[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"mobile-application\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:mobile-application":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,14,0,[8,49,81,122,151,175,214,247,277,313,347,374,402,426],{"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":32,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100635725","development-of-a-mobile-application-called-tansiyoritim-for-hypertension-patients-100635725",false,"NCT07556419","Development of a Mobile Application Called TansiyoRitim for Hypertension Patients","The Effect of a Mobile Application Developed for Hypertension Patients on Blood Pressure Control, Treatment Adherence, and Self-Efficacy: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Diagnosed with hypertension at least 1 year prior to enrollment\n* Currently using antihypertensive medication\n* Able to use a smartphone\n* Able to measure blood pressure at home\n* No severe visual or hearing impairment\n* Able to communicate in Turkish\n* Literate\n* Willing to participate and provide informed consent\n\nExclusion Criteria:\n\n* Age under 18 or over 85 years\n* Presence of severe comorbid chronic disease affecting participation\n* Severe physical or cognitive impairment preventing participation\n* Body mass index (BMI) ≥ 30 kg\u002Fm²","ALL","18 Years","85 Years",{"count":20,"type":21},160,"ESTIMATED","INTERVENTIONAL",[24],"NA","Based on King's Theory of Goal Success, this project is designed to develop a mobile application called TansiyoRitim for individuals over the age of 18 diagnosed with hypertension. The research consists of the following phases: creating educational content, designing the mobile application, and evaluating the application and its effectiveness. Within the scope of the research, participants' blood pressure control, self-efficacy levels, and treatment adherence behaviors will be assessed using valid and reliable measurement tools, and the goal is to support these behaviors through the developed mobile health application. Participants' clinical treatment processes, pharmacological treatment adjustments planned by the physician, and changes in medication dosages will be excluded from the scope of the project. No intervention will be made in the medical treatment currently being administered during the study; participants' routine clinical follow-up and treatment processes will continue within the framework of standard care. Only educational and mobile app-based supportive interventions will be implemented within the scope of the research.",[27,28,29,30,31],"Hypertension","Mobile Application","Blood Pressure Control","Treatment Adherence","Self-Efficacy",[27,33,34,30,31,35],"mobile application","blood pressure control","King's Goal Achievement Theory","NOT_YET_RECRUITING","2026-06-16",{"date":39,"type":40},"2026-06-18","ACTUAL",{"date":42,"type":21},"2026-07-01",{"date":44,"type":21},"2027-03-20",{"name":46,"class":47},"Kafkas University","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":4,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":16,"minAge":56,"maxAge":17,"enrollmentInfo":57,"targetDuration":4,"studyType":22,"phases":59,"briefSummary":60,"conditions":61,"keywords":66,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":48},"100585491","nurse-parental-support-using-a-proactive-mobile-app-in-symptom-management-for-children-with-mechanical-ventilation-100585491","NCT06903052","Nurse Parental Support Using a Proactive Mobile App in Symptom Management for Children With Mechanical Ventilation","Nurse Parental Support Using a Proactive Mobile App in Symptom Management for Children With Medical Complexity Requiring Mechanical Ventilation: an Effectiveness-implementation Hybrid 2 Study","The inclusion criteria for parents are:\n\n1. parent of a child with mechanical ventilation aged 2-18\n2. having a Smartphone\n3. able to communicate in Chinese and read Chinese\n4. living with his\u002Fher child at home.\n\nThe exclusion criteria for parents are:\n\n1. a reported mental health disorder\n2. engaging in other structured programs related to symptom management 3) living in an area with no internet coverage.","2 Years",{"count":58,"type":21},52,[24],"The aims of this study are to test the effectiveness of a nurse support using a proactive mobile app to enhance parental self-efficacy in symptom management for children using mechanical ventilations, and alongside identify factors facilitating or deterring the program implementation.\n\nA single group pre-post quasi-experimental study on parents of CMC requiring mechanical ventilation.\n\nParents will be recruited from a non-government office, with an estimated sample size of 52 parents. Self-administrated questionnaire, and semi-structured interview guide will be used for data collection.",[62,63,64,28,65],"Child With Medical Complexity","Symptom Management","Self Efficacy","Nurse-led Supportive Care",[67,68,69,33,70],"parental self-efficacy","children requiring mechanical ventilation","symptom management","nurse-led parental support","RECRUITING","2026-06-11",{"date":74,"type":40},"2026-06-15",{"date":76,"type":40},"2025-05-06",{"date":78,"type":21},"2028-04-30",{"name":80,"class":47},"The Hong Kong Polytechnic University",{"id":82,"slug":83,"hasResults":11,"nctId":84,"briefTitle":85,"officialTitle":86,"acronym":87,"eligibilityCriteria":88,"healthyVolunteers":89,"sex":90,"minAge":91,"maxAge":92,"enrollmentInfo":93,"targetDuration":4,"studyType":22,"phases":95,"briefSummary":96,"conditions":97,"keywords":109,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":113,"lastUpdatePostDateStruct":114,"startDateStruct":116,"completionDateStruct":118,"leadSponsor":120,"locationsCount":48},"100628155","effectiveness-of-an-mhealth-innovation-on-the-impact-of-menstrual-complaints-in-adolescents-100628155","NCT07457957","Effectiveness of an mHealth Innovation on the Impact of Menstrual Complaints in Adolescents","The Effectiveness of an mHealth Innovation on the Impact of Menstrual Complaints in Adolescents - A Randomised Controlled Trial","MGA","Inclusion Criteria:\n\n* Dutch, English, Turkish or Moroccan-Arabic speaking\n* Post menarche\n* Access to a smartphone or tablet with iOS or Android operating system\n\nExclusion Criteria:\n\n* Amenorrhea\n* Pregnancy\n* No menstrual bleeding or withdrawel bleeding in the 3 months prior to inclusion.\n* Previously or currently under treatment by a health care provider for menstrual complaints",true,"FEMALE","12 Years","21 Years",{"count":94,"type":21},874,[24],"The aim of this study is to improve menstrual health-related quality of life in adolescents by using a mobile menstrual health tracker. We will perform a randomized controlled trial to evaluate the (cost)-effectiveness of this mHealth intervention.",[98,99,100,101,102,103,104,105,28,106,107,108],"Dysmenorrhea","Heavy Menstrual Bleeding","Menstrual Cramps","Menstrual Bleeding, Heavy","Menstrual Discomfort","Menstrual Cycle Abnormal","Menstrual Disorder","Menstrual Health","mHealth","Menstrual Health Intervention","Adolescent",[110,106,111,108,112],"randomized clinical trial","Menstrual health","Menstrual Tracker App","2026-03-04",{"date":115,"type":40},"2026-03-09",{"date":117,"type":21},"2026-02-16",{"date":119,"type":21},"2029-05-31",{"name":121,"class":47},"Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)",{"id":123,"slug":124,"hasResults":11,"nctId":125,"briefTitle":126,"officialTitle":127,"acronym":128,"eligibilityCriteria":129,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":130,"targetDuration":4,"studyType":22,"phases":132,"briefSummary":133,"conditions":134,"keywords":137,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":142,"lastUpdatePostDateStruct":143,"startDateStruct":145,"completionDateStruct":147,"leadSponsor":149,"locationsCount":4},"100620489","mobile-education-and-comfort-in-ostomy-patients-100620489","NCT07358286","MOBILE EDUCATION AND COMFORT IN OSTOMY PATIENTS","THE EFFECT OF KOLCABA'S COMFORT THEORY-BASED MOBILE EDUCATION ON COMFORT LEVELS OF OSTOMY PATIENTS: A RANDOMIZED CONTROLLED TRIAL","STOMA-PLUS","Inclusion Criteria:\n\n* Adults aged 18 years and older\n* Patients with a stoma (colostomy or urostomy)\n* Ability to use a smartphone or mobile device\n* Willingness to participate in the study\n* Ability to provide informed consent\n\nExclusion Criteria:\n\n* Cognitive impairment that prevents understanding of the study procedures\n* Severe psychiatric disorders\n* Inability to use mobile technology\n* Participation in another interventional study during the study period",{"count":131,"type":21},68,[24],"Purpose of the Study\n\nThis study aims to understand whether a mobile education program can improve comfort levels in people living with a stoma. A stoma is a surgical opening created on the abdomen to allow stool or urine to leave the body. Living with a stoma can affect daily life in many ways, including physical comfort, emotional well-being, social life, and the home environment.\n\nThe education program used in this study is based on Kolcaba's Comfort Theory. This theory focuses on comfort as a whole and includes physical, emotional, social, and environmental aspects of a person's life. The study will compare people who receive mobile education with those who receive standard hospital care only.\n\nWho Can Take Part\n\nAdults aged 18 years and older who are scheduled to have colostomy, ileostomy, or urostomy surgery may take part in this study. Participants must be able to communicate in Turkish, read and understand written information, and agree to join the study voluntarily.\n\nPeople with severe cognitive problems, serious communication difficulties, or major vision or hearing problems will not be included.\n\nWhat Will Happen in the Study\n\nParticipants will be randomly assigned to one of two groups:\n\nMobile Education Group\n\nStandard Care Group\n\nBoth groups will receive routine care provided by the hospital.\n\nParticipants in the mobile education group will also receive access to a mobile application designed specifically for people with a stoma. This application includes:\n\nEasy-to-understand information about stoma care\n\nAnimated educational videos showing step-by-step stoma care practices\n\nGuidance on skin care, pouch changing, and hygiene\n\nInformation on common problems and when to seek medical help\n\nReminders to support daily stoma care routines\n\nThe mobile application can be used on smartphones and does not include diagnosis or treatment. It is for education and support only.\n\nParticipants in the standard care group will receive usual hospital education and care. After the study is completed, they will also be offered the mobile education program.\n\nWhat Participants Will Be Asked to Do\n\nAll participants will be asked to answer questionnaires that measure comfort levels at several time points:\n\nBefore surgery\n\nOne day after surgery\n\nFifteen days after discharge (by phone)\n\nOne month after surgery (during a clinic visit)\n\nParticipants in the mobile education group will be shown how to use the application and may use it as often as they wish. Researchers may contact participants to ask about their experience using the app and to identify any difficulties.\n\nPossible Benefits\n\nParticipants may gain better understanding of stoma care and feel more confident managing daily life with a stoma. The mobile education program may help reduce discomfort, support emotional well-being, and improve overall quality of life.\n\nThe results of this study may help healthcare professionals develop better education tools and support programs for people living with a stoma.\n\nRisks and Safety\n\nThis study does not involve experimental medical treatments. The mobile application provides education only. Personal data will not be collected through the app, and all information will be kept confidential. Participants may leave the study at any time without affecting their medical care.\n\nWhy This Study Is Important\n\nAccess to stoma care education can be limited due to time constraints, staff availability, and hospital resources. Mobile education may provide an easy and accessible way for people to receive reliable information whenever they need it.\n\nThis study will help determine whether a comfort-focused mobile education program can support people living with a stoma and improve their overall comfort and well-being.",[135,136,28],"Stoma","Ostomy",[138,139,140,141],"Ostomy Care","Mobile Health","Kolcaba's Comfort Theory","Nursing","2026-01-14",{"date":144,"type":40},"2026-01-22",{"date":146,"type":21},"2026-01",{"date":148,"type":21},"2026-06",{"name":150,"class":47},"Ege University",{"id":152,"slug":153,"hasResults":11,"nctId":154,"briefTitle":155,"officialTitle":156,"acronym":4,"eligibilityCriteria":157,"healthyVolunteers":11,"sex":90,"minAge":17,"maxAge":4,"enrollmentInfo":158,"targetDuration":4,"studyType":22,"phases":160,"briefSummary":161,"conditions":162,"keywords":4,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":165,"lastUpdatePostDateStruct":166,"startDateStruct":168,"completionDateStruct":170,"leadSponsor":172,"locationsCount":174},"100582352","effectiveness-of-digital-intervention-hm4mh-app-on-perinatal-psychological-wellbeing-100582352","NCT06862193","Effectiveness of Digital Intervention (HM4MH-app) on Perinatal Psychological Wellbeing","The Effectiveneness of a Digital Intervention (the HM4MH-app) on Perinatal Psychological Wellbeing: Randomized Controlled Trial","Inclusion Criteria:\n\n(i) pregnant women attending a participating maternity health care centre who (ii) have access to their own mobile phone and BankID and is (iii) currently in gestational week 8-15 and (iv) is 18 years or older.\n\nExclusion Criteria:\n\n* Previous psychotic disorder",{"count":159,"type":21},440,[24],"As many as 25% of pregnant women report mental health problems such as depressiveness and anxiety. This is a major concern as mental illness during pregnancy can have severe and long-lasting consequences for the pregnant woman, the baby, as well as the partner. Digital interventions (e.g., apps) have shown to be promising in promoting mental wellbeing, at scale, however, the majority of tools have been developed and evaluated in a general population rather than tailored for pregnancy. The objective of this trial is to investigate the effectiveness of a new digital tool (HealthyMoms4MentalHealth-app) on mental health outcomes during the perinatal period.",[28,163,164],"Behavior","Perinatal Mental Health","2025-12-15",{"date":167,"type":40},"2025-12-22",{"date":169,"type":40},"2025-03-10",{"date":171,"type":21},"2027-12-31",{"name":173,"class":47},"Karolinska Institutet",4,{"id":176,"slug":177,"hasResults":11,"nctId":178,"briefTitle":179,"officialTitle":180,"acronym":181,"eligibilityCriteria":182,"healthyVolunteers":89,"sex":16,"minAge":183,"maxAge":184,"enrollmentInfo":185,"targetDuration":4,"studyType":22,"phases":187,"briefSummary":188,"conditions":189,"keywords":202,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":205,"lastUpdatePostDateStruct":206,"startDateStruct":208,"completionDateStruct":210,"leadSponsor":212,"locationsCount":48},"100567397","a-mobile-app-to-improve-24-hour-movement-guideline-adherence-in-preschoolers-100567397","NCT06667661","A Mobile App to Improve 24-Hour Movement Guideline Adherence in Preschoolers","A Home-Based Intervention to Improve Adherence to the 24-Hour Movement Guidelines in Young Children","Shining Star","Inclusion (Child):\n\n* Ages 3-4 years.\n* Parent report that they meet 0 or 1 recommendation for physical activity, sleep, and screen-time as defined by the 24-hour movement guidelines. The physical activity recommendation is defined as greater than or equal to 3 hours\u002Fday of total physical activity, including 1 hour of moderate-to-vigorous physical activity. The sleep recommendation is defined as 10-13 hours\u002Fday. The sedentary behavior recommendation is defined as less than or equal to 1 hour\u002Fday of sedentary screen-time.\n\nInclusion (Parents):\n\n* Parents must agree to use their mobile phone for the duration of the study (\\~12 weeks) and download the mobile app onto their phone.\n* The parent\u002Fcaregiver is fluent in English to participate in testing the mobile app.\n* The parent\u002Fcaregiver must be willing to travel to KUMC to complete study visits.\n\nExclusion (child):\n\n* Mobility limitations as reported by the parent.\n* Meeting two or more recommendations for physical activity, sleep, and screen-time.\n* Sibling or household member is participating or participated in the study.","3 Years","4 Years",{"count":186,"type":21},80,[24],"The goal of this clinical trial is to evaluate whether a home-based mHealth intervention can improve adherence to the 24-Hour Movement Guidelines in preschool-aged children (3-4 years old) who currently meet 0 or 1 of the guidelines for physical activity, sedentary behavior, and sleep. The main questions it aims to answer are:\n\n* Can the intervention increase the proportion of children meeting all three 24-Hour Movement Guidelines (physical activity, screen-time, and sleep)?\n* Is the intervention feasible for parents to implement, as measured by a parent feedback survey?\n\nResearchers will compare an intervention group to a waitlist control group to assess whether the intervention leads to increased guideline adherence.\n\nParents and Participants:\n\n* Children will wear an accelerometer to track physical activity and sleep patterns.\n* Parents will use a mobile app that delivers weekly lessons and behavior-related goals to encourage healthy movement behaviors in their children.\n* Parents will complete questionnaires on their child's movement behaviors and development at baseline, 6 weeks, and 12 weeks.\n* Additionally, children will undergo motor skills assessments, and parents will provide feedback on cognitive development and behavioral changes.",[190,191,192,193,194,195,196,197,198,199,28,200,201],"Healthy","24-Hour Movement Guidelines","Feasibility Studies","Sleep","Physical Activity","Screen Time","Sedentary Behaviors","Motor Skills","Cognition","Parent-Child Relations","Health Education","Child Development",[194,203,193,201,197,204,190,191,195,196,198,199,28,200],"Sedentary Behavior","Behavioral problems","2025-12-03",{"date":207,"type":40},"2025-12-11",{"date":209,"type":40},"2025-01-29",{"date":211,"type":21},"2026-12-31",{"name":213,"class":47},"University of Kansas Medical Center",{"id":215,"slug":216,"hasResults":11,"nctId":217,"briefTitle":218,"officialTitle":219,"acronym":4,"eligibilityCriteria":220,"healthyVolunteers":11,"sex":16,"minAge":91,"maxAge":17,"enrollmentInfo":221,"targetDuration":4,"studyType":22,"phases":223,"briefSummary":224,"conditions":225,"keywords":231,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":238,"lastUpdatePostDateStruct":239,"startDateStruct":241,"completionDateStruct":243,"leadSponsor":245,"locationsCount":48},"100610511","cesikids-trial-enhancing-psychological-resilience-in-adolescents-with-cancer-100610511","NCT07228533","CesiKids Trial: Enhancing Psychological Resilience in Adolescents With Cancer","Evaluation of the Effectiveness of a Nursing-Based Co-Design Intervention Program (CesiKids) to Enhance Psychological Resilience in Hospitalized Adolescents Diagnosed With Cancer: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Parents have provided informed consent after receiving information,\n* The child has given assent to participate after being informed,\n* The child is between 12 and 18 years of age,\n* The child has been diagnosed with cancer and is currently receiving inpatient treatment,\n* The child is undergoing chemotherapy and\u002For radiotherapy,\n* The child is able to use a computer and\u002For smartphone,\n* The child can understand and speak Turkish.\n\nExclusion Criteria:\n\n* Receiving hematopoietic stem cell transplantation treatment,\n* Having developed a relapse after remission,\n* Experiencing communication difficulties (e.g., intellectual disability, visual impairment, etc.),\n* Having a psychiatric diagnosis made by a psychiatrist,\n* Having experienced a significant life event affecting psychological well-being within the past four weeks (e.g., death, divorce, etc.).",{"count":222,"type":21},36,[24],"This study will develop and evaluate a mobile-based co-design intervention (CesiKids) to enhance psychosocial resilience in hospitalized adolescents aged 12-18 diagnosed with cancer. The program will be created using Bronfenbrenner's Ecological Systems Theory and designed in collaboration with nurses, recovered adolescents, and parents. A randomized controlled design will be used. The intervention group will participate in a four-week structured program, while the control group will receive standard care. Psychosocial resilience and coping outcomes will be assessed at baseline, post-intervention, and follow-up. This research aims to offer an evidence-based, scalable model to support resilience among adolescents with cancer in clinical settings.",[226,227,28,228,229,230],"Resilience, Psychological","Adolescent Cancer","Pediatric Cancer","Pediatric Nursing","Coping",[108,232,233,234,235,236,237],"Resilience","Coping skills","Neoplasms","Pediatric nursing","Mobile application","Psychosocial intervention","2025-11-13",{"date":240,"type":40},"2025-11-14",{"date":242,"type":21},"2025-11",{"date":244,"type":21},"2027-06",{"name":246,"class":47},"Eskisehir Osmangazi University",{"id":248,"slug":249,"hasResults":11,"nctId":250,"briefTitle":251,"officialTitle":252,"acronym":4,"eligibilityCriteria":253,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":254,"targetDuration":4,"studyType":22,"phases":256,"briefSummary":257,"conditions":258,"keywords":260,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":269,"lastUpdatePostDateStruct":270,"startDateStruct":272,"completionDateStruct":273,"leadSponsor":275,"locationsCount":48},"100609172","evaluation-of-the-effectiveness-of-a-mobile-application-developed-for-hemodialysis-patients-100609172","NCT07211100","Evaluation of the Effectiveness of a Mobile Application Developed for Hemodialysis Patients.","Evaluation of the Impact of a Mobile Application Developed for Hemodialysis Patients on Treatment Adherence, Symptom Management and Clinical Parameters.","Inclusion Criteria:\n\n* Age ≥ 18 years.\n* Diagnosed with end-stage renal disease (ESRD).\n* Receiving maintenance hemodialysis treatment for at least 3 months.\n* Able to use a smartphone and willing to install the mobile health application.\n* Voluntarily agreeing to participate in the study and providing written informed consent.\n\nExclusion Criteria:\n\n* Patients with cognitive impairment, severe psychiatric disorders, or communication barriers that may interfere with participation.\n* Patients with visual or hearing impairments that prevent the use of the mobile application.\n* Patients who have undergone kidney transplantation or are scheduled for transplantation within the study period.\n* Patients with serious comorbid conditions requiring hospitalization (e.g., advanced cancer, severe heart failure).\n* Participation in another interventional clinical trial within the past 3 months.",{"count":255,"type":21},72,[24],"This study aims to evaluate the effectiveness of a mobile health application developed for adult patients undergoing hemodialysis treatment. The mobile application includes modules on adherence to medication, diet, and fluid restrictions, symptom management (fatigue, pain, itching), nutrition guidance, exercise recommendations, and motivational content. It also features reminder notifications, an \"Ask the Expert\" module, and personal symptom tracking.\n\nThe research will be conducted as a single-center, single-blind, randomized controlled experimental study. Participants will be assigned to intervention and control groups using block randomization. The intervention group will receive the mobile application, while the control group will receive standard care. Assessments will be carried out at baseline (T0), 1st month (T1), and 2nd month (T2).\n\nThe measurement tools to be used include the End-Stage Renal Disease Adherence Questionnaire (ESRD-AQ), Post-Dialysis Fatigue Scale, 5-D Itch Scale, Visual Analog Scale (VAS) for pain, and the Mobile Application Usability Scale. In addition, clinical parameters such as serum potassium, phosphorus, and albumin will be evaluated.\n\nA total of 72 patients (36 intervention, 36 control) will be included in the study. This study aims to assess the impact of a mobile health application on treatment adherence, symptom management, and clinical parameters among hemodialysis patients, and to develop a digital health model that can be integrated into nursing care.",[259,28],"End-Stage Renal Disease Requiring Haemodialysis",[261,33,262,263,264,265,266,267,268],"hemodialiysis","mobil health","pain","fatigue","itching","nursingcare","adaptation","esrd","2025-09-29",{"date":271,"type":40},"2025-10-07",{"date":242,"type":21},{"date":274,"type":21},"2026-02",{"name":276,"class":47},"Saglik Bilimleri Universitesi",{"id":278,"slug":279,"hasResults":11,"nctId":280,"briefTitle":281,"officialTitle":282,"acronym":4,"eligibilityCriteria":283,"healthyVolunteers":89,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":284,"targetDuration":4,"studyType":286,"phases":4,"briefSummary":287,"conditions":288,"keywords":296,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":304,"lastUpdatePostDateStruct":305,"startDateStruct":307,"completionDateStruct":309,"leadSponsor":311,"locationsCount":4},"100601744","addressing-pregnant-womens-first-trimester-worries-and-information-needs-with-mhealth-solutions-100601744","NCT07114471","Addressing Pregnant Women's First Trimester Worries and Information Needs With mHealth Solutions","Exploring the Anxieties and Health Information Needs of Women in the First Trimester to Inform mHealth Solutions for Antenatal Care","Pregnant women\n\nInclusion criteria\n\n* To ensure that participants have the first trimester of pregnancy fresh in their minds the sample will include women that are currently pregnant or have had a child within the last 2 years\n* Living in the UK\n* Over the age of 18\n* Able to give informed consent Exclusion criteria\n* Evidence of\u002Fdiagnosis of cognitive impairment\n\nHealthcare professionals\n\nInclusion criteria\n\n\\- Belonging to one of the following professional groups i.e. healthcare professionals involved in the care of pregnant women\n\n* Doctor in obstetrics and gynaecology\n* Midwives\n* Nurses (within the field of obstetrics and gynaecology),\n* Sonographers that scan pregnant women\n* General practitioners\n* Psychologists (that work with pregnant women)\n* Physiotherapists (that work with pregnant women)\n* Living in the UK\n* Over the age of 18\n* Able to give informed consent Exclusion criteria\n* Evidence of\u002Fdiagnosis of cognitive impairment\n\nDigital Health Experts\n\nInclusion criteria\n\n* Professionals with at least 3 year's experience in digital health, health informatics or mobile health application development\n* Based in the United Kingdom Exclusion criteria\n* Evidence of\u002Fdiagnosis of cognitive impairment",{"count":285,"type":21},1450,"OBSERVATIONAL","The first 12 weeks of pregnancy, known as the first trimester, can be one of the most worrying times for women. (Where this lay summary refers to women, it should be taken to include people who do not identify as women but who have the capacity to become pregnant). Many experience nausea, bleeding, or anxiety about whether the pregnancy is progressing normally. Despite this, most women do not see a midwife or doctor until around 10 weeks into the pregnancy. This leaves a gap where they may have important questions but little professional support. As a result, many turn to mobile phone applications or the internet to find answers - but the quality of information online is mixed, and it can be confusing or even unsafe.\n\nThis research aims to understand what support women really need in early pregnancy, what concerns they have, and whether a mobile health application (mHealth app) could help fill this gap in current pregnancy care in a safe and personalised way. The study will also ask healthcare professionals and digital health experts what such an application should include, and how it can be made accessible, and easy to understand for all women - including those with different levels of health knowledge and digital skills.\n\nTo carry out the research, we will use a combination of online surveys and interviews. Women who are currently pregnant or have had a baby in the last two years will be invited to take part, along with healthcare professionals such as midwives and doctors, and experts in digital health. The survey will ask about their experiences in early pregnancy, how they have used digital tools or apps, and whether they felt their questions were answered before their first NHS appointment. The interview stage will allow participants to talk in more depth about what support they wanted and what would have helped them most. All participants will receive information about support services because we realise that discussing unmet information needs or worries in early pregnancy may be upsetting for some women.\n\nThe views collected will inform the design of a new mobile application to support women during early pregnancy. The application will use artificial intelligence (AI) to personalise information based on each woman's needs and background, and to explain things clearly and simply. The content and design of the application will be reviewed by doctors and digital health specialists to make sure it is safe, accurate, and easy to use.\n\nPublic and patient involvement is central to this project. A diverse group of women and representatives from grassroots organisations will be invited to shape the questions we ask, review the design of the application, and help us make it inclusive for people from different backgrounds.\n\nThis research will help us create a practical, trustworthy, and inclusive tool to support women during one of the most vulnerable times in pregnancy when women don't usually see a doctor. If successful, it could be used widely across the NHS to help reduce anxiety, improve understanding, and ensure women get the right support earlier in their pregnancy with the long-term aim of improving outcomes for women, babies, and families across the UK.",[289,290,291,292,293,28,294,295],"Pregnancy Trimester, First","Anxiety","Worries","Health Knowledge, Attitudes, Practice","mHealth Application","Antenatal Care","Patient Education as Topic",[297,298,299,300,301,302,303],"Observational Study","Surveys and Questionnaires","Interview","Digital Health","Health Literacy","Pregnant People","User Centered Design","2025-08-11",{"date":306,"type":40},"2025-08-14",{"date":308,"type":21},"2025-09",{"date":310,"type":21},"2027-10",{"name":312,"class":47},"Bournemouth University",{"id":314,"slug":315,"hasResults":11,"nctId":316,"briefTitle":317,"officialTitle":318,"acronym":319,"eligibilityCriteria":320,"healthyVolunteers":89,"sex":16,"minAge":321,"maxAge":18,"enrollmentInfo":322,"targetDuration":4,"studyType":22,"phases":324,"briefSummary":325,"conditions":326,"keywords":332,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":338,"lastUpdatePostDateStruct":339,"startDateStruct":341,"completionDateStruct":343,"leadSponsor":345,"locationsCount":4},"100596321","effect-of-a-mobile-based-hydration-tracking-program-on-knowledge-attitudes-and-behaviors-in-older-adults-100596321","NCT07043933","Effect of a Mobile-Based Hydration Tracking Program on Knowledge, Attitudes, and Behaviors in Older Adults","The Effect of a Mobile-Compatible Web-Based Hydration Tracking Program on Hydration Knowledge, Attitudes, and Behaviors in Older Adults: A Randomized Controlled Trial","SIVI","Inclusion Criteria:\n\n* Daily water and other fluid intake below the recommended levels: less than 2.0 L\u002Fday for older adult men and less than 1.6 L\u002Fday for older adult women (ESPEN Guidelines, 2024) Aged between 65 and 84 years Having at least a primary school education Having sufficient motor skills Having the cognitive capacity, willingness, and experience necessary to use technology Willing to participate in the study Owning a mobile phone compatible with the application Having prior experience using mobile applications\n\nExclusion Criteria:\n\n* Diagnosed with moderate or severe cognitive impairment (MMSE \\\u003C 24)\n* Having vision or hearing impairments that prevent participation\n* Diagnosed with advanced stage chronic kidney disease (Stage 4-5)\n* Diagnosed with congestive heart failure (NYHA class III-IV)\n* Being on fluid restriction by medical order\n* Having a diagnosed urinary incontinence condition\n* Having a diagnosis of terminal illness or active cancer treatment\n* Participating in another hydration-related clinical study\n* Experiencing a disruption in app usage for one week or longer for any reason","65 Years",{"count":323,"type":21},70,[24],"This randomized controlled trial aims to evaluate the impact of a mobile-friendly, web-based hydration tracking application (named \"SIVI\") on hydration-related knowledge, attitudes, and behaviors in older adults. Inadequate fluid intake is a common and modifiable risk factor for dehydration in the elderly, leading to increased morbidity, hospitalizations, and functional decline. However, many older individuals forget to drink fluids or face barriers such as fear of incontinence, mobility limitations, or cognitive challenges.\n\nThis study will include 70 community-dwelling older adults aged 65-84 years, recruited from a Family Health Center. Participants will be randomly assigned to either the intervention or control group. The intervention group will use the SIVI application for two months. The app is specially designed for older adults and includes features such as personalized fluid goals, reminders, hydration education modules, feedback, and a user-friendly interface with large fonts and high contrast. Participants will log their daily fluid intake, receive motivational messages, and access videos and information about healthy hydration habits. A water bottle will be provided to standardize measurement across groups.\n\nThe control group will receive only routine care. Both groups will complete questionnaires measuring demographics, hydration knowledge, attitudes, behaviors, and fluid consumption habits at baseline, one month, and two months.\n\nData collection will be conducted face-to-face by the researcher, and analysis will be performed using SPSS 22.0. Statistical tests will include descriptive statistics, Shapiro-Wilk for normality, chi-square for categorical data, and t-tests and ANOVA for comparisons over time.\n\nThe results are expected to show that the SIVI application improves older adults' hydration knowledge, fosters positive attitudes, and promotes healthy fluid intake behaviors, thus supporting self-management of hydration and potentially reducing dehydration-related health risks.",[327,328,329,330,28,331],"Dehydration","Older Adults (65 Years and Older)","Hydration Status","Self-management Behavior","Web Based Intervention",[327,333,334,335,336,337],"Aged","Hydration","Older Adults","Mobile Applications","Self-Management","2025-06-21",{"date":340,"type":40},"2025-06-29",{"date":342,"type":21},"2025-10-01",{"date":344,"type":21},"2026-02-01",{"name":346,"class":47},"Ezgi Atasoy",{"id":348,"slug":349,"hasResults":11,"nctId":350,"briefTitle":351,"officialTitle":352,"acronym":353,"eligibilityCriteria":354,"healthyVolunteers":11,"sex":90,"minAge":17,"maxAge":355,"enrollmentInfo":356,"targetDuration":4,"studyType":22,"phases":358,"briefSummary":359,"conditions":360,"keywords":4,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":365,"lastUpdatePostDateStruct":366,"startDateStruct":368,"completionDateStruct":370,"leadSponsor":372,"locationsCount":174},"100560827","enabling-women-with-parkinsons-disease-to-identify-and-better-manage-hormonal-triggers-of-parkinsonian-symptoms-100560827","NCT06582212","Enabling Women with Parkinson's Disease to Identify and Better Manage Hormonal Triggers of Parkinsonian Symptoms","Enabling Women with Parkinson's Disease to Identify and Better Manage Hormonal Triggers","Lady-PD","Inclusion Criteria:\n\n* Non-menopausal women\n* Diagnosis of PD according to the MDS criteria onset of PD symptoms since at least two years before inclusion\n* Age 18-56 years\n* On stable medication regimen for PD for at least two months without foreseen need to modify it within the next three months\n* With and without OCP or intrauterine devices (IUD\n\nExclusion Criteria:\n\n* Post-menopausal women with PD\n* Any condition that, in the opinion of the investigator, will preclude the participant from successfully or safely completing study procedures (i.e., dementia, severe depression, etc.)\n* People not able to give an informed consent.","56 Years",{"count":357,"type":21},100,[24],"Forty percent of people living worldwide with Parkinson's disease (PD) are women. Twenty percent of patients have PD onset under the age of 60 years, a time when women may encounter significant caregiving responsibilities along with occupational and other competing demands.\n\nStudies with surveys of women with PD (WwPD) have reported worsening of PDrelated symptoms especially in the week prior and the week of menses. However, prospective evidence is scarce and clinical guidelines to manage this issue do not exist. As a result, care is either non-existent or fragmented.\n\nThe investigators propose a French multicentre prospective pilot study to capture changes in PD symptoms in relation to the stages of the menstrual cycle aiming at reducing hormonal related worsening in PD symptoms through neurologist intervention and\u002For patient selfmanagement.\n\nDigital technology will remotely enable patient reported outcome (PRO) tracking through the My Moves Matter app changes in PD symptoms during several months. This information will then help neurologists to customize treatment.\n\nChanges in motor symptoms will also be highlighted by tracking through the use of a wearable device (PDMonitor) to objectively detect motor changes together with the app.\n\nThis will further support the reliability of the app. This study will provide evidence for the impact of the menstrual cycle on PD and help neurologists and patients to better manage PD symptoms related to these hormonal changes.",[361,28,362,363,364],"Digital Technology","Motor Fluctuations","Oestrogen","Parkinson Disease","2025-03-24",{"date":367,"type":40},"2025-03-25",{"date":369,"type":40},"2025-03-12",{"date":371,"type":21},"2027-09-12",{"name":373,"class":47},"University Hospital, Grenoble",{"id":375,"slug":376,"hasResults":11,"nctId":377,"briefTitle":378,"officialTitle":379,"acronym":4,"eligibilityCriteria":380,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":381,"enrollmentInfo":382,"targetDuration":4,"studyType":22,"phases":384,"briefSummary":385,"conditions":386,"keywords":389,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":393,"lastUpdatePostDateStruct":394,"startDateStruct":396,"completionDateStruct":398,"leadSponsor":400,"locationsCount":48},"100581488","a-digital-health-intervention-to-promote-self-management-in-patients-with-chronic-obstructive-pulmonary-disease-100581488","NCT06850961","A Digital Health Intervention to Promote Self-management in Patients With Chronic Obstructive Pulmonary Disease","A Digital Health Intervention for Promoting Self-management in Patients With Chronic Obstructive Pulmonary Disease - a Feasibility Study","Inclusion Criteria:\n\n* Clinical diagnosis of Chronic Obstructive Pulmonary Disease\n* Mucus-related issues ≥3 times per week\n* Speak and write Norwegian\n* Ability to independently operate a smartphone and\u002For iPad\n\nExclusion Criteria:\n\n* Severe mental illness\n* Substance abuse that hinder participation in the study","90 Years",{"count":383,"type":21},90,[24],"Dyspnea, cough, and chronic mucus hypersecretion are common symptoms in patients with Chronic Obstructive Pulmonary Disease (COPD), which increases risk of infections followed by exacerbations, often leading to hospitalization, disease progression and mortality. This patient group requires lifelong treatment in healthcare. A mobile application was developed to facilitate adherence to evidence-based guidelines for tailored breathing and airway clearance techniques to enhance self-management. The app is only in Norwegian and has a Norwegian name which is \"Pust Deg Bedre\" (PDB). The PDB app is fully developed and tested and can be downloaded for free. The app seems promising as a treatment tool, but has not yet been clinical evaluated. This project aims to 1) explore the feasibility of providing the app for patients with COPD, 2) explore the patients' with COPD experiences with the use of the PDB-app in treating dyspnea and mucus secretion, 3) explore the physiotherapists' experiences with the use of the PDB-app in treating dyspnea and mucus secretion, 4) explore the physiotherapists' experiences with implementing the PDB-app in treatment of patients with COPD, 5) explore the patients' experiences with the education in use of the PDB-app, and 6) At a 6-month follow up: explore the physiotherapists experiences with the usefulness and applicability of PBD-app, and to generally explore their experiences with participating in the project.",[387,388,28,192],"Chronic Obstructive Pulmonary Disease (COPD)","Self-management",[390,391,392,388,28],"COPD","Digital health intervention","Feasibility","2025-02-24",{"date":395,"type":40},"2025-02-28",{"date":397,"type":40},"2025-01-06",{"date":399,"type":21},"2030-12-31",{"name":401,"class":47},"Western Norway University of Applied Sciences",{"id":403,"slug":404,"hasResults":11,"nctId":405,"briefTitle":406,"officialTitle":407,"acronym":4,"eligibilityCriteria":408,"healthyVolunteers":89,"sex":16,"minAge":17,"maxAge":321,"enrollmentInfo":409,"targetDuration":4,"studyType":22,"phases":410,"briefSummary":411,"conditions":412,"keywords":414,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":418,"lastUpdatePostDateStruct":419,"startDateStruct":421,"completionDateStruct":423,"leadSponsor":425,"locationsCount":48},"100553952","the-effect-of-an-anti-smoking-mobile-application-on-self-efficacy-decision-making-and-breath-carbon-monoxide-levels-100553952","NCT06492772","The Effect of an Anti-Smoking Mobile Application on Self-Efficacy, Decision Making and Breath Carbon Monoxide Levels","The Effect of the Mobile Application Developed Against Smoking Behavior on Teachers' Self-Efficacy, Decision Making and Breath Carbon Monoxide Levels","Inclusion Criteria:\n\n* Having a smartphone and daily internet access\n* Volunteering to participate in the study\n* Getting a score of 5 medium level or above according to the Fagerström Nicotine Dependency Test rules test\n* Not always having any smoking cessation support or a smoking cessation intervention\n\nExclusion Criteria:\n\n* Those who did not agree to participate in the research\n* Those who do not smoke or have quit smoking\n* Those who use any tobacco product other than cigarettes (e-cigarette, hookah, cigar, etc.)\n* Those who have severe chronic health problems (vision-hearing problems, dementia and Alzheimer's, chronic lung diseases)\n* Those who do not use smartphones",{"count":323,"type":21},[24],"Purpose:This research aims to examine the effect of a mobile application developed against smoking behavior on teachers' self-efficacy, decision-making and carbon monoxide levels in breath.The research was planned as a randomized controlled experimental type.Working in public schools in Izmir\u002FNarlıdere District teachers constitute the universe of the research. According to the calculations made, it was decided to include 35 people in the experimental group and 35 people in the control group. After obtaining institutional permissions, teachers who meet the inclusion criteria will be determined.To ensure homogeneity, control and intervention groups will be stratified according to age, gender, and addiction levels.Assignment to intervention and control groups will be made by simple randomization method.The average scores of teachers' self-efficacy, breath carbon monoxide and decision-making levels are the dependent variables of the study.The status of using the mobile application is the independent variable. \"Personal Information Form\", \"Fagerstrom Nicotine Dependency Test (FNBT)\", \"Self-Efficacy Scale\", \"Classification of Stages of Change Scale\", \"Decision Making Scale\" and \"Carbon Monoxide Measurement Values Tracking Form\" will be used in this research. SPSS 26.0 Package program will be used to analyze the data in the study. It will be evaluated statistically at a 95% confidence interval and a significance level of p\\\u003C0.05. Number and percentage distributions for sociodemographic characteristics will be used in the analysis of the data.In comparisons between groups, parametric or nonparametric tests will be used after evaluating the normal distribution feature of the scale scores.\n\nHypotheses 1 H1:There is a difference between the breath CO level scores of intervention and control group teachers according to time (pre-test - 1st month, 3rd month and 6th month).\n\nHypotheses 2 H1:There is a difference between the self-efficacy scale scores of intervention and control group teachers according to time (pre-test, 1st month, 3rd month, 6th month).\n\nHypotheses 3 H1: There is a difference between the decision-making level scores of teachers in the intervention and control groups according to time (pretest-1st month, 3rd month and 6th month).",[413,28],"Smoking",[33,415,416,417],"smoking","breathing carbon monoxide","self-efficacy","2024-07-01",{"date":420,"type":40},"2024-07-09",{"date":422,"type":21},"2024-09",{"date":424,"type":21},"2025-03",{"name":150,"class":47},{"id":427,"slug":428,"hasResults":11,"nctId":429,"briefTitle":430,"officialTitle":431,"acronym":432,"eligibilityCriteria":433,"healthyVolunteers":11,"sex":90,"minAge":17,"maxAge":4,"enrollmentInfo":434,"targetDuration":4,"studyType":22,"phases":435,"briefSummary":436,"conditions":437,"keywords":440,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":445,"lastUpdatePostDateStruct":446,"startDateStruct":448,"completionDateStruct":450,"leadSponsor":452,"locationsCount":4},"100500040","supporting-women-with-breast-cancer-to-practice-dibh-at-home-before-radiation-therapy-100500040","NCT05791084","Supporting Women With Breast Cancer to Practice DIBH at Home Before Radiation Therapy","Supporting Women With Left Sided Breast Cancer to Practice Deep Inspiration Breath Hold (DIBH) at Home Before Radiation Therapy Treatment","DIBHApp","Inclusion Criteria:\n\nInclusion criteria for the study:\n\n* patients \\> 18 years of age\n* with a left-sided breast cancer diagnosis or DCIS\n* who are to receive RT with DIBH technology\n* with curative intention\n* preparatory CT visit minimum 7 days to a maximum of 4 weeks\n* able to speak and understand good enough Swedish to be able to assimilate content in the mobile app and answer surveys and interview questions\n* have access to a smart mobile phone.\n\nExclusion Criteria:\n\n* patients receiving palliative RT or neoadjuvant chemotherap\n* Planning CT starting \\\u003C 7 days\n* people with some form of orthopedic, rheumatological or neurological injury or disease that limits the possibility of carrying out the intervention.",{"count":20,"type":21},[24],"To examine the effect of a preparatory digital tool including a new instruction for deep inspiration breath hold (DIBH), before start of radiation therapy in women diagnosed with left sided breast cancer, compared with usual care.",[301,438,439,28],"Distress, Emotional","Preparedness",[441,442,443,33,444],"DIBH","RCT","radiotherapy","distress","2023-03-16",{"date":447,"type":40},"2023-03-30",{"date":449,"type":21},"2023-09-01",{"date":451,"type":21},"2029-03-30",{"name":453,"class":47},"Jonkoping University"]