[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"psychiatric-hospitalization\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:psychiatric-hospitalization":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,7,0,[8,49,80,104,127,153,188],{"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":30,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100641660","the-green-room-virtual-nature-for-mental-well-being-in-the-acute-psychiatry-ward-100641660",false,"NCT07655063","The Green Room: Virtual Nature for Mental Well-being in the Acute Psychiatry Ward","The Green Room: A Mixed-Methods Randomized Controlled Trial Evaluating Virtual Reality-Based Nature Exposure in an Acute Psychiatry Ward","GREEN ROOM","Inclusion Criteria:\n\nAdults aged 18 to 65 years. Admitted to the Acute Psychiatry Ward (regardless of voluntary or involuntary legal status).\n\nSufficient cognitive and clinical stability to provide informed consent and engage with the VR equipment, as determined by the clinical team.\n\nAbility to communicate effectively in Spanish.\n\nExclusion Criteria:\n\nHistory of photosensitive epilepsy or severe seizure disorders. Presence of active facial injuries, infections, or skin conditions that prevent the hygienic use of the VR headset.\n\nPre-existing severe vertigo, balance disorders, or high susceptibility to motion sickness.\n\nAcute clinical state involving high risk of agitation or behavioral dysregulation that could compromise participant or equipment safety.\n\nSevere visual or hearing impairments that cannot be corrected and would hinder the VR experience.\n\nPatients who have previously participated in the study during a prior admission are not eligible for re-enrolment.","ALL","18 Years",{"count":20,"type":21},120,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study evaluates the feasibility, acceptability and clinical impact of a virtual reality (VR)- based nature intervention in an acute psychiatric inpatient unit. Participants are randomly assigned to recieve VR nature sessions (using Nature Treks VR on Meta Quest 3) in addition to standard care, or standard care alone. The primary outcome is change in percieved stress (PSS-19) from admission to discharge. The study uses a mixed-methods design combining randomized controlled trial with a qualitative phase.",[27,28,29],"Mental Disorders","Psychiatric Hospitalization","Stress (Psychology)",[31,32,33,34,35],"virtual reality","nature exposure","Acute psychiatry","Inpatient","Mental health","NOT_YET_RECRUITING","2026-06-12",{"date":39,"type":40},"2026-06-17","ACTUAL",{"date":42,"type":21},"2026-06-10",{"date":44,"type":21},"2026-12",{"name":46,"class":47},"Hospital Clinic of Barcelona","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":53,"acronym":54,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":17,"minAge":56,"maxAge":57,"enrollmentInfo":58,"targetDuration":4,"studyType":22,"phases":59,"briefSummary":60,"conditions":61,"keywords":63,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":4},"100626048","trauma-exposure-and-suicidal-behaviors-in-adolescents-aged-11-17-hospitalized-in-child-and-adolescent-psychiatry-100626048","NCT07430566","Trauma Exposure and Suicidal Behaviors in Adolescents Aged 11-17 Hospitalized in Child and Adolescent Psychiatry","ATTAQ","Common Inclusion Criteria:\n\n* Age between 11 and 17 years inclusive\n* Admitted for full-time psychiatric hospitalization\n* Obtaining consent from at least one of the adolescent's legal representatives and the adolescent's personal assent\n\nInclusion Criteria - \"Suicidal Group\":\n\n\\- Reason for admission: suicidal behavior (suicide attempt)\n\nInclusion Criteria - \"Non-Suicidal Group\":\n\n\\- Reason for admission: other psychiatric causes (including suicidal thoughts without suicide attempt and non-suicidal self-injurious behavior)\n\nCommon Exclusion Criteria:\n\n\\- Neither parent available to participate in the intervention\n\nExclusion Criterion - \"Non-Suicidal Group\":\n\n\\- History of suicidal behavior prior to the current hospitalization","11 Years","17 Years",{"count":20,"type":21},[24],"It is a comparative monocentric study with longitudinal follow-up at 6 months in adolescents aged between 11 years and 17 years inclusive admitted to complete hospitalization either for suicidal behaviors or for other psychiatric causes. The objective is to explore the experiences of hospitalized adolescents regarding hospitalization, as well as their perceptions of the factors involved in their remission and their experience of the traumatic event(s) if they have been exposed.",[62,28],"Suicidal Ideation and Behavior",[64,65,66,67,68,69,70],"suicide","adolescent","post-traumatic stress disorder","neurodevelopmental disorders","résilience","biomarqueurs","comportements suicidaires","2026-02-18",{"date":73,"type":40},"2026-02-24",{"date":75,"type":21},"2026-03",{"date":77,"type":21},"2027-09",{"name":79,"class":47},"University Hospital, Montpellier",{"id":81,"slug":82,"hasResults":11,"nctId":83,"briefTitle":84,"officialTitle":85,"acronym":4,"eligibilityCriteria":86,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":87,"enrollmentInfo":88,"targetDuration":4,"studyType":90,"phases":4,"briefSummary":91,"conditions":92,"keywords":93,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":98,"completionDateStruct":100,"leadSponsor":102,"locationsCount":4},"100600448","optimal-acute-adult-psychiatric-in-patient-care-in-hong-kong-100600448","NCT07097623","Optimal Acute Adult Psychiatric In-patient Care in Hong Kong","Optimal Acute Adult Psychiatric In-patient Care in Hong Kong: a Mixed-method Study","I. Psychiatric nurses\n\nInclusion Criteria:\n\n* working in the Hospital Authority on a full-time basis,\n* with ≥ 10 years post-registration experience, and\n* able to read and understand English\n\nExclusion Criteria:\n\n* without working experience in adult psychiatry\n\nII. Service users\n\nInclusion Criteria:\n\n* aged 18-64\n* able to read and communicate in Cantonese, and\n* being discharged within a year\n\nExclusion Criteria:\n\n* having a co-morbidity of learning disability, organic\u002Fneurological conditions, or substance misuse disorder\n\nIII. Family caregivers\n\nInclusion Criteria:\n\n* aged 18 or above, and\n* able to read and communicate in Cantonese\n\nExclusion Criteria:\n\n* having active psychiatric conditions","64 Years",{"count":89,"type":21},160,"OBSERVATIONAL","This mixed-method study aims to evaluate the optimal number of hospital beds and quality of acute adult psychiatric inpatient care in Hong Kong using online Delphi surveys for psychiatric nurses and individual interviews for service users with mental health conditions and family caregivers. The main question it aims to answer is:\n\nWhat are the consensus points for quality acute adult psychiatric inpatient care in Hong Kong from psychiatric nurses, service users, and caregivers?\n\nPsychiatric nurses will respond to three rounds of online Delphi surveys, while service users and caregivers will attend individual semi-structured interviews.",[28],[94],"adult psychiatric inpatient care, optimal bed number","2025-07-30",{"date":97,"type":40},"2025-07-31",{"date":99,"type":21},"2025-08-04",{"date":101,"type":21},"2026-08-31",{"name":103,"class":47},"The Hong Kong Polytechnic University",{"id":105,"slug":106,"hasResults":11,"nctId":107,"briefTitle":108,"officialTitle":109,"acronym":110,"eligibilityCriteria":111,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":112,"enrollmentInfo":113,"targetDuration":4,"studyType":22,"phases":115,"briefSummary":116,"conditions":117,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":118,"lastUpdatePostDateStruct":119,"startDateStruct":121,"completionDateStruct":123,"leadSponsor":125,"locationsCount":4},"100585598","effectiveness-of-a-temporal-and-sound-space-in-the-paramedical-management-of-crisis-100585598","NCT06904443","Effectiveness of a Temporal and Sound Space in the Paramedical Management of \"Crisis\"","Effectiveness of a Temporal and Sound Space in the Paramedical Management of \"Crisis\" States of Patients Hospitalized in Psychiatry: Quasi-experimental Study With a Single Arm","PsySon","Inclusion Criteria:\n\n* Be between 18 and 65 years old.\n* Diagnosis of bipolar disorder or schizophrenia DSM5.\n* Be hospitalized full-time in an acute psychiatric ward with or without compulsory care (SPL, SPDT, SPDTU, SPPI, SPDRE).\n* Prior written informed consent of the patient or his legal representative.\n* Benefit from a social protection scheme.\n\nExclusion Criteria:\n\n* Have a severe cognitive disorder assessed during the clinical interview, making it impossible to focus one's attention.\n* Hearing-impaired subjects who do not wear hearing aids.","65 Years",{"count":114,"type":21},172,[24],"This project could potentially lead to better crisis management in psychiatry, using music as a mediator. The integration of a well-designed sound device could help caregivers build trust with patients, alleviate anxiety, and foster an environment conducive to healing. In addition, it would offer a less invasive and more patient-centered alternative, creating an atmosphere that facilitates communication and calming.",[28],"2025-03-24",{"date":120,"type":40},"2025-04-01",{"date":122,"type":21},"2025-07-01",{"date":124,"type":21},"2027-09-01",{"name":126,"class":47},"Centre Hospitalier St Anne",{"id":128,"slug":129,"hasResults":11,"nctId":130,"briefTitle":131,"officialTitle":132,"acronym":133,"eligibilityCriteria":134,"healthyVolunteers":11,"sex":17,"minAge":135,"maxAge":18,"enrollmentInfo":136,"targetDuration":4,"studyType":22,"phases":138,"briefSummary":139,"conditions":140,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":144,"lastUpdatePostDateStruct":145,"startDateStruct":147,"completionDateStruct":149,"leadSponsor":151,"locationsCount":48},"100566909","effects-of-benson-relaxation-exercise-on-anxiety-level-and-sleep-quality-in-adolescents-100566909","NCT06661304","Effects of Benson Relaxation Exercise on Anxiety Level and Sleep Quality in Adolescents","The Effect of Benson Relaxation Exercise on Anxiety Level and Sleep Quality in Adolescents Receiving Inpatient Treatment in a Psychiatric Clinic: A Randomized Controlled Trial","BRE","Inclusion Criteria:\n\n* Being treated in the child and adolescent clinic at the hospital where the study was conducted\n* Being between the ages of 14-18\n* Not diagnosed with psychotic disorder or schizophrenia\n* Scoring between 20 and 59 on the STAI I-II scale\n* Scoring 5 and above on the PSQI scale\n* Being willing to participate in the study\n* Parents giving verbal consent for participation in the study and signing the written voluntary consent form\n\nExclusion Criteria:\n\n* Not receiving treatment in the child-adolescent clinic at the hospital where the study was conducted\n* Not being between the ages of 14-18\n* Being diagnosed with psychotic disorder and schizophrenia\n* Not receiving a score between 20-59 on the STAI I-II scale\n* Receiving a score below 5 on the PSQI scale\n* Not being willing to participate in the study\n* The parent not giving verbal consent for participation in the study and not signing the written voluntary consent form","14 Years",{"count":137,"type":21},60,[24],"Purpose: The purpose of this study is to examine the effects of Benson relaxation exercise applied to children and adolescents receiving inpatient treatment in a psychiatric clinic on anxiety levels and sleep quality.\n\nDesign: The study is a randomized controlled trial with a pretest-posttest control group.\n\nMethod: The study will be conducted in a private psychiatric hospital in Turkey between October 2024 and June 2025. When hospital records were examined, it was determined that 100 patients received inpatient treatment in the last year. Therefore, the universe of the study consisted of 100 patients. The effect of some instructions in the Benson relaxation exercise on delusions and hallucinations is unknown. Therefore, psychosis and schizophrenia patients with delusions and hallucinations will be excluded from the scope of the study. Patients who meet the inclusion criteria will be randomly assigned to the intervention and control groups. The study will be terminated when a total of 60 patients are reached, 30 in the intervention and 30 in the control group. Benson relaxation exercise will be applied to the patients in the intervention group. No application will be made to the patients in the control group. Research data will be collected with the \"State-Trait Anxiety Scale\" and \"Pittsburgh Sleep Quality Index\".\n\nHypotheses:\n\nH1: The anxiety level of patients who applied Benson relaxation exercise is lower than the patients who did not.\n\nH2: The sleep quality of patients who applied Benson relaxation exercise is better than the patients who did not.",[141,142,143,28],"Relaxation Program","Anxiety","Sleep Quality","2024-12-24",{"date":146,"type":40},"2024-12-27",{"date":148,"type":21},"2024-12",{"date":150,"type":21},"2025-10",{"name":152,"class":47},"Uskudar University",{"id":154,"slug":155,"hasResults":11,"nctId":156,"briefTitle":157,"officialTitle":158,"acronym":159,"eligibilityCriteria":160,"healthyVolunteers":11,"sex":17,"minAge":161,"maxAge":18,"enrollmentInfo":162,"targetDuration":164,"studyType":90,"phases":4,"briefSummary":165,"conditions":166,"keywords":171,"overallStatus":176,"whyStopped":4,"lastUpdateSubmitDate":177,"lastUpdatePostDateStruct":178,"startDateStruct":180,"completionDateStruct":182,"leadSponsor":184,"locationsCount":187},"100311328","youth-experiences-and-health-study-100311328","NCT03332966","Youth Experiences and Health Study","Youth Experiences and Health (YEAH) Study - Psychological Symptoms and Resources As Predictors of Mental Health Among Treatment-seeking Adolescents","YEAH","Inclusion Criteria:\n\nStart of care in adolescent mental health clinic\n\nExclusion Criteria:\n\nPrevious diagnosis of psychotic disorder","15 Years",{"count":163,"type":21},1000,"5 Years","This study aims to identify unusual experiences and psychiatric symptoms that indicate a heightened risk for severe mental disorders - especially psychoses. It is important to develop reliable questionnaire methods that are cost-effective in first-stage screening, leading to in-depth assessments and targeted care. However, existing psychosis-risk questionnaires are limited in content, intended for adults, and have been insufficiently tested for actual predictive value. Therefore we will collect a new, large dataset from an unselected group of adolescents entering psychiatric care in three major urban areas of Finland. Comprehensive national health care registers will be used to assess how well the selected experiences and symptoms predict the participants' mental health over the following few years.",[167,28,168,169,170],"Psychotic Disorders","Prodromal Symptoms","Cannabis Use","Trauma, Psychological",[65,172,173,174,175],"outpatients","questionnaire","psychotic-like symptoms","psychosis risk","RECRUITING","2024-09-23",{"date":179,"type":40},"2024-09-25",{"date":181,"type":40},"2019-12-01",{"date":183,"type":21},"2024-12-31",{"name":185,"class":186},"Finnish Institute for Health and Welfare","OTHER_GOV",3,{"id":189,"slug":190,"hasResults":11,"nctId":191,"briefTitle":192,"officialTitle":193,"acronym":4,"eligibilityCriteria":194,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":112,"enrollmentInfo":195,"targetDuration":4,"studyType":90,"phases":4,"briefSummary":197,"conditions":198,"keywords":201,"overallStatus":176,"whyStopped":4,"lastUpdateSubmitDate":206,"lastUpdatePostDateStruct":207,"startDateStruct":209,"completionDateStruct":211,"leadSponsor":212,"locationsCount":48},"100535320","evaluation-of-a-new-recovery-oriented-model-of-psychiatric-inpatient-care-100535320","NCT06250296","Evaluation of a New Recovery-oriented Model of Psychiatric Inpatient Care","Evaluation of a New Recovery-oriented Model of Care on Psychiatric Inpatient Wards.","Inclusion Criteria:\n\n* Patients hospitalized in one of the three participating wards\n\nExclusion Criteria:\n\n* Incapacity to give informed consent\n* Insufficient knowledge of French",{"count":196,"type":21},700,"This project will study the effects of a major reorganization of psychiatric inpatient wards. This reorganization will affect many aspects of day-to-day work, with the aim of improving the individualization of care, the integration of relatives and the participation of the patients in treatment planning. This new organization will initially involve a first pilot ward, before being extended to other wards.\n\nThe aim of this project is to understand whether this new organization has positive effects on the use of coercive measures, the average length of stay, the improvement in patients' clinical condition, as well as on patient satisfaction, their perception of coercion, the wards' atmosphere on the unit and patients' personal recovery.\n\nAll patients admitted to three wards of the Division of adult psychiatry of the Geneva University Hospital aged 18 and over, with a good knowledge of French and being treated for any type of diagnosis except dementia, are invited to take part in the study. They will be assessed at discharge regarding the selected outcomes. The study will last 18 months: during the first 9 months, the new model will be applied on the pilot ward, and the wo other wards will serve as comparison wards. After 9 months, the model will also be applied to these other two wards.",[28,199,200],"Coercion","Recovery",[202,203,204,205],"psychiatric inpatient care","coercion","recovery","patient satisfaction","2024-07-01",{"date":208,"type":40},"2024-07-03",{"date":210,"type":40},"2024-02-15",{"date":150,"type":21},{"name":213,"class":47},"University Hospital, Geneva"]