[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"childbirth-experience\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:childbirth-experience":32},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,63,92],{"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":67,"acronym":4,"eligibilityCriteria":68,"healthyVolunteers":16,"sex":17,"minAge":69,"maxAge":70,"enrollmentInfo":71,"targetDuration":4,"studyType":23,"phases":73,"briefSummary":74,"conditions":75,"keywords":78,"overallStatus":50,"whyStopped":4,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":84,"startDateStruct":86,"completionDateStruct":88,"leadSponsor":90,"locationsCount":4},"100618295","effectiveness-of-a-virtual-reality-intervention-on-pain-anxiety-and-satisfaction-in-laboring-women-100618295","NCT07329764","Effectiveness of a Virtual Reality Intervention on Pain, Anxiety, and Satisfaction in Laboring Women","Women meeting the following criteria were eligible for enrollment:\n\n1. Pregnant.\n2. Aged 18 years or older.\n3. Pregnant for more than 37 weeks.\n4. Single baby born in the cephalic presentation and willing to deliver naturally.\n5. Admitted to the hospital during the latent period.\n6. No major medical conditions or complications during pregnancy for either mother or baby.\n7. Able to hear, speak, read, and write Chinese.\n8. Interested in participating in this study and agreeing to complete the questionnaire.\n\nWomen meeting the above criteria will be enrolled after the researchers explain the research methods and objectives. Exclusion criteria include:\n\n1. Virtual reality sickness.\n2. Vision or hearing problems.\n3. Withdrawal from the study.\n4. Maternal or fetal condition requiring emergency cesarean section.\n5. Those diagnosed with migraine, epilepsy, or mental illness.","18 Years","50 Years",{"count":72,"type":22},92,[25],"This study is designed to evaluate whether a virtual reality (VR) intervention can help reduce pain and anxiety and improve childbirth satisfaction among laboring women.\n\nEligible participants will be randomly assigned to either a VR intervention group or a control group receiving standard intrapartum care. Women in the VR group will use a virtual reality headset that provides immersive natural imagery and music during labor, while women in the control group will receive routine care without VR.\n\nThe study will compare levels of labor pain, anxiety, and childbirth satisfaction between the two groups to determine the effectiveness of the virtual reality intervention as supportive care during labor.",[76,77,32],"Relieve Pain","Anxiety",[79,33,77,80,81,82],"Virtual Reality","Childbirth Satisfaction","Non-pharmacological Pain Management","Intrapartum Care","2025-12-29",{"date":85,"type":54},"2026-01-09",{"date":87,"type":22},"2025-12-12",{"date":89,"type":22},"2026-07-31",{"name":91,"class":61},"Wan-Lin Pan",{"id":93,"slug":94,"hasResults":11,"nctId":95,"briefTitle":96,"officialTitle":96,"acronym":4,"eligibilityCriteria":97,"healthyVolunteers":11,"sex":17,"minAge":69,"maxAge":4,"enrollmentInfo":98,"targetDuration":4,"studyType":100,"phases":4,"briefSummary":101,"conditions":102,"keywords":109,"overallStatus":114,"whyStopped":4,"lastUpdateSubmitDate":115,"lastUpdatePostDateStruct":116,"startDateStruct":118,"completionDateStruct":120,"leadSponsor":122,"locationsCount":62},"100613914","maternal-informing-on-labor-induction-impact-on-childbirth-experience-100613914","NCT07272785","Maternal Informing on Labor Induction: Impact on Childbirth Experience","Inclusion Criteria:\n\n* Planned induction of labor at the antenatal ward or at the outpatient clinic\n* Adequate language skills (Finnish, Swedish, English)\n\nExclusion Criteria:\n\n* Induction at the delivery ward or at the obstetric emergency care clinic\n* Spontaneous onset of labor or a planned cesarean delivery\n* Age below 18 years at the time of recruitment",{"count":99,"type":22},50,"OBSERVATIONAL","The aim of this study is to explore the information provided to mothers about labor induction and its connection to their childbirth experience. In addition, the study examines how the use of social media may influence the birth experience among patients undergoing labor induction.",[103,104,105,106,107,108,32],"Labor, Induced","Labor, Obstetric","Pregnancy","Humans","Prospective Study","Prospective Study , Questionaires",[110,111,105,112,113],"Childbirth experience","Induction of labor","Childbirth","Obstetrics","RECRUITING","2025-12-16",{"date":117,"type":54},"2025-12-23",{"date":119,"type":54},"2025-12-08",{"date":121,"type":22},"2026-06",{"name":123,"class":124},"Turku University Hospital","OTHER_GOV"]