[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"satisfaction-with-care\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:satisfaction-with-care":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,51,85],{"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":33,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":40,"lastUpdatePostDateStruct":41,"startDateStruct":44,"completionDateStruct":45,"leadSponsor":47,"locationsCount":50},"100615087","virtual-reality-as-a-method-for-pain-and-anxiety-control-during-first-trimester-procedural-abortion-100615087",false,"NCT07288047","Virtual Reality as a Method for Pain and Anxiety Control During First Trimester Procedural Abortion","Virtual Reality as an Adjunctive Agent for the Management of Pain and Anxiety During First Trimester Procedural Abortion: a Randomized Controlled Trial","CALM-VR","Inclusion Criteria:\n\n* Patients at Planned Parenthood of Western Pennsylvania who have decided to undergo and are eligible for a procedural abortion.\n* 18 years old or older\n* \\\u003C14 weeks gestation on day of abortion\n* Able to comprehend written English\n* Willing to comply with the study protocol\n* Willing and able to provide informed consent\n\nExclusion Criteria:\n\n* History of vertigo\n* History of epilepsy\n* Claustrophobia\n* Significant hearing or visual impairments (such as deafness or blindness)\n* Require hearing aids\n* Have an implanted medical device, such as cardiac pacemaker or defibrillator\n* Require misoprostol for cervical preparation\n* Prior unsuccessful attempt at abortion during this pregnancy","FEMALE","18 Years",{"count":20,"type":21},72,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this clinical trial is to learn whether use of a virtual reality (VR) headset showing a meditative nature video will help reduce pain and anxiety during a first trimester procedural abortion. Investigators will enroll 72 patients undergoing a first trimester procedural abortion with usual care to manage pain and anxiety compared to use of a VR headset in addition to usual care to see if use of the VR headset will decrease pain and anxiety and increase satisfaction with the procedure.",[27,28,29,30,31,32],"Abortion, First Trimester","Pain Management","Pain After Surgery","Satisfaction","Satisfaction With Care","Anxiety After Surgery",[34,35,36,37,38],"satisfaction","virtual reality","procedural abortion","pain control","anxiety control","RECRUITING","2026-05-01",{"date":42,"type":43},"2026-05-06","ACTUAL",{"date":40,"type":43},{"date":46,"type":21},"2026-10-30",{"name":48,"class":49},"Study Investigator","OTHER",2,{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":56,"acronym":57,"eligibilityCriteria":58,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":59,"targetDuration":4,"studyType":22,"phases":61,"briefSummary":62,"conditions":63,"keywords":67,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":78,"completionDateStruct":80,"leadSponsor":82,"locationsCount":84},"100581207","visual-biofeedback-through-transperineal-ultrasound-during-the-expulsive-phase-of-labour-to-improve-maternal-childbirth-satisfaction-100581207","NCT06847308","Visual Biofeedback Through Transperineal Ultrasound During the Expulsive Phase of Labour to Improve Maternal Childbirth Satisfaction","Visual Biofeedback (VB) Through Trans-Perineal Ultrasound (TPU) During the Active 2nd Stage of Labour to Improve Maternal Childbirth Satisfaction: a Randomised Controlled Trial","RCT:VB-TPU","INCLUSION criteria (all must be met):\n\n1. Voluntary written informed consent of the participant.\n2. Term (37-42w) singleton gestations.\n3. Vaginally nulliparous (no previous vaginal birth \\> 20 weeks of gestation).\n4. Fetus in cephalic presentation, without any major congenital or chromosomal anomalies.\n5. Admitted to the delivery unit in labour, regardless of the onset (spontaneous or induced).\n6. Epidural analgesia in situ.\n7. Non-pathological CTG at the time of recruitment (2015 FIGO classification).\n\nEXCLUSION criteria (if one or more is present):\n\n* Significant psychiatric comorbidity (psychiatric follow-up during pregnancy, or active (psycho-pharmacological) treatment).\n* History of severe PFDs\u002Fsurgery (or any other condition affecting pelvic floor function\u002Fanatomy, besides pregnancy and delivery).\n* Significant neurological disease e.g., spinal injury, multiple sclerosis, diabetic neuropathy, etc.\n* Significant connective tissue disorders (e.g., Ehlers-Danlos syndrome).\n* Severe active maternal (pregnancy-related) comorbidity: non-exhaustive e.g., severe hypertensive disorder, significant antepartum haemorrhage, sepsis, thromboembolism, severe pre-existing cardiac\u002Frespiratory\u002Fneurological disease, etc. Well-controlled comorbidities will not be considered exclusion criteria (non-exhaustive e.g., well-controlled (gestational) diabetes, hypertensive disorders of pregnancy, PROM without signs of intra-amniotic infection, etc.).\n* Linguistic barriers - not able to give written informed consent in Dutch.\n* Severe visual impairment (sufficient to the receipt\u002Fcomprehension of visual biofeedback).",{"count":60,"type":21},488,[24],"Childbirth is generally regarded as a positive life-changing experience. Up to 44% of women may however experience this as a traumatic event, with 3% suffering from post-traumatic stress disorder after childbirth. The aetiology of a traumatic childbirth experience is a complex interplay between pre-birth, intra-partum and postnatal factors. Feelings of loss of control, lack of interaction with the obstetric caregiver and lack of emotional or practical support during labour are important contributing factors. This trial aims to investigate the effect of providing Visual Biofeedback (VB) through Trans-Perineal Ultrasound (TPU) during the active 2nd stage of labour on maternal childbirth satisfaction. The hypothesis is that the intervention will improve patient-caregiver communication and enhance parturient women's sense of control and empowerment, ultimately improving the birth experience.",[64,65,31,66],"Labor Stage, Second","Labor and Delivery","Childbirth",[68,69,70,71,72,73],"2nd stage of labour","visual biofeedback","maternal childbirth satisfaction","obstetrics","ultrasound","trans-perineal ultrasound","NOT_YET_RECRUITING","2025-02-20",{"date":77,"type":43},"2025-02-26",{"date":79,"type":21},"2025-03-01",{"date":81,"type":21},"2028-02-28",{"name":83,"class":49},"Universitaire Ziekenhuizen KU Leuven",1,{"id":86,"slug":87,"hasResults":11,"nctId":88,"briefTitle":89,"officialTitle":90,"acronym":4,"eligibilityCriteria":91,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":92,"targetDuration":4,"studyType":22,"phases":94,"briefSummary":95,"conditions":96,"keywords":99,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":101,"lastUpdatePostDateStruct":102,"startDateStruct":104,"completionDateStruct":106,"leadSponsor":108,"locationsCount":84},"100566141","preoperative-animated-videos-in-patients-undergoing-operative-hysteroscopy-under-anesthesia-100566141","NCT06651320","Preoperative Animated Videos in Patients Undergoing Operative Hysteroscopy Under Anesthesia","Effect of Preoperative Patient Education Via Animated Videos in Patients Undergoing Operative Hysteroscopy Under Anesthesia","Inclusion Criteria:\n\n* Adult patients (above 18 and older),\n* Patients undergoing operative hysteroscopy under anesthesia in our OR due to uterine findings previously diagnosed during diagnostic hysteroscopy.\n\nExclusion Criteria:\n\n* Patients who are not able to watch the audiovisual video\n* Patients who cannot sign a consent form.",{"count":93,"type":21},100,[24],"The goal of this clinical trial is to assess if the use of an audiovisual animated video, describing the gynecological procedure (hysteroscopy) the patient is about to undergo, will help to reduce the patient's level of anxiety, affect her anesthesia parameters and increase their overall satisfaction from the procedure.\n\nOur hypothesis is that patient who will watch the video (intervention group) will experience less anxiety, will have lower heart rate and lower blood pressure during the procedure, and have overall more satisfaction with the procedure, compared to patients who will not watch the preoperative video (control group).\n\nPatients will be asked to rate their anxiety level before the procedure and their satisfaction afterwards.",[97,98],"Anxiety","Satisfaction with Care",[100],"hysteroscopy","2024-10-18",{"date":103,"type":43},"2024-10-21",{"date":105,"type":21},"2024-11-01",{"date":107,"type":21},"2026-02-28",{"name":109,"class":110},"Assaf-Harofeh Medical Center","OTHER_GOV"]