[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"mobile-health\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:mobile-health":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,10,0,[8,45,70,95,121,146,176,207,229,246],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":4},"100642375","gutcheck-optimization-of-a-personalized-mobile-health-app-for-survivors-of-gastrointestinal-cancer-100642375",false,"NCT07661017","GutCheck: Optimization of a Personalized Mobile Health App for Survivors of Gastrointestinal Cancer","Inclusion\n\nSurvivors of GI cancer are eligible if they are:\n\n* ≥18 years old\n* reside in or have received cancer care in Minnesota\n* own a smartphone • consent to install the GutCheck app and discontinue diet tracking in other lifestyle apps (e.g., MyFitness, Fitbit, Noom).\n* are English-speaking\n* have received a GI cancer diagnosis (e.g., esophageal, gastric, colorectal, liver, pancreatic, etc)\n* At least 2 months post-cancer treatment\n\nInclusion criteria for oncology specialists (oncologists, advanced practice providers, nurses, dietitians, and patient navigators) include:\n\n* Have interacted with at least 1 cancer patient or survivor in the past month.\n* Have experience working with electronic health records (EHR).\n\nExclusion\n\n* Currently pregnant (Patient Study ONLY)\n* Pregnancy status may be self-reported by the participant.\n* Individuals who are postmenopausal, surgically sterile, or otherwise unable to become pregnant are not subject to this exclusion.\n* Active cancer or receiving treatment for another cancer.\n* Currently taking or has taken antibiotics in the last 3 months.\n* Diagnosis of inflammatory bowel disease (e.g., Crohn's Disease, ulcerative colitis), and\u002For celiac disease.\n* Involuntary weight loss of 10% or more of usual body weight within 6 months, or involuntary loss of 5% or more of usual body weight in 1 month.\n\nOncology specialists' exclusion criteria include:\n\n* Unable to participate in an interview",true,"ALL","18 Years",{"count":19,"type":20},200,"ESTIMATED","INTERVENTIONAL",[23],"NA","There are two components to the study: a patient and a clinician study. The clinician study will include one-hour semi-structured interviews with oncology specialists to identify facilitators and barriers to integrating digital diet interventions into the clinical workflow, and to understand their needs and preferences for digital diet interventions. The patient study aims to investigate initial feasibility, efficacy and acceptability of the GutCheck app and intervention. It will last 9 weeks and involves 2 study visits and 2 active phases with a transition week and optional transition visit between phases. During active phases, participants will be asked to use the GutCheck app every day. Prior to the first active phase, participants will go through informed consent and app training. The first active phase will last two weeks and will focus on tracking participants' diet, gastrointestinal (GI) symptoms, and stress. The data collected during the first active phase will be used to identify any potential trigger foods that may contribute to GI symptoms, but only if the participant reports experiencing GI symptoms. Between active phases, participants will have one Transition Week, where results from the first phase are given to the participants with the option to attend a Transition Week Visit. The second active phase will last four weeks and will involve the message intervention. A single-blind, micro-randomized trial design will be used to repeatedly randomize participants to different intervention combinations, determining both the timing and frequency of intervention message delivery throughout the day. Lastly, there will be an exit visit and interview within a week from the intervention to collect post-intervention measures and ask about the participant's experience with the GutCheck app.",[26,27,28,29,30,31,32],"Gastrointestinal","Mobile Health","Gastrointestinal Symptoms","Gut Health","Gastrointestinal Cancer","Survivorship","GI Cancer","NOT_YET_RECRUITING","2026-06-16",{"date":36,"type":37},"2026-06-22","ACTUAL",{"date":39,"type":20},"2026-12",{"date":41,"type":20},"2030-06",{"name":43,"class":44},"Masonic Cancer Center, University of Minnesota","OTHER",{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":54,"phases":4,"briefSummary":55,"conditions":56,"keywords":4,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":69},"100512333","long-term-evaluation-of-a-mobile-application-for-follow-up-of-cardiac-patients-cardio2u-study-100512333","NCT05951088","Long-term Evaluation of a Mobile Application for Follow-up of Cardiac Patients (Cardio2U Study)","Long-term Evaluation of a Mobile Application for Follow-up of Cardiac Patients","Cardio2U","Inclusion Criteria:\n\n1. Age ≥ 18 years,\n2. Patients in whom AF or atrial flutter is diagnosed with an electrocardiogram (12-lead, Holter monitor,…) and\u002For patients in whom HF is diagnosed in their medical records,\n3. Patients who are capable of signing the informed consent.\n\nExclusion Criteria:\n\n1. Not able to speak and read Dutch,\n2. Cognitive impaired (e.g. severe dementia),\n3. No smartphone or tablet available.",{"count":19,"type":20},"OBSERVATIONAL","This trial has to aim to evaluate an innovative, in-house developed mobile application supporting patients in their home environment by actively involving them in different aspects of their condition and treatment. The usability, long-term adherence and patient satisfaction will be studied in patients with atrial fibrillation (AF) and\u002For heart failure (HF).",[57,58,27],"Follow-up","Education","RECRUITING","2026-05-04",{"date":62,"type":37},"2026-05-08",{"date":64,"type":37},"2023-05-23",{"date":66,"type":20},"2026-05-30",{"name":68,"class":44},"University Hospital, Antwerp",1,{"id":71,"slug":72,"hasResults":11,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":4,"eligibilityCriteria":76,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":77,"targetDuration":4,"studyType":21,"phases":79,"briefSummary":80,"conditions":81,"keywords":84,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":86,"lastUpdatePostDateStruct":87,"startDateStruct":89,"completionDateStruct":91,"leadSponsor":93,"locationsCount":69},"100538305","text4father-r21-social-media---efficacy-trial-100538305","NCT06289101","text4FATHER R21: Social Media - Efficacy Trial","Adapting text4FATHER to Directly Link to First-time Expectant Fathers Using Social Media to Improve Infant and Family Health","Inclusion Criteria:\n\n* Aged ≥18 years\n* Live in the U.S.\n* Speak English\n* Mother gestational age at enrollment less than 25 weeks\n* First-time father-to-be\n* Willing\u002Fable to receive texts.\n\nExclusion Criteria:\n\n* Individuals who are minors\n* Do not speak English\n* Unable to provide informed consent\n* Not a first-time father\n* Not willing\u002Funable to receive texts\n* In the past 12 months, any safety concern reported between father-to-be and the mother-to-be, including report of any physical, emotional, sexual harm, threatening behaviors, police involvement, restraining or protective order",{"count":78,"type":20},180,[23],"This project will be the first to examine the efficacy of a text messaging intervention designed to recruit first-time fathers-to-be using social media across the U.S. to become involved during pregnancy through two months of postnatal age to support infant, mother, and father well-being.",[82,27,83],"Fathers","Nuclear Family",[85],"Fatherhood","2025-09-17",{"date":88,"type":37},"2025-09-18",{"date":90,"type":37},"2024-09-10",{"date":92,"type":20},"2026-08",{"name":94,"class":44},"Johns Hopkins University",{"id":96,"slug":97,"hasResults":11,"nctId":98,"briefTitle":99,"officialTitle":100,"acronym":4,"eligibilityCriteria":101,"healthyVolunteers":11,"sex":16,"minAge":102,"maxAge":4,"enrollmentInfo":103,"targetDuration":4,"studyType":21,"phases":105,"briefSummary":106,"conditions":107,"keywords":4,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":112,"lastUpdatePostDateStruct":113,"startDateStruct":115,"completionDateStruct":117,"leadSponsor":119,"locationsCount":69},"100583679","mhealth-person-centred-self-care-support-for-homebound-older-adults-a-hybrid-effectiveness-implementation-study-100583679","NCT06879457","mHealth Person-centred Self-care Support for Homebound Older Adults: A Hybrid Effectiveness-implementation Study","Empowering Homebound Older Adults in Self-care Using a Mobile Health-assisted, Person-centred Care Approach: A Hybrid Effectiveness-implementation Design","Inclusion Criteria:\n\n* Aged 60 years or older;\n* Unable to leave home more than twice per week due to physical or functional health problems;\n* Own and have basic proficiency in using a smartphone;\n* Speak Cantonese;\n* Indicate sufficient cognitive ability; and\n* Be moderately frail or below.\n\nExclusion Criteria:\n\n* Unable to hear, see, or communicate effectively;\n* Be completely bed-bound; or\n* Reside in an area without stable internet coverage.","60 Years",{"count":104,"type":20},130,[23],"The aim of the study is to evaluate the effectiveness and implementation of the mobile health (mHealth)-assisted, person-centred care (PCC) self-care support programme for homebound older adults. The researcher will compare PCC approach to a conventional care provider-led model. Participants (n = 130) will receive the intervention of six bi-weekly WhatsApp video call sessions over three months with nurse case managers (NCMs).",[27,108,109,110,111],"Person-Centred Care","Self-Care","Homebound","Older Adults","2025-09-08",{"date":114,"type":37},"2025-09-15",{"date":116,"type":37},"2025-03-10",{"date":118,"type":20},"2027-12-31",{"name":120,"class":44},"The Hong Kong Polytechnic University",{"id":122,"slug":123,"hasResults":11,"nctId":124,"briefTitle":125,"officialTitle":126,"acronym":127,"eligibilityCriteria":128,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":129,"targetDuration":4,"studyType":21,"phases":130,"briefSummary":131,"conditions":132,"keywords":135,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":137,"lastUpdatePostDateStruct":138,"startDateStruct":140,"completionDateStruct":142,"leadSponsor":144,"locationsCount":69},"100596360","digital-follow-up-program-after-discharge-home-following-thoracic-surgery-100596360","NCT07044440","Digital Follow-up Program After Discharge Home Following Thoracic Surgery","The Development and Evaluation of a Digital Follow-up Program During the Initial Four Weeks After Discharge Home Following Thoracic Surgery. A Confirmatory, Single-center, Prospective, Non-blinded, Randomized, Controlled Study","DFP","Inclusion Criteria:\n\n* Patients who have signed an informed consent form and underwent a surgery performed at the Thoracic Surgery Department of the University Hospital Basel\n* Age ≥ 18 years at the time of informed consent\n* First participation in the Study\n* Patient operated under general anesthesia\n* Patients who are in possession of a smart phone or personal computer and have an e-mail account and are able to answer a digital questionnaire. Or an immediate caretaker in the same household owns a smartphone or personal computer and is familiar with the use\n* Patients who understand verbal and written German or French\n* Patients discharged at home after surgery\n* Hospital stay \\> 3 nights after surgery\n\nExclusion Criteria:\n\n* Patients under preoperative opioid\u002Fcortisone therapy\n* Patients who are unable to follow the procedure of the study, e. g. read or understand German or French, psychological disorders, dementia, etc.\n* Enrolment of the investigator, his\u002Fher family members, employees and other dependent person\n* Patients with polytrauma or who underwent mediastinoscopy",{"count":19,"type":20},[23],"The aim of the study is to evaluate whether a digital follow-up program can improve postoperative pain management and quality of life in patients during the first 28 days after discharge home following thoracic surgery, compared to standard follow-up care.",[133,27,134,57],"Thoracic Surgery","Post Operative Recovery",[136,133],"Electronic Follow-up","2025-08-04",{"date":139,"type":37},"2025-08-05",{"date":141,"type":37},"2025-07-30",{"date":143,"type":20},"2026-06",{"name":145,"class":44},"University Hospital, Basel, Switzerland",{"id":147,"slug":148,"hasResults":11,"nctId":149,"briefTitle":150,"officialTitle":151,"acronym":152,"eligibilityCriteria":153,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":154,"enrollmentInfo":155,"targetDuration":4,"studyType":21,"phases":157,"briefSummary":158,"conditions":159,"keywords":166,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":167,"lastUpdatePostDateStruct":168,"startDateStruct":170,"completionDateStruct":172,"leadSponsor":174,"locationsCount":69},"100508571","electronic-patient-decision-support-system-for-patients-with-type-2-diabetes-diapadess-100508571","NCT05902156","Electronic Patient Decision Support System for Patients with Type 2 Diabetes (DiaPaDeSS)","The Effect of Electronic Patient Decision Support System Developed for Use Patients with Type 2 Diabetes (DiaPaDeSS) on Self-Management, Patient Activation and Metabolic Parameters","DiaPaDeSS","Inclusion Criteria:\n\n* Patients with type 2 diabetes who had been followed up and treated at the Endocrinology and Metabolic Diseases Polyclinic\n* Aged between 18-65 years\n* Patients who know their diagnosis and can verbally express it\n* Have been diagnosed with type 2 diabetes for at least six months\n* Who are literate\n* Who have internet access at home, who have one of the tools such as a computer, tablet or smartphone and can use these tools\n* Consented to participate in the study\n* Had no other psychiatric or mental barriers to answering the questions, language or cognitive difficulties, and barriers to verbal or written communication\n\nExclusion Criteria:\n\n* Diagnosed with myocardial infarction, stroke or diabetic foot in the last six months\n* Diagnosed with type 1 diabetes or gestational diabetes\n* Diagnosed with terminal illness\n* Using steroid therapy\n* Had pregnant\n* Having dementia and cognitive deficits\n* Having retinopathy or advanced neuropathy\n* Patients whose information is not allowed to be accessed","65 Years",{"count":156,"type":20},72,[23],"This study evaluates the effects of an electronic patient decision support system developed for the use of patients with type 2 diabetes (DiaPaDeSS) on self-management, patient activation, and metabolic parameters. To manage type 2 diabetes after discharge, patients must continue to perform interventions at home, such as blood glucose monitoring, blood pressure measurement, weight measurement, medication use, and foot care. To achieve this, patient's self-management and activation levels should be increased. This can also lead to positive improvements in the metabolic parameters. It would be beneficial to develop DiaPaDeSS that can increase the self-management and activation levels of patients with type 2 diabetes. The investigators will develop the DiaPaDeSS intervention protocol. Our content includes patient education information about type 2 diabetes, self-management practice tasks (daily, weekly, quarterly), a type 2 diabetes patient education program according to DiaPaDeSS algorithms, and measurement questionnaires. The content of the DiaPaDeSS will be evaluated by 10 experts in the fields of medicine, nursing, and informatics. A feasibility test with seven patients will be conducted to evaluate the usability of DiaPaDeSS. A single-blind, randomized controlled trial design will be used. Patients with type 2 diabetes will be pretested and randomized (intervention 36, control 36) to the DiaPaDeSS intervention and control groups. Both the DiaPaDeSS intervention and control groups will use the DiaPaDeSS for three months. While participants in the DiaPaDeSS intervention group can reach all contents of the DiaPaDeSS, others can reach only these fields: self-management practice tasks (daily, weekly, quarterly), and measurements questionnaires. The effectiveness of the DiaPaDeSS will be evaluated at baseline and at month 3.",[27,160,161,162,163,164,165],"Type 2 Diabetes","Patient Activation","Self-Management","Decision Support System","Nursing","Randomized Controlled Trial",[27,160,161,163,162,164,165],"2025-02-04",{"date":169,"type":37},"2025-02-06",{"date":171,"type":20},"2025-03-30",{"date":173,"type":20},"2025-11-01",{"name":175,"class":44},"Akdeniz University",{"id":177,"slug":178,"hasResults":11,"nctId":179,"briefTitle":180,"officialTitle":181,"acronym":4,"eligibilityCriteria":182,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":183,"enrollmentInfo":184,"targetDuration":4,"studyType":21,"phases":186,"briefSummary":187,"conditions":188,"keywords":191,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":198,"lastUpdatePostDateStruct":199,"startDateStruct":201,"completionDateStruct":203,"leadSponsor":205,"locationsCount":69},"100570165","effectiveness-and-implementation-of-mobile-health-platform-for-medication-management-and-e-labeling-edrugsafe-100570165","NCT06703697","Effectiveness and Implementation of Mobile Health Platform for Medication Management and E-Labeling (eDrugSafe)","Evaluating the Effectiveness and Implementation of Mobile Health Platform for Medication Management and E-Labeling (eDrugSafe): a Cluster Randomized Trial","Inclusion Criteria:\n\n1. Adults aged 18 to 79 years.\n2. Individuals who can speak and understand Korean.\n3. Possession of a personal electronic device capable of accessing mobile applications and web services over wireless internet (bring participants' own device, BYOD).\n4. Patients taking three or more medications with at least one medication prescribed for 28 days or longer.\n5. Individuals who have provided direct consent to participate in the study.\n\nExclusion Criteria:\n\n1. Individuals using any mobile web platform other than eDrugSafe for medication safety information purposes after enrollment.\n2. Individuals who do not consent to participate in the study or who withdraw their consent.","79 Years",{"count":185,"type":20},360,[23],"The goal of this cluster randomized trial is to learn if eDrugSafe, a mobile web platform for drug electronic labeling (e-labeling) and medication management, can improve medication adherence and self-efficacy in adults who take multiple medications. This study will also assess whether eDrugSafe is feasible and acceptable for use in real clinical settings, especially in local pharmacies.\n\nThe main questions it aims to answer are:\n\n* Can eDrugSafe improve medication adherence, self-efficacy, and quality of life for adults taking multiple medications and reduce hospitalizations?\n* Is eDrugSafe acceptable and feasible for implementing drug e-labeling and supporting medication management in community settings?\n\nResearchers will compare eDrugSafe to usual care (traditional paper methods) to see if eDrugSafe is effective in supporting adults who take multiple medications, and if it can be feasibly implemented in local pharmacies.\n\nParticipants will:\n\n* Visit a local pharmacy randomly assigned to use eDrugSafe or traditional care methods and decide if they wish to join the study.\n* Use either eDrugSafe to access medication information and manage their medication history, or receive usual care with paper-based methods, for 6 months.\n* Complete surveys at the start of the study, at 3 months, and at 6 months to measure effectiveness and implementation outcomes.",[27,189,190],"Medication Management","Drug Labelling",[27,189,192,193,194,195,196,197],"Drug E-label","electronic labeling","hybrid study","implementation","cluster randomized trial","Electronic Medicinal Product Information (ePI)","2024-11-25",{"date":200,"type":37},"2024-11-27",{"date":202,"type":37},"2024-08-12",{"date":204,"type":20},"2025-07-31",{"name":206,"class":44},"Seoul National University",{"id":208,"slug":209,"hasResults":11,"nctId":210,"briefTitle":211,"officialTitle":212,"acronym":4,"eligibilityCriteria":213,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":214,"targetDuration":4,"studyType":21,"phases":216,"briefSummary":217,"conditions":218,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":220,"lastUpdatePostDateStruct":221,"startDateStruct":223,"completionDateStruct":225,"leadSponsor":227,"locationsCount":69},"100559894","ai-powered-chatbot-vs-human-counselors-in-smoking-cessation-100559894","NCT06570070","AI-powered Chatbot vs. Human Counselors in Smoking Cessation","Effectiveness of Artificial Intelligence (AI)-Powered Chatbot vs. Human Counselors in Smoking Cessation","Inclusion Criteria:\n\n1. aged 18 and above, reside in Zhuhai for the next 6 months;\n2. smoke at least 1 cigarette or use e-cigarettes daily;\n3. Having a smartphone and a WeChat account, being able to use WeChat skillfully.\n\nExclusion Criteria:\n\n1. Smokers who have communication barrier (either physically or cognitively);\n2. Smokers who are currently participating in other SC programmes or services",{"count":215,"type":20},300,[23],"This study aims to explore the feasibility and preliminary effectiveness of AI-powered chatbot support in community smokers.",[219,27],"Smoking Cessation","2024-08-22",{"date":222,"type":37},"2024-08-26",{"date":224,"type":20},"2024-09-01",{"date":226,"type":20},"2025-12-30",{"name":228,"class":44},"Beijing Normal University",{"id":230,"slug":231,"hasResults":11,"nctId":232,"briefTitle":233,"officialTitle":234,"acronym":4,"eligibilityCriteria":235,"healthyVolunteers":11,"sex":16,"minAge":102,"maxAge":4,"enrollmentInfo":236,"targetDuration":4,"studyType":21,"phases":237,"briefSummary":238,"conditions":239,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":220,"lastUpdatePostDateStruct":241,"startDateStruct":242,"completionDateStruct":243,"leadSponsor":245,"locationsCount":69},"100559895","mobile-based-intervention-to-promote-physical-activity-among-the-elderly-100559895","NCT06570083","Mobile-Based Intervention to Promote Physical Activity Among the Elderly","Mobile-Based Intervention to Promote Physical Activity Among the Elderly With Chronic Diseases","Inclusion Criteria:\n\n1. Age ≥60 years and diagnosed with at least one chronic disease\n2. Owns a smartphone and is proficient in using WeChat\n3. Daily sedentary time ≥6 hours\n\nExclusion Criteria:\n\n1. recent surgeries, injuries, or other conditions that would prevent simple physical activity\n2. hearing, vision, or physical disabilities",{"count":19,"type":20},[23],"This study aims to explore the feasibility and preliminary effectiveness of a mobile phone-based intervention among elderly individuals with chronic diseases.",[27,240],"Physical Activity",{"date":222,"type":37},{"date":224,"type":20},{"date":244,"type":20},"2026-09-30",{"name":228,"class":44},{"id":247,"slug":248,"hasResults":11,"nctId":249,"briefTitle":250,"officialTitle":250,"acronym":4,"eligibilityCriteria":251,"healthyVolunteers":15,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":252,"targetDuration":4,"studyType":54,"phases":4,"briefSummary":254,"conditions":255,"keywords":257,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":260,"lastUpdatePostDateStruct":261,"startDateStruct":263,"completionDateStruct":265,"leadSponsor":267,"locationsCount":69},"100527338","mobile-health-applications-in-pediatric-patient-management-clinicians-perceptions-expectations-and-experiences-100527338","NCT06146465","Mobile Health Applications in Pediatric Patient Management: Clinicians' Perceptions, Expectations and Experiences","Inclusion Criteria:\n\n* Being a medical doctor involved in the management of pediatric patients (0-18 years old)\n\nExclusion Criteria:\n\n* Other specialists outside of pediatrics and family medicine.",{"count":253,"type":20},368,"The goal of this observational study is to to determine the perceptions, expectations and experiences of physicians involved in pediatric patient management about mHealth applications. The main questions it aims to answer are:\n\n* Is the use of mHealth applications in pediatric patient management different between pediatricians and other specialties?\n* What are the most commonly used mHealth applications in pediatric patient management? Participants will fill out an online survey form.",[27,256],"Pediatrics",[258,259],"mobile health","pediatric","2024-08-05",{"date":262,"type":37},"2024-08-06",{"date":264,"type":37},"2023-10-01",{"date":266,"type":20},"2024-10-01",{"name":268,"class":44},"Dr. Behcet Uz Children's Hospital"]