[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"primiparity\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:primiparity":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,63,97],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":37,"overallStatus":50,"whyStopped":4,"lastUpdateSubmitDate":51,"lastUpdatePostDateStruct":52,"startDateStruct":55,"completionDateStruct":57,"leadSponsor":59,"locationsCount":62},"100641975","use-of-perineal-mirror-during-the-second-stage-of-labor-100641975",false,"NCT07659249","USE OF PERINEAL MIRROR DURING THE SECOND STAGE OF LABOR","THE EFFECT OF PERİNEAL MİRROR USE DURİNG THE SECOND STAGE OF LABOR ON THE DURATİON OF THE SECOND STAGE, RECOVERY, AND PERCEİVED PAİN, SUPPORT, AND CONTROL LEVELS DURİNG DELİVERY","Inclusion Criteria:\n\n* Women aged 19 and over\n* Women with term pregnancy (38+0 - 41+6)\n* Women with singleton pregnancy\n* Women who have had spontaneous vaginal delivery\n* Primiparous pregnant women\n* Women who voluntarily agree to participate in the study will be included.\n\nExclusion Criteria:\n\n* Women with high-risk pregnancies\n* Women with multiple pregnancies",true,"FEMALE","19 Years","49 Years",{"count":21,"type":22},80,"ESTIMATED","INTERVENTIONAL",[25],"NA","Objective: This study was designed to evaluate the effect of perineal mirror use during the second stage of labor on the duration of the second stage, postpartum recovery, and perceived pain, support, and control levels during delivery.\n\nMethod: The study was designed as a randomized controlled experimental study to examine the effect of perineal mirror use on delivery outcomes in primiparous women. The study population consisted of primiparous pregnant women admitted to the maternity clinic between June 29, 2026, and October 30, 2026. The sample size was calculated using the G\\*Power 3.1.9.2 program with an effect size of 0.50, 5% Type I error, and 95% power level; a total of 72 participants were selected, 36 in the intervention group and 36 in the control group. Considering potential losses, the sample size was increased by 10%, and a total of 80 pregnant women were planned to be included in the study. Participants were randomly assigned to the intervention group using a perineal mirror and the control group receiving routine care. The following instruments will be used as data collection tools: Pregnancy Demographic Information Form, REEDA Scale, Visual Analog Scale (VAS), and Perceived Support and Control in Childbirth Scale.\n\nExpected Outcome: It is predicted that the perineal mirror may increase the woman's active participation, motivation, and perceived control by allowing her to see the fetal descent and the progress of labor; consequently, it may reduce the duration of active pushing and the duration of the second stage. It is also thought that it may have positive effects on the birth experience, postpartum recovery, and perceived level of support and control. The research results are expected to provide evidence for non-invasive and low-cost applications that can be used in childbirth care.",[28,29,30,31,32,33,34,35,36],"Labor, Second Stage","Vaginal Delivery","Primiparity","Perineal Mirror Use","Childbirth Experience","Labor Pain","Perceived Support During Childbirth","Perceived Control During Childbirth","Postpartum Perineal Healing",[38,39,40,41,42,43,44,45,46,47,48,49],"Midwifery","Perineal mirror","Second stage of labor","Vaginal birth","Primiparous women","Labor duration","Childbirth pain","Perceived support","Perceived control","REEDA scale","Maternal outcomes","Non-invasive intervention","NOT_YET_RECRUITING","2026-06-18",{"date":53,"type":54},"2026-06-22","ACTUAL",{"date":56,"type":22},"2026-06-29",{"date":58,"type":22},"2026-10-30",{"name":60,"class":61},"Sakarya University","OTHER",1,{"id":64,"slug":65,"hasResults":11,"nctId":66,"briefTitle":67,"officialTitle":68,"acronym":4,"eligibilityCriteria":69,"healthyVolunteers":16,"sex":17,"minAge":70,"maxAge":71,"enrollmentInfo":72,"targetDuration":4,"studyType":23,"phases":74,"briefSummary":75,"conditions":76,"keywords":80,"overallStatus":87,"whyStopped":4,"lastUpdateSubmitDate":88,"lastUpdatePostDateStruct":89,"startDateStruct":91,"completionDateStruct":93,"leadSponsor":95,"locationsCount":62},"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.","18 Years","35 Years",{"count":73,"type":22},64,[25],"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.",[77,78,79,30],"Breast Feeding","Exclusive Breast Feeding","Maternal-Fetal Attachment",[81,82,83,84,85,86],"Breastfeeding Education","Hybrid Education","Primiparous Women","Antenatal Attachment","Breastfeeding Self-Efficacy","Mother-Infant Bonding","RECRUITING","2026-03-13",{"date":90,"type":54},"2026-03-17",{"date":92,"type":54},"2025-12-30",{"date":94,"type":22},"2026-08-01",{"name":96,"class":61},"Emel GÜÇLÜ CİHAN",{"id":98,"slug":99,"hasResults":11,"nctId":100,"briefTitle":101,"officialTitle":102,"acronym":4,"eligibilityCriteria":103,"healthyVolunteers":16,"sex":17,"minAge":70,"maxAge":4,"enrollmentInfo":104,"targetDuration":4,"studyType":23,"phases":106,"briefSummary":107,"conditions":108,"keywords":109,"overallStatus":87,"whyStopped":4,"lastUpdateSubmitDate":114,"lastUpdatePostDateStruct":115,"startDateStruct":117,"completionDateStruct":119,"leadSponsor":121,"locationsCount":62},"100557832","breastfeeding-education-using-the-card-game-method-100557832","NCT06543238","Breastfeeding Education Using the Card Game Method","The Effect of Breastfeeding Education Using the Card Game Method on Breastfeeding Success, Breastfeeding Self-efficacy and Satisfaction in Primiparous Mothers: A Randomized Controlled Trial","Inclusion Criteria:\n\n* The conditions for volunteering to participate in the study are being over the age of 18, being able to read and write, being able to read and understand Turkish, not having hearing, speaking or visual impairments, having received breastfeeding training at a pregnancy school, being healthy in the 34th to 38th week of primiparous pregnancy, having a planned cesarean section, having a live birth and having a healthy baby.\n\nExclusion Criteria:\n\n* Obstacles to communication include having a visual, hearing or perception disorder, not being able to read or write, having a psychiatric illness, being multiparous and having a vaginal birth, having a risky pregnancy, not having a live birth and not having a live baby after birth.",{"count":105,"type":22},60,[25],"This study aims to determine the effects of breastfeeding education using the card game method on breastfeeding success and breastfeeding self-efficacy in primiparous breastfeeding mothers.",[30],[30,110,77,111,112,113],"Mothers","Self Efficacy","Education","Game","2025-02-28",{"date":116,"type":54},"2025-03-04",{"date":118,"type":54},"2024-09-09",{"date":120,"type":22},"2025-06",{"name":122,"class":61},"Çankırı Karatekin University"]