[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"expectations\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:expectations":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,49,77],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":31,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100591412","neural-mechanisms-of-interpersonal-expectations-on-negative-affect-100591412",false,"NCT06980090","Neural Mechanisms of Interpersonal Expectations on Negative Affect","Inclusion Criteria:\n\n'Doctors' are recruited from medical students at the Geisel School of Medicine and resident physicians at Dartmouth Hitchcock Medical Center (DHMC).\n\nExclusion Criteria:\n\n* No self-reported current or history of depression, bipolar disorder, or other psychiatric diagnosis\n* No self-reported current seizure disorder (i.e., seizure within past 10 years), or history of stroke or other major neurological diagnosis that can cause cognitive impairment\n* No self-reported current chronic pain, or acute pain within three months of the study period\n* No current migraine disorder (i.e., 15 headache days or more in 1 month)\n* No use of central nervous system-effective medication or other medication for neurological\u002Fpsychiatric treatment\n* No self-reported substance abuse within the last six months\n* No contraindication to MRI or tTIS (e.g., pregnancy, claustrophobia, pacemakers, ear\u002Fcochlear implants, shrapnel injuries, clips, or other ferromagnetic\u002Felectrical objects\u002Fdevices, diagnosed brain abnormality such as tumor, or skin lesions on the scalp.)\n* No contraindications for induced pain (e.g., no heart disease, high blood pressure, heart surgery, heart problems of any kind, severe asthma, respiratory problems of any kind, fibromyalgia, Raynaud's Syndrome or Disease, chronic pain, diabetes)\n* Participants must be capable of performing experimental tasks (e.g., are able to read), are fluent or native speakers of English\n* Participants must be able to tolerate the maximum level of thermal pain stimuli (for thermal stimuli)",true,"ALL","18 Years","55 Years",{"count":20,"type":21},196,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this clinical trial is to learn whether non-invasive brain stimulation, called transcranial temporal interference stimulation (tTIS), can reduce negative affect, and how expectations shaped by care providers influence these effects.\n\nThe main questions this study aims to answer are: (1)Does active tTIS reduce negative affect more effectively than sham (inactive) tTIS? (2)Do positive treatment expectations enhance the effects compared to negative expectations?\n\nParticipants will: (1) Receive either active or sham tTIS. (2) Be provided with positive or negative messaging regarding treatment effectiveness. (3) Interact with care providers and complete assessments measuring negative affect and physiological responses.",[27,28,29,30],"Negative Affectivity","Non-invasive Brain Stimulation","Placebo Effect","Expectations",[32,33,34,35],"Transcranial temporal interference stimulation","Pain","Fear","Cognitive effort","RECRUITING","2026-06-08",{"date":39,"type":40},"2026-06-11","ACTUAL",{"date":42,"type":40},"2025-09-01",{"date":44,"type":21},"2028-03-03",{"name":46,"class":47},"Trustees of Dartmouth College","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":55,"minAge":17,"maxAge":4,"enrollmentInfo":56,"targetDuration":4,"studyType":58,"phases":4,"briefSummary":59,"conditions":60,"keywords":63,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":48},"100615441","maternal-expectations-on-labor-analgesia-and-risk-of-postpartum-depression-an-observational-study-100615441","NCT07292649","Maternal Expectations on Labor Analgesia and Risk of Postpartum Depression: An Observational Study","Inclusion Criteria:\n\n* Signed informed consent\n* Planned vaginal delivery (spontaneous or induced)\n* Pregnancy\n* Age \\> 18 years\n\nExclusion Criteria:\n\n* Allergy to local anesthetics\n* Language barrier\n* Contraindications to labor analgesia\n* Delivery by Cesarean section\n* Known history of psychiatric disorders (including major depression)","FEMALE",{"count":57,"type":21},3640,"OBSERVATIONAL","Postpartum Depression (PPD) is defined as the development of depression at any time during the first year after childbirth¹. Its prevalence ranges from 15% to 20%. It can manifest with symptoms such as depressed mood, loss of interest and energy, insomnia, anxiety, and may even lead to suicidal ideation. The consequences are numerous, both physical and psychological, with long-term repercussions on the mother-infant bond, family dysfunction, and the development of emotional and cognitive disorders in children. The etiology of PPD is multifactorial, but numerous recent studies have focused on the role of labor pain and its management with labor analgesia techniques. The aim of the present study is therefore to assess whether there is a difference in the incidence of PPD between parturients whose expectations regarding labor analgesia were met ('expectations met' group) versus those whose expectations were unmet.",[61,62,30],"Postpartum Depression (PPD)","Labor Analgesia",[64,65,66,67],"postpartum depression","labor analgesia","epidural","expectations","2026-04-28",{"date":70,"type":40},"2026-04-29",{"date":72,"type":40},"2026-01-08",{"date":74,"type":21},"2029-06",{"name":76,"class":47},"University of Padova",{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":4,"eligibilityCriteria":83,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":84,"enrollmentInfo":85,"targetDuration":4,"studyType":58,"phases":4,"briefSummary":87,"conditions":88,"keywords":91,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":94,"lastUpdatePostDateStruct":95,"startDateStruct":97,"completionDateStruct":99,"leadSponsor":101,"locationsCount":48},"100522313","patients-expectations-before-spinal-surgery-100522313","NCT06080997","Patients' Expectations Before Spinal Surgery","Patients' Expectations Before, and Their Experiences After Spinal Surgery, Regarding Pain, Rehabilitation and Quality of Life","Inclusion Criteria:\n\nPatients undergoing elective spinal surgery. Patients able to read and understand Danish.\n\nExclusion Criteria:\n\nPatients with cognitive deficits, such as dementia. Patients with alcohol and drug dependence.","100 Years",{"count":86,"type":21},300,"With this study the investigators want to perform a prospective observational cohort study at Zealand University Hospital, Koege, Denmark.\n\nThe purpose of this study is twofold:\n\n1. to investigate how expectations predict patients' pain, rehabilitation and quality of life after spinal surgery.\n2. to explore the patients' expectations before, and their experiences after, spinal surgery regarding pain, rehabilitation and quality of life.",[30,89,33,90],"Surgery","Quality of Life",[30,33,92,93],"Rehabilitation","Quality of life","2025-02-17",{"date":96,"type":40},"2025-02-18",{"date":98,"type":40},"2024-01-01",{"date":100,"type":21},"2026-11-30",{"name":102,"class":47},"Zealand University Hospital"]