[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100635725":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":30,"centralContacts":38,"locations":46,"responsibleParty":59,"collaborators":25,"id":62,"slug":63,"hasResults":64,"nctId":65,"briefTitle":66,"officialTitle":67,"acronym":25,"eligibilityCriteria":68,"healthyVolunteers":64,"sex":69,"minAge":70,"maxAge":71,"enrollmentInfo":72,"targetDuration":25,"studyType":75,"phases":76,"briefSummary":78,"conditions":79,"keywords":85,"overallStatus":89,"whyStopped":25,"lastUpdateSubmitDate":90,"lastUpdatePostDateStruct":91,"startDateStruct":94,"completionDateStruct":96,"leadSponsor":98,"locationsCount":99},{"fullName":5,"class":6},"Kafkas University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Mobile Application Group","EXPERIMENTAL","Patients meeting the sampling inclusion criteria will be informed about the study and invited to participate. Verbal and written consent will be obtained from patients who meet the inclusion criteria and agree to participate in the study. The follow-up period for patients included in the mobile application process varies in the literature from 1.5 months (Yildirim Keskin et al., 2025), 3 months (Lee et al., 2024), to 6 months (Bozorgi et al., 2021). Accordingly, the duration of the application has been determined as 3 months (12 weeks). Follow-up periods vary in the literature. To determine the appropriate follow-up time for patients, studies in the literature were reviewed. The follow-up period in these studies ranges from 2 to 8 weeks (Bozorgi et al., 2021; Lee et al., 2024; Yildirim Keskin et al., 2025). Therefore, the follow-up period in this study has been determined as 2 weeks. A total of 7 measurements will be taken: pre-test, post-test, and 5 interim measurements.",[13],"Behavioral: Mobile application",{"label":15,"type":10,"description":16,"interventionNames":17},"Control Group","Patients meeting the sampling inclusion criteria will be informed about the study and invited to participate. Verbal and written consent will be obtained from patients who meet the inclusion criteria and agree to participate. No intervention will be performed on the patients. Therefore, the follow-up period in this study has been set at 2 weeks. A total of 7 measurements will be taken: a pre-test, a post-test, and 5 interim measurements. Post-tests will be conducted after 3 months.",[18],"Behavioral: control group",[20,26],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":25},"BEHAVIORAL","Mobile application","The mobile application will be developed for patients with hypertension. It will include educational videos, educational texts, and reminders.",[9],null,{"type":21,"name":27,"description":28,"armGroupLabels":29,"otherNames":25},"control group","The control group will not be interfered with.",[15],[31,34],{"name":32,"affiliation":5,"role":33},"Rabia Bayrambey, 1","PRINCIPAL_INVESTIGATOR",{"name":35,"affiliation":36,"role":37},"Yeliz Akkuş, 2","Nigde Omer Halisdemir University","STUDY_DIRECTOR",[39,43],{"name":32,"role":40,"phone":41,"phoneExt":25,"email":42},"CONTACT","+905059809499","rabia_byrmby36@outlook.com",{"name":35,"role":40,"phone":44,"phoneExt":25,"email":45},"+905052598458","yelizakkus@gmail.com",[47],{"facility":5,"status":25,"city":48,"state":25,"zip":49,"country":50,"countryCode":25,"cosmosGeoPoint":51,"geoPoint":56,"contacts":57},"Kars","36000","Turkey (Türkiye)",{"type":52,"coordinates":53},"Point",[54,55],43.08548,40.59825,{"lat":55,"lon":54},[58],{"name":25,"role":40,"phone":41,"phoneExt":25,"email":42},{"type":33,"investigatorFullName":60,"investigatorTitle":61,"investigatorAffiliation":5,"oldNameTitle":25,"oldOrganization":25},"Rabia BAYRAMBEY","Research Assistant","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":73,"type":74},160,"ESTIMATED","INTERVENTIONAL",[77],"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.",[80,81,82,83,84],"Hypertension","Mobile Application","Blood Pressure Control","Treatment Adherence","Self-Efficacy",[80,86,87,83,84,88],"mobile application","blood pressure control","King's Goal Achievement Theory","NOT_YET_RECRUITING","2026-06-16",{"date":92,"type":93},"2026-06-18","ACTUAL",{"date":95,"type":74},"2026-07-01",{"date":97,"type":74},"2027-03-20",{"name":5,"class":6},1]