[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"stress-disorder-post-traumatic\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:stress-disorder-post-traumatic":68},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,53,85,106,147,173],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":30,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100637380","psychological-stress-and-support-needs-of-volunteer-first-responders-after-smartphone-based-cardiac-arrest-alerts-100637380",false,"NCT07607808","Psychological Stress and Support Needs of Volunteer First Responders After Smartphone-based Cardiac Arrest Alerts","Burden and Resilience After Volunteer Engagement in Out-of-Hospital Cardiac Arrest","BRAVE","Inclusion Criteria:\n\n* Volunteer first responders alerted through the \"Corhelper\" smartphone application\n* Sufficient German language skills to understand the study information and to participate in the debriefing conversation and questionnaires\n* Written informed consent for study participation\n* Actual arrival at the scene with direct exposure to the resuscitation situation (e.g., visual contact with the patient or active participation in resuscitation measures)\n\nExclusion Criteria:\n\n* Age below 18 years\n* Anticipated severe post-traumatic stress symptoms during the course of the study, in order to avoid possible retraumatization\n* Already enrolled in the study following a different Corhelper alert event",true,"ALL","18 Years",{"count":21,"type":22},75,"ESTIMATED","INTERVENTIONAL",[25],"NA","Out-of-hospital cardiac arrest is a serious emergency. In many areas, trained volunteers are alerted by a smartphone app to help before emergency services arrive. While this can save lives, these situations can also be emotionally stressful for the volunteers. This study looks at how these experiences affect volunteer first responders and how they cope with them. It also examines whether a structured follow-up conversation after an event can help reduce stress.\n\nPeople who respond to a cardiac arrest alert can take part in the study. Participants will answer short questionnaires about their well-being about four weeks and ten weeks after the event. Some participants will also be offered a guided conversation to talk about their experience, while others will not.\n\nThe researchers will compare both groups to see if the conversation helps reduce stress over time. The study will also explore which factors may increase or reduce emotional burden.\n\nParticipants can stop answering the questionnaires at any time. If signs of increased stress are identified, support options are available. With consent, the study team may contact participants to offer further information and help connect them with support services.\n\nThe results of this study may help improve support for volunteer first responders in the future.",[28,29],"Mental Health","Stress Disorder, Post Traumatic",[31,32,33,28,34,35,36,37,38,39],"First Responders","Cardiac Arrest","Psychological Stress","Debriefing","Volunteer Responders","Out-of-Hospital Cardiac Arrest","Resilience","Smartphone-based alert system","Mobile App Alert System","NOT_YET_RECRUITING","2026-05-21",{"date":43,"type":44},"2026-05-26","ACTUAL",{"date":46,"type":22},"2026-05-01",{"date":48,"type":22},"2027-11-01",{"name":50,"class":51},"University Hospital, Aachen","OTHER",1,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":4,"eligibilityCriteria":59,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":60,"targetDuration":4,"studyType":23,"phases":62,"briefSummary":63,"conditions":64,"keywords":69,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":78,"completionDateStruct":80,"leadSponsor":82,"locationsCount":52},"100477021","acceptability-and-feasibility-of-work-oriented-social-cognitive-skills-training-for-veterans-with-serious-mental-illness-100477021","NCT05491538","Acceptability and Feasibility of Work-Oriented Social-Cognitive Skills Training for Veterans With Serious Mental Illness","Acceptability and Feasibility of Work-Oriented, Veteran-Centric, Social-Cognitive Skills Training","Inclusion Criteria:\n\n* Veterans who are outpatients and enrolled to receive supported services at the Minneapolis VA Health Care System.\n* Veterans are eligible for this program if they are receiving services from a mental health team at the Minneapolis VA Health Care System, are motivated to pursue employment, and are seeking employment within 30 miles of the medical center.\n* Veterans will be eligible for the study if they have a DSM-5 diagnosis of Schizophrenia, Schizoaffective Disorder, Bipolar I Disorder, Bipolar II Disorder, Recurrent Major Depressive Disorder, or PTSD.\n\nExclusion Criteria:\n\nStudy exclusion criteria are:\n\n* presence of a moderate or severe traumatic brain injury\n* presence of a cognitively compromising neurological disease\n* understanding of English that is not sufficient for comprehension of testing procedures\n* premorbid IQ less than 70\n* behavior that prevents participation in a group intervention\n* hearing or visual impairment that prevents completion of intervention and testing procedures\n* clinical instability, defined as active suicidal ideation or hospitalization in the previous 4 weeks\n* current diagnosis of alcohol or substance use disorder, severe\n* current participation in another mental health intervention study\n* inability to commit to 7-9 months of study participation due to a planned move or unstable housing\n* inability to provide informed consent\n* presence of a guardian of person",{"count":61,"type":22},20,[25],"Many individuals with serious mental illness have difficulty accurately interpreting interpersonal cues and effectively engaging in social exchanges. Difficulties related to the interpersonal aspects of work can lead to isolation, poor productivity, and job loss. The goals of this study are to: 1) adapt an evidence-based social cognitive skills intervention for work settings and use with Veterans, 2) examine the acceptability of the work focused skills training intervention, 3) assess the feasibility of combining the social cognitive skills training program with supported employment, and 4) examine change on functional outcomes.\n\nThe current study will use feedback from veteran and employment specialist stakeholders to adapt an evidence-based social cognitive skills training program, Social Cognition and Interaction Training (SCIT). The intervention will be modified to tailor it to work relationships and to address any unique relationship concerns among Veterans that are identified by stakeholders. SCIT-Work Edition (SCIT-WE) will add: 1) education about work-related social norms; 2) examples of work-related social interactions that require perspective taking and problem- solving; 3) individual sessions with the study therapist to enhance learning and relevance to each participant's goals; 4) structured interactions with the participant's employment specialist to practice skills outside of group; and 5) skill application sessions with the participant's employment specialist that prompt use of skills after training is completed.\n\nSCIT-WE will be developed and piloted in an open trial with 20 Veterans enrolled in the supported employment program at the Minneapolis VA who have a qualifying serious mental illness diagnosis. SCIT-WE will be offered for 2 hours weekly over 13 weeks, when most participants are in the job development and job search phases of supported employment. While participating in the group skills training, participants will have weekly, individual homework review sessions with the group facilitator to promote understanding of the skills and to discuss relevance of the skills to personal goals. Participants also will practice skills weekly with their employment specialist for 10-15 minutes to promote use of skills outside of group sessions. In the 3-months following skills training completion, participants will complete 10 15-minute skills review sessions with their employment specialist to encourage continued skill application in a work setting.\n\nParticipants will complete assessments at baseline, before receiving the intervention; 3-months post-enrollment, after participating in a weekly skills training group; and 6-months post-enrollment, after receiving 10 additional individual skills review sessions with their employment specialist. Accessibility will be measured with rate of treatment uptake, rate of treatment completion, and participant attitudes toward the intervention. Feasibility of the intervention will be assessed by examining retention in supported employment and the study at 3- and 6-months post-enrollment. Impact of the intervention will be examined with measures of quality of life, social adjustment, self-efficacy, and work relationship quality. It is hypothesized that the intervention will be acceptable to Veterans. The investigators predict a 50% treatment uptake rate, a 70% intervention completion rate, and positive ratings on measures of satisfaction, interest, and value. The investigators hypothesize that it will be feasible to complete this intervention in combination with supported employment activities. The investigators predict that retention in both skills training and supported employment will be 75% at 3-months post-enrollment and 60% 6-months post enrollment. The investigators hypothesize that positive change will be seen at 3-months post-enrollment and sustained at 6-months post-enrollment on measures of quality of life and social adjustment. The investigators predicted that self-efficacy regarding return to work will be improved at 3-months post-enrollment. The investigators predict that Veterans will report being productive and having positive work relationships 6-months post-enrollment.\n\nThe findings will inform the development of a novel intervention targeting the social and functional impairments associated with serious mental illness. The knowledge gained from this study will guide the development of the next generation of interventions. Given that employment is a critical part of recovery, advancement in therapeutic interventions that support Veterans in this process will be of significance.",[65,66,67,68],"Schizophrenia","Bipolar Disorder","Depressive Disorder, Major","Stress Disorder, Post-Traumatic",[70,71,72,73],"social cognition","employment, supported","psychotherapy, group","mental health","RECRUITING","2025-10-08",{"date":77,"type":44},"2025-10-09",{"date":79,"type":44},"2022-12-01",{"date":81,"type":22},"2027-11-30",{"name":83,"class":84},"VA Office of Research and Development","FED",{"id":86,"slug":87,"hasResults":11,"nctId":88,"briefTitle":89,"officialTitle":89,"acronym":90,"eligibilityCriteria":91,"healthyVolunteers":11,"sex":18,"minAge":92,"maxAge":19,"enrollmentInfo":93,"targetDuration":4,"studyType":23,"phases":95,"briefSummary":96,"conditions":97,"keywords":4,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":98,"lastUpdatePostDateStruct":99,"startDateStruct":101,"completionDateStruct":103,"leadSponsor":104,"locationsCount":4},"100589895","development-of-follow-up-nursing-consultations-for-children-at-risk-of-post-resuscitation-syndrome-100589895","NCT06960356","Development of Follow-up Nursing Consultations for Children at Risk of Post-resuscitation Syndrome","SURVIPED","Inclusion Criteria:\n\n* Patients aged between 1 and 17.5 years at inclusion\n* Having stayed in a paediatric intensive care unit in one of the 2 participating centers: Lyon or Grenoble\n* Requiring mechanical ventilation (invasive or non-invasive) for more than 24 hours\n\nExclusion Criteria:\n\n* Patients already under the care of a psychologist or psychiatrist\n* patients who died during their stay in intensive care\n* Patients who died between discharge and 3 months\n* Patients suspected of abuse\n* Patient and\u002For parent refusal to participate\n* No social security affiliation\n* Patients \u002F parents who do not speak French","1 Year",{"count":94,"type":22},115,[25],"The investigator hypothesize that, during an IPDE consultation 3 months after discharge from critical care, the investigator will identify PTSD in approximately one-third of children, and show an association between this syndrome and quality of life in children admitted to pediatric intensive care.",[29],"2025-04-28",{"date":100,"type":44},"2025-05-07",{"date":102,"type":22},"2025-12",{"date":102,"type":22},{"name":105,"class":51},"University Hospital, Grenoble",{"id":107,"slug":108,"hasResults":11,"nctId":109,"briefTitle":110,"officialTitle":111,"acronym":112,"eligibilityCriteria":113,"healthyVolunteers":11,"sex":18,"minAge":114,"maxAge":4,"enrollmentInfo":115,"targetDuration":4,"studyType":117,"phases":4,"briefSummary":118,"conditions":119,"keywords":125,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":137,"lastUpdatePostDateStruct":138,"startDateStruct":140,"completionDateStruct":142,"leadSponsor":144,"locationsCount":146},"100584246","parental-well-being-after-childbirth-in-switzerland-100584246","NCT06886841","Parental Well-being After Childbirth in Switzerland","Stress Of Co-parents Related to A Traumatic Experience of Birth Across Switzerland","SOCRATES","Inclusion criteria:\n\n* Women who give birth in a participating maternity unit or birth center during the study period.\n* Partner of a participating women: the partner must be designated by the mother, live with her at the time of birth, and only one partner can be included per mother.\n* Gestational age at birth: ≥22+0 weeks and\u002For birthweight ≥500 grams\n* Age: Participants must be 14 years or older.\n* Language Proficiency: Participants must have sufficient proficiency in one of Switzerland's main official languages (German, French, Italian) or English to ensure accurate communication and comprehension of study materials.\n\nExclusion Criteria:\n\n* Refusal to participate\n* Inability to provide informed consent","14 Years",{"count":116,"type":22},4200,"OBSERVATIONAL","Improving maternal and child health is a global priority, with increasing emphasis on ensuring women and their families not only survive but also thrive after childbirth. While high-income countries like Switzerland provide strong antenatal and intrapartum care, the quality of postnatal care often lags behind, despite the critical physical, mental, and social needs of the postpartum period. Studies indicate high rates of mental distress, physical pain, and sexual discomfort among mothers, alongside a lack of research on the well-being of co-parents.\n\nThe main question this cohort study aims to answer is: how do the health and well-being of mothers and co-parents evolve during the first year after childbirth? Participants will complete four online questionnaires: the first within the first few days after birth, followed by additional assessments at 2, 6, and 12 months postpartum.\n\nThis comprehensive approach seeks to inform policy and improve evidence-based postnatal care practices, benefiting approximately 80,000 families annually in Switzerland.",[28,120,121,122,123,124,29],"Physical Health","Postpartum","Parents","Quality of Life","Quality of Care",[126,73,127,128,129,130,131,132,133,134,135,136],"childbirth-related post-traumatic stress disorder","postpartum","parental wellbeing","physical health","sexual health","social support","quality of life","quality of care","postpartum depression","mothers","coparents","2025-03-19",{"date":139,"type":44},"2025-03-20",{"date":141,"type":44},"2025-03-17",{"date":143,"type":22},"2026-06",{"name":145,"class":51},"Laurent Gaucher",2,{"id":148,"slug":149,"hasResults":11,"nctId":150,"briefTitle":151,"officialTitle":152,"acronym":4,"eligibilityCriteria":153,"healthyVolunteers":11,"sex":18,"minAge":154,"maxAge":155,"enrollmentInfo":156,"targetDuration":4,"studyType":23,"phases":158,"briefSummary":159,"conditions":160,"keywords":161,"overallStatus":74,"whyStopped":4,"lastUpdateSubmitDate":141,"lastUpdatePostDateStruct":164,"startDateStruct":166,"completionDateStruct":168,"leadSponsor":170,"locationsCount":146},"100584644","eeg-based-personalized-transcranial-magnetic-stimulation-etms-to-treat-post-traumatic-stress-disorder-100584644","NCT06892028","EEG-based Personalized Transcranial Magnetic Stimulation (eTMS) to Treat Post-Traumatic Stress Disorder","A Randomized Controlled Trial of Electroencephalogram (EEG) Personalized Transcranial Magnetic Stimulation (eTMS) for Post-Traumatic Stress Disorder","Inclusion Criteria:\n\n* Willing and able to consent to participate in the study via signed Informed Consent\n* Age 22 - 65 years\n* Diagnosis of PTSD according to DSM-5 criteria via the Clinician-Administered PTSD Scale (CAPS).\n* Onset of symptoms meeting the DSM-5 criteria for PTSD symptoms persisting for a minimum of 6 months prior to the Screening Visit\n* Veterans Administration PCL-5 cut point score of 31 or above\n* Positive identification as either a Veteran, or First Responder (e.g., emergency medical service provider, firefighter, or any other emergency response personnel)\n\nExclusion Criteria:\n\n* Uncontrolled medical, psychological or neurological condition\n* Pregnant, or female unwilling to use effective birth control during the course of the trial\n* Metal objects in the head\n* Past exposure to metal fragments, permanent piercings, and\u002For other possible metal sources in the head and neck\n* Current participation in any interventional research protocol\n* History of any type of Electroconvulsive Therapy (ECT) or repetitive Transcranial Magnetic Stimulation (rTMS)\n* History of stroke or intracranial lesion or increased intracranial pressure\n* History of epilepsy of seizure\n* Family history of epilepsy or seizure in 1st degree relative\n* An elevated risk of suicide or violence to others","22 Years","65 Years",{"count":157,"type":22},110,[25],"This is a randomized, sham controlled study of the Electroencephalogram (EEG) based Transcranial Magnetic Stimulation (eTMS) treatment for Post-Traumatic Stress Disorder (PTSD). The recruitment goal is 110 participants who are United States Military veterans or first responders (e.g., firefighters, police, paramedics, etc.). The Study includes an EEG recording in order to determine the optimal treatment parameters for the eTMS system, followed by 15 in-office visits that take place over 21-28 total days. Two eTMS treatment sessions are administered during each office visit.",[29],[162,163,31],"PTSD","Veterans",{"date":165,"type":44},"2025-03-24",{"date":167,"type":44},"2025-02-12",{"date":169,"type":22},"2026-01-31",{"name":171,"class":172},"Wave Neuroscience","INDUSTRY",{"id":174,"slug":175,"hasResults":11,"nctId":176,"briefTitle":177,"officialTitle":177,"acronym":178,"eligibilityCriteria":179,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":180,"targetDuration":4,"studyType":117,"phases":4,"briefSummary":182,"conditions":183,"keywords":185,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":190,"lastUpdatePostDateStruct":191,"startDateStruct":193,"completionDateStruct":195,"leadSponsor":197,"locationsCount":4},"100574155","evaluation-of-the-effect-of-an-emergency-department-information-video-on-the-risk-of-post-traumatic-stress-disorder-30-days-after-an-emergency-visit-100574155","NCT06755606","Evaluation of the Effect of an Emergency Department Information Video on the Risk of Post-Traumatic Stress Disorder 30 Days After an Emergency Visit.","VISU","Inclusion Criteria:\n\n* Age ≥ 18 years\n* Triage level 1, 2, 3 by the triage nurse (according to CIMU, FRENCH or other scale used locally)\n* Non-opposition to participation in the study after information and delivery of the information note\n* Possibility of 30-day follow-up (self-questionnaire to be completed by e-mail)\n* Patient with cognitive or sensory capacity to view and understand information videos\n\nExclusion Criteria :\n\n* Inability to consent (neurological disorder, coma, acute intoxication, cognitive impairment)\n* Patient does not have a good understanding of the French language.\n* Estimated life expectancy less than 6 months\n* Participation in other clinical intervention research",{"count":181,"type":22},750,"Post-traumatic stress disorder (PTSD) is a psychological disorder characterized by the re-experiencing of distressing symptoms, avoidance of traumatic memories and physiological hyperarousal in people who have been exposed to a traumatic event. The consequences of PTSD are manifold: financial, quality of life, absenteeism, morbidity, and mortality.\n\nAn emergency department visit can be a traumatic event and associated with anxiety.\n\nStudies have explored the prevalence and factors associated with the occurrence of PTSD among a selected population of patients admitted to the emergency department for either cardiological or traumatological reasons. The prevalence of PTSD at 1 month varied among these populations, from 12% to 25%.\n\nSeveral factors have been described that could be independently associated with an increased risk of developing PTSD: factors linked to the patient himself (basal state and severity of acute pathology) or to the patient pathway (care structure, care modalities, waiting time). Given the serious medical, psycho-social and economic consequences of PTSD, it is important to identify the risk factors that can be controlled during a patient's stay in the emergency department.\n\nIn 2025, a general information procedure for patients and next of kin will be deployed in three emergency departments.\n\nThe aim of this procedure is to improve the quality of the information provided to emergency patients, thereby enhancing the experience of patients and those accompanying them. It will consist of video support delivering standardized information to patients from the moment they arrive in the emergency department until they are discharged. These videos will describe the patient's journey through the emergency department.\n\nThe aim of this study is to evaluate the effect of this information procedure on the risk of developing PTSD.",[184,29],"PTSD - Post Traumatic Stress Disorder",[186,187,188,189],"stress disorders","interventions","communication","emergency medicine","2024-12-24",{"date":192,"type":44},"2025-01-01",{"date":194,"type":22},"2025-02",{"date":196,"type":22},"2026-01",{"name":198,"class":51},"Assistance Publique - Hôpitaux de Paris"]