[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"mobile-health-technology-mhealth\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:mobile-health-technology-mhealth":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,51,85,110],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":31,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":50},"100644239","mobile-app-based-yoga-and-meditation-in-rheumatoid-arthritis-100644239",false,"NCT07666594","Mobile App-Based Yoga and Meditation in Rheumatoid Arthritis","Effectiveness of a Mobile Application-Based Yoga and Meditation Program in Patients With Rheumatoid Arthritis: A Single-Blind Randomized Controlled Trial.","Inclusion Criteria:\n\n* Adults aged between 18 and 65 years.\n* Diagnosed with Rheumatoid Arthritis (RA) by a rheumatologist.\n* Disease in a stable phase (remission or low disease activity).\n* Access to a smartphone or tablet and sufficient proficiency in using mobile applications.\n* Cognitive sufficiency to provide written and verbal informed consent in Turkish.\n\nExclusion Criteria:\n\n* Presence of acute RA flare-ups.\n* Severe psychiatric diagnoses (e.g., psychosis, bipolar disorder, or severe major depression).\n* Severe cognitive impairment or dementia.\n* Pregnancy.\n* Regular practice of meditation or mindfulness within the last 6 months.\n* Participation in any other stress management program within the last 3 months.\n* Receipt of mental health services within the last 6 months.","ALL","18 Years","65 Years",{"count":20,"type":21},102,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this single-blind, randomized controlled trial is to evaluate the clinical effectiveness and short-term economic impact of a mobile application-based, personalized yoga and meditation program in adult patients with Rheumatoid Arthritis (RA).\n\nThe main questions it aims to answer are:\n\nDoes an 8-week digital yoga and meditation intervention reduce anxiety and improve other clinical\u002Fpsychological outcomes (such as depression, pulmonary function, reaction time, quality of life, and stress) compared to standard medical care? Does this digital intervention reduce short-term healthcare utilization and associated direct medical costs?\n\nResearchers will compare the Mobile App Group (receiving personalized yoga and meditation via the Meditopia app) to a Control Group (receiving usual medical care) to evaluate the effectiveness and cost-efficiency of the intervention.\n\nParticipants in the experimental group will:\n\nUse a mobile application to practice 15-30 minutes of yoga and 15-30 minutes of meditation daily, at least 4 days a week over an 8-week period.\n\nComplete clinical, psychometric, and economic assessments at baseline, week 4, and week 8.",[27,28,29,30],"Rheumatoid Arthritis (RA)","Anxiety","Depression Anxiety Disorder","Mobile Health Technology (mHealth)",[32,33,34,35,36,37],"Rheumatoid Arthritis","Yoga","Mobile Health (mHealth)","Meditation","Cost Analysis","Psychological Stress","NOT_YET_RECRUITING","2026-06-18",{"date":41,"type":42},"2026-06-24","ACTUAL",{"date":44,"type":21},"2026-06",{"date":46,"type":21},"2027-06",{"name":48,"class":49},"Tugba Civi Karaaslan","OTHER",1,{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":56,"acronym":57,"eligibilityCriteria":58,"healthyVolunteers":11,"sex":16,"minAge":59,"maxAge":60,"enrollmentInfo":61,"targetDuration":4,"studyType":22,"phases":63,"briefSummary":64,"conditions":65,"keywords":70,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":76,"lastUpdatePostDateStruct":77,"startDateStruct":79,"completionDateStruct":81,"leadSponsor":83,"locationsCount":50},"100636769","digitally-enhanced-cognitive-behavioral-therapy-100636769","NCT07569991","Digitally Enhanced Cognitive-Behavioral Therapy","Digitally Enhanced Cognitive-Behavioral Therapy for Adolescents With Depression and Obesity","CBT+","Inclusion Criteria:\n\n* Age 12-17 years\n* Body mass index (BMI) ≥85th percentile for age and sex\n* Elevated depression symptoms, Center for Epidemiologic Studies-Depression Scale (CES-D) ≥21\n\nExclusion Criteria:\n\n* Type 2 diabetes; Fasting glucose ≥126 mg\u002FdL or HbA1c ≥6.5\n* Major developmental (e.g., intellectual developmental disability) or medical or genetic condition (e.g. cancer, Bardet-Biedhl)\n* Pregnancy\u002Fbreastfeeding (females)\n* Bariatric surgery, weight loss medication, or weight loss \\>3% in the past 3 months\n* Active suicidality or self-harm","12 Years","17 Years",{"count":62,"type":21},60,[24],"Adolescent depression is a major public health problem. Depression affects adolescents' emotional well-being now and in the future, and it also affects their physical health, especially the risk for heart disease and other cardiovascular and metabolic health problems. In adolescents with depression and obesity, evidence-based programs for depression, like cognitive-behavioral therapy (CBT), might improve physical health, in part by supporting healthy behaviors such as physical activity, nutritious eating, and getting enough sleep. Our preliminary studies provide support for this overarching hypothesis. If adolescents have access to a digital app to support practicing CBT skills in between program sessions, it might especially help them to learn skills that help to feel better and be healthier in their day-to-day lives. We are tailoring a digital app for this purpose and we will make changes to the app based on feedback from adolescents, their parents, and their doctors. Once the app is well-liked and helpful, and works well as a support for taking part in CBT, we will randomly assign 60 adolescents with depression and overweight\u002Fobesity to either \"CBT+\" - a CBT group program plus the app, or \"CBT-only\" - the CBT group program only. We will pilot test whether this research is feasible, likeable, and credible, learning information that will inform a larger study to test of CBT+ can support emotional well-being, health behavior, and cardiovascular and metabolic health in adolescents.",[66,67,68,30,69],"Depression in Adolescence","Obesity & Overweight","Cognitive-behavioral Therapy","Health Behavior",[71,72,73,74,75],"cognitive-behavioral therapy","depression","adolescents","cardiometabolic health","mHealth","2026-06-03",{"date":78,"type":42},"2026-06-05",{"date":80,"type":21},"2027-01-01",{"date":82,"type":21},"2028-08-01",{"name":84,"class":49},"Colorado State University",{"id":86,"slug":87,"hasResults":11,"nctId":88,"briefTitle":89,"officialTitle":90,"acronym":91,"eligibilityCriteria":92,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":93,"targetDuration":4,"studyType":22,"phases":95,"briefSummary":96,"conditions":97,"keywords":4,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":101,"lastUpdatePostDateStruct":102,"startDateStruct":104,"completionDateStruct":106,"leadSponsor":108,"locationsCount":50},"100625533","ed-plwdcare-partner-text-messaging-100625533","NCT07423871","ED PLWD\u002FCare Partner Text Messaging","Development and Pilot Testing of a Novel Text Messaging Intervention to Improve Emergency Department Care Transitions Among Care Partners of Persons Living With Cognitive Impairment","CAPTURE","Inclusion Criteria:\n\n* Care partners (family members or close contacts) of persons living with cognitive impairment (PLWCI) who were evaluated and discharged from the emergency department (ED)\n* Age 18 years or older\n* Able to read and understand English or Spanish\n* Owns a mobile phone capable of receiving SMS text messages\n* Provides informed consent to participate in the study\n* Care recipient (PLWCI) resides in a community setting (i.e., not in a long-term care facility)\n\nExclusion Criteria:\n\n* Care partner of a patient who is admitted to the hospital from the ED or transferred to a facility (e.g., skilled nursing facility)\n* Care partner who is already enrolled in another caregiving support trial or intervention study\n* Care partner who does not have regular access to a mobile phone with SMS capabilities\n* Care partner who is unable or unwilling to participate in follow-up over 30 days\n* Care partner of a patient enrolled in hospice or receiving end-of-life care",{"count":94,"type":21},80,[24],"The purpose of this research study is to develop and test a text-messaging intervention for emergency department (ED) discharge care transitions experienced by caregivers of older adults with cognitive impairment.",[98,99,100,30],"Dementia","Caregiver","Emergency Department","2026-02-19",{"date":103,"type":42},"2026-02-23",{"date":105,"type":21},"2027-03",{"date":107,"type":21},"2030-06-30",{"name":109,"class":49},"Yale University",{"id":111,"slug":112,"hasResults":11,"nctId":113,"briefTitle":114,"officialTitle":115,"acronym":116,"eligibilityCriteria":117,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":118,"targetDuration":4,"studyType":22,"phases":120,"briefSummary":121,"conditions":122,"keywords":132,"overallStatus":141,"whyStopped":4,"lastUpdateSubmitDate":142,"lastUpdatePostDateStruct":143,"startDateStruct":145,"completionDateStruct":147,"leadSponsor":149,"locationsCount":50},"100566450","efficiency-of-the-medidux-smartphone-app-for-demission-management-in-patients-medicated-in-acute-admission-unit-aau-100566450","NCT06655337","Efficiency of the \"Medidux\" Smartphone App for Demission Management in Patients Medicated in Acute Admission Unit (AAU)","Efficiency of the \"Medidux\" Smartphone App for Demission Management in Patients Medicated in Acute Admission Unit (AAU): a Randomized Controlled Trial.","EffiDux","Inclusion Criteria:\n\n* Signed Informed Consent Form (ICF)\n* Age ≥ 18 years\n* (Self-)admission to the involved Acute Admissions Unit (AAU)\n* \"Lead symptom\" identified as coughing, back pain or abdominal discomfort\n* Participant within ESI triage system group 4 (standard) and 5 (non-urgent)\n* German-speaking\n* Ownership of a smartphone or other mobile device with iOS or Android operating system\n\nExclusion Criteria:\n\n* Age \\\u003C 18 years\n* Participant whose compliance to the study's protocol, e.g. due to mental health problems, physical problems, or the private life situation, can be justifiably doubted\n* Participant with insufficient knowledge about the use of a smartphone or other mobile device with iOS or Android operating system\n* Participant already using or planning to use another comparable electronic patient-reported symptom monitoring system (e.g. CANKADO) during this trial",{"count":119,"type":21},417,[24],"The goal of this clinical trial is to evaluate whether the use of the medidux™ smartphone app can optimize post-discharge management for patients admitted to Acute Admission Units (AAU) with non-urgent health complaints. This trial includes adult patients (age ≥ 18) in Emergency Severity Index (ESI) triage system groups 4 (standard) or 5 (non-urgent), presenting with primary symptoms such as cough, back pain, or abdominal discomfort.\n\nThe main question it aims to answer is:\n\nCan the medidux™ app reduce the incidence of AAU readmissions, emergency hospitalizations, or consultations with other medical providers within 7 days after initial admission?\n\nResearchers will compare participants using the medidux™ app (intervention arm) with those receiving standard care (control arm) to observe potential differences in the rates of readmissions, emergency hospitalizations, and medical consultations.\n\nParticipants will:\n\n* use the medidux™ app to monitor their symptoms and vital parameters for 7 days after discharge (intervention arm).\n* receive follow-up consultations at day 7 and at day 28 to assess symptom progression and any healthcare interactions (both arms).",[123,124,125,126,127,128,129,130,30,131],"Acute Disease","Acute Hospitalization","Coughing","Back Pain","Abdominal Pain (AP)","Patient Discharge","Patient Readmission","Mobile Health Apps","Patient Reported Outcome (PRO)",[123,128,129,125,126,133,134,135,136,137,138,139,140],"Abdominal Pain","Mobile Health Applications","Remote Monitoring","Post-discharge Care","Symptom Monitoring","Health Behaviour","Telemedicine","Randomized Controlled Trial","RECRUITING","2025-09-29",{"date":144,"type":42},"2025-10-03",{"date":146,"type":42},"2025-09-28",{"date":148,"type":21},"2027-03-28",{"name":150,"class":151},"Mobile Health AG","INDUSTRY"]