[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100608379":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":25,"centralContacts":29,"locations":25,"responsibleParty":35,"collaborators":25,"id":39,"slug":40,"hasResults":41,"nctId":42,"briefTitle":43,"officialTitle":44,"acronym":25,"eligibilityCriteria":45,"healthyVolunteers":41,"sex":46,"minAge":47,"maxAge":25,"enrollmentInfo":48,"targetDuration":25,"studyType":51,"phases":52,"briefSummary":54,"conditions":55,"keywords":25,"overallStatus":58,"whyStopped":25,"lastUpdateSubmitDate":59,"lastUpdatePostDateStruct":60,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":25},{"fullName":5,"class":6},"Fenerbahce University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"experimental arm(ıntervention group): Mobile application and usual care","EXPERIMENTAL","Participants in this group will receive routine nursing care and the standard hospital educational booklet. In addition, they will use a mobile application developed to support chemotherapy-related symptom management. The app includes modules for symptom tracking, short educational videos (approx. 2 minutes each), and written\u002Fvisual brochures. Before use, participants will be trained on installation and navigation. They can also contact a nurse or researcher via the app for questions.",[13],"Behavioral: Mobile Application",{"label":15,"type":16,"description":17,"interventionNames":18},"Control Arm: Usual Care Only","ACTIVE_COMPARATOR","Participants in this group will receive routine nursing care and the standard hospital educational booklet. No additional intervention will be provided.",[19],"Behavioral: Usual Care Only",[21,26],{"type":22,"name":23,"description":11,"armGroupLabels":24,"otherNames":25},"BEHAVIORAL","Mobile Application",[9],null,{"type":22,"name":27,"description":17,"armGroupLabels":28,"otherNames":25},"Usual Care Only",[15],[30],{"name":31,"role":32,"phone":33,"phoneExt":25,"email":34},"Demet DEMET SEMİZ","CONTACT","05457120188","demet.semiz@fbu.edu.tr",{"type":36,"investigatorFullName":37,"investigatorTitle":38,"investigatorAffiliation":5,"oldNameTitle":25,"oldOrganization":25},"PRINCIPAL_INVESTIGATOR","Demet SEMİZ","Lecturer","100608379","the-effect-of-mobile-application-assisted-nursing-services-on-symptom-control-in-breast-cancer-patients-100608379",false,"NCT07200791","The Effect of Mobile Application-Assisted Nursing Services on Symptom Control in Breast Cancer Patients","Effect of Mobile Application-Supported Nursing Service on Symptom Management in Breast Cancer Patients During Chemotherapy: A Randomized Controlled Trial","Inclusion Criteria:\n\n* 18 yaş ve üzerinde olan,\n* Çalışmaya katılmayı kabul eden,\n* Meme kanseri tanısı alan kadınlar,\n* 4AC-12 Paklitaksel tedavi protokolü uygulana,\n* Okuma yazma bilen ve iletişim problemi olmayan,\n* Akıllı telefonu olan bireyler\n* Akıllı telefonu kullanabilen bireyler\n* Verileri eksiksiz olarak dolduran bireyler\n\nExclusion Criteria:\n\n* Kardiyak problemi olan bireyler\n* Karaciğer ve böbrek yetmezliği olan bireyler\n* Mobil uygulama kullanamayan bireyler\n* Akıllı telefon kullanamayan bireyler\n* Araştırmadan ayrılmak isteyen bireyler\n* Araştırmada çeşitli sebeplerle eksik veri toplanan bireyler","FEMALE","18 Years",{"count":49,"type":50},74,"ESTIMATED","INTERVENTIONAL",[53],"NA","Breast cancer is the most common type of cancer in women, accounting for approximately one-quarter of all female cancers in Turkey. Chemotherapy is widely used in treatment, but it also affects healthy cells, leading to numerous side effects such as fatigue, nausea, hair loss, sleep problems, and skin and nail changes. These side effects complicate symptom management and negatively impact patients' self-efficacy and quality of life.\n\nMobile health applications allow patients to track their symptoms, communicate with healthcare professionals, and implement recommended non-pharmacological methods. Literature demonstrates that these applications reduce symptoms, improve quality of life, and enhance self-efficacy.\n\nThis research is a randomized controlled experimental trial designed to evaluate the effect of mobile app-assisted nursing services on symptom management in women diagnosed with breast cancer and undergoing chemotherapy. The research will be conducted in the chemotherapy unit of a training and research hospital in Istanbul.\n\nThe study will consist of two groups: an intervention group and a control group. Randomization will be conducted using a computer-assisted method (random.org). Based on the power analysis, 74 patients will be included in the sample for 85% power at a 95% confidence interval, a significance level of p\\\u003C0.05, and a medium effect size.\n\nInclusion criteria include individuals aged 18 years and older, female, diagnosed with breast cancer, undergoing the 4AC-12 Paclitaxel protocol, owning and using a smartphone, and consenting to participate in the study. Exclusion criteria include patients with cardiac problems, liver or kidney failure, inability to use the mobile app, or providing incomplete data.\n\nStudy data will be collected online via a mobile app. The results of the study will demonstrate the effectiveness of mobile health apps in symptom management, increasing self-efficacy, and improving quality of life.",[56,57],"Symptom Management","Quality of Life","NOT_YET_RECRUITING","2025-12-02",{"date":61,"type":62},"2025-12-09","ACTUAL",{"date":64,"type":50},"2025-12",{"date":66,"type":50},"2026-08",{"name":5,"class":6}]