[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Bilecik Seyh Edebali Universitesi\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":269},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,10,0,[8,49,79,108,136,156,176,202,229,251],{"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":28,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100643150","early-phase-1-botulinum-toxin-a-for-bruxism-using-digital-occlusal-analysis-100643150",false,"NCT07640035","Botulinum Toxin-A for Bruxism Using Digital Occlusal Analysis","Objective Assessment of Bruxism and Treatment Response Using Digital Occlusal Analysis: A Clinical Study of Botulinum Toxin-A","Inclusion Criteria:\n\n* Adults aged 18 years and older\n* Diagnosis of bruxism based on self-report and clinical assessment\n* Systemically healthy individuals\n* Angle Class I occlusion\n* Ability and willingness to provide written informed consent and comply with study procedures\n\nExclusion Criteria:\n\n* Presence of temporomandibular joint pathology\n* Neuromuscular disorders\n* Pregnancy or lactation\n* Known allergy or hypersensitivity to Botulinum Toxin-A\n* Use of medications that may affect muscle function\n* Missing posterior teeth\n* Ongoing orthodontic treatment\n* Angle Class II or Class III malocclusion\n* Previous Botulinum Toxin injection into the masseter muscles","ALL","18 Years","64 Years",{"count":20,"type":21},36,"ESTIMATED","INTERVENTIONAL",[24],"EARLY_PHASE1","Bruxism is a repetitive jaw-muscle activity that may lead to tooth wear, muscle pain, headaches, and functional limitations. Current diagnostic approaches mainly rely on self-reported symptoms and clinical examination findings, which may not accurately reflect ongoing muscle activity. Digital occlusal analysis systems offer an objective method for evaluating bite force and occlusal function.\n\nThe aim of this randomized, placebo-controlled clinical trial is to investigate whether a digital occlusal analysis system can objectively assess bruxism and monitor treatment response following Botulinum Toxin-A (BTX-A) injections. Thirty-six adults diagnosed with bruxism will be randomly assigned to receive either BTX-A injections or placebo injections into the masseter muscles.\n\nClinical examinations, patient-reported outcomes, and digital occlusal measurements will be collected at baseline and at 2 weeks, 3 months, and 6 months after treatment. Primary outcomes include bite force characteristics, force distribution, occlusion time, disocclusion time, and center of force. Secondary outcomes include pain intensity, maximum mouth opening, muscle tenderness, functional limitation scores, and self-reported bruxism-related symptoms.\n\nThis study aims to provide objective evidence regarding the usefulness of digital occlusal analysis in the diagnosis and follow-up of bruxism and to evaluate the effectiveness of Botulinum Toxin-A treatment using both objective and subjective outcome measures.",[27],"Bruxism",[27,29,30,31,32,33,34,35],"Digital Occlusal Analysis","Bite Force","Masseter Muscle","Occlusal Force Distribution","Botulinum Toxin Type A","Masticatory Muscle Activity","Placebo-Controlled Trial","NOT_YET_RECRUITING","2026-06-05",{"date":39,"type":40},"2026-06-10","ACTUAL",{"date":42,"type":21},"2026-07-20",{"date":44,"type":21},"2027-07-20",{"name":46,"class":47},"Bilecik Seyh Edebali Universitesi","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":4,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":56,"minAge":17,"maxAge":4,"enrollmentInfo":57,"targetDuration":4,"studyType":22,"phases":59,"briefSummary":61,"conditions":62,"keywords":65,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":48},"100632719","vacuum-assisted-clipper-in-preoperative-hair-removal-effects-on-contamination-and-skin-integrity-100632719","NCT07517341","Vacuum-Assisted Clipper in Preoperative Hair Removal: Effects on Contamination and Skin Integrity","An Evaluation of the Effects of Using a Vacuum-Assisted Electric Shaver for Preoperative Hair Removal on Microbial Environmental Contamination and the Skin","Inclusion Criteria:\n\n* Male patients aged 18 years and older\n* Scheduled for elective laparoscopic surgery\n* Require preoperative hair removal at the surgical site\n* Classified as ASA I, ASA II, or ASA III\n* Able and willing to provide written informed consent\n\nExclusion Criteria:\n\n* Female patients\n* Patients who do not require preoperative hair removal\n* ASA IV or higher risk classification\n* Presence of active skin lesions at the surgical site that may affect assessment (e.g., dermatitis, psoriasis, open wounds, prominent scars, recent sunburn)\n* Use of any of the following within the last 7 days:\n* Antimicrobial soap, lotion, or shampoo\n* Topical or systemic antibiotics\n* Steroid therapy\n* Exposure to biocide-containing pools or thermal\u002Fspa waters\n* Severe immunosuppression (e.g., absolute neutropenia, high-dose steroid therapy)\n* Requirement for emergency surgery\n* Known allergy to any products or procedures used in the study","MALE",{"count":58,"type":21},120,[60],"NA","This randomized controlled study aims to evaluate the effectiveness of a vacuum-assisted electric trimmer (VD-ETM) compared with a standard electric trimmer (ETM) for preoperative hair removal. The study will assess microbial and environmental contamination, surgical site infection (SSI), procedure duration, skin integrity, patient safety, and patient satisfaction. Preoperative hair removal is a critical step in preventing SSI; however, conventional ETM devices may contribute to environmental contamination due to dispersed hair particles. VD-ETM systems are designed to reduce this risk by simultaneously removing hair and capturing particles. This study will provide evidence on whether VD-ETM improves operating room hygiene and patient outcomes.",[63,64],"Microbial Contamination","Environmental Contamination",[66,67,68,69,70],"Vacuum-assisted electric hair removal system","Surgical site infection","Hair removal","Microbial contamination","Skin integrity","2026-04-01",{"date":73,"type":40},"2026-04-08",{"date":75,"type":21},"2026-05-01",{"date":77,"type":21},"2026-12-30",{"name":46,"class":47},{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":83,"acronym":4,"eligibilityCriteria":84,"healthyVolunteers":85,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":86,"targetDuration":4,"studyType":22,"phases":88,"briefSummary":89,"conditions":90,"keywords":94,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":100,"lastUpdatePostDateStruct":101,"startDateStruct":103,"completionDateStruct":105,"leadSponsor":107,"locationsCount":4},"100628464","evaluation-of-the-effects-of-traditional-and-e-learning-methods-in-cancer-pain-care-education-on-learning-outcomes-and-institutional-costs-100628464","NCT07461974","Evaluation of the Effects of Traditional and E-Learning Methods in Cancer Pain Care Education on Learning Outcomes and Institutional Costs","Inclusion Criteria:\n\n* Students who have access to the internet and a computer\u002Fmobile phone,\n* Students who have successfully completed the Fundamentals of Nursing course,\n* Students who are taking the Internal Medicine Nursing course for the first time,\n* Students who voluntarily agree to participate in the study.\n\nExclusion Criteria:\n\n* Students who are repeating the Internal Medicine Nursing course,\n* Students who have taken the Palliative Care and Nursing or Oncology Nursing courses,\n* Students who have been diagnosed with cancer themselves or have a relative diagnosed with cancer,\n* Students who were admitted to the nursing department through the Vertical Transfer Exam (DGS) after graduating from an associate degree program in a health-related field,\n* Students who graduated from a Vocational Health High School,\n* Students who were admitted through the International Student Examination.",true,{"count":87,"type":21},100,[60],"Cancer pain is a significant clinical problem that directly affects patients' quality of life and requires nurses to be equipped with adequate knowledge and skills to provide effective care. The current shift in knowledge and skill acquisition from traditional teaching methods toward e-learning-based approaches has increased the importance of comparing the effects of these educational methods on learning outcomes in cancer pain management education.\n\nWithin this context, the course content on cancer pain management will be developed using both traditional and e-learning methods based on the ADDIE instructional design model. The effects of these two methods on students' learning outcomes and institutional teaching costs will be evaluated. Thus, this study aims to contribute to identifying effective and cost-efficient teaching strategies in nursing education.",[91,92,93],"Cancer Pain","Nursing Students","Nursing Education",[95,96,97,98,99],"Nursing","Traditional Learning Methods","E-Learning Methods","Education","Cost","2026-03-09",{"date":102,"type":40},"2026-03-10",{"date":104,"type":21},"2026-06-01",{"date":106,"type":21},"2026-12-31",{"name":46,"class":47},{"id":109,"slug":110,"hasResults":11,"nctId":111,"briefTitle":112,"officialTitle":113,"acronym":4,"eligibilityCriteria":114,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":115,"enrollmentInfo":116,"targetDuration":117,"studyType":118,"phases":4,"briefSummary":119,"conditions":120,"keywords":125,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":128,"lastUpdatePostDateStruct":129,"startDateStruct":131,"completionDateStruct":133,"leadSponsor":135,"locationsCount":4},"100618312","fear-of-hypoglycemia-in-patients-with-diabetes-100618312","NCT07329985","FEAR of HYPOGLYCEMIA in PATIENTS WITH DIABETES","THE EFFECT OF FEAR OF HYPOGLYCEMIA ON DIET AND MEDICATION ADHERENCE IN PATIENTS WITH DIABETES","Inclusion Criteria:\n\nDiagnosed with diabetes Aged 18-65 Having experienced at least one hypoglycemic attack previously, Using antidiabetic medication (oral pills and\u002For insulin), Volunteered to participate in the study\n\nExclusion Criteria:\n\nunable to communicate in the same language having cognitive impairment wanting to leave the study at any stage","65 Years",{"count":87,"type":21},"1 Day","OBSERVATIONAL","Fear of hypoglycemia has a significant impact on both medication and dietary adherence in individuals with diabetes. Through avoidance behaviors, it can disrupt metabolic control, prevent the achievement of glycemic targets, and increase the risk of long-term complications. Therefore, monitoring only biochemical parameters is insufficient in diabetes management. It is crucial for healthcare professionals to systematically assess the fear of hypoglycemia.",[121,122,123,124],"Diabetes Mellitus","Diet, Healthy","Medication Adherence","Hypoglycemia",[126,123,95,127],"Diabetes","Diet","2026-02-19",{"date":130,"type":40},"2026-02-20",{"date":132,"type":21},"2026-04-15",{"date":134,"type":21},"2026-12-15",{"name":46,"class":47},{"id":137,"slug":138,"hasResults":11,"nctId":139,"briefTitle":140,"officialTitle":141,"acronym":4,"eligibilityCriteria":142,"healthyVolunteers":85,"sex":16,"minAge":17,"maxAge":143,"enrollmentInfo":144,"targetDuration":4,"studyType":118,"phases":4,"briefSummary":145,"conditions":146,"keywords":4,"overallStatus":147,"whyStopped":4,"lastUpdateSubmitDate":148,"lastUpdatePostDateStruct":149,"startDateStruct":151,"completionDateStruct":153,"leadSponsor":155,"locationsCount":48},"100578588","jigsaw-technique-and-stroke-patient-care-100578588","NCT06813248","Jigsaw Technique and Stroke Patient Care","Effect of Jigsaw Technique on Learning Knowledge About Stroke Patient Care in Nursing Students","Inclusion Criteria:\n\n* Those who were attending class at the time the research data were collected,\n* had not received any previous training in stroke patient care,\n* agreed to participate in the research\n\nExclusion Criteria:\n\n* Absenteeism from class","40 Years",{"count":87,"type":21},"In the literature, problem-based learning, case discussions and case scenarios, and simulation applications are used in stroke patient care nursing education. However, the use of the jigsaw technique is quite limited. Based on this information, it is anticipated that stroke patient care education provided with the Jigsaw technique can increase nursing students' cooperation and communication skills, allowing them to acquire more effective and comprehensive knowledge in clinical care.",[95,98],"RECRUITING","2025-12-29",{"date":150,"type":40},"2025-12-30",{"date":152,"type":40},"2024-12-15",{"date":154,"type":21},"2026-01-01",{"name":46,"class":47},{"id":157,"slug":158,"hasResults":11,"nctId":159,"briefTitle":160,"officialTitle":161,"acronym":4,"eligibilityCriteria":162,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":163,"enrollmentInfo":164,"targetDuration":4,"studyType":118,"phases":4,"briefSummary":166,"conditions":167,"keywords":4,"overallStatus":147,"whyStopped":4,"lastUpdateSubmitDate":148,"lastUpdatePostDateStruct":171,"startDateStruct":172,"completionDateStruct":173,"leadSponsor":175,"locationsCount":48},"100577429","neuropathic-pain-and-type-ii-diabetic-patients-100577429","NCT06798181","Neuropathic Pain and Type II Diabetic Patients","The Effect of Neuropathic Pain on Self-Care Ability and Quality of Life in Type II Diabetic Patients","Inclusion Criteria:\n\n* 18 years and older,\n* Diagnosed with type II diabetes,\n* Reading and writing,\n* No physical or psychological communication barriers,\n* Can read and speak Turkish,\n* Volunteers\n\nExclusion Criteria:\n\n* Diagnosed with type I diabetes","100 Years",{"count":165,"type":21},128,"Diabetes Mellitus (DM) is a common metabolic disease characterized by hyperglycemia resulting from insufficiency, deficiency or absence of the insulin hormone. Chronic hyperglycemia, secondary metabolic and microvascular changes resulting in diabetic neuropathy are among the most common complications encountered in DM patients.\n\nDiabetic neuropathy is called peripheral, autonomic or spinal depending on the region of involvement. Peripheral involvement is more common than other region involvement and its prevalence in DM patients is observed to be 16-87%. Diabetic peripheral neuropathy (DPN) presents with numbness, tingling, paresthesia, muscle weakness and pain. These symptoms can start from the toes and progress to the leg and even the upper extremities.\n\nIn diabetic peripheral neuropathy, pain is seen as burning, electric shock or sharp cold pain, increases at night and affects sleep quality. In these patients, daily living activities such as walking, climbing stairs, and sleeping are negatively affected by progressive DPN and pain, falls are observed, mood disorders are experienced, and the quality of life decreases.",[168,169,170],"Neuropathic Pain","Quality of Life","Diabetic Neuropathies",{"date":150,"type":40},{"date":152,"type":40},{"date":174,"type":21},"2026-01-30",{"name":46,"class":47},{"id":177,"slug":178,"hasResults":11,"nctId":179,"briefTitle":180,"officialTitle":181,"acronym":4,"eligibilityCriteria":182,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":183,"enrollmentInfo":184,"targetDuration":4,"studyType":22,"phases":185,"briefSummary":186,"conditions":187,"keywords":189,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":194,"lastUpdatePostDateStruct":195,"startDateStruct":197,"completionDateStruct":199,"leadSponsor":201,"locationsCount":4},"100607616","sleep-hygiene-in-undergraduate-students-studying-in-the-field-of-health-100607616","NCT07190872","Sleep Hygiene in Undergraduate Students Studying in the Field of Health","Sleep Hygiene Among Undergraduate Students Studying in the Health Field: A Study on Awareness and Behavioural Change","Inclusion Criteria:\n\n* Being an associate degree student at Bilecik Şeyh Edebali University School of Health Services.\n\nBeing a student who has started clinical practice and is actively doing an internship in the clinic.\n\nBeing between the ages of 18 and 25\n\nScoring ≥ 30 on the Sleep Hygiene Index (UHI) (poor sleep hygiene score)\n\nAgreeing to volunteer for the study and signing the informed consent form\n\nNot having received any sleep hygiene training in the last 3 months.\n\nBeing able to participate regularly in the research process (pre-test, training intervention, and post-tests).\n\nExclusion Criteria:\n\n* Having been diagnosed with a sleep disorder (e.g., insomnia, sleep apnea, narcolepsy, etc.).\n\nReceiving a diagnosis of a psychiatric illness that can affect mental health and\u002For taking psychiatric medication regularly.\n\nHaving a chronic illness and taking regular medication (e.g., diabetes, epilepsy, cardiovascular diseases).\n\nWorking nite shifts or having irregular sleep schedules (e.g., students on duty).\n\nDeclaring that they will be unable to regularly participate in the study process or failing to comply with interventions during the study.","25 Years",{"count":87,"type":21},[60],"This study looks at sleep hygiene-the daily habits and environment that help people sleep well-among 2nd-year students at the Health Services Vocational School of Bilecik Şeyh Edebali University (Türkiye). Many health sciences students have busy schedules, clinical practice, and exam stress, which may reduce sleep quality. Good sleep is important for learning, attention, mood, and overall health.\n\nPurpose:\n\nThe aim is to assess the current sleep hygiene and quality of students, and determine whether a brief, in-person education program can enhance their knowledge, habits, and sleep quality in the upcoming weeks.\n\nWho can take part:\n\nThe program is designed for daytime (normal education) 2nd-year students in programs such as Operating Room Services, Paramedic, Opticianry, Pharmacy Services, Medical Laboratory Techniques, Medical Documentation and Secretariat, and Child Development who volunteer and give written consent. Participation is voluntary, and you may leave the study at any time without any penalty.\n\nWhat will happen if you join:\n\nYou will complete short forms before the education session to measure sleep habits and sleep quality (for example, bedtime, caffeine use, and screen time).\n\nYou will attend four classroom sessions (each about 40 minutes). These sessions explain practical sleep tips (regular bed\u002Fwake times, reducing evening caffeine and screen time, preparing a quiet\u002Fdark room, simple relaxation after clinical shifts) and help you create a personal sleep plan.\n\nYou will fill out the same forms again 2 weeks and 4 weeks after the education to see changes over time.\n\nWhat we measure:\n\nSleep hygiene behaviors (how often helpful\u002Funhelpful habits are used)\n\nSleep quality refers to how restful sleep feels, the time it takes to fall asleep, the frequency of night awakenings, and overall daytime functioning.\n\nKnowledge about sleep hygiene (a short quiz) We will also look at factors like stress level, evening screen use, and caffeine intake.\n\nPossible benefits:\n\nYou may learn practical ways to improve sleep, which can help with attention, mood, and daily performance.\n\nPossible risks\u002Fdiscomforts:\n\nThis is an educational program. Risks are minimal (for example, brief discomfort when answering personal questions about sleep). You can skip any question you do not want to answer.\n\nPrivacy:\n\nAll information will be kept confidential and used only for research. Reports will not include names or identifying details.\n\nCosts and payment:\n\nThere is no cost to taking part, and there is no payment for participation.\n\nWithdrawal:\n\nParticipation is voluntary. You may stop at any time without affecting your courses or grades.",[188],"Sleep Hygiene",[190,191,192,193],"sleep hygiene","sleep quality","behavior change","transtheoretical model","2025-09-17",{"date":196,"type":40},"2025-09-24",{"date":198,"type":21},"2025-10-30",{"date":200,"type":21},"2026-04-30",{"name":46,"class":47},{"id":203,"slug":204,"hasResults":11,"nctId":205,"briefTitle":206,"officialTitle":207,"acronym":4,"eligibilityCriteria":208,"healthyVolunteers":85,"sex":16,"minAge":209,"maxAge":4,"enrollmentInfo":210,"targetDuration":4,"studyType":22,"phases":212,"briefSummary":213,"conditions":214,"keywords":216,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":221,"lastUpdatePostDateStruct":222,"startDateStruct":224,"completionDateStruct":226,"leadSponsor":228,"locationsCount":48},"100580629","the-effect-of-retirement-education-on-individuals-retirement-planning-and-quality-of-life-100580629","NCT06839781","The Effect of Retirement Education on Individuals' Retirement Planning and Quality of Life","The Effect of Retirement Education According to Meleis' Transition Theory on Individuals' Retirement Planning and Quality of Life","Inclusion Criteria for the Study\n\n* Literacy\n* Being over 50 years old\n* Not having any verbal communication disabilities (language, speech, vision or -hearing problems) Retirement Planning Process Scale score falling outside the cut-off value Exclusion criteria for the study\n* Having previously received retirement training on the subjects covered by the study Criteria for termination of the study\n* Individual not attending two or more training sessions for any reason\n* Individual retiring due to disability during the program period","50 Months",{"count":211,"type":21},106,[60],"The aim of this study is to learn the effects of retirement education applied to individuals aged 50 and over approaching retirement, according to Meleis's Transition Theory, on their retirement planning processes and quality of life.\n\nThe hypotheses of the study are as follows:\n\nH01: There is no difference in retirement planning perception between the experimental group applied with Meleis's Transition Theory and the control group not applied in terms of retirement planning perception.\n\n* There is no difference in financial planning perception of individuals in the experimental group applied with Meleis's Transition Theory and the control group not applied in terms of retirement education.\n* There is no difference in psychosocial perception of individuals applied with Meleis's Transition Theory and retirement education in terms of retirement planning.\n* There is no difference in health perception of individuals applied with Meleis's Transition Theory and retirement education in terms of retirement planning.\n* There is no difference in lifestyle perception of individuals applied with Meleis's Transition Theory and retirement education in terms of retirement planning.\n\nH02: There is no difference in quality of life between the experimental group applied with Meleis's Transition Theory and the control group not applied in terms of retirement education.\n\nTo evaluate the effectiveness of the training, researchers will collect data from the same number of people with similar characteristics at the beginning and end of the training.\n\nParticipants will (initiative group):\n\nAnswer the pre-test before the intervention Attend retirement education for 1 hour per week for 6 weeks Answer the post-test after the intervention Answer the follow-up test 1 month after the post-test",[215],"Healthy",[217,218,219,220],"quality of life","nursing","occupational health","transition theory","2025-02-20",{"date":223,"type":40},"2025-02-21",{"date":225,"type":21},"2025-03-01",{"date":227,"type":21},"2025-05-30",{"name":46,"class":47},{"id":230,"slug":231,"hasResults":11,"nctId":232,"briefTitle":233,"officialTitle":233,"acronym":4,"eligibilityCriteria":234,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":235,"targetDuration":4,"studyType":22,"phases":237,"briefSummary":238,"conditions":239,"keywords":241,"overallStatus":147,"whyStopped":4,"lastUpdateSubmitDate":244,"lastUpdatePostDateStruct":245,"startDateStruct":247,"completionDateStruct":249,"leadSponsor":250,"locationsCount":48},"100554151","effect-of-immunization-education-program-on-parental-vaccine-hesitation-100554151","NCT06495359","Effect of Immunization Education Program on Parental Vaccine Hesitation","Inclusion Criteria:\n\n* Having a child between the ages of 0-6,\n* admitted to the pediatric ward,\n* who have not previously received training on immunization\n* Parents who volunteered to participate in the study\n\nExclusion Criteria:\n\n* illiterate\n* parents with mental retardation, vision and hearing impairment",{"count":236,"type":21},60,[60],"Not administering vaccines due to vaccine hesitancy is both a potential public health problem and a difficult and risky situation for healthcare professionals. Health sector workers play a very important role in vaccinating families. As public awareness increases, interest in these vaccines is likely to increase. Made works; It shows that healthcare professionals and physicians establishing trust and communicating effectively with vaccine recipients and parents is one of the most effective ways to eliminate vaccine hesitations. They stated that in order for childhood vaccines to be administered at a high rate, effective communication should first be established with parents. This project aimed to determine the effect of the immunization education program on parents' vaccine hesitancy. The project is designed as a randomized controlled study and will consist of experimental and control groups. An education program regarding immunization will be applied to the parents in the experimental group. The originality of this project is the evaluation of the effect of the immunization education program applied to parents whose children are hospitalized on vaccine hesitancy. Although studies on vaccine hesitancy in parents have increased in recent years, most of them consist of descriptive studies aimed at determining the level of vaccine hesitancy and affecting factors. No intervention studies on the effect of immunization education in parents on vaccine hesitancy have been found.",[240],"Nurse's Role",[242,243,98],"Immunization","Parents","2024-07-09",{"date":246,"type":40},"2024-07-10",{"date":248,"type":40},"2024-03-01",{"date":225,"type":21},{"name":46,"class":47},{"id":252,"slug":253,"hasResults":11,"nctId":254,"briefTitle":255,"officialTitle":255,"acronym":4,"eligibilityCriteria":256,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":257,"targetDuration":4,"studyType":22,"phases":258,"briefSummary":259,"conditions":260,"keywords":262,"overallStatus":147,"whyStopped":4,"lastUpdateSubmitDate":244,"lastUpdatePostDateStruct":265,"startDateStruct":266,"completionDateStruct":267,"leadSponsor":268,"locationsCount":48},"100554148","effect-of-rational-drug-education-on-the-attitudes-of-parents-of-hospitalized-children-100554148","NCT06495320","Effect of Rational Drug Education on the Attitudes of Parents of Hospitalized Children","Inclusion Criteria:\n\n* Having a child between the ages of 0-12,\n* admitted to the pediatric ward,\n* who have not previously received training on rational drug use\n* Parents who volunteered to participate in the study\n\nExclusion Criteria:\n\n* illiterate\n* parents with mental retardation, vision and hearing impairment",{"count":236,"type":21},[60],"In this project, it was aimed to determine the effect of the rational drug management training program on parents' attitudes towards rational drug use. The project is designed as a randomized controlled study and will consist of experimental and control groups. An education program on rational drug use will be applied to the parents in the experimental group. The originality of this project is the evaluation of the effect of the education program on rational drug use applied to parents whose children are hospitalized. Although studies on rational drug use in parents have increased in recent years, most of them consist of descriptive studies aimed at evaluating knowledge and attitudes towards rational drug use. It seems that the number of intervention studies on rational drug use in parents is limited. No intervention studies aimed at the rational drug use attitudes of parents whose children are hospitalized have been found. This study has the feature of revealing the effectiveness of the rational drug use education program to be applied to parents in cases of illness and hospitalization where the importance of rational drug use becomes evident.",[261],"Nursing Caries",[263,264,243],"Rational drug use","Hospitalized Children",{"date":246,"type":40},{"date":248,"type":40},{"date":225,"type":21},{"name":46,"class":47},""]