[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"technology\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:technology":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,45,70,96,120],{"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":30,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100461830","optimizing-technology-to-improve-medication-adherence-and-bp-control-optima-bp-100461830",false,"NCT05293756","OPtimizing Technology to Improve Medication Adherence and BP Control (OPTIMA-BP)","OPtimizing Technology to Improve Medication Adherence and Blood Pressure Control","Inclusion Criteria:\n\n1. Self-identify as African American\n2. 50 years of age or older\n3. Diagnosed with hypertension, with a systolic blood pressure≥ 130 mmHg but less than 170 mmHg\n4. Prescribed at least two hypertensive, one of which is a diuretic\u002Fthiazide and or calcium channel blocker antihypertensive medication\n5. Own a smartphone with a data plan, the capability to download the Medisafe app, or view videos\n6. Able to read\u002Funderstand English\n\nExclusion Criteria:\n\n1. Unable to give informed consent or judged to have impaired cognitive ability or severe memory\n2. Currently using a medication management application (app)\n3. Experienced a major CVD event or procedure (e.g., myocardial infarction, stroke, heart surgery) within the past year\n4. Patients with a diagnosis of chronic kidney disease (defined as estimated glomerular filtration rate (eGFR) \\\u003C 60 ml\u002Fmin\u002F1.73m2) and\u002For receiving dialysis.","ALL","50 Years",{"count":19,"type":20},208,"ESTIMATED","INTERVENTIONAL",[23],"NA","Hypertension (HTN) has a greater impact on African Americans (AA) than any other U.S. racial group. Uncontrolled blood pressure (BP) contributes to higher rates of disability, death, and health resource use among AA. HTN is the single most influential risk factor for cardiovascular disease (CVD), as well as a risk factor for the incidence of stroke, diabetes, chronic kidney disease, and dementia. Importantly, older adults account for 15% of the U.S. population, and two-thirds of older adults over age 60 have HTN, with higher rates observed in AA older adults. Strategies to support self-managing HTN and BP control are crucial as the older population is projected to age considerably and become more racially and ethnically diverse. Research has documented the negative effects on health and health outcomes of poorly controlled BP and is one of the most important modifiable CVD risk factors. Lower BP targets will require aggressive management and an increase in antihypertensive medications. Therefore, to achieve lower targets in this population, greater efforts, including patient-centered methods will be needed to support self-managing HTN, especially in terms of medication adherence.\n\nAs we shifted into the digital age, the use of mHealth technologies (smart phones, applications, SMS or text messaging) has been a powerful approach and mechanism for the treatment and management of chronic diseases. However, behavioral interventions that incorporate technology do not reach minorities or disadvantaged AA older adults with HTN. OPtimizing Technology to Improve Medication Adherence and BP Control (OPTIMA-BP) will leverage existing knowledge of effective technology-based components for HTN self-management to support and improve BP control using unique aspects of mHealth platforms in AA older adults. Findings from this study, if confirmed, will improve BP control and support self-managing HTN, as well as has the potential to close the health disparity gap between AA and non-AA older adults with HTN.",[26,27,28,29],"Hypertension","Self-Management","Technology","Quality of Life",[26,27,31],"Home Blood Pressure Monitoring","RECRUITING","2026-03-30",{"date":35,"type":36},"2026-04-03","ACTUAL",{"date":38,"type":36},"2021-02-14",{"date":40,"type":20},"2027-05-31",{"name":42,"class":43},"Case Western Reserve University","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":52,"sex":16,"minAge":53,"maxAge":4,"enrollmentInfo":54,"targetDuration":4,"studyType":21,"phases":56,"briefSummary":57,"conditions":58,"keywords":4,"overallStatus":60,"whyStopped":4,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":4},"100411232","video-home-visits-for-dietary-counselling-100411232","NCT04634851","Video Home Visits for Dietary Counselling","Optimizing Dietary Habits for Kidney Stone Formers Using Telehealth Directed Individualized Nutritional Counseling","Inclusion Criteria:\n\n* Patients known to have a history of calcium-based kidney stone disease verified by stone analysis (stones containing calcium oxalate(CaOx) or calcium phosphate(CaP) on stone analysis), or patients with a diagnosis of kidney stone disease verified by imaging (computerized tomography, ultrasound, or plain film\u002Fx-ray) and a prior 24-hour urine results with elevated SS CaOx\\>8 or SS CaP\\>1.25.\n* Patients 18 years or older.\n* Patients with a smartphone, internet capable tablet, or video capable laptop.\n* Patients with a household member with a smartphone, internet capable tablet, or video capable laptop.\n\nExclusion Criteria:\n\n* Pregnant patients.\n* Patients unable to produce a urine sample.\n* Patients who have previous surgical reconstruction involving incorporation of bowel in the urinary tract.\n* Patients with known sodium regulation abnormalities (adrenal tumors, pituitary tumors, glucocorticoid deficiency, hypothyroidism, syndrome of inappropriate antidiuretic hormone secretion, nephrotic syndrome, severe congestive heart failure, severe hepatic impairment, etc.).\n* Patients on medications significantly affecting urinary sodium levels (lithium, amphotericin, vasopressin V2-receptor antagonists, lactulose, for example).",true,"18 Years",{"count":55,"type":20},100,[23],"This pilot study aims to develop a protocol for home video informed dietary counseling with the goal of reducing overall sodium consumption among kidney stone formers. To accomplish this the investigators will: 1)Assess which data available on video visits are most informative to convey patient sodium consumption, and 2) Administer virtual home visits with informed dietary counseling in our intervention arm and compare this to standard dietary counseling looking specifically at the outcome of 24-hour urine sodium excretion results over time. This study will benefit dramatically from the rapid growth of telehealth medical visits as a consequence of the SARS-CoV-2 pandemic, with the ultimate goal to improve and adapt patient dietary counseling for the prevention of kidney stone disease in the new and evolving era of telehealth.",[28,59],"Diet Habit","NOT_YET_RECRUITING","2026-01-29",{"date":63,"type":36},"2026-02-02",{"date":65,"type":20},"2027-07-01",{"date":67,"type":20},"2029-06-30",{"name":69,"class":43},"University of California, San Francisco",{"id":71,"slug":72,"hasResults":11,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":4,"eligibilityCriteria":76,"healthyVolunteers":52,"sex":16,"minAge":77,"maxAge":78,"enrollmentInfo":79,"targetDuration":4,"studyType":21,"phases":81,"briefSummary":82,"conditions":83,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":88,"startDateStruct":90,"completionDateStruct":92,"leadSponsor":94,"locationsCount":44},"100445924","evaluation-of-trauma-center-based-intervention-for-adolescent-traumatic-injury-survivors-100445924","NCT05086757","Evaluation of Trauma Center-Based Intervention for Adolescent Traumatic Injury Survivors","Evaluation of Trauma Center-Based, Technology Enhanced Stepped Care Intervention for Adolescent Traumatic Injury Survivors.","Inclusion Criteria:\n\n* adolescent ages 12-17 admitted following traumatic injury\n* scored significantly on the peritraumatic distress scale (PDI \u002F ITSS)\n\nExclusion Criteria:\n\n* if the injury was self-inflicted\n* injuries are so severe, they prevent participation (e.g., head or spinal cord injuries that prevent verbal communication)","12 Years","17 Years",{"count":80,"type":20},300,[23],"Pediatric traumatic injury (i.e., injury of sudden onset and severity requiring immediate attention) is the leading cause of death and morbidity among US adolescents and are associated with mental health and health risk outcomes, including posttraumatic stress and depression (affecting between 19-42%), deficits in physical recovery, social functioning and quality of life, which if unaddressed, may contribute to increased use of health care services. The investigators partnered with three accredited Level I and II pediatric trauma centers to conduct a multi-site hybrid 1 effectiveness-implementation trial with 300 adolescent (ages 12-17) traumatic injury patients to assess the extent to which the Trauma Resilience and Recovery Program (TRRP), a scalable and sustainable, technology-enhanced, multidisciplinary stepped model of care, promotes improvement in quality of life and emotional recovery and gather preliminary data on the potential for TRRP to be implemented in other Level I trauma centers. Directly in line with NICHD's Pediatric Trauma and Critical Illness Research and Training (PTCIB) Strategic Research and Training agenda, this study will provide valuable data on the efficacy, preliminary effectiveness and potential for implementation of an innovative, cost-effective, sustainable technology-enhanced intervention designed to address the unique needs of adolescent injury patients and mitigate short- and long-term impact of injury on mental health, quality of life, and overall well-being.",[84,28,85,86],"Traumatic Injury","Posttraumatic Stress Disorder","Adolescents","2025-08-08",{"date":89,"type":36},"2025-08-11",{"date":91,"type":36},"2022-07-01",{"date":93,"type":20},"2027-08-30",{"name":95,"class":43},"Medical University of South Carolina",{"id":97,"slug":98,"hasResults":11,"nctId":99,"briefTitle":100,"officialTitle":101,"acronym":4,"eligibilityCriteria":102,"healthyVolunteers":11,"sex":16,"minAge":103,"maxAge":4,"enrollmentInfo":104,"targetDuration":4,"studyType":106,"phases":4,"briefSummary":107,"conditions":108,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":110,"lastUpdatePostDateStruct":111,"startDateStruct":113,"completionDateStruct":115,"leadSponsor":117,"locationsCount":44},"100486529","comparison-between-exactech-guided-personalized-surgery-gps-and-conventional-instrumentation-of-shoulder-arthroplasty-100486529","NCT05615259","Comparison Between Exactech Guided Personalized Surgery (GPS) and Conventional Instrumentation of Shoulder Arthroplasty","A Prospective, Multi-Center, Randomized Clinical Study of Total Shoulder Arthroplasty Comparing Exactech Guided Personalized Surgery (GPS) vs. Conventional Instrumentation","Inclusion Criteria:\n\n* Patient is at least 21 years of age at the time of surgery\n* Patient is indicated for reverse shoulder arthroplasty\n* Patient is willing to participate by complying with pre- and postoperative visit requirements\n* Patient is willing to participate for the entire length of the prescribed follow-up (minimum 2 years)\n* Patient is willing and able to review and sign a study informed consent form\n* Preop CT scan is within 3 months of the date of surgery\n\nExclusion Criteria:\n\n* Revision shoulder arthroplasty\n* Reverse shoulder arthroplasty for fracture\n* Need for structural glenoid bone graft\n* Osteomyelitis of the proximal humerus or scapula; if a systemic infection or a secondary remote infection is suspected or confirmed, implantation should be delayed until infection is resolved\n* Inadequate or malformed bone that precludes adequate support or fixation of the prosthesis\n* Neuromuscular disorders that do not allow control of the joint\n* Significant injury to the brachial plexus\n* Non-functional deltoid muscles\n* The patient is unwilling or unable to comply with the post-operative care instructions\n* Patients who are a known drug or alcohol abuser, or have a psychological disorder (e.g. schizophrenia major depression, bipolar disorder, etc.) as defined by the DSM4 that affect follow-up care or treatment outcomes.\n* Alcohol, drug, or other subtance abuse\n* Any disease state that could adversaly affect the function or longevity of the implant\n* Patient is pregnant\n* Patient is a prisoner\n* Patient who are currently involved in any personal injury litigation, medical-legal or worker's compensation claims","21 Years",{"count":105,"type":20},260,"OBSERVATIONAL","The primary objective of this study is to examine the optimization of Reverse Shouder Arthroplasty implant position between GPS and conventional techniques. The secondary objective is to assess the effect of implant position using GPS vs. conventional techniques on ROM and patient reported outcomes. Long-term follow-up to 10 years with minimum 2 year follow-up for patients.",[28,109],"Comparison","2025-02-26",{"date":112,"type":36},"2025-02-28",{"date":114,"type":36},"2020-09-23",{"date":116,"type":20},"2031-09-30",{"name":118,"class":119},"Exactech","INDUSTRY",{"id":121,"slug":122,"hasResults":11,"nctId":123,"briefTitle":124,"officialTitle":125,"acronym":4,"eligibilityCriteria":126,"healthyVolunteers":11,"sex":16,"minAge":53,"maxAge":4,"enrollmentInfo":127,"targetDuration":4,"studyType":21,"phases":129,"briefSummary":130,"conditions":131,"keywords":136,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":141,"lastUpdatePostDateStruct":142,"startDateStruct":144,"completionDateStruct":146,"leadSponsor":148,"locationsCount":44},"100553420","assessment-of-pain-using-a-pain-diagnostic-system-that-measurs-facial-movement-using-100553420","NCT06485856","ASSESSMENT OF PAIN USING A PAIN DIAGNOSTIC SYSTEM THAT MEASURS FACIAL MOVEMENT USING","Cukurova University","Inclusion Criteria:\n\n* 18 years and over,\n* Those with intubation\u002Ftracheostomy,\n* Conscious, unable to communicate verbally,\n* Glaskow coma score 13-15,\n* Patients who agreed to participate in the study\n\nExclusion Criteria:\n\n* Those with any facial abnormality that may alter facial expression analysis (facial paralysis, Poland-mobius syndrome)\n* Those with neurological and mental disorders,\n* Having a history of chronic pain,\n* Those who have a condition that requires them to be in the prone position all the time (Pilonidal Sinus, ARDS, etc.),\n* Patients who cannot speak the same language as the healthcare professional",{"count":128,"type":20},46,[23],"Pain is a subjectively difficult, abstract and comprehensive concept that is at the core of the whole study, emerging in relation to various advancements, and detailed description. For non-controlling, stress-free, stress-or-thickness training for thromboembolic, pulmonary and other organ modalities, re-admission from discharge, thromboembolic, pulmonary and other reasons.\n\nThe scales of use in the assessment of pain in the conscious surgical patient who cannot communicate verbally, into the pain, are physically subjective. Ekman and Friesen are planning the movements of their muscles to be performed by an Action Coding process that could be experienced in 1978. system; It has been applied in pain, in the evaluation of pain in the postoperative period and in children, in the new clinical practice, and in the new and clinical practice.\n\nHealth professionals may be biased in diagnosing pain, especially in intensive care patients, and may underestimate pain. In the literature, it is seen that the child who is made with pain in his patients in education in the field of medicine is not used in his experiences, similar to the pain that measures the tastes of the faces of the single scales. In this context, standardized, continuous, objective and scalable pain measures indicate the practice environment. The aim of these people is to evaluate the pain in our surgical patients who cannot communicate clearly and clearly with pain diagnosis that measures facial movement.",[132,133,134,28,135],"Nursing","Pain Assessment","Critical Care","Facial Recognition",[137,138,139,140,28],"Nurse","Pain assessment","Intensive care","Facial diagnosis","2024-06-26",{"date":143,"type":36},"2024-07-03",{"date":145,"type":36},"2024-05-15",{"date":147,"type":20},"2024-12-15",{"name":149,"class":43},"Fatmagül Üstünel"]