[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"maternal-behavior\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:maternal-behavior":32},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,11,0,[8,47,79,103,138,158,185,232,266,295,317],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100553095","patient-clinical-linkages-to-improve-trust-and-engagement-in-postpartum-healthcare-100553095",false,"NCT06481631","Patient-clinical Linkages to Improve Trust and Engagement in Postpartum Healthcare","Empowering Women for Postpartum Care and Reproductive Health in Mississippi Delta","Inclusion Criteria:\n\n* Identified as high risk pregnancy\n* Postpartum mothers\u002Fparents 18-45 years\n* Resident of the one of 5 target counties (Washington, Bolivar, Scott, Humphreys, and Carroll)\n* Maternal healthcare providers in target counties\n* Maternal community health leaders\n\nExclusion Criteria:\n\n* not identified as high risk pregnancy\n* 18 years of age postpartum\n* cesarean birth\n* non-resident of the 5 target counties","FEMALE","18 Years","45 Years",{"count":20,"type":21},250,"ESTIMATED","INTERVENTIONAL",[24],"NA","Maternal mortality in the United States is higher than in peer nations and has not decreased since 1990. Beyond mortality, severe maternal mortality impacts far too many women. Not only are these high rates alarming, but notable racial\u002Fethnic and socioeconomic disparities exist. These inequities are highly regional, with women living in the rural southeast part of the United States, including the Mississippi Delta, having the highest rates of maternal mortality and morbidity. Unfortunately, these disparities have proven to be stubbornly resistant to interventions, necessitating an innovative multifaceted approach focused on community practice, building trust, and prioritizing patient voices. To meet this need, this proposal aims to establish the Mississippi Delta Research Center of Excellence for Maternal Health with the goal of addressing preventable maternal mortality, decreasing severe maternal morbidity, and promoting maternal health equity in partnership with the Mississippi Delta community. This patient-clinical linkages intervention study will evaluate the effectiveness of a multilevel and multisector communication and health literacy strategy to increase trust and engagement in postpartum healthcare among women in the Mississippi Delta, with a specific focus on Black women, their families, and their communities.\n\nThese research projects both have the overarching goal of partnering with the community to determine and meet the needs of pregnant and postpartum women in the Mississippi Delta and address the disparities within maternity health and health care outcomes.",[27,28,29,30,31,32,33],"Family Dynamics","Trust in Healthcare System","Family Structure","Health Literacy","Contraception","Maternal Behavior","Postpartum Mood Disturbance","RECRUITING","2026-06-04",{"date":37,"type":38},"2026-06-08","ACTUAL",{"date":40,"type":38},"2025-06-01",{"date":42,"type":21},"2030-06-30",{"name":44,"class":45},"Jackson State University","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":4,"eligibilityCriteria":53,"healthyVolunteers":54,"sex":16,"minAge":17,"maxAge":55,"enrollmentInfo":56,"targetDuration":4,"studyType":22,"phases":58,"briefSummary":59,"conditions":60,"keywords":64,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":4},"100632957","short-term-mindfulness-intervention-for-anxiety-and-maternal-attachment-in-nicu-mothers-100632957","NCT07520435","Short-Term Mindfulness Intervention for Anxiety and Maternal Attachment in NICU Mothers","Effect of a Short-Term Mindfulness-Based Stress Reduction Program on Anxiety and Maternal Attachment in Mothers With Infants Admitted to the Neonatal Intensive Care Unit: A Randomized Controlled Trial","Inclusion Criteria:\n\nMothers aged 18 to 50 years Mothers whose newborns are admitted to the Neonatal Intensive Care Unit (NICU) Mothers of infants without congenital anomalies Mothers who have not previously participated in any mindfulness-based or psychological support program Mothers without cognitive impairment Mothers who are willing to participate voluntarily and comply with all study procedures Mothers who are able to communicate in Turkish\n\nExclusion Criteria:\n\nMothers who wish to withdraw from the study voluntarily Mothers whose infants are discharged from the NICU during the intervention period Mothers receiving MBSR or any other psychological therapy Mothers using psychopharmacological medication",true,"50 Years",{"count":57,"type":21},66,[24],"This randomized controlled study aims to evaluate the effects of a short-term mindfulness-based stress reduction (MBSR) program on anxiety levels and maternal attachment in mothers whose infants are admitted to the Neonatal Intensive Care Unit (NICU). A total of 33 mothers will be recruited and assigned to intervention and control groups. The intervention group will receive a structured four-session mindfulness program, while the control group will receive standard care. Data will be collected using the Maternal Attachment Scale and the State-Trait Anxiety Inventory. The findings are expected to provide evidence on the effectiveness of mindfulness-based interventions in reducing anxiety and improving maternal-infant bonding during the postpartum period.",[61,62,32,63],"Postpartum Anxiety","Postpartum Period","Psychological Stress",[65,66,67,68],"Mindfulness","Mindfulness-Based Stress Reduction","Anxiety Disorders","Randomized Controlled Trial","NOT_YET_RECRUITING","2026-04-03",{"date":72,"type":38},"2026-04-09",{"date":74,"type":21},"2026-04-27",{"date":76,"type":21},"2026-07-01",{"name":78,"class":45},"Saglik Bilimleri Universitesi",{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":4,"eligibilityCriteria":85,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":86,"targetDuration":4,"studyType":88,"phases":4,"briefSummary":89,"conditions":90,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":94,"lastUpdatePostDateStruct":95,"startDateStruct":97,"completionDateStruct":99,"leadSponsor":101,"locationsCount":46},"100598135","breastfeeding-myths-and-mothers-motivation-100598135","NCT07067554","Breastfeeding Myths and Mothers' Motivation","An Investigation of the Relationship Between Mothers' Susceptibility to Breastfeeding Myths and Their Motivation to Breastfeed","Inclusion Criteria:\n\n* Having an infant aged 0-6 months\n* Having breastfed the baby at least once\n* Voluntarily agreeing to participate in the study\n\nExclusion Criteria:\n\n* Having a physical or psychiatric health condition that prevents breastfeeding\n* Having had a multiple (twin or more) pregnancy\n* Exclusively formula-feeding the baby",{"count":87,"type":21},191,"OBSERVATIONAL","Breast milk is a unique and irreplaceable source of nutrition for infants, offering protection against many common childhood diseases due to its natural sterility, accessibility, and immune-boosting antibodies. Exclusive breastfeeding for the first six months of life is critical for healthy growth, development, and immune support. Despite global recommendations by WHO and UNICEF, lack of knowledge and inadequate support continue to hinder optimal breastfeeding practices.\n\nOne major barrier is the persistence of cultural myths and misconceptions, such as \"colostrum should be discarded,\" or \"infants need water after every feeding.\" These unfounded beliefs may reduce mothers' confidence and lead to early cessation of breastfeeding or premature introduction of complementary foods.\n\nThis study aims to examine the relationship between mothers' belief in breastfeeding myths and their motivation to breastfeed. While prior research has explored each factor individually, no known studies have analyzed their interaction.",[91,32,92,93],"Breastfeeding","Health Knowledge, Attitudes, Practice","Motivation","2025-09-25",{"date":96,"type":38},"2025-09-30",{"date":98,"type":38},"2025-09-09",{"date":100,"type":21},"2026-07-30",{"name":102,"class":45},"Acibadem University",{"id":104,"slug":105,"hasResults":11,"nctId":106,"briefTitle":107,"officialTitle":108,"acronym":4,"eligibilityCriteria":109,"healthyVolunteers":54,"sex":110,"minAge":111,"maxAge":112,"enrollmentInfo":113,"targetDuration":4,"studyType":22,"phases":115,"briefSummary":116,"conditions":117,"keywords":122,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":129,"lastUpdatePostDateStruct":130,"startDateStruct":132,"completionDateStruct":134,"leadSponsor":136,"locationsCount":46},"100505449","combined-oral-motor-stimulation-and-language-on-preterm-infant-feeding-100505449","NCT05861531","Combined Oral Motor Stimulation and Language on Preterm Infant Feeding","The Combined Association of an Oral Motor Stimulation and Language Intervention on Preterm Infant Feeding","Inclusion Criteria:\n\n* 23-30 weeks\n* English and Spanish speaking\n\nExclusion Criteria:\n\n* Major congenital anomalies\n* Surgical necrotizing enterocolitis\n* Non-English and Non-Spanish speaking","ALL","23 Weeks","30 Weeks",{"count":114,"type":21},124,[24],"This is a randomized controlled trial to study an oromotor stimulation in combination with a reading curriculum in the NICU among preterm infants using oral muscle exercises, Language Environment Analysis (LENA) recordings, linguistic feedback, and a language curriculum to improve the neonatal inpatient oral feeding and language outcomes for preterm infants.",[118,119,120,121,32],"Language Delay","Language Development","Feeding; Difficult, Newborn","Mother-Infant Interaction",[123,124,125,126,127,128],"Neonatal feeding","Neonatal language","Oromotor stimulation","Newborn reading","Parent infant interaction","LENA","2025-09-10",{"date":131,"type":38},"2025-09-17",{"date":133,"type":38},"2025-07-01",{"date":135,"type":21},"2030-07-01",{"name":137,"class":45},"Women and Infants Hospital of Rhode Island",{"id":139,"slug":140,"hasResults":11,"nctId":141,"briefTitle":142,"officialTitle":143,"acronym":144,"eligibilityCriteria":145,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":146,"targetDuration":4,"studyType":22,"phases":148,"briefSummary":25,"conditions":149,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":150,"lastUpdatePostDateStruct":151,"startDateStruct":153,"completionDateStruct":155,"leadSponsor":156,"locationsCount":157},"100593429","mississippi-delta-community-care-home-visits-program-100593429","NCT07006324","Mississippi Delta Community Care Home Visits Program","Community Care Home Visiting Program to Reduce Maternal Health Inequities","Time4Mom","Inclusion Criteria:\n\n* Identified as high risk pregnancy\n* Postpartum mothers\u002Fparents 18-45 years\n* Resident of the one of 5 target counties (Washington, Bolivar, Scott, Humphreys, and Carroll)\n\nExclusion Criteria:\n\n* not identified as high risk pregnancy\n* 18 years of age postpartum\n* cesarean birth\n* non-resident of the 5 target counties",{"count":147,"type":21},500,[24],[32,33],"2025-08-25",{"date":152,"type":38},"2025-09-02",{"date":154,"type":38},"2025-08-01",{"date":42,"type":21},{"name":44,"class":45},2,{"id":159,"slug":160,"hasResults":11,"nctId":161,"briefTitle":162,"officialTitle":163,"acronym":164,"eligibilityCriteria":165,"healthyVolunteers":54,"sex":16,"minAge":166,"maxAge":4,"enrollmentInfo":167,"targetDuration":4,"studyType":22,"phases":169,"briefSummary":170,"conditions":171,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":175,"lastUpdatePostDateStruct":176,"startDateStruct":178,"completionDateStruct":180,"leadSponsor":182,"locationsCount":184},"100508069","the-mother-in-norway-study-100508069","NCT05895604","The Mother in Norway Study","The Mother in Norway Study - A Randomised Trial of Nurse-Family Partnership (NFP)","MiNS","Inclusion Criteria: Female; No previous live births; Currently pregnant; Gestation period less than 28 weeks (i.e., less than or equal to 27 weeks, 6 days) at time of recruitment; Live within an area serviced by a NFP Implementing Agency; Not currently enrolled in the study; professionals are concerned about the pregnancy \u002F impending parenthood\n\nExclusion Criteria: Women who have had a previous live birth; Women who are not currently pregnant; Women who are past their 28th week of gestation (i.e., greater than or equal to 28 weeks, 0 days) at time of recruitment; Women who live outside of an area serviced by a NFP Implementing Agency; Women who are currently enrolled in the study; professionals are not concerned about the pregnancy \u002F impending parenthood","16 Years",{"count":168,"type":21},700,[24],"The Norwegian government is implementing the Nurse Family Partnership program (NFP) to combat child abuse and social inequality. This study will examine NFP with an individually randomized controlled parallel-group trial. The study will enroll 700 mothers over three years, with half receiving NFP services and the other half receiving standard care. The primary outcome is violence towards mothers and their children, assessed through questionnaires and observation tests. The study will also evaluate the program's effects on various health-related outcomes using administrative data. Cost-effectiveness analyses will be conducted to compare NFP to existing services and improve its delivery efficiency.",[32,172,173,174],"Injuries","Violence","Mental Health Wellness","2025-08-05",{"date":177,"type":38},"2025-08-11",{"date":179,"type":38},"2023-06-01",{"date":181,"type":21},"2042-12-31",{"name":183,"class":45},"Oslo Metropolitan University",5,{"id":186,"slug":187,"hasResults":11,"nctId":188,"briefTitle":189,"officialTitle":190,"acronym":191,"eligibilityCriteria":192,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":55,"enrollmentInfo":193,"targetDuration":4,"studyType":22,"phases":195,"briefSummary":196,"conditions":197,"keywords":215,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":223,"lastUpdatePostDateStruct":224,"startDateStruct":226,"completionDateStruct":228,"leadSponsor":230,"locationsCount":46},"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",{"count":194,"type":21},784,[24],"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.",[198,199,200,201,202,203,204,205,206,207,208,32,209,210,211,212,213,214],"Maternal Health Services","Infant, Newborn","Postnatal Care","Breast Feeding","Maternal-Child Relations","Postpartum Depression (PPD)","Mental Health","Lactation","Breast Feeding, Exclusive","Patient Satisfaction and Experience With Integrative Therapies","Neonatal Jaundice","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",[216,217,218,219,220,221,222],"Postnatal care","inpatient","maternity competence","satisfaction","integrative care","breastfeeding","maternal behavior","2025-07-12",{"date":225,"type":38},"2025-07-22",{"date":227,"type":21},"2025-10-01",{"date":229,"type":21},"2026-12-31",{"name":231,"class":45},"Medical University of Vienna",{"id":233,"slug":234,"hasResults":11,"nctId":235,"briefTitle":236,"officialTitle":237,"acronym":238,"eligibilityCriteria":239,"healthyVolunteers":54,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":240,"targetDuration":4,"studyType":22,"phases":242,"briefSummary":243,"conditions":244,"keywords":250,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":257,"lastUpdatePostDateStruct":258,"startDateStruct":260,"completionDateStruct":262,"leadSponsor":264,"locationsCount":46},"100557963","improving-maternal-sleep-and-mental-health-100557963","NCT06544941","Improving Maternal Sleep and Mental Health","Improving Maternal Mental Health in Military-Affiliated Pregnant Women: Effectiveness of a Smart Bassinet","SHINE","Inclusion Criteria:\n\n* Pregnant women with a singleton gestation who have a military affiliation\n* Ages 18-45 years\n* Ability to communicate during the screening process\n* Access to a computer, smart phone or tablet with internet service\n* Willing to use bassinet they are randomized to\n* Willing to travel to a local Quest for blood draw\n\nExclusion Criteria:\n\n* Presence of depression assessed over the phone using the Structured Clinical Interview for DSM Disorders - Clinical Version, Mood Disorders Section (SCID-I). Current active suicidal ideation, medical or psychiatric instability, or active substance abuse or dependence during the last 90 days. Since this is a study about risk for recurrent PPMD, actively depressed women will be excluded.\n* Plans to co-sleep with infant. The goal is to compare two bassinets; therefore co-sleeping would prohibit extensive use of a bassinet.\n* Under the age of 18 years or \\> 45 years. The goal is to include women of childbearing age.\n* Multiple gestations, Type 1 diabetes, congenital fetal anomalies. Women with these factors will likely have major disruption of sleep, require 2 bassinets, or a disrupted home life. These would skew the data and make interpretations and comparisons difficult.\n* Tobacco use (current). Smoking is associated with poor sleep and inflammation.\n* Self-reported, untreated comorbid sleep disorders including narcolepsy, periodic leg movement disorder, and\u002For obstructive sleep apnea. These disorders contribute to poor sleep and often require medications for treatment.\n* Current use of psychotropic or sleep medications. These are associated with altered sleep and inflammation.",{"count":241,"type":21},342,[24],"The goal of this clinical trial is to test the effectiveness of a Smart Bassinet to prevent\u002Fmitigate postpartum mood disorders by augmenting maternal sleep and\u002For enhancing infant sleep. The investigators will conduct a 2-arm randomized controlled trial (RCT) to compare infant and maternal sleep of infants who use a smart bassinet (SB) or a standard commercially available bassinet (Halo Bassinest Swivel Sleeper 3.0) (usual\u002Ftraditional care (TAU)). After confirmation of eligibility, participants (N = 342) will randomly be assigned to either the SB or TAU. The investigators hypothesize that use of the SB will be associated with better infant and maternal sleep over a 6-month period, and these mothers will report fewer depressive and anxiety symptoms across the postpartum. The main question\\[s\\] it aims to answer \\[is\u002Fare\\]:\n\nAim 1: Determine the effect of the SB on infant sleep and maternal sleep. \\[primary hypothesis or outcome measure 2\\]? Aim 2: Determine the effect of the SB on maternal postpartum depressive symptoms and evaluate the model that the association between the SB and postpartum depressive symptoms is mediated by both infant and maternal sleep Aim 3: Compare trajectory of immune system function from late pregnancy through postpartum between PPD and non-PPD and between SB and TAU groups Exploratory Aim. Evaluate whether the elevated risk demonstrated by previously identified PPD epigenetic biomarkers at the TTC9B and HP1BP3 genes can be modified by using a SB. The investigators hypothesize that the elevated risk will be reduced in the SB condition compared to TAU.\n\nMilitary-affiliated pregnant women will be recruited from across the US via social media and advertising. Monthly online questionnaires will be completed by the mother. Objective sleep data will be collected monthly using an actigraph for 1-week from both mother and baby. Blood samples for assay of inflammatory markers will be collected at enrollment, 3- and 6- months postpartum.",[245,61,246,247,32,248,249],"Postpartum Depression","Sleep Disturbance","Infant Behavior","Inflammation","Military Family",[251,252,253,254,255,256],"sleep","postpartum","intervention","inflammation","depression","anxiety","2025-02-06",{"date":259,"type":38},"2025-02-10",{"date":261,"type":38},"2025-01-15",{"date":263,"type":21},"2028-06",{"name":265,"class":45},"University of Colorado, Colorado Springs",{"id":267,"slug":268,"hasResults":11,"nctId":269,"briefTitle":270,"officialTitle":271,"acronym":4,"eligibilityCriteria":272,"healthyVolunteers":54,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":273,"targetDuration":4,"studyType":22,"phases":275,"briefSummary":276,"conditions":277,"keywords":280,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":286,"lastUpdatePostDateStruct":287,"startDateStruct":289,"completionDateStruct":291,"leadSponsor":293,"locationsCount":46},"100563432","nurse-implemented-infant-mother-attachment-security-program-100563432","NCT06616090","Nurse Implemented Infant-Mother Attachment Security Program","Investigating the Effectiveness of Nurse Implemented Attachment-Based Maternal Sensitivity Program in Primary Family Health Care Services","Inclusion Criteria:\n\n* mothers with 9- to 12-month infants\n* having a normally developing infant.\n\nExclusion Criteria:\n\n* mothers with infants who have a chronic pediatric health problem\n* mother with infants whose developmental problems are detected during routine evaluations\n* mothers with temporary protection status (i.e., immigrants) due to potential communication problems\n* if the mother is not the primary caregiver",{"count":274,"type":21},120,[24],"This study focuses on adapting and evaluating an attachment-based intervention program implemented by nurses in Family Health Centers (FHCs) in Turkey. The program aims to enhance parental sensitivity and infant-mother attachment security. Evidence suggests that such programs, developed in Western countries, effectively improve parenting behaviors and attachment quality. Despite the positive effects of similar programs in Turkey, their integration into primary healthcare for wider public benefit remains unexplored. The project will develop an intervention protocol based on effective methods from previous attachment-based programs into routine childcare visits at FHCs. A randomized controlled trial involving 120 mothers with 9- to 12-month-old babies in Istanbul will be recruited. FHCs will be randomly assigned to intervention and control groups, with 60 mother-infant dyads in each condition. Nurses will deliver the program during childcare visits at 9, 12, 15, and 18 months. Intervention FHCs will also use reminders like posters and short films in the waiting rooms to reinforce the concepts. Effectiveness will be evaluated through pretest, posttest, and follow-up home visits using observational and self-report measures on attachment security, maternal sensitivity, as well as maternal psychological characteristics, along with infant socioemotional measures. Upon completion of the project, control FHC nurses will receive training to deliver a condensed version of the program.",[278,279,32],"Nurse's Role","Infant Development",[281,282,283,284,285],"attachment-based program","maternal sensitivity","attachment security","nurse-based","primary healthcare","2024-09-24",{"date":288,"type":38},"2024-09-27",{"date":290,"type":21},"2024-10-01",{"date":292,"type":21},"2026-11-01",{"name":294,"class":45},"Sabanci University",{"id":296,"slug":297,"hasResults":11,"nctId":298,"briefTitle":299,"officialTitle":300,"acronym":4,"eligibilityCriteria":301,"healthyVolunteers":54,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":302,"targetDuration":4,"studyType":22,"phases":304,"briefSummary":305,"conditions":306,"keywords":4,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":309,"lastUpdatePostDateStruct":310,"startDateStruct":312,"completionDateStruct":313,"leadSponsor":315,"locationsCount":46},"100557427","this-study-aimed-to-examine-the-effects-of-individualized-care-and-counseling-given-to-mothers-in-the-first-trimester-of-pregnancy-on-maternal-attachment-maternal-self-efficacy-and-maternal-function-100557427","NCT06537973","This Study Aimed to Examine the Effects of Individualized Care and Counseling Given to Mothers in the First Trimester of Pregnancy on Maternal Attachment, Maternal Self-efficacy and Maternal Function.","The Effect of Individualized Care and Counseling Given to Primiparous Mothers in the Postpartum Period on Maternal Attachment, Maternal Self-Efficacy and Maternal Function: Randomized Controlled Trial","Inclusion Criteria:\n\n* Being primiparous\n* Having a vaginal birth\n* Having given birth at term\n* Being 18 years or older\n* Having a single, healthy baby\n* Must be at least a primary school graduate\n* The mother does not have a diagnosed chronic or psychiatric disease.\n* Volunteering to participate in the study\n\nExclusion Criteria:\n\n* • Having a history of risky pregnancy\n\n  * Participated in any birth preparation training program\n  * The mother shows signs of mental or physical illness (self-report\u002Fclinical diagnosis).\n  * Inability to communicate effectively with the mother\n  * The baby has a health problem",{"count":303,"type":21},54,[24],"Purpose of the research:\n\nThis study aimed to examine the effects of individualized care and counseling given to mothers in the first trimester after birth on maternal attachment, maternal self-efficacy and maternal function.\n\nIn this context, the hypotheses of the research are as follows:\n\n1. Individualized care and counseling does not have a significant effect on the level of maternal attachment.\n2. Individualized care and counseling does not have a positive effect on mothers\\' self-efficacy perceptions.\n3. Individualized care and counseling does not have a significant effect on the gain of maternal function.\n\nThe study consists of experimental and control groups. The mothers of the experimental group will be interviewed in the 2nd, 4th, 6th, 8th and 12th postpartum weeks, and various surveys will be administered through counseling.\n\nControl group mothers will not be given any training or counseling by the researcher other than the standard care and services offered in the hospital. The measurement tools applied to the experimental group mothers will be simultaneously applied to the control group mothers.",[32,307,308],"Self Efficacy","Maternal Care Patterns","2024-07-31",{"date":311,"type":38},"2024-08-05",{"date":309,"type":21},{"date":314,"type":21},"2024-09-15",{"name":316,"class":45},"Necmettin Erbakan University",{"id":318,"slug":319,"hasResults":11,"nctId":320,"briefTitle":321,"officialTitle":322,"acronym":4,"eligibilityCriteria":323,"healthyVolunteers":54,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":324,"targetDuration":4,"studyType":88,"phases":4,"briefSummary":326,"conditions":327,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":330,"lastUpdatePostDateStruct":331,"startDateStruct":333,"completionDateStruct":335,"leadSponsor":337,"locationsCount":46},"100515056","early-life-feeding-exposure-and-infant-immune-and-health-status-100515056","NCT05986539","Early Life Feeding Exposure and Infant Immune and Health Status.","Mechanistic Effects of Early Life Feeding Exposure on Infant Inflammatory and Health Status","Inclusion Criteria:\n\n* Mother at least 18 years of age\n* Mother is in third trimester (week 27 of gestation) or biological infant is 5 weeks of age or younger\n* Mother plans to continue to provide your infant breastmilk (by breastfeeding or by pumping) for at least 18 weeks (4.5 months) from your delivery date or mother plans to continue to provide formula exclusively to infant for at least 18 weeks of life.\n* Mother lives within a 45-mile radius of Study Site, or is willing to deliver samples for visits 2, 4, and 6.\n* Mother willing to meet at (designated sample collection site) for visits 3 and 5 for sample collection and visit activities.\n* Mother willing to consent and comply with all aspects of the study protocol and methods, save the optional activities and optional sample collections.\n* Mother and infant are considered healthy by Principle Investigator.\n* For Formula Fed Group: Mother-Infant dyad is able to match to a Breastfed dyad using maternal BMI and infant sex.\n\nExclusion Criteria:\n\n* Mother or Infant have participated or are currently participating in an interventional drug or device (non-observational) research study before.\n* Mother reports that they, or the infant, have had an adverse effect during a venous blood collection.\n* Infant was born less than 36 weeks of gestation.\n* Infant or mother have health conditions that increase the risk of study procedures.",{"count":325,"type":21},60,"Background: Although breastfeeding has known protective effects, such as preventing childhood obesity, the specific mechanisms remain unclear. Idaho has a high breastfeeding initiation rate (92%) but a significant prevalence of childhood obesity (30.5% overweight\u002Fobese). Limited research exists on the impact of maternal inflammation, maternal body mass index (BMI), C-reactive protein (CRP), and interleukin-6 (IL-6) concentrations in breastmilk on infant health outcomes, especially in healthy full-term infants.\n\nObjective: This study aims to expand understanding of the role of maternal inflammation on breastmilk composition and its effect on infant immune development. The investigators seek to investigate the relationship between maternal health status, breastmilk inflammatory concentrations, and balanced immune development in infants. Additionally, the investigators aim to explore the potential influence of early diet exposure, including maternal inflammatory status, on the risk of obesity and other inflammatory conditions.\n\nMethods: Healthy full-term infants (breastfed\u002Fformula-fed) and their mothers will be recruited. Maternal inflammation markers (BMI, CRP, IL-6) and immune markers in infants will be analyzed. Flow cytometry will assess immune populations. Correlations between maternal systemic inflammation, infant inflammation, and breastmilk inflammatory markers will be examined for breastfeeding mothers.\n\nOutcomes: The investigators hypothesize breastfed infants will display a more favorable anti-inflammatory profile. This study will identify factors influencing immune development and potential pathways linking early-life exposures to long-term health outcomes. Findings will inform strategies for promoting balanced immune development and elucidate the role of early diet exposure, including maternal inflammation, as a protective or risk factor for obesity and inflammatory conditions.",[32,328,329,279],"Maternal Obesity","Breast Milk Collection","2024-07-24",{"date":332,"type":38},"2024-07-26",{"date":334,"type":38},"2024-01-12",{"date":336,"type":21},"2025-04-30",{"name":338,"class":45},"University of Idaho"]