[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"birth\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:birth":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,8,0,[8,46,80,112,134,163,191,221],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":28,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100617030","trial-of-underwater-birth-100617030",false,"NCT07313319","Trial of Underwater Birth","Trial of Underwater Birth: A Randomized Control Trial","TUB","Inclusion Criteria: Inclusion criteria based on A model practice template for hydrotherapy in labor and birth (2016):\n\nPrenatal inclusion criteria (to be assessed at the time of enrollment):\n\n* ≥18 years of age\n* Able to speak and understand English or Spanish\n* Singleton gestation\n* Vertex presentation\n* Able to ambulate with no mobility restrictions (i.e., no difficulty getting from seated to standing)\n* Less than class III obesity (BMI \\\u003C40 kg\u002Fm2) at initiation of prenatal care\n\nLabor inclusion criteria (to be assessed at time of admission):\n\n* Greater than 37 weeks 0 days through and less than 412 completed weeks 6 days gestation with fetus in vertex presentation\n* Normal blood pressure and normal temperature (obstetric criteria for exclusion: two blood pressures 140\u002F90 four hours apart; two fevers of over 100.4 one hour apart)\n\nExclusion Criteria: based on A model practice template for hydrotherapy in labor and birth (2016):\n\nPrenatal exclusion criteria (to be assessed at the time of enrollment):\n\n* Active infections such as HIV, Hepatitis B, Hepatitis C, HSV outbreak (on prophylaxis acceptable) (GBS positive is acceptable)\n* Pre-existing medical conditions including heart disease, uncontrolled asthma, preexisting diabetes, chronic hypertension, or activity restrictions\n* High-risk pregnancy conditions including preeclampsia, gestational hypertension, preterm gestation, multiple gestation, gestational diabetes type A2, estimated fetal weight of 5000g for non-diabetics or \\>4500 for GDM-A1, unstable substance use disorder (i.e. not in remission), placental abruption or other unexplained vaginal bleeding, previous cesarean section, fetal growth restriction (\\\u003C10th percentile), fetal anomaly, or other neonatal condition that may complicate neonatal transition to extrauterine life.\n* Existing contraindication to vaginal birth\n\nLabor exclusion criteria (to be assessed at the time of admission):\n\n* Meconium-stained amniotic fluid\n* Preterm rupture of membranes (PROM) greater than 24 hours without the start of any labor contractions (those whose have PROM greater than 24 hours but are in labor can continue to be included in the study)\n* Immediate need for operative delivery at time of admission","FEMALE","18 Years",{"count":20,"type":21},230,"ESTIMATED","INTERVENTIONAL",[24],"NA","Evaluate maternal perinatal outcomes in adult low-risk laboring people randomized to waterbirth compared to those randomized to birth on land.",[27],"Birth",[29,30,31,32],"waterbirth","landbirth","epidural use","birth outcomes","RECRUITING","2026-04-22",{"date":36,"type":37},"2026-04-23","ACTUAL",{"date":39,"type":37},"2026-04-21",{"date":41,"type":21},"2028-12",{"name":43,"class":44},"University of New Mexico","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":52,"eligibilityCriteria":53,"healthyVolunteers":54,"sex":17,"minAge":55,"maxAge":56,"enrollmentInfo":57,"targetDuration":4,"studyType":22,"phases":59,"briefSummary":60,"conditions":61,"keywords":65,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":45},"100632821","binaural-beat-music-virtual-reality-and-hormones-in-childbirth-100632821","NCT07518667","Binaural Beat Music, Virtual Reality, and Hormones in Childbirth","The Effect of Binaural Rhythm-Supported Music and Virtual Reality Experience on Labor Pain and Hormones","VR","Inclusion Criteria:\n\n* Able to speak Turkish and communicate verbally\n* No hearing or visual impairments\n* The pregnancy is at term (37-42 weeks of gestation) and labor has begun\n* Single fetus with cephalic presentation\n* No chronic disease\n* Not taking hormone therapy\n* Pregnant women who do not have any obstetric risks and are expected to give birth normally\n\nExclusion Criteria:\n\n* Diagnosed with risky pregnancy\n* Complications during birth\n* Those with vision and hearing problems\n* Any pharmacological pain-reducing method applied\n* Cesarean section planned\n* Those who have experienced any alternative methods for preparing for birth or managing labor pain (such as yoga, meditation, breathing exercises, hypnosis)",true,"20 Years","35 Years",{"count":58,"type":21},90,[24],"This study aims to investigate the effects of Binaural Beats-supported music and virtual reality experience on the levels of oxytocin, prolactin, catecholamine, endorphin, prostaglandin E and cortisol, which are hormones that play an active role in birth, using the Elisa method. Additionally, the study will examine the effects of virtual reality experience and Binaural Beats-supported music during labor on labor pain and some birth outcomes (such as the presence of an episiotomy, the onset of labor, the duration of labor, and the newborn Apgar score).The randomized controlled study will consist of three groups: a virtual reality group, a Binaural Beats-supported music group, and a control group. The research will be completed with a total of 90 people, with 30 people in each group. The research will be conducted at the Maternity Ward of Istanbul Gaziosmanpaşa Training and Research Hospital. Ethics committee approval has been received for the research. Data collection has not yet begun. An application has been made to the hospital administration for institutional permission. The research will begin once the permissions are received.",[27,62,63,64],"Hormones","Virtual Reality","Music",[27,66,67,68,69],"hormones","virtual reality","Binaural beats","music","NOT_YET_RECRUITING","2026-04-02",{"date":73,"type":37},"2026-04-08",{"date":75,"type":21},"2026-05",{"date":77,"type":21},"2027-07",{"name":79,"class":44},"Medipol University",{"id":81,"slug":82,"hasResults":11,"nctId":83,"briefTitle":84,"officialTitle":84,"acronym":85,"eligibilityCriteria":86,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":87,"enrollmentInfo":88,"targetDuration":4,"studyType":22,"phases":90,"briefSummary":91,"conditions":92,"keywords":96,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":103,"lastUpdatePostDateStruct":104,"startDateStruct":106,"completionDateStruct":108,"leadSponsor":110,"locationsCount":45},"100615525","the-impact-of-virtual-doula-services-on-birth-outcomes-in-rural-communities-100615525","NCT07293741","The Impact of Virtual Doula Services on Birth Outcomes in Rural Communities","RIVER","Inclusion Criteria:\n\n* 18-45 years of age\n* pregnant (second or early third trimester) with their first child\n* reside in a rural zip codes in the U.S.\n\nExclusion Criteria:\n\n* non-singleton pregnancy\n* police custody or incarceration\n* infant to be separated from mother (e.g., placed for adoption, protective custody)\n* working with a doula prior to enrollment.","45 Years",{"count":89,"type":21},614,[24],"This study will assess the impact of virtual doula care on birth and postnatal outcomes among rural mothers. The goal of virtual doula services is to improve access to care in underserved communities and decrease urban-rural differences in key maternal health outcomes including mode of birth (cesarean vs vaginal) and birth satisfaction. By implementing a digital randomized controlled trial, the study team will efficiently recruit a national sample of rural pregnant women to provide evidence of the effectiveness of virtual doula care, the appropriateness of virtual visits for different care and support needs, and the role of virtual care in improving maternal health.",[27,93,94,95],"Telehealth","Pregnancy","Maternal Health",[97,98,99,100,101,102],"telehealth","virtual","doula","pregnancy","birth","maternal health","2025-12-18",{"date":105,"type":37},"2025-12-22",{"date":107,"type":21},"2026-09",{"date":109,"type":21},"2029-12",{"name":111,"class":44},"RAND",{"id":113,"slug":114,"hasResults":11,"nctId":115,"briefTitle":116,"officialTitle":117,"acronym":4,"eligibilityCriteria":118,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":119,"targetDuration":4,"studyType":22,"phases":121,"briefSummary":122,"conditions":123,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":125,"lastUpdatePostDateStruct":126,"startDateStruct":128,"completionDateStruct":130,"leadSponsor":132,"locationsCount":45},"100613263","combined-intravenous-tramadol-and-paracetamol-versus-intramuscular-pethidine-for-pain-relief-during-the-first-stage-of-labor-compare-the-efficacy-and-adverse-effects-100613263","NCT07264309","Combined Intravenous Tramadol and Paracetamol Versus Intramuscular Pethidine for Pain Relief During the First Stage of Labor. Compare the Efficacy and Adverse Effects","Combined Intravenous Tramadol and Paracetamol Versus Intramuscular Pethidine for Pain Relief During the First Stage of Labor","Inclusion Criteria:\n\nSingleton Term pregnancy First stage of labor including at least 4 painful contractions in 30 min with cervical dilatation less or equal to 1 cm or 50% effacement Spontaneous or induced labor -\n\nExclusion Criteria:\n\n* Previous cesarean delivery\n* Malpresentation\n* Multiple pregnancies\n* Suspected intrauterine growth restriction \\\u003C 3 percentile\n* Suspected placental abruption\n* History of allergy to paracetamol, tramadol or pethidine\n* Women with sleep apnea disorder\n* Morbid obesity BMI≥40\n* History of significant cardiac, liver and renal diseases\n* Anti-convulsive medication consumption\n* MAO inhibitors medication consumption within the last 14 days\n* Non reassuring fetal heart rate monitoring (type II or III)\n* Tense use",{"count":120,"type":21},140,[24],"The goal of this intervention study is to compare the efficacy and adverse effects of pain relief during the first stage of labor using 75 mg IM pethidine versus the combination of IV 100 mg tramadol and 1000 mg paracetamol.\n\nThe investigator assume that the combination of IV tramadol and paracetamol will be more effective with less adverse effects than IM pethidine in pain relief at the first stage of labor.\n\nThe investigator primary outcome is The effect on pain relief according to numeric rating scale (NTS) in the study groups Before the administration of the drugs, fetal heart rate patterns and contractions will be recorded with cardiotocography monitor for at least 20 min. The investigator will evaluate vigilance at 30 minutes following drug administration.\n\nNRS pain score (0-10) will be collected before administration and one hour after drug administration",[124,27],"Pain Management","2025-12-07",{"date":127,"type":37},"2025-12-15",{"date":129,"type":37},"2025-11-01",{"date":131,"type":21},"2027-12",{"name":133,"class":44},"Zohar Nachum",{"id":135,"slug":136,"hasResults":11,"nctId":137,"briefTitle":138,"officialTitle":139,"acronym":4,"eligibilityCriteria":140,"healthyVolunteers":54,"sex":17,"minAge":141,"maxAge":56,"enrollmentInfo":142,"targetDuration":4,"studyType":22,"phases":144,"briefSummary":145,"conditions":146,"keywords":148,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":154,"lastUpdatePostDateStruct":155,"startDateStruct":157,"completionDateStruct":159,"leadSponsor":161,"locationsCount":45},"100610869","the-effect-of-wireless-electronic-fetal-monitoring-on-labor-pain-and-birth-experiences-100610869","NCT07233187","The Effect of Wireless Electronic Fetal Monitoring on Labor Pain and Birth Experiences","The Effect of Continuous Wireless Fetal Monitoring During the Intrapartum Period on Labor Pain and Birth Experience: A Randomized Controlled Single-Blind Study","Inclusion Criteria:\n\n* The study included healthy primiparous or multiparous pregnant women who agreed to participate in the study, were between the ages of 18 and 35, had a gestational age greater than 37+0, had cervical dilation greater than 4 cm, had a single, live fetus, were not using uterotonic agents, spoke Turkish, had no comprehension, perception, or communication problems, and were healthy.\n\nExclusion Criteria:\n\n* Pregnant women who were diagnosed with a risky pregnancy, who were illiterate, who had a contagious disease, or who had a risky disease were not included in the study.","19 Years",{"count":143,"type":21},112,[24],"This study is using Electronic Fetal Monitoring (EFM) to assess fetal health in pregnant women in labor. This will be compared with continuous wired EFM and continuous wireless EFM. The effects of wireless and continuous wireless EFM on labor pain levels and labor experiences will be measured.",[27,147],"Intrapartum",[149,150,151,152,153],"Fetal Monitoring","intrapartum","pain","birth experience","Continuous Wireless Fetal Monitoring","2025-11-14",{"date":156,"type":37},"2025-11-18",{"date":158,"type":21},"2025-11-15",{"date":160,"type":21},"2026-01-15",{"name":162,"class":44},"Tokat Gaziosmanpasa University",{"id":164,"slug":165,"hasResults":11,"nctId":166,"briefTitle":167,"officialTitle":168,"acronym":4,"eligibilityCriteria":169,"healthyVolunteers":54,"sex":17,"minAge":18,"maxAge":56,"enrollmentInfo":170,"targetDuration":4,"studyType":22,"phases":172,"briefSummary":173,"conditions":174,"keywords":178,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":182,"lastUpdatePostDateStruct":183,"startDateStruct":185,"completionDateStruct":187,"leadSponsor":189,"locationsCount":45},"100598516","childbirth-education-classes-spousal-support-birth-memory-choice-of-the-birth-method-and-birth-satisfaction-100598516","NCT07072507","Childbirth Education Classes, Spousal Support, Birth Memory, Choice of the Birth Method, and Birth Satisfaction","The Effect of Childbirth Preparation Classes on Spousal Support, Birth Preference, Birth Memory, and Birth Satisfaction","Inclusion Criteria:\n\n* Being able to speak and write Turkish\n* Nulliparous\n* Being in 30-32 weeks of pregnancy\n* Having a singleton pregnancy\n\nExclusion Criteria:\n\n* Having communication and psychological problems\n* Having multiple pregnancies\n* Being overweight and obese\n* Being divorced or having lost a spouse\n* Not attending more than one session of childbirth preparation classes with\u002Fwithout a spouse\n* Filling out incomplete forms",{"count":171,"type":21},93,[24],"The research questions of this study are listed below.\n\n1. Is the mean spouse support score of pregnant women who attend childbirth preparation education with their spouses higher than that of women in the group with unique participation in childbirth preparation education and the control group who were left to usual care?\n2. Is the mean birth satisfaction scale score of pregnant women who attend childbirth preparation education with their spouses higher than that of women in the group with unique participation in childbirth preparation education and the control group who were left to usual care?\n3. Is the mean birth memory and recall scale score of pregnant women who attend childbirth preparation education with their spouses higher than that of women in the group with unique participation in childbirth preparation education and the control group who were left to usual care?\n4. Are the birth preferences of pregnant women who attend childbirth preparation education with their spouses significantly different from those of women in the group with unique participation in childbirth prep",[27,175,94,176,177],"Education","Birth Memory","Birth Satisfaction",[179,180,176,177,181],"Childbirth Education Classes","Partner Support","choice of the birth method","2025-07-16",{"date":184,"type":37},"2025-07-18",{"date":186,"type":37},"2025-06-28",{"date":188,"type":21},"2025-10-30",{"name":190,"class":44},"Aydin Adnan Menderes University",{"id":192,"slug":193,"hasResults":11,"nctId":194,"briefTitle":195,"officialTitle":195,"acronym":196,"eligibilityCriteria":197,"healthyVolunteers":54,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":198,"targetDuration":4,"studyType":200,"phases":4,"briefSummary":201,"conditions":202,"keywords":209,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":212,"lastUpdatePostDateStruct":213,"startDateStruct":215,"completionDateStruct":217,"leadSponsor":219,"locationsCount":45},"100580954","birth--breastfeeding-support-study-100580954","NCT06844019","Birth & Breastfeeding Support Study","BABSS","Inclusion Criteria: 18 years, intention to breastfeed, single gestation, reads and understands Danish -\n\nExclusion Criteria: Twin gestation, less than 18 years, no intention to breastfeed, does not read and understand Danish\n\n\\-",{"count":199,"type":21},1628,"OBSERVATIONAL","The goal of this observational study is to learn about the effects of birth practices such as cesarean section and vacuum assisted birth and diseases such as gestational diabetes and preeclampsia on exclusive breastfeeding. The main question it aims to answer is:\n\n• Does cesarean section, vacuum assisted birth, gestational diabetes and preeclampsia affect exclusive breastfeeding three months after birth? Participants answer eight online survey questions. One survey is distributed before birth and the remaining seven surveys are distributed after birth at three, seven and four-teen days, as well as one, three, six and twelve months after birth.",[203,204,205,27,206,207,208],"Breastfeeding","Breastfeeding Initiation","Breastfeeding Duration","Birth Practices","Gestational Diabetes Mellitus (GDM)","Preeclampsia",[210,211],"Birth, birth practices, gestational diabetes, preeclampsia","breastfeeding","2025-05-22",{"date":214,"type":37},"2025-05-28",{"date":216,"type":37},"2025-01-06",{"date":218,"type":21},"2028-01",{"name":220,"class":44},"Herlev Hospital",{"id":222,"slug":223,"hasResults":11,"nctId":224,"briefTitle":225,"officialTitle":226,"acronym":4,"eligibilityCriteria":227,"healthyVolunteers":54,"sex":17,"minAge":18,"maxAge":87,"enrollmentInfo":228,"targetDuration":4,"studyType":22,"phases":230,"briefSummary":231,"conditions":232,"keywords":234,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":240,"lastUpdatePostDateStruct":241,"startDateStruct":242,"completionDateStruct":244,"leadSponsor":246,"locationsCount":45},"100591760","effect-of-snoezelen-room-on-birth-process-100591760","NCT06984614","Effect of Snoezelen Room on Birth Process","Effect of Snoezelen Room on Birth Process: a Randomized Controlled Study","Inclusion Criteria:\n\n* Pregnant women who are planned to give birth vaginally in their 37th-42nd weeks of pregnancy,\n* who are in their first pregnancy, who do not have any vision,\n* hearing or communication problems,\n* who can speak Turkish and express themselves in Turkish,\n* who volunteer will be included in the study.\n\nExclusion Criteria:\n\n* Women with multiple pregnancies,\n* women who are planned to give birth by cesarean section,\n* women who give birth by cesarean section for any reason during the study,\n* women who develop any complications during pregnancy,\n* women with chronic diseases,\n* women with verbal, mental, etc. communication disabilities will not be included in the study.\n* Women who have instrumental delivery (with vacuum or forceps),\n* postpartum complications in the newborn, or complications related to episiotomy (such as 3rd and 4th degree laceration, hematoma) from the control or intervention groups will be excluded from the study.",{"count":229,"type":21},104,[24],"Aromatherapy, visual and auditory stimuli are used together in the Snoezelen room. Aromatherapy increases the production of endorphins, reduces the intensity of pain and distracts the attention from the pain. Music also blocks the transmission of nerve impulses to the spinal cord.Considering these effects, the study emerges as a new technology for the midwifery field in our country. Although the use of snoezelen rooms in the delivery environment is becoming increasingly widespread abroad, it has not been used in delivery services in any hospital in our country. The primary purpose of this study is to convert a room in the delivery room of the hospital into a Snoezelen room and have women complete their delivery process in this room, and the secondary purpose is to determine the effect of the Snoezelen room on the delivery process.\n\nThe primiparous pregnant women selected for the intervention and control groups will be informed about the purpose of the study and the applications by the research midwife or gynecologist following the birth and will be administered the \"Pregnant Information Form\", \"Visual Analog Scale (VAS)\", \"Fear of Childbirth Scale\", \"Birth Comfort Scale\", and after birth, the \"Birth Information Form\", \"Birth Satisfaction Scale\". The Beta Endorphin Level Recording Form will be filled out.",[233,27],"Birth Outcomes",[235,236,237,238,239,100],"midwifery","birth process","snoezelen room","fear of birth","birth satisfaction","2025-05-20",{"date":212,"type":37},{"date":243,"type":37},"2025-01-11",{"date":245,"type":21},"2025-06-30",{"name":247,"class":44},"Sakarya University"]