[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"patient-empowerment\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:patient-empowerment":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,43,73],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100591930","phase-4-perineal-massage-using-a-pelvic-wand-during-pregnancy-100591930",false,"NCT06986824","Perineal Massage Using A Pelvic Wand During Pregnancy","A Pilot Study To Assess The Effect Of Antepartum Perineal Massage Using A Pelvic Wand On Labor Agency And Pelvic Health","Inclusion Criteria:\n\n* Pregnant\n* Plan to give birth at BIDMC\n* Age ≥18 years old\n* English language preference\n* 32-36 weeks 'gestation\n\nExclusion Criteria:\n\n* Contraindication to vaginal birth, active genital herpes infection, fetal anomaly requiring cesarean birth).","FEMALE","18 Years",{"count":19,"type":20},140,"ESTIMATED","INTERVENTIONAL",[23],"PHASE4","There is limited research on the optimal strategy to reduce obstetric laceration, postpartum urinary retention, and postpartum pelvic pain. In systematic reviews, clinician-directed massage of the perineal muscles at the time of birth and patient directed massage of the perineal muscles in the third trimester to inconsistently reduce the incidence of severe obstetric laceration.1,2 However, there is significant heterogeneity of these studies is due in large part to the lack of a standardized protocols and unpredictability of clinician availability to perform perineal massage around the time of birth.\n\nThe purpose of this study is to understand how perineal massage with a pelvic wand in late pregnancy and during labor influences one's sense of self-control over the labor process and birth experience.",[26,27,28,29],"Pregnancy Related","Pelvic Floor Disorders","Obstetric; Injury","Patient Empowerment","RECRUITING","2026-03-06",{"date":33,"type":34},"2026-03-09","ACTUAL",{"date":36,"type":34},"2025-10-01",{"date":38,"type":20},"2026-09-01",{"name":40,"class":41},"Beth Israel Deaconess Medical Center","OTHER",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":50,"sex":51,"minAge":17,"maxAge":52,"enrollmentInfo":53,"targetDuration":4,"studyType":21,"phases":55,"briefSummary":57,"conditions":58,"keywords":62,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":42},"100549946","management-of-chronic-non-cancer-pain-with-non-pharmacological-therapies-100549946","NCT06440668","Management of Chronic Non-Cancer Pain With Non-Pharmacological Therapies","Management of Chronic Non-Cancer Pain With Non-Pharmacological Therapies: Randomized Clinical Trial.","Inclusion Criteria:\n\n* Patients aged 18 years or older,\n* Residing in the areas served by HSJDA,\n* With non-cancer chronic pain already diagnosed and treated for at least 6 months but not relieved by the usual treatment,\n* Who have explicitly and in writing expressed their desire to participate in the workshops and the study through the Informed Consent document,\n* And who complete the initial documentation necessary for their evaluation.\n\nExclusion Criteria:\n\n* Patients in the diagnostic phase,\n* Patients with pain exclusively associated with cancer pathology,\n* Patients with a life expectancy of less than one year,\n* Patients with severe cognitive or mental illnesses that prevent them from understanding both the content of the workshops and the measurement instruments.",true,"ALL","75 Years",{"count":54,"type":20},128,[56],"NA","A randomized controlled clinical trial will be conducted, involving a psychoeducational activity as the intervention. There will be a control group of patients with non-cancer chronic pain who will continue their usual treatment.\n\nThe trial will end after 3 months. Pain, well-being, medication management, mood, self-esteem, and quality of life will be compared just before starting the workshop with the status at the end of the workshop (one month later) to assess the immediate effect, and three months later to evaluate the medium-term effect. These measurements will be taken in both the control and intervention groups.\n\nAdditionally, for the intervention group, a follow-up will be conducted six months after the workshop ends to assess the long-term effect duration.\n\nThis study does not allow blinding of patients or professionals conducting the intervention, but the person analyzing the data to compare the effect produced in the control and intervention groups will be blinded. Therefore, it is an observer-blind evaluation.",[59,60,61,29],"Chronic Pain Syndrome","Sensitization, Central","Quality of Life",[59,60,61,29],"NOT_YET_RECRUITING","2024-06-04",{"date":66,"type":34},"2024-06-05",{"date":68,"type":20},"2024-06-10",{"date":70,"type":20},"2025-10-31",{"name":72,"class":41},"Hospital San Juan de Dios del Aljarafe de Sevilla",{"id":74,"slug":75,"hasResults":11,"nctId":76,"briefTitle":77,"officialTitle":78,"acronym":79,"eligibilityCriteria":80,"healthyVolunteers":11,"sex":51,"minAge":81,"maxAge":52,"enrollmentInfo":82,"targetDuration":4,"studyType":21,"phases":84,"briefSummary":85,"conditions":86,"keywords":4,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":91,"lastUpdatePostDateStruct":92,"startDateStruct":94,"completionDateStruct":96,"leadSponsor":98,"locationsCount":100},"100385501","urinary-proteomics-combined-with-home-blood-pressure-telemonitoring-for-health-care-reform-100385501","NCT04299529","Urinary Proteomics Combined With Home Blood Pressure Telemonitoring for Health Care Reform","Urinary Proteomics Combined With Home Blood Pressure Telemonitoring for Health Care Reform: a Randomised Controlled Trial","UPRIGHT-HTM","Inclusion Criteria:\n\n* Patients must have at least three additional guideline-defined risk factors, preferably including hypertension, type 2 diabetes mellitus (T2DM), or both;\n* Patients should be willing patients to engage for the duration of the study in home blood pressure telemonitoring (1 reading per day);\n* Patients must have an email address and internet access via smartphone, tablet, or laptop or desktop computer;\n* Patients should comply with the study protocol during the run-in phase.\n\nExclusion Criteria:\n\n* Type 1 diabetes mellitus;\n* Absence of a practicable echocardiographic window;\n* Previous or concurrent severe cardiovascular or non-cardiovascular disease;\n* Cancer within 5 years of enrolment;\n* Suspected substance abuse;\n* Psychiatric illness;\n* Use of nephrotoxic drugs;\n* Particpation in another clinical study.","55 Years",{"count":83,"type":20},1000,[56],"UPRIGHT-HTM will compare risk stratification, treatment efficiency and health economic outcomes of a diagnostic approach based on home blood pressure telemonitoring combined with urinary proteomic profiling with home blood pressure telemonitoring alone",[87,88,89,90,29],"Protein Deregulation","Blood Pressure","Health Care Utilization","Cost Effectiveness","2020-03-05",{"date":93,"type":34},"2020-03-06",{"date":95,"type":20},"2020-04-01",{"date":97,"type":20},"2026-07-31",{"name":99,"class":41},"KU Leuven",12]