satisfaction and Maternal Attachment\"","The Effect of the Use of Natural Landscape Pictures Accompanied by Music on Breastfeeding, Breastfeeding Satisfaction and Maternal Attachment to Lactation-Period Mothers During Breastfeeding","Inclusion Criteria:\n\n* Voluntarily agreeing to participate in the research\n* Being over 18 years old\n* Being at least a primary school graduate\n* Not having a diagnosed psychiatric disease\n* Without mental disability\n* Turkish speakers and those who do not have communication problems\n* Primiparous mothers\n* The mother does not have any problems that would prevent her from breastfeeding (e.g., nipple cracks)\n* The child is not premature\n* Mothers who gave birth at term\n* The baby is not low birth weight\n* Mothers who do not have any problems that would prevent the baby from breastfeeding\n\nExclusion Criteria:\n\n* Being illiterate\n* Being under 18 years old\n* Having a diagnosed psychiatric illness\n* Having mental disability and communication problems\n* Those who do not speak Turkish and have communication problems\n* Non-primiparous mothers\n* The mother has any problems that may prevent her from breastfeeding (e.g., nipple cracks)\n* Having a premature baby\n* Mothers who did not give birth at term\n* Low birth weight of the baby\n* Mothers who have any problems that may prevent the baby from breastfeeding",{"count":593,"type":22},90,[60],"The study was planned as a randomized controlled study to evaluate the effect of using natural landscape pictures accompanied by music during breastfeeding for lactating mothers on breastfeeding, breastfeeding satisfaction and maternal attachment.",[27],[27,598,599,600],"Maternal attachment","Music therapy","Maternal Satisfaction","2024-07-25",{"date":603,"type":39},"2024-07-26",{"date":605,"type":39},"2024-01-18",{"date":607,"type":22},"2024-08-10",{"name":609,"class":46},"Hasan Kalyoncu University",{"id":611,"slug":612,"hasResults":11,"nctId":613,"briefTitle":614,"officialTitle":615,"acronym":616,"eligibilityCriteria":617,"healthyVolunteers":17,"sex":232,"minAge":4,"maxAge":4,"enrollmentInfo":618,"targetDuration":4,"studyType":58,"phases":620,"briefSummary":621,"conditions":622,"keywords":629,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":634,"lastUpdatePostDateStruct":635,"startDateStruct":636,"completionDateStruct":637,"leadSponsor":638,"locationsCount":47},"100556240","sumamos-excelencia-project-implementation-of-best-practices-in-clinical-practice-thrid-edition-100556240","NCT06522529","Sumamos Excelencia Project: Implementation of Best Practices in Clinical Practice (Thrid Edition)","SUMAMOS EXCELENCIA Project: Assessment of Implementation of Best Practices in a National Health System (Thrid Edition)","SE24","Inclusion Criteria:\n\n1. Unit inclusion criteria:\n\n   * NHS units and nursing homes which voluntary adhere to the project.\n   * NHS units and nursing homes providing direct patient care and commit to implement evidence-based recommendations on hand hygiene and one of the following topics: pain assessment and management, urinary incontinence management, obesity prevention and breastfeeding promotion, Smoking Cessation, falls prevention, pressure injuries prevention. For the purposes of this study, a \"unit\" is defined as any service, centre or institution that delivers health services to a homogeneous group of patients who share similar characteristics.\n2. Patient inclusion criteria: The study will include all patients attended in the units participating in the study, who meet the following criteria, depending on the recommendations to be implemented in each unit:\n\n   1. Pain:\n\n      * People susceptible to suffering some type of pain regardless of age.\n      * Patients treated in acute or chronic health institutions (Hospitals, Nursing Homes or Primary Care).\n   2. Urinary incontinence:\n\n      \\- Patients 18 years or older.\n\n      \\- Patients with uncomplicated stress, urge or mixed urinary incontinence\n\n      \\- At least 7 days of admission or possibility of continuity of care preferably up to 6 weeks.\n   3. Obesity:\n\n      * Babies and preschool children up to 12 years old.\n      * For ages 2 to 12 years (inclusive), children must not be overweight or obese 1 year prior to baseline measurement (in February 2021 or at the closest review to February 2021 at which BMI is recorded).\n      * Good general health.\n   4. Breastfeeding:\n\n      * Lactating people.\n      * Healthy neonates of gestational age greater than 36 weeks, with birth weight greater than or equal to 2500 gr.\n      * Couples and relatives within the support network.\n      * Postpartum period and up to 6 months of life of the baby (183 days of life, included).\n      * In primary care, only non-urgent care will be included.\n   5. Smoking Cessation:\n\n      \\- ≥ 18 years of age\n      * Smokers\n   6. Pressure injury prevention:\n\n      \\- Adults population (≥ 18 years).\n      * Admitted to hospitals, nursing homes or included in home care programmes.\n      * Patients at risk of developing pressure injuries.\n   7. Falls prevention:\n\n      * Adults aged 65 years or older, and adults aged 18 years or older who may potentially present problems in walking as a result of neurological or traumatic diseases, medication, or who suffer from loss of strength or drowsiness.\n   8. Hand hygiene:\n\n      \\- All health professionals who care for patients in the units participating in the study.\n\n      Exclusion Criteria:\n\n      \\-",{"count":619,"type":22},400,[60],"There is a gap between research and clinical practice, leading to variability in decision-making. Multifaceted implementation strategies are for improving implementation of best practices. Quasi-experimental, multicentre, before and after. Primary care, hospital units and nursing homes, and the patients attended at both. Implementation of evidence-based recommendations by application of a multifaceted implementation strategy (training, audit, context analysis, local strategies design, feedback, facilitation). Data will be collected at baseline and, during the first year of follow up, at months (4,8,12)",[623,624,27,625,626,627,628],"Pain","Obesity, Childhood","Incontinence, Urinary","Smoking Cessation","Pressure Injury","Fall",[630,631,632,496,633],"Implementation","Implementation science","Evidence-based practice","Quality of Health Care","2024-07-24",{"date":603,"type":39},{"date":555,"type":22},{"date":186,"type":22},{"name":639,"class":640},"Instituto de Salud Carlos III","OTHER_GOV",{"id":642,"slug":643,"hasResults":11,"nctId":644,"briefTitle":645,"officialTitle":646,"acronym":647,"eligibilityCriteria":648,"healthyVolunteers":17,"sex":18,"minAge":4,"maxAge":649,"enrollmentInfo":650,"targetDuration":4,"studyType":58,"phases":652,"briefSummary":653,"conditions":654,"keywords":4,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":655,"lastUpdatePostDateStruct":656,"startDateStruct":658,"completionDateStruct":660,"leadSponsor":661,"locationsCount":47},"100554006","peer-assisted-breastfeeding-education-program-100554006","NCT06493474","Peer Assisted Breastfeeding Education Program","Effect of Peer Assisted Breastfeeding Education Program (PABEP) on Breastfeeding Self-Efficacy and Breastfeeding Levels: Randomized Controlled Study","PABEP","Inclusion Criteria:\n\n* being in the antenatal period\n* having their first pregnancy\n* not having received breastfeeding counseling before.\n\nExclusion Criteria:\n\n* mothers with previous birth history\n* previously educated women","36 Weeks",{"count":651,"type":22},170,[60],"It was aimed to evaluate the effect of the Peer Supported Breastfeeding Education Program given during the antenatal period on the breastfeeding knowledge and attitude levels, breastfeeding self-efficacy and breastfeeding levels of postpartum women. For this purpose, the hypotheses created in our study are as follows.\n\n1. H1: Breastfeeding knowledge and attitudes of mothers in the PABEP group are significantly higher than those in the control group.\n2. H1: Breastfeeding proficiency levels of mothers in the PABEP group are significantly higher than those in the control group.\n3. H1: Breastfeeding success of mothers in the PABEP group is significantly higher than the control group, according to the breastfeeding evaluation results.",[27],"2024-07-06",{"date":657,"type":39},"2024-07-10",{"date":659,"type":22},"2024-07-20",{"date":659,"type":22},{"name":662,"class":46},"Akdeniz University",{"id":664,"slug":665,"hasResults":11,"nctId":666,"briefTitle":667,"officialTitle":668,"acronym":4,"eligibilityCriteria":669,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":670,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":672,"conditions":673,"keywords":675,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":680,"lastUpdatePostDateStruct":681,"startDateStruct":683,"completionDateStruct":685,"leadSponsor":687,"locationsCount":47},"100514517","a-study-in-lactating-mothers-and-their-newborns-to-analyse-the-composition-of-human-milk-100514517","NCT05979532","A Study in Lactating Mothers and Their Newborns to Analyse the Composition of Human Milk","A Longitudinal Prospective, Observational, Cohort Study in Lactating Mothers and Their Newborns to Further Unravel the Complexity of Human Milk","Inclusion Criteria:\n\n* Pregnant women in the third trimester of pregnancy (≥28 weeks) who have the intention to provide breastfeeding for at least 6 months post-partum.\n* Age ≥ 18 years.\n* Willingness to provide residual human milk.\n* Living in proximity of NCRU (clinical site in NL).\n* Dutch speaking and reading.\n* Freezer -18°C available.\n* Having mobile phone, tablet, or computer available.\n* Signed informed consent from the subject (pregnant woman).\n* Signed informed consent from the other parent and\u002For legally acceptable representative, of the unborn baby(s), aged ≥ 18 years.\n\nExclusion Criteria:\n\n* Pregnant women known positive for human immunodeficiency virus (HIV), hepatitis B (HBV), or hepatitis C (HCV).\n* Multiple pregnancy \\> 2.\n* Incapability of subjects to comply with study protocol as per the judgment of the site staff (e.g. fluency in local language, access to laptop\u002Fsmartphone devices and internet connection required for data collection).\n* Women (and their unborn baby(s)) with current or intended participation in any other clinical study involving investigational or marketed products.\n* Employees and\u002For children\u002Ffamily members or relatives of employees of Nutricia Research or the participating site.\n\nContinuation exclusion criteria (after birth)\n\n* Stillbirth\n* Newborn having any congenital abnormality, chromosomal disorder or severe disease that would prevent the infant from breastfeeding and\u002For growing normally based on the opinion of a health care professional and\u002For study physician.\n* No donation of any milk sample within the first 8 weeks postpartum (timepoints week 1, week 1.5, and week 4).",{"count":671,"type":22},172,"The current longitudinal (max. 2-year) observational cohort study in 120 lactating mothers and their newborns will make it possible to explore human milk composition across different lactation stages, between different human milk groups, and in relation to maternal, perinatal, infant, and sample characteristics as well as to the microbiota of the infant.",[27,674],"Milk, Human",[27,676,677,63,678,679],"Human milk","Research","Human Milk Oligosaccharide","HMO","2024-03-14",{"date":682,"type":39},"2024-03-15",{"date":684,"type":39},"2024-02-13",{"date":686,"type":22},"2027-08-31",{"name":688,"class":689},"Nutricia Research","INDUSTRY"]