[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Kafkas University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":187},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,49,77,106,133,161],{"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":53,"acronym":54,"eligibilityCriteria":55,"healthyVolunteers":56,"sex":57,"minAge":58,"maxAge":59,"enrollmentInfo":60,"targetDuration":4,"studyType":22,"phases":62,"briefSummary":63,"conditions":64,"keywords":67,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":48},"100619755","the-effect-of-a-health-belief-model-based-education-program-on-breast-self-examination-practice-behavior-breast-cancer-fear-and-awareness-levels-in-women-a-randomized-controlled-trial-100619755","NCT07348744","The Effect of a Health Belief Model-Based Education Program on Breast Self-Examination Practice Behavior, Breast Cancer Fear, and Awareness Levels in Women: A Randomized Controlled Trial","KAU-BSE-RCT","Inclusion Criteria:\n\n* Being affiliated with Family Health Center No. 1 in Ardahan Province,\n* Being a woman between the ages of 20 and 69,\n* Being literate,\n* Not having been diagnosed with breast cancer,\n* Not having a mental or communication disorder,\n* Having a phone available for communication,\n* Women who voluntarily agree to participate in the study.\n\nExclusion Criteria:\n\n* Difficulty communicating,\n* Wanting to drop out of the study,\n* Not wanting to participate in the study.\n* Women who did not fill out the data form despite reminders via message and phone call.",true,"FEMALE","20 Years","69 Years",{"count":61,"type":21},76,[24],"The study titled \"The Effect of a Health Belief Model-Based Training Program on Women's Self-Breast Examination Behavior, Breast Cancer Fear and Awareness Levels: A Randomized Controlled Study\" aimed to increase breast cancer awareness and the application of breast self-examination techniques among women by providing the necessary training through a training program based on the Health Belief Model.",[65,66],"Breast Self-Examination","Breast Cancer",[65,66,68],"Health Belief Model","2026-01-09",{"date":71,"type":40},"2026-01-16",{"date":73,"type":21},"2026-01",{"date":75,"type":21},"2026-08",{"name":46,"class":47},{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":81,"acronym":82,"eligibilityCriteria":83,"healthyVolunteers":56,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":84,"targetDuration":4,"studyType":22,"phases":86,"briefSummary":87,"conditions":88,"keywords":91,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":98,"lastUpdatePostDateStruct":99,"startDateStruct":101,"completionDateStruct":103,"leadSponsor":105,"locationsCount":4},"100589861","the-effect-of-arteriovenous-fistula-care-training-given-to-hemodialysis-patients-on-quality-of-life-comfort-and-self-care-behaviours-100589861","NCT06959914","The Effect of Arteriovenous Fistula Care Training Given to Hemodialysis Patients on Quality of Life, Comfort and Self-Care Behaviours","Fistula care","Inclusion Criteria:\n\n* -Volunteering to participate in the research,\n* Speaking Turkish.\n* 18 years of age or older\n* Having AVF\n* Receiving HD treatment 3 times a week for at least 6 months\n* Not having cognitive and mental problems that prevent participation in the study\n\nExclusion Criteria:\n\n* Not consenting to participate in the study\n\n  * Being a diagnosed psychiatric individual,\n  * Having a visual, hearing, speech, physical or mental disability,\n  * Being incomplete in their education.",{"count":85,"type":21},60,[24],"This study will be conducted to evaluate the effect of Arterio-Venous Fistula (AVF) care training given to hamodialysis patients on quality of life, comfort and self-care behaviours. Patient education is one of the practices that help patients to gain self-care behaviours as well as reducing the cost of health expenditures. Nurses are health professionals who play an important role in patient education. Nurses provide patient education by using different materials. These materials can sometimes be mobile phones, videos, web-based applications, sometimes face-to-face interviews with patients, brochures or written materials. In this study, a training programme for AVF care will be developed. In addition, it is expected that the AVF care training to be given to HD patients will increase the quality of life and comfort areas, and increase the awareness and well-being levels of patients in self-care behaviours. The effectiveness of the study will be expanded by presenting the results of the research as a paper in an international comprehensive congress. An article of the study will be published in a journal scanned in international indexes and will be included in the literature.",[89,90],"Hemodialysis Patient","Hemodialysis Catheter",[92,93,94,95,96,97],"Arteriovenous Fistula","Qualitiy of life","Comfort","Self-care","Hemodialysis","Hemodialysis access","2025-05-07",{"date":100,"type":40},"2025-05-13",{"date":102,"type":21},"2025-09",{"date":104,"type":21},"2026-09",{"name":46,"class":47},{"id":107,"slug":108,"hasResults":11,"nctId":109,"briefTitle":110,"officialTitle":111,"acronym":4,"eligibilityCriteria":112,"healthyVolunteers":56,"sex":16,"minAge":17,"maxAge":113,"enrollmentInfo":114,"targetDuration":4,"studyType":22,"phases":116,"briefSummary":117,"conditions":118,"keywords":120,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":125,"lastUpdatePostDateStruct":126,"startDateStruct":128,"completionDateStruct":130,"leadSponsor":132,"locationsCount":48},"100568020","the-effect-of-conscious-awareness-development-psychoeducation-program-prepared-for-caregivers-100568020","NCT06675773","The Effect of Conscious Awareness Development Psychoeducation Program Prepared for Caregivers","The Effect of Conscious Awareness Development Psychoeducation Program Prepared for Caregivers on Conscious Awareness, Job Stress and Compassion Fatigue.","Inclusion Criteria:\n\n* Being over 18 years of age,\n* Being actively working as a care worker in relevant institutions.\n\nExclusion Criteria:\n\n* Having received similar training before\n* Having been diagnosed with a mental illness\n* Wanting to leave the study at any stage.\n* Not having attended more than two sessions.","65 Years",{"count":115,"type":21},40,[24],"This study aimed to increase the conscious awareness of caregivers and reduce work stress and compassion fatigue.",[119],"Mental Health Issue",[121,122,123,124],"Mindfulness,","Work stress","Compassion Fatigue","Psychoeducation","2024-11-11",{"date":127,"type":40},"2024-11-13",{"date":129,"type":21},"2024-12-15",{"date":131,"type":21},"2025-11-15",{"name":46,"class":47},{"id":134,"slug":135,"hasResults":11,"nctId":136,"briefTitle":137,"officialTitle":138,"acronym":4,"eligibilityCriteria":139,"healthyVolunteers":11,"sex":57,"minAge":17,"maxAge":4,"enrollmentInfo":140,"targetDuration":4,"studyType":22,"phases":142,"briefSummary":143,"conditions":144,"keywords":149,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":153,"lastUpdatePostDateStruct":154,"startDateStruct":156,"completionDateStruct":158,"leadSponsor":160,"locationsCount":4},"100559813","the-effect-of-artificial-intelligence-supported-and-nurse-led-online-breastfeeding-counseling-100559813","NCT06569017","The Effect of Artificial Intelligence Supported and Nurse-Led Online Breastfeeding Counseling","The Effect of Artificial Intelligence Supported and Nurse-Led Online Breastfeeding Counseling on Mothers' Breastfeeding Competence: A Randomized Controlled Study","Inclusion Criteria:\n\n* The pregnant woman is willing to participate in the research,\n* The pregnant woman must have an informed written voluntary consent form,\n* The pregnant woman is over 18 years of age,\n* The pregnant woman speaks and understands Turkish,\n* Having the pregnant woman\\'s first baby (primiparous),\n* The pregnant woman is planning to give birth in the hospital where she came for pregnancy check-up,\n* The pregnant woman must have received breastfeeding training at the family health center to which she is affiliated.\n* The baby does not have a disease that would prevent sucking (cleft palate, cleft lip, etc.),\n* The baby is born older than the 37th week of pregnancy,\n* The baby\\'s birth weight is 2500 g and above, and the APGAR score is 7 and above at the 5th minute.\n\nExclusion Criteria:\n\n* The pregnant woman has mental retardation that affects her ability to understand and comprehend,\n* Multiple pregnancy,\n* The pregnant woman has gestational disorders such as preeclampsia, eclampsia and a history of gestational diabetes,\n* The pregnant woman has a diagnosed psychiatric disorder,\n* The pregnant woman receives support from a private breastfeeding consultant,\n* Taking the baby to the neonatal intensive care unit after birth,\n* The baby is born before the 37th week of pregnancy,\n* Loss of communication with pregnant women who were contacted before birth, after birth,\n* Pregnant women who do not use smartphones,\n* Pregnant women who have an application installed on their phones but have never used the application until the birth,\n* Pregnant women who were given an educational booklet but did not look at the booklet until the birth,\n* Pregnant women who do not attend the 1.5-hour training or who have to leave the training halfway will be excluded.",{"count":141,"type":21},90,[24],"Breastfeeding is the gold standard in infant nutrition in the first 12 months of life (1). Breastfeeding self-efficacy perception is one of the most important factors affecting mothers\\' breastfeeding duration and success in the postpartum period (2,3).Although AI has traditionally been the domain of powerful mainframes and data centers, new approaches have the capacity to put the power of AI directly into the hands of patients (4).Therefore, considering the importance of breastfeeding education and counseling, this study will determine the effect of training and use of a mobile application-supported artificial intelligence tool and nurse-led online breastfeeding counseling on mothers; breastfeeding self-efficacy perception, breastfeeding success, infant feeding attitude and postpartum depression levels. Thus, the effectiveness of the artificial intelligence tool and nurse-led breastfeeding counseling will be compared.",[145,146,147,148],"Artificial Intelligence","Nursing Caries","Breastfeeding","Breast Feeding, Exclusive",[150,151,152],"artificial intelligence","nurse led","breastfeeding","2024-08-21",{"date":155,"type":40},"2024-08-23",{"date":157,"type":21},"2024-09-01",{"date":159,"type":21},"2025-12-01",{"name":46,"class":47},{"id":162,"slug":163,"hasResults":11,"nctId":164,"briefTitle":165,"officialTitle":166,"acronym":4,"eligibilityCriteria":167,"healthyVolunteers":11,"sex":57,"minAge":17,"maxAge":168,"enrollmentInfo":169,"targetDuration":4,"studyType":22,"phases":171,"briefSummary":172,"conditions":173,"keywords":4,"overallStatus":179,"whyStopped":4,"lastUpdateSubmitDate":180,"lastUpdatePostDateStruct":181,"startDateStruct":183,"completionDateStruct":185,"leadSponsor":186,"locationsCount":48},"100525059","the-effects-of-laughter-yoga-and-mindfulness-based-stress-reduction-mbsr-practices-applied-to-women-with-breast-cancer-100525059","NCT06116812","The Effects of Laughter Yoga and Mindfulness-Based Stress Reduction (MBSR) Practices Applied to Women With Breast Cancer","The Effects of Laughter Yoga and Mindfulness-based Stress Reduction (MBSR) Practices Applied to Women With Breast Cancer Receiving Chemotherapy on Anxiety, Depression, Quality of Life and Spiritual Well-being Levels: A Randomized Controlled Study","Inclusion Criteria:\n\n* Women who are 18 years of age or older, do not have communication problems, have and can use a smartphone, do not have internet problems to participate in group sessions, volunteer to participate in the study, receive chemotherapy at least once a month and will continue to receive chemotherapy during the study. Women with stage 1 and stage 2 breast cancer, women with primary and secondary education, women within the first year of treatment in terms of the number of cycles, women with a score of 8 or more on the Hospital anxiety and depression scale (0-7 points are normal, 8- A score of 10 is borderline, 11 and above indicates abnormality).\n\nExclusion Criteria:\n\n* Women who did not meet the inclusion criteria, refused to participate in the study, and participated in less than 80% of the research practices (It is recommended to participate in at least 6 out of 8 sessions in the literature (Liu et al. 2022).),\n* Women who use mindfulness therapy, laughter therapy or any complementary or integrative medicine in their daily lives outside the research, women who have a diagnosed psychological disease, metastasis or recurrence, and whose chemotherapy treatment was terminated before the study was completed,\n* Women with stage 3 and stage 4 breast cancer, women who have been receiving chemotherapy for more than 1 year, women whose scores are 8 or below on the Hospital anxiety and depression scale (0-7 points indicate normal, 8-10 points indicate borderline, 11 and above indicate abnormality ).","60 Years",{"count":170,"type":21},105,[24],"Breast cancer is defined as the most common type of cancer that causes death among women (Siegel et al. 2019). It constitutes 24% of cancers and 15% of cancer-related deaths in women (T.R. Ministry of Health 2020). According to statistics made towards the end of 2020, there are 7.8 million women in the world who were diagnosed with breast cancer in the last 5 years and are alive. It is estimated that one in every 8 women will develop breast cancer in developed countries (WHO 2021).\n\nThe Ministry of Health reported the frequency of breast cancer in our country as 45.6\u002F100,000 in women in 2018. The incidence of breast cancer is reported to be higher, especially in the 45-54 age range (TC Ministry of Health 2020).\n\nChemotherapy is one of the most frequently preferred treatment methods in the treatment of breast cancer and can cause serious side effects such as pain, nausea and vomiting, loss of appetite, shortness of breath, mouth sores, fatigue, insomnia, anxiety and depression, and may lead to a deterioration in the quality of life of patients (Waks and Winer 2019, Samami et al. 2021, Sajadian et al. 2017, McFarland et al. 2018, Hamer et al. 2017).\n\nIn the international and national literature, no study has been found comparing the effects of laughter and mindfulness therapy on the anxiety, depression, quality of life and spiritual well-being experienced by breast cancer patients. In this study, it is planned to investigate the effects of laughter and mindfulness therapy applications on the anxiety, depression, quality of life and spiritual well-being levels of women with breast cancer receiving chemotherapy.",[66,174,175,176,177,178],"Laughter Therapy","Mindfulness Therapy","Life Quality","Anxiety and Depression","Spiritual Well-being","RECRUITING","2024-08-11",{"date":182,"type":40},"2024-08-14",{"date":184,"type":40},"2024-01-01",{"date":157,"type":21},{"name":46,"class":47},""]