[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"bonding\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:bonding":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,7,0,[8,52,77,107,138,161,189],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":34,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":21},"100614171","the-effect-of-the-cesarean-eras-protocol-on-mother-infant-and-father-infant-bonding-a-multicenter-randomized-controlled-clinical-trial-100614171",false,"NCT07276126","The Effect of the Cesarean ERAS Protocol on Mother-Infant and Father-Infant Bonding: a Multicenter, Randomized Controlled Clinical Trial.","ERAS-CS-BOND-1","IInclusion Criteria:\n\nPregnant women aged 18-60 years.\n\nSingleton, live fetus, and ≥37 weeks of gestation.\n\nUndergoing elective or medically indicated cesarean delivery.\n\nAbility to read and understand Turkish (for questionnaire validity).\n\nMothers and fathers willing and able to complete postpartum follow-up assessments (2 hours, 24 hours, day 4, day 7).\n\nProvision of written informed consent by mother and, if participating, by father\u002Fpartner.\n\nMaternal postpartum clinical stability (no condition precluding questionnaire completion).\n\n❌ Exclusion Criteria (Dışlanma Kriterleri)\n\nExclusion Criteria:\n\nPreterm birth (\\\u003C37 weeks) or multiple gestation (twins, triplets).\n\nStillbirth, early neonatal death, or major congenital anomaly.\n\nNewborn requiring prolonged NICU stay preventing bonding assessments.\n\nMaternal severe obstetric complications:\n\nMassive postpartum hemorrhage\n\nHysterectomy\n\nSevere preeclampsia or eclampsia\n\nSevere postpartum infection\n\nMaternal active psychiatric disorder or use of psychotropic medication.\n\nMaternal need for high-dose opioid analgesia or sedation interfering with bonding assessments.\n\nInability to read\u002Funderstand Turkish or cognitive impairment preventing questionnaire completion.\n\nFailure to complete follow-up visits (2 hours, 24 hours, day 4, day 7).\n\nWithdrawal of consent at any time.",true,"ALL","18 Years","60 Years",{"count":21,"type":22},1,"ESTIMATED","INTERVENTIONAL",[25],"NA","This is a multicenter, 1:1 parallel-group, randomized controlled trial designed to compare the effect of the Enhanced Recovery After Cesarean (ERAS) protocol versus standard perioperative care on mother-infant and father-infant bonding in women undergoing cesarean delivery. The study will initially be conducted as a single-center trial at Istanbul Okan University Hospital. Once adequate site preparation is completed, additional centers will be added to expand the study to a multicenter setting.\n\nPrimary Outcome:\n\nThe primary outcome is the total score on the Postpartum Bonding Questionnaire (PBQ) assessed on postpartum day 7, reflecting mother-infant bonding.\n\nSecondary Outcomes:\n\nSecondary outcomes include:\n\nMaternal\u002FParental Postnatal Attachment Scale (MIBS) score at 2 hours postpartum (mother)\n\nPBQ score at 24 hours postpartum (mother)\n\nPBQ score at day 4 postpartum (mother)\n\nPBQ score at day 7 postpartum (father-infant bonding)\n\nEdinburgh Postnatal Depression Scale (EPDS) scores for mothers at 2 hours and 7 days postpartum\n\nTime to initiation of breastfeeding\n\nRequirement for neonatal intensive care unit (NICU) admission\n\nSample Size:\n\nThe total multicenter target sample size is n=300, with 150 participants in the ERAS group and 150 in the standard care group. The initial single-center phase at Okan University Hospital will enroll a target of n=100 participants (50 per group).\n\nRandomization:\n\nParticipants will be randomized using a block and stratified randomization approach based on parity (primiparous vs multiparous) and planned type of anesthesia.\n\nBlinding (Masking):\n\nDue to the nature of the intervention, care providers cannot be blinded to group assignment. However, outcome assessors and data analysts will remain blinded to treatment allocation to minimize bias.\n\nStudy Timeline and Visits:\n\nParticipants will be evaluated at multiple time points following cesarean delivery: 2 hours postpartum, 24 hours postpartum, day 4 postpartum, and day 7 postpartum. All primary and secondary outcomes will be collected at the specified time points.\n\nSignificance and Rationale:\n\nThe ERAS protocol for cesarean delivery is designed to optimize perioperative care, enhance recovery, and potentially improve early parent-infant bonding. While previous studies have focused on maternal recovery and clinical outcomes, evidence regarding the impact of ERAS on both mother-infant and father-infant bonding remains limited. This trial aims to provide high-quality evidence on whether ERAS implementation can improve early bonding experiences, maternal mental health, breastfeeding initiation, and neonatal outcomes compared with standard perioperative care. The findings may guide future clinical practice and contribute to optimizing family-centered care in cesarean deliveries.\n\nKey Features:\n\nMulticenter, randomized controlled design\n\nParallel 1:1 allocation\n\nStratified randomization by parity and anesthesia type\n\nBlinded outcome assessment and data analysis\n\nMultiple postpartum evaluation points\n\nFocus on psychosocial and clinical outcomes\n\nExpected Contributions:\n\nThis study will provide comprehensive data on the feasibility and effectiveness of ERAS protocols in cesarean deliveries and their potential benefits for both maternal and paternal bonding with the newborn. The inclusion of both mother-infant and father-infant outcomes, as well as maternal mental health and breastfeeding indicators, ensures a holistic assessment of early family-centered outcomes.",[28,29,30,31,32,33],"Bonding","ERAS","Cesarean Section","Maternal Care","Father - Child Relations","Mother-Infant Interaction",[35,36,37,38,39],"eras","erac","cesarean","maternal bonding","paternal bonding","RECRUITING","2026-04-27",{"date":43,"type":44},"2026-04-28","ACTUAL",{"date":46,"type":44},"2025-12-13",{"date":48,"type":22},"2026-04-20",{"name":50,"class":51},"Okan University","OTHER",{"id":53,"slug":54,"hasResults":11,"nctId":55,"briefTitle":56,"officialTitle":57,"acronym":4,"eligibilityCriteria":58,"healthyVolunteers":16,"sex":59,"minAge":18,"maxAge":4,"enrollmentInfo":60,"targetDuration":4,"studyType":23,"phases":62,"briefSummary":63,"conditions":64,"keywords":4,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":4},"100580442","effects-of-music-on-post-cesarean-pain-anxiety-breastfeeding-and-mother-infant-attachment-impact-100580442","NCT06837350","Effects of Music on Post-Cesarean Pain, Anxiety, Breastfeeding and Mother Infant Attachment Impact","Music on Post-cesarean","Inclusion Criteria:\n\n* Being 18 years of age or older\n* Being in the third trimester (up to 2 weeks before the planned cesarean delivery date)\n* Being primigravida\n* Having a single fetus\n* Not having a hearing problem\n* Voluntarily participating in the study\n\nExclusion Criteria:\n\n* Having any chronic disease\n* Having a risky pregnancy condition (gestational diabetes, gestational hypertension, preeclampsia, etc.)\n* Having a psychiatric medical diagnosis and using medication.","FEMALE",{"count":61,"type":22},70,[25],"The physiological effects of music therapy include creating a behavioral change and changing the mood by reducing psychophysiological stress, pain, anxiety and isolation. Music has the ability to create deep relaxation. It is known to have relieving effects on insomnia. In addition, it has been reported that music therapy application before and during birth reduces labor pain and reduces postpartum anxiety and depression levels. The postpartum period, which begins with the birth of the newborn, covers the 6-8 week period that it takes for the changes that occur in the woman's body during pregnancy to return to its pre-pregnancy state. This period is an important transition period in which physical, social and emotional changes occur in mothers. In addition to rapid anatomical and physiological changes, mothers experience a difficult process in which the transition to motherhood is experienced, new roles and responsibilities are assumed, and relationships with their spouses and other family members are reorganized. Although a woman begins to feel the changes that having a baby creates in her daily life during pregnancy, she usually experiences the biggest change after the baby is born. The period when the first emotional bond between the newborn and her family is formed and a sense of trust develops is defined as mother-baby bonding. Many factors affect mother-baby bonding in the postpartum period, which is the most important time when the bond established between the expectant mother and the baby during pregnancy, referred to as prenatal bonding, is strengthened after birth. It is particularly affected by the mother's upbringing, as well as her experiences during pregnancy, birth, puerperium, and the baby's first months. Healthy and early interaction between mother and baby initiates a healthy bonding process.",[65,28,66,67],"Cesarian Section","Pain","Anxiety","NOT_YET_RECRUITING","2026-04-22",{"date":43,"type":44},{"date":72,"type":22},"2026-04-23",{"date":74,"type":22},"2026-12-30",{"name":76,"class":51},"Sinop University",{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":81,"acronym":82,"eligibilityCriteria":83,"healthyVolunteers":11,"sex":59,"minAge":18,"maxAge":4,"enrollmentInfo":84,"targetDuration":4,"studyType":23,"phases":86,"briefSummary":87,"conditions":88,"keywords":93,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":98,"lastUpdatePostDateStruct":99,"startDateStruct":101,"completionDateStruct":103,"leadSponsor":105,"locationsCount":21},"100633372","optimizing-sleep-maternal-offspring-bonding-and-sleep-in-the-maternity-ward-100633372","NCT07525830","Optimizing Sleep Maternal-Offspring Bonding and Sleep in the Maternity Ward","COSMOS","Inclusion Criteria:\n\n* Maternal inclusion criteria:\n* Mother over 18 years of age;\n* Mother for whom vaginal delivery is planned\n* Mother who has chosen to breastfeed exclusively;\n* Mother who has a single pregnancy;\n* Mother with no history of sleep disorders.\n* Mother able to understand, read and speak French or, failing that, who has someone in her immediate circle who can understand, read and speak French;\n* Mother affiliated to the social security system;\n* Having signed the consent to participate in the study\n* Newborn inclusion criteria:\n* Newborns born at term, i.e. ≥ 37+0 weeks of amenorrhea (SA).\n\nExclusion Criteria:\n\n* Non-inclusion criterion relating to the mother:\n* Mother for whom a cesarean section is scheduled\n* Mother under legal protection ;\n* Mother presenting with an acute or chronic non-stabilized condition;\n* Mother with a history of sleep disorders;\n* Mother exposed to substances that can alter sleep (alcohol, sedative drugs).\n\nSecondary exclusion criteria:\n\n* Mother who gave birth by emergency cesarean section\n* Mother with a major post-partum medical complication requiring follow-up in a unit other than the maternity unit;\n* Newborn with a major medical complication requiring follow-up in a unit other than the maternity unit.",{"count":85,"type":22},132,[25],"The quality of sleep in maternity wards is crucial for the mental and physical health of the mother, as well as for the development of secure mother to infant bonding. The introduction of \"co-dodo\" cribs, although scarcely studied, may influence sleep quality in both the mother and the newborn infant. Objective : This study aims at evaluating the impact of a co-dodo crib on the sleep quality of the newborn infant, her mother and the mother-infant bonding, compared to a control group with mother using a standard crib.\n\nThis observational, randomized, controlled, multicenter study will include adult mother, breastfeeding and hospitalized in maternity wards after full-term delivery (≥ 37 weeks of gestation). Participant will be randomly assigned in a 1:1 ratio to receive either a co-dodo crib or a standard crib for their newborn infant during their maternity STAI-Y. Actigraphic data will be used for non-invasive sleep assessment in both the newborn infant and the mother. Validated self-reported questionnaires will evaluate maternal stress, sleep quality, post-partum depression risk and mother-infant bonding. • Hypothesis : We hypothesize that using a co-dodo crib compared to a standard crib may improve the newborn and mother sleep quality, decrease the mother stress and enhance the mother to infant bonding.",[89,90,91,92,28],"Co-spleeping","Spleeping Quality","Newborn","Breastfeeding Mothers",[89,94,95,96,97],"spleeping quality","newborn","breastfeeding mothers","bonding","2026-04-07",{"date":100,"type":44},"2026-04-13",{"date":102,"type":44},"2026-02-16",{"date":104,"type":22},"2027-08",{"name":106,"class":51},"Centre Hospitalier Universitaire, Amiens",{"id":108,"slug":109,"hasResults":11,"nctId":110,"briefTitle":111,"officialTitle":112,"acronym":4,"eligibilityCriteria":113,"healthyVolunteers":11,"sex":59,"minAge":18,"maxAge":114,"enrollmentInfo":115,"targetDuration":4,"studyType":23,"phases":117,"briefSummary":118,"conditions":119,"keywords":122,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":129,"lastUpdatePostDateStruct":130,"startDateStruct":132,"completionDateStruct":134,"leadSponsor":136,"locationsCount":21},"100611882","feasibility-and-efficacy-of-gtep-for-birth-trauma-100611882","NCT07246356","Feasibility and Efficacy of GTEP for Birth Trauma","A Study to Explore the Feasibility and Efficacy of Group Traumatic Episode Protocol (GTEP) for Reducing Trauma Symptoms Following a Traumatic Birthing Experience","Inclusion Criteria:\n\n* Aged between 18-65 years.\n* Currently under the Black Country Perinatal Mental Health Service\n* Experiencing self-reported trauma symptoms related to a birthing experience within the last 18 months (this includes the birth itself, the postnatal hospital stay, and\u002For any neonatal admissions).\n* Access to technology (e.g., laptop, internet connection) to be able to access the online group.\n* Access to a confidential space within their home, and childcare for their baby\u002Fany other existing children.\n* Proficient levels of English Language to engage with the group.\n* Ability to engage in group therapy based on clinical presentation.\n* Capacity to consent to engage in the GTEP group and research study.\n\nExclusion Criteria:\n\n* Women\u002Fbirthing people whose baby is no longer under their care.\n* Severe and enduring mental health presentations (i.e., diagnosis of bipolar, psychosis and\u002For schizophrenia.\n* Significant sensory impairment (e.g., needing a British Sign Language interpreter).","65 Years",{"count":116,"type":22},10,[25],"This clinical study aims to evaluate the feasibility and initial efficacy of Group Traumatic Episode Protocol (GTEP) for reducing trauma symptoms (measured by the PCL-5 and City BiTS) for individuals following a traumatic birthing experience. A secondary aim is to evaluate the efficacy of GTEP in improving parental wellbeing (measured through the CORE-10) and parent-infant bonding (measured through the PBQ) following a traumatic birthing experience.\n\nParticipants (those who have experienced a traumatic birthing experience) will complete the GTEP intervention, delivered online. They will be asked to complete outcome measures and give feedback on their experience of the group.",[120,121,28],"PTSD (Childbirth-Related)","Psychological Wellbeing",[123,124,125,126,127,128],"GTEP","Group EMDR","Birth trauma","Psychological wellbeing","Perinatal","Parent infant bonding","2026-02-18",{"date":131,"type":44},"2026-02-19",{"date":133,"type":44},"2025-06-19",{"date":135,"type":22},"2026-06-30",{"name":137,"class":51},"University of Birmingham",{"id":139,"slug":140,"hasResults":11,"nctId":141,"briefTitle":142,"officialTitle":142,"acronym":4,"eligibilityCriteria":143,"healthyVolunteers":16,"sex":59,"minAge":18,"maxAge":4,"enrollmentInfo":144,"targetDuration":4,"studyType":23,"phases":146,"briefSummary":147,"conditions":148,"keywords":4,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":152,"lastUpdatePostDateStruct":153,"startDateStruct":155,"completionDateStruct":157,"leadSponsor":159,"locationsCount":21},"100621392","the-effect-of-lullaby-during-bath-time-on-mother-infant-bonding-postpartum-depression-and-parental-self-efficacy-in-infants-100621392","NCT07370025","The Effect of Lullaby During Bath Time on Mother-Infant Bonding, Postpartum Depression, and Parental Self-Efficacy in Infants","Inclusion Criteria:\n\n* Mothers who have had an uncomplicated pregnancy and delivery\n* Mothers who are healthy enough to care for their baby\n* Mothers who have suitable conditions at home to bathe their baby\n* Babies born at term (≥ 37 weeks of gestation) and with stable general health after birth\n\nExclusion Criteria:\n\n* Mothers with a history of serious postpartum complications (such as postpartum hemorrhage)\n* Mothers diagnosed with psychiatric illness\n* Mothers who are unable to participate directly in the care of their baby (due to severe disability, mandatory bed rest, etc.)\n* Mothers who cannot participate in the lullaby program due to hearing impairment\n* Infants who experience serious respiratory, cardiac, or neurological problems at birth or thereafter, who have a skin disease or dermatological condition that limits bathing, who have a history of admission to the neonatal intensive care unit, or who have a chronic disease or congenital anomaly",{"count":145,"type":22},98,[25],"This randomized, single-blind controlled trial aims to evaluate the effects of maternal lullaby singing during infant bathing on mother-infant bonding, postpartum depressive symptoms, and perceived parenting self-efficacy in mothers of healthy term infants. The postpartum period represents a critical phase for maternal psychological adjustment, during which stress, depressive symptoms, and low parenting confidence may negatively affect the quality of mother-infant interaction and bonding. Low-cost, culturally meaningful, and non-pharmacological interventions that support maternal well-being and early bonding are therefore of particular importance.\n\nThe study will be conducted with mothers who have delivered healthy term infants in a public hospital. Eligible participants will be randomly assigned to either an intervention group or a control group. Mothers in the intervention group will receive a structured bathing education and will be instructed to bathe their infants three times per week for two consecutive weeks while singing a lullaby using their own voice in a calm and quiet home environment. Live-recorded music will not be used. The intervention emphasizes sensory interaction, emotional closeness, and maternal voice as key components. Each bathing session is expected to last approximately 10-15 minutes. The control group will receive routine postpartum care without a structured lullaby-based bathing intervention.\n\nOutcome measures include mother-infant bonding, postpartum depressive symptoms, and perceived maternal parenting self-efficacy. Data will be collected at two time points: prior to hospital discharge (within the first 24 hours postpartum) and at the end of the two-week intervention period. Validated self-report instruments will be used for all outcome assessments.\n\nThe findings of this study are expected to provide evidence on the effectiveness of a simple, culturally embedded caregiving practice in supporting maternal mental health, strengthening mother-infant bonding, and enhancing parenting confidence during the early postpartum period. Results may inform postpartum care practices, parental counseling programs, and midwife-led supportive interventions.",[149,28,150,151],"Newborn Infant","Self Efficacy","Postpartum Depression (PPD)","2026-01-28",{"date":154,"type":44},"2026-01-30",{"date":156,"type":22},"2026-05-15",{"date":158,"type":22},"2027-01-15",{"name":160,"class":51},"Istanbul University - Cerrahpasa",{"id":162,"slug":163,"hasResults":11,"nctId":164,"briefTitle":165,"officialTitle":165,"acronym":166,"eligibilityCriteria":167,"healthyVolunteers":16,"sex":59,"minAge":18,"maxAge":4,"enrollmentInfo":168,"targetDuration":4,"studyType":23,"phases":170,"briefSummary":171,"conditions":172,"keywords":176,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":180,"lastUpdatePostDateStruct":181,"startDateStruct":183,"completionDateStruct":185,"leadSponsor":187,"locationsCount":21},"100566917","the-effects-of-video-based-and-practical-newborn-bathing-education-provided-to-primiparous-pregnant-women-during-the-third-trimester-on-knowledge-anxiety-and-bonding-during-the-first-bath-a-randomized-controlled-trial-100566917","NCT06661408","The Effects of Video-Based and Practical Newborn Bathing Education Provided to Primiparous Pregnant Women During the Third Trimester on Knowledge, Anxiety, and Bonding During the First Bath: A Randomized Controlled Trial","NewbornBathing","Inclusion Criteria:\n\n* Can speak and understand Turkish,\n* 18 years of age or older,\n* Literate,\n* Primiparous,\n* In the third trimester of pregnancy,\n* A singleton pregnancy,\n* No psychiatric illness,\n* Who have not received any training on newborn bathing before,\n* Her baby was not diagnosed with a fetal anomaly,\n* With a smartphone and internet,\n* Residing in the province of Kahramanmaras and\n* Who agreed to participate in the research\n\nExclusion Criteria:\n\n* Preterm labor (\\<37 weeks gestation),\n* Stillbirth,\n* The baby needs intensive care or is hospitalized,\n* The baby has a low birth weight (\\<2500 grams),\n* The one whose baby\\'s first bath was given by someone else,\n* A newborn bathing program was organized at the pregnancy school.\n* Wishing to leave at any stage of the study.",{"count":169,"type":22},144,[25],"This study will be conducted in a randomized controlled experimental research design with pretest, posttest control group.",[173,174,67,28,175],"Newborn Bathing","Primiparous Pregnant Women","Knowledge",[91,177,178,179],"Bathing","Primipar","Education","2024-10-25",{"date":182,"type":44},"2024-10-28",{"date":184,"type":22},"2024-12-15",{"date":186,"type":22},"2025-08-15",{"name":188,"class":51},"Kahramanmaras Sutcu Imam University",{"id":190,"slug":191,"hasResults":11,"nctId":192,"briefTitle":193,"officialTitle":194,"acronym":195,"eligibilityCriteria":196,"healthyVolunteers":11,"sex":17,"minAge":197,"maxAge":198,"enrollmentInfo":199,"targetDuration":4,"studyType":23,"phases":201,"briefSummary":202,"conditions":203,"keywords":208,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":210,"lastUpdatePostDateStruct":211,"startDateStruct":213,"completionDateStruct":215,"leadSponsor":217,"locationsCount":21},"100493764","preterm-delayed-cord-clamping-and-early-skin-to-skin-contact-predecess-100493764","NCT05709392","Preterm DElayed Cord Clamping and Early Skin-to-Skin Contact: PreDECESS","Preterm DElayed Cord Clamping and Early Skin-to-Skin Contact","PreDECESS","Inclusion Criteria:\n\nInfants born in gestational weeks 30+0-34+6 through vaginal delivery and admitted to neonatal ward in Sweden.\n\nParents must be able to read Swedish.\n\nExclusion Criteria:\n\nInfants with known disease when an expanded blood volume is expected will be excluded as early cord clamping is recommended (severe anemia, cardiac disease etc).\n\nInfants with known malformations. Infants with severe or moderate asphyxia (defined as APGAR \\\u003C 4 at 5 minutes of age).\n\nInfants where the physician in charge find it inappropriate with delayed cord clamping.\n\nNo time for cord clamping has been registered.","30 Weeks","34 Weeks",{"count":200,"type":22},126,[25],"The PreDECESS trial is a prospective study where that will evaluate a new method taking care of premature infants in gestational weeks 30+0 to 34+6 at birth. The new method includes delayed cord clamping and early skin-to-skin contact with a parent. Two populations of infants with their parents will be compared. Infants taken care of in the traditional way before the new method is introduced, and infants taken care of with the new method when it is being introduced.\n\nPrimary question:\n\nDoes delayed cord clamping and early skin-to skin contact (SSC) lead to better bonding between parents and their infants?\n\nSecondary questions:\n\nAre there any potential adverse effects with delayed cord clamping and early skin-to skin contact (SSC)? Is there a difference in infants level of bilirubin, haemoglobin or proBNP? Is there a difference in infants growth? Is there a difference in infants neurological development? Is there a difference in infants and parents level of stress? Is there a difference in mothers production of breastmilk, frequency of breastfeeding or experience of breastfeeding? Is there a difference in parents mood? How do parents of preterm infants experience giving birth of their preterm baby before and after the introduction of the new method?",[28,204,205,206,207],"Stress","Breastfeeding","Child Development","Adverse Events",[209],"adverse events","2023-01-23",{"date":212,"type":44},"2023-02-02",{"date":214,"type":44},"2022-12-12",{"date":216,"type":22},"2028-12-11",{"name":218,"class":51},"Ostergotland County Council, Sweden"]