[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Halmstad University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":103},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,49,81],{"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":4,"briefSummary":24,"conditions":25,"keywords":27,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100631667","ai-assisted-fall-prevention-through-evidence-100631667",false,"NCT07503665","AI-assisted Fall Prevention Through Evidence","Safe AI-assisted Fall Prevention Through Evidence","SAFE","Individual interviews with key actors in the implementation\n\nInclusion criteria:\n\n1. Be employed at one of the participating hospitals\n2. Hold a role as a key stakeholder in the implementation work\n3. Have experience with the implementation of the AI-assisted fall prevention\n4. Have the ability to understand and communicate in Swedish\n\nExclusion criteria:\n\n1\\. Have insufficient proficiency in Swedish to participate in an interview or observation and to understand the purpose and content of the study\n\nIndividual interviews with managers\n\nInclusion criteria:\n\n1. Be employed as a manager at one of the participating hospitals\n2. Have experience with the implementation or use of the AI-assisted fall prevention\n3. Have the ability to understand and communicate in Swedish\n\nExclusion criteria:\n\n1\\. Have insufficient proficiency in Swedish to participate in an interview or observation and to understand the purpose and content of the study\n\nIndividual interviews with staff\n\nInclusion criteria:\n\n1. Be employed as staff on a ward at one of the participating hospitals where the AI-assisted fall prevention has been decided to be implemented\n2. Have experience with the implementation or use of the AI-assisted fall prevention\n3. Have the ability to understand and communicate in Swedish\n\nExclusion criteria:\n\n1\\. Have insufficient proficiency in Swedish to participate in an interview or observation and to understand the purpose and content of the study\n\nObservations of staff work\n\nInclusion criteria:\n\n1. Be employed as staff on a ward at one of the participating hospitals where the AI-assisted fall prevention has been decided to be implemented\n2. Have experience with the implementation or use of the AI-assisted fall prevention\n3. Have the ability to understand and communicate in Swedish\n\nExclusion criteria:\n\n1\\. Have insufficient proficiency in Swedish to participate in an interview or observation and to understand the purpose and content of the study\n\nIndividual interviews with patients and family members:\n\nInclusion criteria (for family members, only inclusion criterion 1b applies):\n\n1. Either (a) have been a patient on a ward at one of the participating hospitals where the AI-assisted fall prevention has been implemented, or (b) be a family member involved in the care of a patient who meets the inclusion criteria but lacks the ability to provide informed consent. The family member must be able to understand and communicate in Swedish\n2. Have experience with the AI-assisted fall prevention as part of their care\n3. Have the ability to understand and communicate in Swedish\n4. Be 18 years of age or older\n5. Have the ability to provide informed consent. If there is any uncertainty regarding a patient's ability to provide informed consent, the research team will refrain from conducting the interview.\n\nExclusion criteria:\n\n1. Have insufficient proficiency in Swedish to participate in an interview or observation and to understand the purpose and content of the study\n2. Lack the ability to provide informed consent\n\nWeb-based surveys with staff:\n\nInclusion criteria:\n\n1. Be employed as staff on a ward at one of the participating hospitals where the AI-assisted fall prevention is decided to be implemented.\n\nExclusion criteria:\n\n1. Not being employed on a ward at one of the participating hospitals where the AI-assisted fall prevention is decided to be implemented\n2. Lack the ability to access information and respond to the survey in Swedish\n\nRetrospective medical record data:\n\nInclusion criteria:\n\n1\\. Patients who have been cared for on a ward at one of the participating hospitals where the AI-assisted fall prevention has been implemented, either (a) up to 24 months after implementation or (b) up to 12 months before implementation.\n\nExclusion criteria:\n\n1\\. Patients who have only received care outside the defined time period, meaning not within 24 months after or 12 months before the implementation of the AI-assisted fall prevention\n\nLearning labs:\n\nInclusion criteria:\n\n1. (a) Be employed at one of the participating hospitals and hold a role as a key stakeholder in the implementation work, or be staff or a manager with experience of the implementation or use of the AI-assisted fall prevention; or (b1) have been a patient cared for on a ward at one of the participating hospitals where the AI-assisted fall prevention has been implemented and have experience with the AI-assisted fall prevention as part of their care; or (b2) be a family member of a patient with such experience; or (c) be a patient representative for a patient group, patient organization, or user organization where falls are an identified issue\n2. Have the ability to understand and communicate in Swedish\n\nExclusion criteria:\n\n1. Have insufficient proficiency in Swedish to participate in an interview or observation and to understand the purpose and content of the study\n2. Lack the ability to provide informed consent",true,"ALL","18 Years",{"count":21,"type":22},23425,"ESTIMATED","OBSERVATIONAL","The goal of this multi-method study is to investigate how AI-assisted fall-prevention are implemented in routine hospital care what their effects are. The main questions it aims to answer are how these AI systems influence patient safety outcomes, how they affect healthcare professionals work and healthcare resource use, and what factors support or hinder their sustainable integration into hospital environments.",[26],"Fall",[28,29,30,31,32,33,34,35],"fall prevention","artificial intelligence","hospital","work","patient safety","resource use","implementation","effects","RECRUITING","2026-03-25",{"date":39,"type":40},"2026-03-31","ACTUAL",{"date":42,"type":40},"2026-01-01",{"date":44,"type":22},"2028-12",{"name":46,"class":47},"Halmstad University","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":18,"minAge":55,"maxAge":56,"enrollmentInfo":57,"targetDuration":4,"studyType":59,"phases":60,"briefSummary":62,"conditions":63,"keywords":68,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":73,"lastUpdatePostDateStruct":74,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":48},"100578217","intervention-with-weighted-blankets-for-children-with-adhd-and-sleep-problems-implementation-and-effectiveness-100578217","NCT06808425","Intervention With Weighted Blankets for Children With ADHD and Sleep Problems: Implementation and Effectiveness","Inclusion Criteria:\n\n* Children diagnosed with ADHD (DSM-5) and sleep problems (defined by screening instrument).\n* Being a patient at child and adolescent mental health service (CAMHS) in Region Halland, Sweden.","6 Years","14 Years",{"count":58,"type":22},200,"INTERVENTIONAL",[61],"NA","The aim is to study a sleep intervention with weighted blankets in children with ADHD and sleep problems regarding 1) short- and long-term effects on sleep and health-related outcomes in comparison with standard treatment (melatonin), 2) barriers and facilitators to implementation in routine clinical practice, and 3) health-economic outcomes.",[64,65,66,67],"ADHD","Sleep Disturbances","Sleep","Sleep Problems",[34,69,70,71,72],"sleep intervention","weighted blankets","children with ADHD","sleep problems","2025-03-12",{"date":75,"type":40},"2025-03-14",{"date":77,"type":40},"2025-02-03",{"date":79,"type":22},"2034-02",{"name":46,"class":47},{"id":82,"slug":83,"hasResults":11,"nctId":84,"briefTitle":85,"officialTitle":86,"acronym":4,"eligibilityCriteria":87,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":88,"enrollmentInfo":89,"targetDuration":4,"studyType":59,"phases":91,"briefSummary":92,"conditions":93,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":98,"completionDateStruct":100,"leadSponsor":102,"locationsCount":48},"100499323","high-intensity-training-in-patients-with-spondyloarthritis-a-randomized-controlled-trial-100499323","NCT05781763","High-intensity Training in Patients With Spondyloarthritis: a Randomized Controlled Trial","High-intensity Exercise Based on Self-management With Digital Coaching in Patients With Spondyloarthritis: a Randomized Controlled Trial","Inclusion Criteria:\n\n* Axial SpA (ICD10 diagnosis of M45, M46.0, M46.1, M46.8 and M46.9).\n* Fulfilling recommendations for physical activity\n\nExclusion Criteria:\n\n* Changed TNF and anti-inflammatory medication the previous three months\n* Cardiovascular disease\n* Comorbidities making high-intensity training inappropriate\n* Performing high-intensity interval training on a regular basis","67 Years",{"count":90,"type":22},100,[61],"Project summary\n\nBackground: For people diagnosed with a spondyloarthritis (SpA) e.g. ankylosing spondylitis or undifferentiated spondyloarthritis, physical activity and exercise are important components in the self-management. Exercise, in addition to physical and mental symptoms related to the disease can easily feel overwhelming to exercise, and low adherence may result. By studying the effects of high-intensity interval training (HIIT) in comparison with training as usual on physiological, inflammatory, and self-reported disease parameters in patients with SpA, we intend to further investigate the short-term and longitudinal training effects, and refine the knowledge to tailor, coach, and stimulate to self-performed HIIT.\n\nObjective: The purpose of this study is to investigate the short- and long-term effects of high- intensity interval training (HIIT) on physiological, inflammatory, and self-reported health parameters in patients with SpA. The aim is also to study the adherence to physical activity and exercise recommendations.\n\nDesign: A randomized controlled trial (RCT) design. Participants: One hundred adults with a confirmed axial SpA from rheumatology clinics in southern Sweden will be recruited and randomized into two groups, the intervention group and the control group.\n\nIntervention: Three high-intensity training sessions per week for three months, of which two interval sessions, with coaching both from a clinical physiotherapist and digital devices (watch and app) followed by nine months with sporadic coaching. The control group will go on with exercise as usual.\n\nPrimary outcome: Self-reported disease activity, inflammatory biomarkers (acute phase proteins).\n\nSecondary outcomes: Physical fitness (aerobic capacity (VO2max), blood pressure, grep strength), body composition and self-reported physical function, health status, well-being, pain, fatigue, adherence to physical activity and exercise recommendations, and confidence in one's own ability to manage pain, symptoms and high-intensity exercise, and additional serum biomarkers.",[94],"Axial Spondyloarthritis","2023-03-12",{"date":97,"type":40},"2023-03-23",{"date":99,"type":40},"2022-03-21",{"date":101,"type":22},"2026-12",{"name":46,"class":47},""]