[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Hospital Universitario Virgen Macarena\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":138},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,46,79,114],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":31,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100650020","effectiveness-of-a-mindfulness-based-intervention-for-pain-management-in-patients-with-multiple-sclerosis-mpims-100650020",false,"NCT07741864","Effectiveness of a Mindfulness-Based Intervention for Pain Management in Patients With Multiple Sclerosis (MPIMS).","Effectiveness of a Mindfulness-Based Intervention for Pain Management in Patients With Multiple Sclerosis","MPIMS","Inclusion Criteria:\n\n* Adults aged 18 to 80 years.\n* Diagnosis of multiple sclerosis with an Expanded Disability Status Scale (EDSS) score between 1.0 and 7.0.\n* Presence of pain.\n* Ability to provide written informed consent.\n\nExclusion Criteria:\n\n* Severe cognitive impairment.\n* Diagnosed psychiatric disorders (e.g., schizophrenia or personality disorders).\n* Participation in another non-pharmacological intervention specifically aimed at pain management.\n* If receiving stable pain medication, treatment must have been maintained for at least 4 months before enrollment.\n* Unwillingness to provide informed consent.","ALL","18 Years","80 Years",{"count":21,"type":22},84,"ESTIMATED","INTERVENTIONAL",[25],"NA","The goal of this clinical trial is to evaluate whether a mindfulness-based intervention is effective for reducing pain in adults with multiple sclerosis. It will also assess whether this intervention improves other symptoms commonly associated with pain, such as fatigue, sleep disturbances, anxiety, depression, and quality of life.\n\nThe main questions it aims to answer are:\n\n* Does a mindfulness-based intervention reduce pain intensity in people with multiple sclerosis?\n* Does the intervention improve fatigue, sleep quality, emotional well-being, quality of life?\n* Does the effectiveness of the intervention differ according to the type of pain experienced by participants? Researchers will compare a mindfulness-based intervention with an educational program to determine whether mindfulness provides additional benefits for pain management in people with multiple sclerosis.\n\nParticipants will:\n\n* Be randomly assigned to either the mindfulness intervention group or the educational control group.\n* Complete assessments before the intervention, immediately after the intervention, and at 1-month and 3-month follow-up visits.\n* If assigned to the mindfulness group, attend eight weekly 2.5-hour group sessions plus one 6-hour retreat, either in person or online.\n* If assigned to the control group, attend two 2-hour educational sessions during the study period.\n* Complete questionnaires evaluating pain, fatigue, physical function, anxiety, depression, sleep quality, quality of life, and mindfulness throughout the study.",[28,29,30],"Multiple Sclerosis","Pain","Pain Management",[28,29,32],"Mindfulness","NOT_YET_RECRUITING","2026-07-30",{"date":36,"type":37},"2026-08-03","ACTUAL",{"date":39,"type":22},"2026-09-02",{"date":41,"type":22},"2027-04-30",{"name":43,"class":44},"Hospital Universitario Virgen Macarena","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":52,"eligibilityCriteria":53,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":54,"targetDuration":4,"studyType":56,"phases":4,"briefSummary":57,"conditions":58,"keywords":62,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":45},"100641203","virtual-stroke-units-versus-conventional-stroke-unit-care-in-non-thrombectomy-candidate-patients-100641203","NCT07635498","Virtual Stroke Units Versus Conventional Stroke Unit Care in Non-Thrombectomy-Candidate Patients.","Virtual Stroke Units Versus Conventional Stroke Unit Care in Non-Thrombectomy-Candidate Patients: A Non-Inferiority Prospective Cohort Study","VSU","Inclusion Criteria\n\n* Age ≥ 18 years.\n* Diagnosis of acute stroke (ischemic or hemorrhagic) confirmed by clinical assessment and neuroimaging (CT and\u002For MRI) within 24 hours of symptom onset or last-seen-well.\n* Not a candidate for mechanical thrombectomy according to current clinical guidelines.\n* Admission to a participating hospital (Hospital de Riotinto, Hospital San Juan de Dios del Aljarafe, or Hospital Universitario Virgen Macarena).\n* Signed informed consent by the participant or legal representative. Exclusion Criteria\n* Pre-stroke modified Rankin Scale (mRS) ≥ 4.\n* Life expectancy \\\u003C 6 months due to non-stroke comorbid conditions.\n* Inability to complete protocolized follow-up (geographical, social, or clinical reasons).\n* Concurrent participation in another interventional clinical trial that may affect study endpoints.\n* Refusal to provide informed consent.",{"count":55,"type":22},726,"OBSERVATIONAL","Stroke is the leading cause of acquired disability in adults and a major cause of mortality worldwide; in Spain, Andalusia shows the highest stroke-related mortality rate. Comprehensive Stroke Units (SU) are the gold-standard organizational model for acute stroke care; however, only a fraction of patients have direct access to an SU, particularly those not eligible for mechanical thrombectomy who are admitted to regional or district hospitals without on-site SU capacity.\n\nThe Virtual Stroke Unit (VSU) concept extends specialized stroke care to non-SU hospitals by combining standardized in-hospital monitoring boxes with synchronous remote multidisciplinary assessment by a stroke neurologist and stroke nurse from a reference center, via the regional telemedicine platform (CATI).\n\nThis prospective, multicenter, non-inferiority cohort study compares effectiveness, safety, and feasibility of VSU care versus conventional SU care in patients with acute ischemic or hemorrhagic stroke who are not candidates for mechanical thrombectomy. Recruitment targets 363 patients per arm (726 total). The primary outcome is death or dependency at 3 months (modified Rankin Scale 3-6) - the canonical measure of stroke-unit effectiveness - with functional independence (mRS 0-2), adherence to the stroke-unit care quality bundle, safety, mortality, recurrence, length of stay, satisfaction (TUQ\u002FTSQ\u002FTMPQ) and cost-effectiveness as secondary outcomes.",[59,60,61],"Stroke","Stroke Hemorrhagic","Ischemic Stroke",[63,64,65,66,67,68,69],"Virtual Stroke Unit","Telemedicine","Telestroke","Stroke Unit","Healthcare delivery system","Non-inferiority","Modified Rankin Scale","RECRUITING","2026-06-16",{"date":73,"type":37},"2026-06-18",{"date":75,"type":37},"2026-04-01",{"date":77,"type":22},"2028-03-31",{"name":43,"class":44},{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":83,"acronym":84,"eligibilityCriteria":85,"healthyVolunteers":11,"sex":86,"minAge":87,"maxAge":88,"enrollmentInfo":89,"targetDuration":4,"studyType":56,"phases":4,"briefSummary":91,"conditions":92,"keywords":97,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":106,"lastUpdatePostDateStruct":107,"startDateStruct":109,"completionDateStruct":111,"leadSponsor":113,"locationsCount":4},"100592890","caramel-retrospective-study-for-personalized-risk-assessment-of-cardiovascular-disease-in-menopausal-and-perimenopausal-women-using-real-world-data-100592890","NCT06999317","CARAMEL: Retrospective Study for Personalized Risk Assessment of Cardiovascular Disease in Menopausal and Perimenopausal Women Using Real World Data","CARAMEL RS","Inclusion Criteria:\n\nSelf-identified as female in the electronic health record (EHR). Age between 40 and 60 years at the time of data collection\u002Findex date. Availability of at least 5-6 years of retrospective data in the EHR, depending on the research objective.\n\nAt least one healthcare encounter (visit, imaging, lab test, diagnosis, etc.) within the defined age range.\n\nFor imaging substudies (e.g., RO3-RO5): availability of at least one relevant imaging test (e.g., DXA, digital mammography, cMRI, CCTA, US) during the age range.\n\nFor signal-based analysis (RO6): presence of ECG monitoring data from implanted devices and at least 2 years of follow-up.\n\nExclusion Criteria:\n\nPrior diagnosis of cardiovascular disease before the observation window (only applicable to specific ROs, e.g., RO2, RO4).\n\nInsufficient data quality or missing key variables needed for modeling (e.g., absence of blood pressure or lipid profile).\n\nPatients with incomplete or inconsistent records (e.g., duplicate IDs, mismatched time frames).\n\nFor signal-based RO6: hospitalizations or diagnoses unrelated to cardiovascular health that may bias AI model training.","FEMALE","40 Years","60 Years",{"count":90,"type":22},1500000,"This retrospective observational study, part of the EU-funded CARAMEL project, aims to develop and validate personalized cardiovascular disease (CVD) risk assessment models specifically designed for menopausal and perimenopausal women (ages 40-60). The study leverages Real World Data (RWD) collected from multiple international clinical partners, including electronic health records (EHR), diagnostic imaging data, and signal data.\n\nThe main objective is to improve the prediction of CVD precursors such as hypertension and dyslipidemia, as well as mid- and long-term risk of CVD events, through advanced artificial intelligence (AI) models. These models will be trained on multimodal data to capture complex, individualized risk trajectories that current risk calculators fail to address, particularly in women. Special focus is placed on under-researched, women-specific risk factors and their interactions with traditional predictors.\n\nThe study includes several research objectives: (1) predicting the onset of hypertension and dyslipidemia using EHR data; (2) modeling the long-term risk of fatal and non-fatal cardiovascular events and disease trajectories; (3) identifying novel imaging biomarkers from routine screening tests such as mammography, DXA, ultrasound, and cardiac MRI; (4) developing multimodal prediction models combining imaging and clinical data; (5) creating automated AI tools for imaging biomarker extraction; and (6) using signal data from cardiac devices to predict disease progression and events.\n\nThe study population consists of middle-aged women with retrospective data available across different health systems. The expected outcome is a validated set of stratified, personalized CVD risk models that can support targeted prevention strategies and enable more equitable, sex-specific care. This will contribute to reducing the burden of CVD in women and addressing critical gaps in early detection, clinical decision-making, and health policy.\n\nThis project has received funding from the European Union's Horizon Europe Research and Innovation Programme under Grant Agreement No 101156210.",[93,94,95,96],"Cardiovascular Risk Factors","Menopausal Women","Perimenopausal Women","Real World Data",[98,99,100,101,102,103,104,105],"Cardiovascular Disease","Cardiovascular risk factors","Menopausal women","Perimenopausal women","real world data","personalised prevention","computational modelling","women-specific risks","2026-01-13",{"date":108,"type":37},"2026-01-15",{"date":110,"type":22},"2026-03-01",{"date":112,"type":22},"2028-04-30",{"name":43,"class":44},{"id":115,"slug":116,"hasResults":11,"nctId":117,"briefTitle":118,"officialTitle":118,"acronym":119,"eligibilityCriteria":120,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":121,"enrollmentInfo":122,"targetDuration":4,"studyType":56,"phases":4,"briefSummary":124,"conditions":125,"keywords":128,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":130,"lastUpdatePostDateStruct":131,"startDateStruct":133,"completionDateStruct":135,"leadSponsor":137,"locationsCount":45},"100567140","evaluation-of-the-efficacy-and-safety-of-portal-pressure-gradient-ppg-measurement-guided-by-endoscopic-ultrasound-eus-in-the-therapeutic-algorithm-of-patients-with-liver-cirrhosis-100567140","NCT06664307","Evaluation of the Efficacy and Safety of Portal Pressure Gradient (PPG) Measurement Guided by Endoscopic Ultrasound (EUS) in the Therapeutic Algorithm of Patients with Liver Cirrhosis.","GPP-USE","Inclusion Criteria:\n\n* Patients diagnosed with advanced liver disease with an indication for primary prophylaxis with NSBBs\n\nExclusion Criteria:\n\n\\- Age \\\u003C 18 years. 2. Advanced stage hepatocellular carcinoma not eligible for curative treatment. 3. Pregnancy. 4. Esophageal stenosis. 5. INR \\> 1.5. 6. Platelets \\\u003C 50,000 µL. 7. Ascites. 8. Patients with any contraindication for performing an upper gastrointestinal endoscopy.\n\n9\\. Patients with contraindication to NSBB treatment. 10. Refusal to sign the informed consent form to participate in the study","85 Years",{"count":123,"type":22},35,"The development of Clinical significant PH (CSPH) is a major driver of complications. PPG is the strongest predictor of decompensation . The shortcomings of GPVH measurements and invasiveness has resulted in an area of unmet clinical need. Non-selective beta-blockers (NSBB) have demonstrated efficacy in reducing PH. However, this requires a second invasive procedure, and there is high interindividual variability in the hemodynamic response to NSBB. EUS-guided GPP measurement emerges as a more accurate, accessible and less invasive technique to potentially predict chronic hemodynamic response. The aim of this project is to assess the safety and efficacy of EUS-derived GPP measurement (EUS-GPP) in patients diagnosed with cirrhosis, to assess the acute hemodynamic response through EUS-derived GPP to intravenous propranolol administration in order to determine the patients who would benefit from NSBB treatment in primary prophylaxis to prevent decompensation using a strategy guided by EUS-GPP measurement.",[126,127],"Portal Pressure Gradient (PPG) Measurement Guided by Endoscopic Ultrasound (EUS)","Hepatic Cirrhosis",[129],"Portal pressure gradient (PPG), endoscopic ultrasound (EUS) ,.the acute hemodynamic response","2024-10-28",{"date":132,"type":37},"2024-10-29",{"date":134,"type":22},"2024-11-01",{"date":136,"type":22},"2027-11-01",{"name":43,"class":44},""]