[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"hemodialysis-patient\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:hemodialysis-patient":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,9,0,[8,42,67,101,130,159,184,210,231],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":27,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100645120","a-theory-based-fluid-self-management-program-100645120",false,"NCT07677605","A Theory-based Fluid Self-management Program","Effects of Self-Management Program on Interdialytic Weight Gain Control in Hemodialysis Patients: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Receiving maintenance hemodialysis for ≥ 3 months\n* Undergoing hemodialysis two times per week on a regular schedule\n* Possession of a smartphone with active WhatsApp use\n* Ability to read and understand Indonesian, with support provided in Javanese where necessary.\n* Provision of written informed consent\n\nExclusion Criteria:\n\n* Severe cognitive impairment or diagnosed psychiatric disorders affecting comprehension or participation, as documented in the medical record.\n* Severe visual, hearing, or communication impairments not corrected by assistive devices\n* Current hospitalisation or unstable medical condition\n* Planned kidney transplantation or dialysis modality change during the study period\n* Participation in another interventional study related to fluid management or self-management\n* Inability to engage with the WhatsApp Channel follow-up","ALL","18 Years",{"count":19,"type":20},160,"ESTIMATED","INTERVENTIONAL",[23],"NA","This study aims to evaluate the efficacy of an intervention guided by the IFSMT, in which structured education and digitally delivered reinforcement strategies are designed to enhance self-management processes, including knowledge and beliefs, self-regulation skills, and social facilitation, among patients undergoing maintenance hemodialysis. The intervention, delivered via a mobile platform three times daily over two months, seeks to improve fluid control adherence and hemodialysis self-management behaviours, and to reduce interdialytic weight gain and stabilise pre-hemodialysis mean arterial pressure, compared with standard education alone.",[26],"Hemodialysis Patient",[28,29],"Fluid-Self Management Program","Interdialytic Weight Gain Control","NOT_YET_RECRUITING","2026-06-24",{"date":33,"type":34},"2026-07-01","ACTUAL",{"date":33,"type":20},{"date":37,"type":20},"2027-02-28",{"name":39,"class":40},"National Taipei University of Nursing and Health Sciences","OTHER",1,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":46,"acronym":4,"eligibilityCriteria":47,"healthyVolunteers":11,"sex":16,"minAge":48,"maxAge":49,"enrollmentInfo":50,"targetDuration":4,"studyType":52,"phases":4,"briefSummary":53,"conditions":54,"keywords":55,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":66},"100635656","gender-based-differences-in-dynamic-balance-among-hemodialysis-patients-100635656","NCT07555522","Gender-Based Differences In Dynamic Balance Among Hemodialysis Patients","Inclusion Criteria:\n\n* Age 20 to 60 years (both sexes)\n* Body mass index (BMI) 18.5 to 29.9 kg\u002Fm²\n* Undergoing hemodialysis three times per week\n* Duration of hemodialysis ≥1 year\n* No exercise therapy within the last 3 months\n* Able to walk independently for at least 2 minutes without assistive devices\n\nExclusion Criteria:\n\n* Recent myocardial infarction (within 6 weeks)\n* Malignant arrhythmia or unstable angina\n* History of major surgery or fracture of the hip\u002Fknee, or hip\u002Fknee replacement\n* Severe respiratory or cardiovascular conditions affecting cardiopulmonary function\n* Severe hypotension during or after hemodialysis\n* Neurological disorders affecting balance","20 Years","60 Years",{"count":51,"type":20},155,"OBSERVATIONAL","Aim of the study is to investigate gender-based differences in dynamic balance in form of Timed-Up-and-Go and Five Times-sit-to-Stand-to-sit tests among hemodialysis patients. The main question it aims to answer is:\n\nAre there gender-based differences in dynamic balance in form of Timed-Up-and-Go and Five Times-sit-to-Stand-to-sit tests among hemodialysis patients?",[26],[56],"Balance","2026-04-24",{"date":59,"type":34},"2026-04-29",{"date":61,"type":20},"2026-04-16",{"date":63,"type":20},"2026-05-25",{"name":65,"class":40},"Cairo University",2,{"id":68,"slug":69,"hasResults":11,"nctId":70,"briefTitle":71,"officialTitle":72,"acronym":4,"eligibilityCriteria":73,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":74,"enrollmentInfo":75,"targetDuration":4,"studyType":21,"phases":77,"briefSummary":78,"conditions":79,"keywords":84,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"locationsCount":4},"100631332","the-effects-of-circadian-rhythm-based-progressive-relaxation-exercises-in-hemodialysis-patients-100631332","NCT07499297","THE EFFECTS OF CIRCADIAN RHYTHM-BASED PROGRESSIVE RELAXATION EXERCISES IN HEMODIALYSIS PATIENTS","THE EFFECTS OF CIRCADIAN RHYTHM-BASED PROGRESSIVE RELAXATION EXERCISES ON SYMPTOM MANAGEMENT, SLEEP QUALITY, COMFORT, AND MENTAL WELL-BEING IN HEMODIALYSIS PATIENTS","Inclusion Criteria:\n\n* 18 and 65 years of age,\n* have no mental or physical disabilities that would prevent them from answering the questions,\n* have no problems related to touch, temperature perception, hearing, or vision,\n* are relatively independent in performing daily activities,\n* do not use any pharmacological or non-pharmacological methods to facilitate sleep,\n* have been receiving hemodialysis (HD) treatment for at least 3 months,\n* are able to communicate and cooperate.\n\nExclusion Criteria:\n\n* are bedridden,\n* have physical limitations preventing them from performing relaxation exercises,\n* have been practicing relaxation exercises (such as breathing exercises, meditation, yoga, etc.) within the last 6 months,\n* are classified as intermediate type (neither type) according to the Morningness-Eveningness Questionnaire,\n* engage in regular exercise,\n* have been diagnosed with psychiatric disorders such as depression or schizophrenia,\n* do not consent to participate in the study.","65 Years",{"count":76,"type":20},75,[23],"The aim of this study is to determine the effect of Progressive Relaxation Exercise (PGE) applied according to the circadian rhythms of hemodialysis (HD) patients on symptom management, sleep quality, comfort and mental well-being levels and to examine the experiences of HD patients regarding PGE application. A sequential mixed method research design will be used in the study. The quantitative part of the study was planned as a randomized controlled double-blind experimental study. The qualitative part will be conducted as a qualitative research to be carried out with individual in-depth interview method in order to examine the opinions of the individuals in the intervention group regarding the 8-week PGE applied according to the circadian rhythm. In the collection of research data, the Introductory Information Form, Morningness-Eveningness Questionnaire (MEQ), Dialysis Symptom Index, Hemodialysis Comfort Scale - Version II, Pittsburg Sleep Quality Index (PSQI), Warwick-Edinburgh Mental Well-Being Scale (WEMIOÖ), Individual Follow-up Form, Progressive Relaxation Exercise Application Guideline (PGEUY) and In-Depth Interview Form with Individuals in the Intervention Group will be used.",[80,26,81,82,83],"Nursing","Circadian Rhythm","Relaxation Exercise","Symptom Management",[80,85,86,87,88,89,90,91],"hemodialysis","circadian rhythm","relaxation exercise","symptom management","sleep quality","comfort","mental well-being","2026-04-02",{"date":94,"type":34},"2026-04-08",{"date":96,"type":20},"2026-04-01",{"date":98,"type":20},"2026-09-22",{"name":100,"class":40},"Karamanoğlu Mehmetbey University",{"id":102,"slug":103,"hasResults":11,"nctId":104,"briefTitle":105,"officialTitle":106,"acronym":4,"eligibilityCriteria":107,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":108,"targetDuration":4,"studyType":21,"phases":110,"briefSummary":111,"conditions":112,"keywords":114,"overallStatus":119,"whyStopped":4,"lastUpdateSubmitDate":120,"lastUpdatePostDateStruct":121,"startDateStruct":123,"completionDateStruct":125,"leadSponsor":127,"locationsCount":129},"100628523","the-effectiveness-of-education-in-diabetic-hemodialysis-patients-100628523","NCT07462741","The Effectiveness of Education in Diabetic Hemodialysis Patients","The Health Belief Model Approach in Diabetic Foot Management: The Effectiveness of Education for Diabetic Hemodialysis Patients","Inclusion criteria:\n\n* Voluntary participation in the study\n* Literacy\n* Absence of psychiatric distress\n* Being over 18 years of age\n* Open to communication and cooperation, no speech problems\n* Receiving continuous hemodialysis treatment\n* Having been diagnosed with diabetes for at least 6 months\n\nExclusion criteria:\n\n* Unwillingness to participate in the study or desire to withdraw from the study\n* Receiving acute hemodialysis treatment\n* Being under 18 years of age\n* Open to communication and cooperation, no speech problems",{"count":109,"type":20},50,[23],"Diabetes is a significant health problem affecting approximately half a billion people worldwide, reaching alarming levels. Diabetic foot ulcers are among the most common and serious complications of diabetes. Diabetes is the most common cause of end-stage renal failure, and diabetic nephropathy is identified as a major risk factor for foot ulcers and amputation. The health belief model is a model that explains behavior. Focusing on the necessary motivational resources for the development of positive health behaviors in individuals is crucial for positive patient outcomes in the education of diabetic hemodialysis patients. It is necessary for hemodialysis nurses to educate diabetic patients on foot care knowledge, improve foot care behaviors, and prevent the development of foot ulcers and lower extremity amputations. However, the lack of studies in the literature on nurse-led foot care education interventions based on the health belief model for diabetic patients undergoing hemodialysis constitutes the strength and unique aspect of this study. The research will be conducted using a randomized controlled pretest-posttest design.",[26,113],"Diabetes Foot Care",[115,116,85,117,118],"Diabetic foot","patient education","self-efficacy","health belief model","RECRUITING","2026-03-05",{"date":122,"type":34},"2026-03-10",{"date":124,"type":34},"2026-01-26",{"date":126,"type":20},"2026-03-09",{"name":128,"class":40},"Inonu University",3,{"id":131,"slug":132,"hasResults":11,"nctId":133,"briefTitle":134,"officialTitle":135,"acronym":136,"eligibilityCriteria":137,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":74,"enrollmentInfo":138,"targetDuration":4,"studyType":21,"phases":140,"briefSummary":141,"conditions":142,"keywords":145,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":150,"lastUpdatePostDateStruct":151,"startDateStruct":153,"completionDateStruct":155,"leadSponsor":157,"locationsCount":4},"100616065","ai-integrated-mobile-education-and-self-management-in-hemodialysis-100616065","NCT07300761","AI-Integrated Mobile Education and Self-Management in Hemodialysis","A Randomized Controlled Trial to Evaluate the Effect of an Artificial Intelligence-Supported Mobile Education Application on Self-Care Behaviors, Arteriovenous Fistula Care, and Biochemical Parameters in Hemodialysis Patients","AI-MOBI-HEMODI","Inclusion Criteria:\n\nMust be 18 years of age or older.\n\nMust have an Arteriovenous Fistula (AVF).\n\nMust not have a communication-hindering problem.\n\nMust be receiving outpatient Hemodialysis (HD) treatment.\n\nMust have been receiving HD treatment for longer than 6 months.\n\nMust own a smartphone and have internet access.\n\nExclusion Criteria:\n\nPatients who do not agree to participate in the research.\n\nPatients who have been diagnosed with advanced cerebrovascular and peripheral vascular insufficiency.\n\nPatients who do not complete the mobile education application",{"count":139,"type":20},76,[23],"This randomized controlled trial aims to evaluate the effectiveness of an Artificial Intelligence-supported mobile education application designed to enhance self-care behaviors, arteriovenous fistula (AVF) care practices, and key biochemical parameters among adult hemodialysis (HD) patients. Chronic Kidney Disease (CKD) and its most common renal replacement therapy, hemodialysis, impose a substantial physical, psychological, and socioeconomic burden on patients. HD patients frequently experience fatigue, pain, cramping, sleep disturbances, thirst and fluid restriction challenges, dietary limitations, AVF-related complications, and emotional distress. These difficulties highlight the importance of strengthening patients' self-care abilities and promoting active involvement in disease management.\n\nDespite the prevalence of mobile health (mHealth) technologies in chronic disease management, existing applications for HD patients remain limited, and none have integrated personalized artificial intelligence-based educational support. The absence of AI-driven patient education represents a significant gap in nursing science and digital health innovation. This project addresses that gap by developing and testing a structured, evidence-based mobile education program supported by artificial intelligence, designed specifically for HD patients.\n\nThe study will enroll 76 eligible hemodialysis patients from Bitlis State Hospital and Bitlis Tatvan State Hospital. Participants will be randomly assigned to either the intervention group or the control group using simple randomization. The intervention group will receive access to the AI-supported mobile application for six weeks, which includes modules on kidney function, CKD and treatment options, symptom management, dietary adherence, fluid management, treatment adherence, and AVF care. Each module incorporates written content, videos, visuals, voice-supported reading features, and an integrated \"Ask a Question\" function allowing patients to communicate directly with the research team. The control group will receive routine clinical care without additional intervention.\n\nThe artificial intelligence component will assist with content personalization, monitoring of patient engagement, data storage, automated reminders for non-active users, and supportive feedback based on learning progress and biochemical trends. The development of the mobile application will be guided by expert opinions from nephrology specialists, dialysis nurses, academicians, and dietitians. Readability of educational materials will be assessed using the Ateşman Readability Formula. A pilot study will be conducted prior to the trial to evaluate usability using the Web Analysis and Measurement Inventory (WAMMI).\n\nData collection will include a Patient Identification Form, the Hemodialysis Arteriovenous Fistula Self-Care Behavior Scale, the Hemodialysis Self-Management Scale, and a Biochemical Parameters Tracking Form. Pre-test data will be collected before the intervention; post-test data will be collected at the end of the six-week intervention period. Biochemical parameters will include BUN, creatinine, albumin, potassium, phosphorus, hemoglobin, uric acid levels, Kt\u002FV, and dry weight, obtained from routine clinical records without additional blood sampling.\n\nThe primary outcomes will assess changes in self-care and self-management behaviors based on validated scales. Secondary outcomes will examine changes in biochemical parameters between the intervention and control groups. Data analysis will be performed using SPSS, employing descriptive statistics, normality testing, and appropriate statistical comparison tests, with significance set at p \\\u003C 0.05.\n\nEthical approval will be obtained from the appropriate institutional ethics committee, and written informed consent will be secured from all participants. Data confidentiality will be ensured using encrypted login systems and secure storage processes.\n\nThis trial is expected to contribute significantly to the scientific literature by being the first AI-supported mobile education intervention tailored for hemodialysis patients. Anticipated benefits include improved self-care behaviors, increased patient autonomy, reduced AVF complications, better adherence to dietary and fluid restrictions, and improved biochemical outcomes. Broader impacts of the project include the potential reduction of hospitalization rates, decreased healthcare costs, increased quality of life for HD patients, and the establishment of a digital model that can be adapted for other chronic disease populations.\n\nUltimately, this study aims to demonstrate that integrating artificial intelligence with mobile health education can create a transformative approach to patient empowerment, clinical care, and chronic disease management within the field of nephrology and nursing.",[26,143,144],"Patient Education","Self Care",[146,143,147,148,149],"Artificial Intelligence","Mobile Application","Self-Care, Hemodialysis","Nursing Care","2025-12-18",{"date":152,"type":34},"2025-12-24",{"date":154,"type":20},"2026-01-02",{"date":156,"type":20},"2026-08-02",{"name":158,"class":40},"Ataturk University",{"id":160,"slug":161,"hasResults":11,"nctId":162,"briefTitle":163,"officialTitle":164,"acronym":4,"eligibilityCriteria":165,"healthyVolunteers":11,"sex":16,"minAge":166,"maxAge":167,"enrollmentInfo":168,"targetDuration":4,"studyType":21,"phases":170,"briefSummary":171,"conditions":172,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":176,"lastUpdatePostDateStruct":177,"startDateStruct":179,"completionDateStruct":181,"leadSponsor":183,"locationsCount":41},"100614225","effect-of-autogenic-training-on-hemodialysis-patients-100614225","NCT07276828","Effect of Autogenic Training on Hemodialysis Patients","Effect Of Autogenic Training On Restless Leg Syndrome And Sleep Disturbance In Hemodialysis","Inclusion Criteria\n\n* Age between 45 and 55 years.\n* Body Mass Index (BMI) between 25.0 and 29.9 kg\u002Fm².\n* Clinically and medically stable.\n* On hemodialysis for at least 6 months prior to enrollment.\n* Diagnosed with chronic kidney disease (CKD), defined by one or more of the following:\n\nEvidence of kidney damage (e.g., albuminuria), or\n\nDecreased kidney function with glomerular filtration rate (GFR) \\\u003C 60 mL\u002Fmin\u002F1.73 m² for ≥ 3 months, irrespective of clinical diagnosis.\n\n\\*Systolic blood pressure \\\u003C 140 mmHg, diastolic blood pressure \\\u003C 90 mmHg, and heart rate \\\u003C 80 bpm.\n\nExclusion Criteria\n\nUncontrolled pulmonary disease.\n\nSevere vascular complications (e.g., critical limb ischemia).\n\nUnstable angina.\n\nUncontrolled cardiac arrhythmia.\n\nDecompensated heart failure.\n\nCognitive impairment.\n\nParticipants who miss more than two weeks of the program or request termination.","45 Years","55 Years",{"count":169,"type":20},54,[23],"goal of this interventional study to investigate the effect of autogenic training on sleep disturbance , restless leg syndrome and fatigue on hemodialysis patient Is there any significant effect of autogenic training on restless leg syndrome, sleep disturbance and fatigue in patients with hemodialysis?\n\nThe intervention will include structured autogenic training sessions, and outcomes such as sleep quality and RLS severity and fatigue will be evaluated after 8 weeks of autogenic training on hemodialysis patients .",[26,173,174,175],"Restless Leg Syndrome (RLS)","Fatigue","Sleep Disturbance","2025-12-16",{"date":178,"type":34},"2025-12-22",{"date":180,"type":20},"2025-12-15",{"date":182,"type":20},"2027-05-15",{"name":65,"class":40},{"id":185,"slug":186,"hasResults":11,"nctId":187,"briefTitle":188,"officialTitle":189,"acronym":4,"eligibilityCriteria":190,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":191,"targetDuration":4,"studyType":21,"phases":193,"briefSummary":194,"conditions":195,"keywords":196,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":202,"lastUpdatePostDateStruct":203,"startDateStruct":205,"completionDateStruct":206,"leadSponsor":208,"locationsCount":41},"100612883","the-effects-of-an-app-based-acupressure-on-alleviating-fatigue-pruritus-and-sleep-quality-among-hemodialysis-patients-100612883","NCT07259369","The Effects of an App-based Acupressure on Alleviating Fatigue, Pruritus, and Sleep Quality Among Hemodialysis Patients","The Effects of an App-based Acupressure Intervention on Alleviating Fatigue, Pruritus, and Sleep Quality Among Hemodialysis Patients","Inclusion Criteria: The patients are\n\n* 18 years old or over\n* are able to speak and understand Vietnamese,\n* receive hemodialysis at least three times a week for three months or longer\n* have a score equal to or greater than 4 on a numeric rating scale (NRS, 0-10)\n* has a smartphone or tablet\n* can provide written informed consent. Exclusion Criteria: The patients who have\n* advanced cancer\n* cognitive impairment\n* chronic obstructive pulmonary disease\n* severe edema\n* have already used or plan to use acupressure or acupuncture in the following 3 months\n* have soft tissue or vascular disease in their lower extremities",{"count":192,"type":20},70,[23],"Objectives: To evaluate the effectiveness of an app-based self-guided acupressure intervention in alleviating fatigue and pruritus, and in improving sleep quality among hemodialysis patients.\n\nDesign and subjects: The parallel randomized controlled trial will be employed in one hospital. Block randomization in a 1:1 ratio will be used to assign the patients to the intervention and control groups. It is estimated that 50 to 100 participants receiving hemodialysis will be recruited.\n\nInstrument: The demographic and health-related information questionnaire, the Post-dialysis Fatigue (PDF), 5-D Itch, and Pittsburgh Sleep Quality Index will be used in this study.\n\nInterventions: The intervention group will use an app-based self-guided acupressure program to do the acupressure by themselves once daily for 4 weeks. Participants in the control group will receive usual care and no other intervention.\n\nData analysis: Both intention-to-treat and per-protocol analysis approaches will be performed. Generalized Estimating Equations (GEE) analysis will be used to assess the effectiveness of the interventions. Sensitivity analysis will be conducted to assess the impact of missing data on the treatment effect if necessary.\n\nExpected outcomes: Participants in the intervention group will know how to do the self-guided acupressure by themselves. If the intervention is effective, the App can be introduced to the hemodialysis patients who need it.",[26,174],[197,198,199,200,201,89],"chronic kidney disease","fatigue","App","pruritus","self-acupressure","2025-11-26",{"date":204,"type":34},"2025-12-02",{"date":180,"type":20},{"date":207,"type":20},"2026-03-15",{"name":209,"class":40},"Taipei Medical University",{"id":211,"slug":212,"hasResults":11,"nctId":213,"briefTitle":214,"officialTitle":215,"acronym":4,"eligibilityCriteria":216,"healthyVolunteers":11,"sex":16,"minAge":217,"maxAge":4,"enrollmentInfo":218,"targetDuration":4,"studyType":52,"phases":4,"briefSummary":220,"conditions":221,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":222,"lastUpdatePostDateStruct":223,"startDateStruct":225,"completionDateStruct":227,"leadSponsor":229,"locationsCount":41},"100598366","high-neutrophil-to-lymphocyte-ratio-and-patients-with-hemodialysis-100598366","NCT07070557","High Neutrophil-to-Lymphocyte Ratio and Patients With Hemodialysis","High Neutrophil-to-Lymphocyte Ratio and Platelet-to-Lymphocyte Ratio Are Associated With Poor Survival in Patients With Hemodialysis","Inclusion Criteria:\n\n* All cases with age ≥ 18 years from both sexes female and male, having end-stage renal disease (ESRD), who have been on hemodialysis for at least three months and divided to 4 groups according to the median of NLR and PLR\n\nExclusion Criteria:\n\n* • Patients aged \\\u003C 18 years old.\n\n  * Patient with autoimmune disease.\n  * Patient with liver cirrhosis.\n  * Patients with immunodeficiency.\n  * Patients with malignancy.","18 Months",{"count":219,"type":20},100,"To explore the role of neutrophil-to-lymphocyte ratio ( NLR ) and platelet-to-lymphocyte ratio ( PLR ) in predicting mortality in hemodialysis (HD) patients.",[26],"2025-07-16",{"date":224,"type":34},"2025-07-17",{"date":226,"type":20},"2025-07-15",{"date":228,"type":20},"2026-05-01",{"name":230,"class":40},"Sohag University",{"id":232,"slug":233,"hasResults":11,"nctId":234,"briefTitle":235,"officialTitle":235,"acronym":236,"eligibilityCriteria":237,"healthyVolunteers":238,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":239,"targetDuration":4,"studyType":21,"phases":241,"briefSummary":242,"conditions":243,"keywords":245,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":252,"lastUpdatePostDateStruct":253,"startDateStruct":255,"completionDateStruct":257,"leadSponsor":259,"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.",true,{"count":240,"type":20},60,[23],"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.",[26,244],"Hemodialysis Catheter",[246,247,248,249,250,251],"Arteriovenous Fistula","Qualitiy of life","Comfort","Self-care","Hemodialysis","Hemodialysis access","2025-05-07",{"date":254,"type":34},"2025-05-13",{"date":256,"type":20},"2025-09",{"date":258,"type":20},"2026-09",{"name":260,"class":40},"Kafkas University"]