[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Amasya University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":420},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,16,0,[8,38,68,91,115,144,169,190,215,240,267,293,318,345,369,396],{"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":21,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":4,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":27,"lastUpdatePostDateStruct":28,"startDateStruct":31,"completionDateStruct":33,"leadSponsor":35,"locationsCount":4},"100642182","clinical-outcomes-of-intubation-techniques-in-anesthesia-100642182",false,"NCT07661186","Clinical Outcomes of Intubation Techniques in Anesthesia","Clinical Outcomes of Intubation Techniques in Anesthesia; an Observational Study.","Inclusion Criteria:\n\n* Patients over 18 years of age ASA 1-2-3 patients undergoing elective laparoscopic cholecystectomy surgery Patients who agreed to participate in the study\n\nExclusion Criteria:\n\n* Patients for whom difficult intubation is considered Patients with neurological disorders Patients with mental retardation Patients who refused to participate in the study.","ALL","18 Years",{"count":19,"type":20},165,"ESTIMATED","1 Day","OBSERVATIONAL","Before surgery, patients will be evaluated by an anesthesiologist at the anesthesia clinic and informed in detail about the study. Patients who do not wish to participate in the study will absolutely not be included, and this will not affect the patients' treatment process in any way. The anesthesia method to be applied to patients who agree to participate in the study will not differ from routine anesthesia application. In other words, no additional medication, procedure, or different anesthesia method will be applied to patients within the scope of the study. After the surgery is completed, patients will be monitored in the recovery room and during their hospital stay. During this monitoring, it will be observed and recorded whether patients have complaints such as sore throat, cough, or hoarseness.",[25],"Laparoscopic","NOT_YET_RECRUITING","2026-06-18",{"date":29,"type":30},"2026-06-22","ACTUAL",{"date":32,"type":20},"2026-06-14",{"date":34,"type":20},"2026-12-15",{"name":36,"class":37},"Amasya University","OTHER",{"id":39,"slug":40,"hasResults":11,"nctId":41,"briefTitle":42,"officialTitle":43,"acronym":4,"eligibilityCriteria":44,"healthyVolunteers":45,"sex":46,"minAge":17,"maxAge":47,"enrollmentInfo":48,"targetDuration":4,"studyType":50,"phases":51,"briefSummary":53,"conditions":54,"keywords":4,"overallStatus":58,"whyStopped":4,"lastUpdateSubmitDate":59,"lastUpdatePostDateStruct":60,"startDateStruct":62,"completionDateStruct":64,"leadSponsor":66,"locationsCount":67},"100641038","the-effect-of-student-midwife-support-circle-intervention-on-burnout-resilience-and-professional-belonging-levels-of-midwifery-students-100641038","NCT07583199","The Effect of Student-Midwife Support Circle Intervention on Burnout, Resilience, and Professional Belonging Levels of Midwifery Students","The Effect of the Student Midwife Support Circle (SMSC) Intervention on Burnout, Resilience, and Professional Belongingness Levels of Midwifery Students: A Mixed-Method Study","Inclusion Criteria:\n\n* Individuals who agree to participate voluntarily in the study\n* Individuals studying in the field of midwifery\n\nExclusion Criteria:\n\n* Individuals who do not agree to participate voluntarily in the study,\n* Individuals who have previously received Student Midwife Support Circle Intervention",true,"FEMALE","49 Years",{"count":49,"type":20},80,"INTERVENTIONAL",[52],"NA","Midwifery students are exposed to multifaceted stressors such as traumatic and unsupportive clinical experiences and psychosocial burdens; this can negatively impact emotional well-being, leading to secondary traumatic stress, burnout, compassion fatigue, and decreased sense of belonging. In this context, there is a growing need for structured and supportive interventions aimed at strengthening students' self-efficacy, resilience, and perceptions of social support. The aim of this research is to determine the effect of the Student Midwife Support Circle Intervention on midwifery students' levels of burnout, resilience, and professional belonging.",[55,56,57],"Burnout","Resilience","Professional Identification","RECRUITING","2026-05-12",{"date":61,"type":30},"2026-05-14",{"date":63,"type":30},"2026-04-06",{"date":65,"type":20},"2026-09-01",{"name":36,"class":37},1,{"id":69,"slug":70,"hasResults":11,"nctId":71,"briefTitle":72,"officialTitle":73,"acronym":4,"eligibilityCriteria":74,"healthyVolunteers":45,"sex":16,"minAge":17,"maxAge":75,"enrollmentInfo":76,"targetDuration":4,"studyType":50,"phases":78,"briefSummary":79,"conditions":80,"keywords":82,"overallStatus":58,"whyStopped":4,"lastUpdateSubmitDate":84,"lastUpdatePostDateStruct":85,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":90,"locationsCount":67},"100639025","assertiveness-training-for-communication-skills-100639025","NCT07575048","Assertiveness Training for Communication Skills","Strengthening the Communication Skills of Oncology Nurses Through Virtual Reality-Based Assertiveness Training","Inclusion Criteria:\n\n* Those who agree to participate in the study,\n* Those who are 18 years of age or older,\n* Those who have been working in oncology clinics for at least 6 months.\n\nExclusion Criteria:\n\n* Those who gave incomplete answers to the scales used in the study,\n* Those who have previously participated in assertiveness skills training.","65 Years",{"count":77,"type":20},60,[52],"This study aims to determine the effect of virtual reality-based assertiveness training on strengthening the communication skills of oncology nurses.",[81],"Communication",[83],"Education","2026-05-03",{"date":86,"type":30},"2026-05-08",{"date":88,"type":30},"2026-03-30",{"date":34,"type":20},{"name":36,"class":37},{"id":92,"slug":93,"hasResults":11,"nctId":94,"briefTitle":95,"officialTitle":96,"acronym":4,"eligibilityCriteria":97,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":98,"enrollmentInfo":99,"targetDuration":21,"studyType":22,"phases":4,"briefSummary":101,"conditions":102,"keywords":4,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":106,"lastUpdatePostDateStruct":107,"startDateStruct":109,"completionDateStruct":111,"leadSponsor":113,"locationsCount":114},"100635803","relationship-between-induction-burst-suppression-and-bispectral-index-100635803","NCT07557433","Relationship Between Induction Burst Suppression and Bispectral Index","The Relationship Between Burst Suppression Observed During Anesthesia Induction and the Bispectral Index Value During the Maintenance Phase of Anesthesia","Inclusion Criteria:\n\n* Age between 18 and 75 years\n* American Society of Anesthesiologists (ASA) physical status I-III\n* Scheduled for elective surgery\n* Surgery planned to be performed under total intravenous anesthesia (TIVA)\n\nExclusion Criteria:\n\n* Presence of neurological disease\n* Chronic use of sedative medications or antiepileptic drugs\n* Severe hepatic or renal dysfunction\n* Intraoperative administration of ketamine or dexmedetomidine","75 Years",{"count":100,"type":20},200,"The purpose of this study is to understand whether certain brain activity patterns that can appear at the beginning of anesthesia are related to how deep anesthesia remains during the operation.\n\nThe main question of the study is:\n\nDo patients who show a pattern called burst suppression during the start of anesthesia experience deeper anesthesia during surgery?\n\nPatients who are scheduled for elective surgery under total intravenous anesthesia (TIVA) may take part in this study. During the operation, brain activity will be monitored using a sensor placed on the forehead (Bispectral Index, BIS monitor), which is already commonly used during anesthesia. Information such as BIS values and the doses of anesthesia medications given during the operation will be recorded.\n\nParticipation in this study will not change the type of anesthesia or the routine care that patients receive during surgery. The study only involves recording and analyzing information collected during standard anesthesia monitoring.",[103,104,105],"Bispectral Index Monitoring","Burst Suppression","Total Intravenous Anesthesia","2026-04-23",{"date":108,"type":30},"2026-04-29",{"date":110,"type":20},"2026-06-01",{"date":112,"type":20},"2027-08-01",{"name":36,"class":37},2,{"id":116,"slug":117,"hasResults":11,"nctId":118,"briefTitle":119,"officialTitle":120,"acronym":4,"eligibilityCriteria":121,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":122,"enrollmentInfo":123,"targetDuration":4,"studyType":50,"phases":125,"briefSummary":126,"conditions":127,"keywords":131,"overallStatus":58,"whyStopped":4,"lastUpdateSubmitDate":137,"lastUpdatePostDateStruct":138,"startDateStruct":140,"completionDateStruct":141,"leadSponsor":143,"locationsCount":67},"100620651","bifes-vs-ipack-in-postoperative-knee-arthroplasty-analgesia-100620651","NCT07360392","BiFeS vs. iPACK in Postoperative Knee Arthroplasty Analgesia","Comparison of Postoperative Analgesic Effects of Two Different Anesthesia Techniques in Knee Arthroplasty: Nerve Blocks Named BiFeS and iPACK","Inclusion Criteria:\n\n* Scheduled for unilateral total knee arthroplasty\n* Classified as ASA physical status I-III\n\nExclusion Criteria:\n\n* Scheduled for revision arthroplasty or bilateral surgery\n* Allergy to local anesthetics or contraindication to regional blocks\n* Neurological disorders, peripheral neuropathy, or conditions affecting lower extremity muscle strength\n* Coagulopathy or receiving anticoagulant therapy\n* History of severe liver, kidney, or heart failure\n* Chronic opioid use or history of substance abuse\n* Patients experiencing intraoperative complications (e.g., excessive bleeding)\n* Cases in which adequate sensory blockade is not achieved after the block","80 Years",{"count":124,"type":20},88,[52],"The Biceps Femoris Short Head (BiFeS) block is a new fascial plane block technique targeting the sensory innervation of the posterolateral capsule of the knee while preserving motor function. The aim of this study is to evaluate the postoperative analgesic efficacy of the BiFeS block combined with the adductor canal block (ACB) in patients undergoing total knee arthroplasty, compared to ACB + iPACK block. The study is planned as a prospective, randomized, double-blind, parallel two-group trial. Patients will be randomized in a 1:1 ratio to receive ACB + iPACK (Group A) or ACB + BiFeS (Group B). Postoperative pain scores (VAS), opioid consumption, early mobilization, and quality of recovery (QoR-15) outcomes will be compared.",[128,129,130],"Arthroplasty, Replacement, Knee","Pain, Postoperative","Anesthesia, Regional",[132,133,134,135,136],"Pain Management","Knee Arthroplasty","BiFes","iPACK","Nerve Block","2026-04-20",{"date":139,"type":30},"2026-04-22",{"date":137,"type":30},{"date":142,"type":20},"2027-06-01",{"name":36,"class":37},{"id":145,"slug":146,"hasResults":11,"nctId":147,"briefTitle":148,"officialTitle":149,"acronym":4,"eligibilityCriteria":150,"healthyVolunteers":45,"sex":46,"minAge":17,"maxAge":4,"enrollmentInfo":151,"targetDuration":4,"studyType":50,"phases":153,"briefSummary":154,"conditions":155,"keywords":157,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":162,"lastUpdatePostDateStruct":163,"startDateStruct":164,"completionDateStruct":166,"leadSponsor":168,"locationsCount":4},"100632385","the-effect-of-using-nature-sounds-and-virtual-reality-during-the-non-stress-test-100632385","NCT07512999","The Effect of Using Nature Sounds and Virtual Reality During the Non-Stress Test","The Effect of Using Nature Sounds and Virtual Reality During the Non-Stress Test on Fetal Well-Being, Maternal Anxiety, Comfort, and Satisfaction","Inclusion Criteria:\n\n* Being 18 years of age or older\n* Being at 32 weeks of gestation or beyond\n* Having a healthy pregnancy\n* Having a singleton and viable pregnancy\n* Not using tobacco or alcohol\n* Having eaten at least two hours before the NST procedure\n\nExclusion Criteria:\n\n* Having any communication impairment (language, vision, hearing, speech, etc.)\n* Having a physical or cognitive condition that prevents the use of the virtual reality application and nature sound Having a diagnosis of a high-risk pregnancy Having a diagnosis of a significant chronic (cardiac, renal, neurological, etc.) or psychiatric disorder (psychosis, neurosis, substance dependence, etc.) Having a multiple pregnancy Having a fetus with an anomaly Experiencing fetal distress requiring emergency intervention Having uterine contractions",{"count":152,"type":20},150,[52],"The aim of this study is to examine the effect of using nature sounds and virtual reality during the non-stress test on fetal well-being, maternal anxiety, comfort, and satisfaction. The study sample will consist of all pregnant women admitted to the Non-Stress Test (NST) unit. A total of 150 women will be included in the sample: 50 for the virtual reality group, 50 for the nature sounds group, and 50 for the control group.",[156],"Pregnancy - Prenatal Testing",[158,159,160,161],"Non-Stress Test","Pregnancy","Anxiety","Fetal health","2026-04-03",{"date":63,"type":30},{"date":165,"type":20},"2026-07-01",{"date":167,"type":20},"2027-03-31",{"name":36,"class":37},{"id":170,"slug":171,"hasResults":11,"nctId":172,"briefTitle":173,"officialTitle":174,"acronym":4,"eligibilityCriteria":175,"healthyVolunteers":45,"sex":46,"minAge":17,"maxAge":4,"enrollmentInfo":176,"targetDuration":4,"studyType":50,"phases":178,"briefSummary":179,"conditions":180,"keywords":181,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":162,"lastUpdatePostDateStruct":185,"startDateStruct":187,"completionDateStruct":188,"leadSponsor":189,"locationsCount":4},"100632197","the-effect-of-a-mindfulness-based-stress-reduction-program-applied-to-nulliparous-pregnant-women-100632197","NCT07510555","The Effect of a Mindfulness-Based Stress Reduction Program Applied to Nulliparous Pregnant Women","The Effect of a Mindfulness-Based Stress Reduction Program Applied to Nulliparous Pregnant Women on Prenatal Anxiety, Fetal Health Concern, and Psychological Well-Being","Inclusion Criteria:\n\n* Be 18 years of age and older,\n* Have at least a primary school graduate\n* Not having given birth before\n* Be between the 12th and 28th weeks of pregnancy,\n* Have internet access\n\nExclusion Criteria:\n\n* Having any communication problems (language, hearing, vision, speech, etc.),\n* Having a diagnosis of high-risk pregnancy, or having a diagnosis of a psychiatric illness (depression, psychosis, etc.)",{"count":177,"type":20},100,[52],"Mindfulness-based stress reduction programs are among the effective methods that can contribute to managing anxiety during pregnancy, strengthening mother-fetus interaction, and supporting psychological well-being. In this context, this study will examine the effect of a mindfulness-based stress reduction program on prenatal anxiety, fetal health concerns, and psychological well-being. The aim of this study is to determine the effect of a mindfulness-based stress reduction program applied to pregnant women who have not previously given birth on prenatal anxiety, fetal health concerns, and psychological well-being.",[159],[159,182,183,184],"Mindfulness","Well-being","Concerns",{"date":186,"type":30},"2026-04-08",{"date":165,"type":20},{"date":167,"type":20},{"name":36,"class":37},{"id":191,"slug":192,"hasResults":11,"nctId":193,"briefTitle":194,"officialTitle":195,"acronym":4,"eligibilityCriteria":196,"healthyVolunteers":45,"sex":46,"minAge":17,"maxAge":4,"enrollmentInfo":197,"targetDuration":4,"studyType":50,"phases":199,"briefSummary":200,"conditions":201,"keywords":204,"overallStatus":58,"whyStopped":4,"lastUpdateSubmitDate":208,"lastUpdatePostDateStruct":209,"startDateStruct":211,"completionDateStruct":213,"leadSponsor":214,"locationsCount":67},"100630293","the-effects-of-yoga-on-pregnant-women-100630293","NCT07485790","The Effects of Yoga on Pregnant Women","The Effects of Yoga on Stress, Sexual Life Quality, and Sleep Habits in Pregnant Women: A Randomized Controlled Study","Inclusion Criteria:\n\n* In their third trimester,\n* Able to read and write in Turkish,\n* Use a smartphone and have internet access,\n* Have no communication barriers,\n* Voluntarily agree to participate in the research.\n\nExclusion Criteria:\n\n* Pregnant women with any risk factors during pregnancy,\n* Pregnant women with any chronic illness,\n* Pregnant women with a diagnosed psychological problem,\n* Pregnant women with any exercise restrictions imposed by a physician,\n* Pregnant women participating in a different training program (meditation, relaxation, etc.)",{"count":198,"type":20},70,[52],"It is thought that a yoga intervention administered to pregnant women will reduce stress levels, enhance sexual quality of life, and positively affect sleep habits. According to the power analysis results, the study must include at least 70 pregnant women (35 in the experimental group and 35 in the control group). Data will be collected through a Personal Information Form, the Perceived Stress Scale (PSS), the Sexual Quality of Life Questionnaire-Female (SQLQ-F), and a Sleep Habits Form. In this study, the yoga practice will be administered to the pregnant women in the experimental group by the researcher.",[202,203],"Sleep Disorder","Stress",[205,206,207],"sexual quality of life","pregnant women","yoga","2026-03-17",{"date":210,"type":30},"2026-03-20",{"date":212,"type":30},"2026-03-15",{"date":65,"type":20},{"name":36,"class":37},{"id":216,"slug":217,"hasResults":11,"nctId":218,"briefTitle":219,"officialTitle":220,"acronym":4,"eligibilityCriteria":221,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":98,"enrollmentInfo":222,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":224,"conditions":225,"keywords":230,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":232,"lastUpdatePostDateStruct":233,"startDateStruct":235,"completionDateStruct":237,"leadSponsor":239,"locationsCount":67},"100619345","effect-of-anesthesia-technique-on-surgical-view-in-shoulder-arthroscopy-100619345","NCT07343414","Effect of Anesthesia Technique on Surgical View in Shoulder Arthroscopy","Impact of Anesthesia Method on Surgical View and Surgeon Satisfaction During Shoulder Arthroscopy: A Prospective Observational Study","Inclusion Criteria:\n\n* Volunteers aged 18 to 75 years.\n* Patients scheduled for elective shoulder arthroscopy.\n* Patients with an ASA (American Society of Anesthesiologists) physical status score of I, II, or III.\n* Patients capable of providing informed consent.\n\nExclusion Criteria:\n\n* Previous surgical procedure performed on the same shoulder.\n* Presence of medical contraindications that could affect the choice of anesthesia (coagulopathy, active infection, severe pulmonary diseases)\n* Known allergy to local anesthetics or general anesthesia agents\n* History of opioid dependence or chronic pain syndrome\n* Presence of neurological disorders, particularly those involving the brachial plexus",{"count":223,"type":20},82,"This prospective observational study evaluates the effect of the anesthesia method (general anesthesia versus regional anesthesia \\[interscalene nerve block\u002Fsuperficial cervical block\\] with sedation) on the operating clarity of the surgical view and the surgeon's satisfaction during elective shoulder arthroscopy. The study investigates how these different anesthesia techniques influence intraoperative conditions, specifically bleeding amounts and the visibility of the surgical field, which are critical for the success of this minimally invasive procedure. Additionally, the research will monitor patient-centered outcomes, including postoperative pain levels, recovery time, and potential side effects such as nausea or vomiting, to determine which anesthesia strategy provides the optimal balance of surgical efficiency and patient comfort.",[226,227,228,229],"Shoulder Arthroscopy","Interscalene Nerve Block","Surgical View Quality","Surgeon Satisfaction",[226,229,228,227,231],"Rotator Cuff Repair","2026-01-07",{"date":234,"type":30},"2026-01-15",{"date":236,"type":20},"2026-02-01",{"date":238,"type":20},"2027-05-01",{"name":36,"class":37},{"id":241,"slug":242,"hasResults":11,"nctId":243,"briefTitle":244,"officialTitle":245,"acronym":4,"eligibilityCriteria":246,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":247,"targetDuration":4,"studyType":50,"phases":248,"briefSummary":249,"conditions":250,"keywords":252,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":259,"lastUpdatePostDateStruct":260,"startDateStruct":262,"completionDateStruct":264,"leadSponsor":266,"locationsCount":67},"100615360","exercise-effects-on-pain-sleep-and-depression-in-diabetic-peripheral-neuropathy-100615360","NCT07291596","Exercise Effects on Pain, Sleep and Depression in Diabetic Peripheral Neuropathy","The Effect of Foot-Ankle Exercises on Pain, Sleep Quality and Depression in Individuals With Diabetic Peripheral Neuropathy","Inclusion Criteria:\n\n* 18 years of age and older\n* Diagnosed with diabetic peripheral neuropathy for at least 6 months S-LANSS pain score ≥ 12\n* Able to perform the exercise program\n* Voluntary participation and informed consent\n\nExclusion Criteria:\n\n* Pregnancy\n* Severe cardiovascular or musculoskeletal disease\n* Cognitive impairment preventing participation\n* Receiving physiotherapy or another structured exercise program during the study\n* Any other condition deemed inappropriate by the investigator",{"count":198,"type":20},[52],"It is known that the pain experienced by individuals with diabetic neuropathy negatively impacts sleep and quality of life, leading to numerous psychosocial problems such as anxiety and depression. Studies in the literature indicate that exercise, a non-pharmacological method, improves pain and sleep quality in individuals with diabetic neuropathy. However, no studies have been found evaluating the effects of foot-ankle exercises on pain, sleep quality, and depression in individuals with diabetic neuropathy.\n\nThis research aims to examine the effects of foot-ankle exercises on pain, sleep quality, and depression in individuals with diabetic peripheral neuropathy.\n\nThis randomized controlled experimental study will be conducted with 70 individuals with diabetes diagnosed with diabetic neuropathy, registered in the patient information systems of two public hospitals. The foot-ankle exercises will be performed by the patients in their homes, twice a day, three days a week, for eight weeks. The research data are as follows: The Introductory Information Form will be collected using the S-Lanns (Self-Leeds Assessment of Neuropathic Symptoms and Sign) Pain Scale, VAS-Visual Analog Scale, Pittsburgh Sleep Quality Index (PSQI), and Beck Depression Inventory (BDI).\n\nThis study is important because it will determine the effects of foot and ankle exercises on pain, sleep disturbances, and depression, which are common problems experienced by individuals with diabetic neuropathy.",[251],"Diabetic Peripheral Neuropathy",[253,254,255,256,257,258],"diabetes","neuropathy","Exercise","Pain","Sleep Quality","Depression","2025-12-05",{"date":261,"type":30},"2025-12-18",{"date":263,"type":20},"2025-12-22",{"date":265,"type":20},"2026-06-30",{"name":36,"class":37},{"id":268,"slug":269,"hasResults":11,"nctId":270,"briefTitle":271,"officialTitle":272,"acronym":4,"eligibilityCriteria":273,"healthyVolunteers":45,"sex":46,"minAge":4,"maxAge":4,"enrollmentInfo":274,"targetDuration":4,"studyType":50,"phases":276,"briefSummary":277,"conditions":278,"keywords":281,"overallStatus":58,"whyStopped":4,"lastUpdateSubmitDate":286,"lastUpdatePostDateStruct":287,"startDateStruct":289,"completionDateStruct":291,"leadSponsor":292,"locationsCount":67},"100614572","effect-of-hypnobreastfeeding-education-in-high-risk-pregnant-women-100614572","NCT07281339","Effect of Hypnobreastfeeding Education in High-Risk Pregnant Women","The Effect of Hypnobreastfeeding Education Given to High-Risk Pregnant Women on Anxiety Levels, Infant Feeding Intention, Postpartum Perception of Insufficient Milk, and Breastfeeding Adaptation","Inclusion Criteria:\n\n* High-risk primiparous pregnant women\n* Those with 28-34 weeks of pregnancy\n* Those who volunteered to participate in the study\n* Those who can read and write Turkish\n\nExclusion Criteria:\n\n* Those with communication disabilities\n* Those with psychiatric and mental illnesses\n* Those who have an obstacle to breastfeeding\n* Those who have previously attended a birth preparation class\n* Those who receive breastfeeding-related training and consultancy\n* Those who gave birth prematurely\n* Those with anomalies in their babies",{"count":275,"type":20},68,[52],"It is thought that hypnobreastfeeding training given to high-risk pregnant women will reduce anxiety levels, increase lactation, encourage breastfeeding, reduce the perception of insufficient milk, and facilitate adaptation to the postpartum breastfeeding process. According to the results of the power analysis, at least 68 high-risk pregnant women, 34 experimental and 34 control, should be included in the study. Data will be collected with the \"Pregnancy Information Form\", \"Anxiety Assessment Scale\", \" Infant Feeding Intention Instrument\", \"Postpartum Information Form\", \"Perception of Insufficient Milk Questionnaire\" and \"Breastfeeding Adaptation Scale\". In the research, hypnobreastfeeding training will be applied by the researcher to the high-risk pregnant women in the experimental group.",[279,280],"High-risk Pregnancy","Breast Feeding",[282,160,283,284,285],"Hypnobreastfeeding","Infant Feeding Intention","Perception of Insufficient Milk","Breastfeeding Adaptation","2025-12-01",{"date":288,"type":30},"2025-12-15",{"date":290,"type":30},"2025-10-15",{"date":265,"type":20},{"name":36,"class":37},{"id":294,"slug":295,"hasResults":11,"nctId":296,"briefTitle":297,"officialTitle":298,"acronym":4,"eligibilityCriteria":299,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":300,"targetDuration":4,"studyType":50,"phases":301,"briefSummary":302,"conditions":303,"keywords":305,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":310,"lastUpdatePostDateStruct":311,"startDateStruct":313,"completionDateStruct":315,"leadSponsor":317,"locationsCount":4},"100582625","music-therapy-applied-during-hemodialysis-100582625","NCT06865742","Music Therapy Applied During Hemodialysis","Effects of Music Therapy Applied During Hemodialysis on Fatigue, Sleep Quality and Mental Well-Being","Inclusion Criteria:\n\n* Being 18 years of age or older\n* Being on HD treatment for at least 6 months\n* Being cooperative and having no verbal communication disabilities (hearing or speaking)\n* Not having a psychiatric disorder\n\nExclusion Criteria:\n\n* Having recently attended a similar program\n* Not agreeing to participate in the study",{"count":77,"type":20},[52],"Many symptoms are encountered during the hemodialysis treatment process, and fatigue and insomnia are two of the most common symptoms. The management of these symptoms, which negatively affect the quality of life and mental well-being of individuals, is very important. It is known that the effects of pharmacological treatments are limited in the management of symptoms encountered during the HD treatment process, and the tendency towards non-pharmacological methods in symptom management is increasing.\n\nThis study will be conducted to determine the effects of music therapy to be applied to individuals receiving HD treatment on fatigue, sleep quality and mental well-being.\n\nThis randomized controlled experimental study will be conducted with 60 individuals receiving treatment in the hemodialysis clinic of a public hospital. Individuals will receive 30 minutes of music therapy after the 2nd hour of each hemodialysis session for 4 weeks. Research data will be collected using the Introductory Information Form, Chalder Fatigue Scale, Pittsburgh Sleep Quality Scale and Warwick-Edinburgh Mental Well-Being Scale.\n\nThis study is important because it is the first study to evaluate the effects of music therapy on fatigue, sleep quality and mental well-being of individuals receiving HD treatment. It is thought that music therapy applied to individuals receiving HD treatment will contribute to the literature on evidence.",[304],"Hemodialysis",[304,306,307,257,308,309],"Music Therapy","Fatigue","Mental Well-Being","nursing","2025-09-30",{"date":312,"type":30},"2025-10-01",{"date":314,"type":20},"2025-11-03",{"date":316,"type":20},"2025-12-31",{"name":36,"class":37},{"id":319,"slug":320,"hasResults":11,"nctId":321,"briefTitle":322,"officialTitle":323,"acronym":4,"eligibilityCriteria":324,"healthyVolunteers":11,"sex":16,"minAge":325,"maxAge":122,"enrollmentInfo":326,"targetDuration":4,"studyType":50,"phases":328,"briefSummary":329,"conditions":330,"keywords":332,"overallStatus":58,"whyStopped":4,"lastUpdateSubmitDate":338,"lastUpdatePostDateStruct":339,"startDateStruct":340,"completionDateStruct":342,"leadSponsor":344,"locationsCount":67},"100570088","effect-of-aronia-berry-consumption-on-inflammatory-parameters-100570088","NCT06702696","Effect of Aronia Berry Consumption on Inflammatory Parameters","Consumption of Anti-Inflammatory Effects of Aronia (Aronia Melanocarpa) Berry in Patients With Chronic Obstructive Pulmonary Disease","Inclusion Criteria:\n\n* Aged 50-80 years\n* Diagnosed with COPD\n* Not following a vegetarian or vegan diet\n* Willing to consume the provided aronia berry (black chokeberry)\n* Non-smokers\n* Have signed the informed consent form\n* Has not undergone endobronchial tube or valve surgery in the last two years.\n\nExclusion Criteria:\n\n* Presence of associated chronic inflammatory\u002Frheumatic diseases\n* Chronic infections that may create a prothrombotic state\n* Chronic kidney disease (CKD)\n* Malignancy\n* Hereditary thrombophilia\n* Essential thrombocythemia\n* Diagnosed endocrine disorders\n* Malabsorption disorders\n* Allergy to any food or berry fruits\n* Smoking\n* Participants who did not sign the informed consent form","50 Years",{"count":327,"type":20},50,[52],"The study will aim to evaluate the effects of consuming freeze-dried aronia berries as an adjunct to medical treatment in patients with chronic obstructive pulmonary disease (COPD), focusing on anti-inflammatory, respiratory, and biochemical parameters.\n\nIt will be conducted at a research hospital in Istanbul, involving 50 participants aged 50-80 diagnosed with COPD. Participants will be randomly assigned to two groups: the aronia group (AG, n=25) and the placebo group (PG, n=25). The AG will receive 30 g of freeze-dried aronia powder daily, while the PG will receive 30 g of placebo powder, both for a duration of 8 weeks. Baseline demographic data will be collected through face-to-face interviews, while biochemical, respiratory, anthropometric, and body composition parameters will be assessed both before and after the intervention. Dietary intake records will also be collected and analyzed.",[331],"COPD (Chronic Obstructive Pulmonary Disease)",[333,334,335,336,337],"anti-inflammatory","black chokeberry","COPD","aronia melanocarpa","cytokines","2025-09-29",{"date":312,"type":30},{"date":341,"type":30},"2024-11-15",{"date":343,"type":20},"2025-11-15",{"name":36,"class":37},{"id":346,"slug":347,"hasResults":11,"nctId":348,"briefTitle":349,"officialTitle":350,"acronym":4,"eligibilityCriteria":351,"healthyVolunteers":45,"sex":46,"minAge":17,"maxAge":75,"enrollmentInfo":352,"targetDuration":4,"studyType":50,"phases":353,"briefSummary":354,"conditions":355,"keywords":358,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":361,"lastUpdatePostDateStruct":362,"startDateStruct":364,"completionDateStruct":366,"leadSponsor":368,"locationsCount":67},"100595858","the-impact-of-the-nurse-led-my-baby-is-safe-educational-program-100595858","NCT07037914","The Impact of the Nurse-Led \"My Baby is Safe\" Educational Program","The Impact of the Nurse-Led \"My Baby is Safe\" Educational Program on Mothers' Knowledge, Skills, and Self-Efficacy","Inclusion Criteria:\n\n* Aged 18 years or older,\n* Having a healthy newborn,\n* Having one or more children,\n* Having at least a primary school education,\n* Having a smartphone and mobile internet access,\n* Being able to speak, read, listen, and understand Turkish, able to follow instructions, and having no communication barriers,\n* Voluntarily agreeing to participate in the study.\n\nExclusion Criteria:\n\n* Mothers whose newborns have any health problems will be excluded from the study.\n* Mothers who wish to withdraw from the study at any point during the research process will be removed from the study.\n* did not complete the process of the assessment and intervention of this study.",{"count":327,"type":20},[52],"The aim of this study is to determine the effect of the My Baby is Safe Educational Program on mothers' knowledge, skills, and self-efficacy levels.The objectives of the study are to ensure that mothers acquire sufficient knowledge and skills regarding SIDS and SBS, and to enhance their self-efficacy levels.The participants were randomly assigned to one group that received only the My Baby is Safe Educational Program (Group I), or to another group that received standard care (Group II).",[356,357],"Sudden Infant Death Syndrome","Shaken Baby Syndrome",[356,357,359,360,83],"Safe Sleep","Pediatric Nursing","2025-06-23",{"date":363,"type":30},"2025-06-26",{"date":365,"type":20},"2025-07",{"date":367,"type":20},"2026-08",{"name":36,"class":37},{"id":370,"slug":371,"hasResults":11,"nctId":372,"briefTitle":373,"officialTitle":374,"acronym":4,"eligibilityCriteria":375,"healthyVolunteers":45,"sex":46,"minAge":376,"maxAge":75,"enrollmentInfo":377,"targetDuration":4,"studyType":50,"phases":379,"briefSummary":380,"conditions":381,"keywords":385,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":388,"lastUpdatePostDateStruct":389,"startDateStruct":391,"completionDateStruct":393,"leadSponsor":395,"locationsCount":4},"100554022","the-effect-of-motivational-interviewing-in-womens-health-100554022","NCT06493682","The Effect of Motivational Interviewing in Women's Health","The Effect of Motivational Interviewing on Behaviour of Healthcare Demand Procrastination, Health Beliefs Regarding Cervical Cancer Screenings, and Screening Participation in Women","Inclusion Criteria:\n\n* The ages of 30-65,\n* Having not had cervical cancer screening before,\n* Having not had a hysterectomy operation,\n* Being literate,\n* Volunteering to participate in the study\n\nExclusion Criteria:\n\n* Those who have communication problems,\n* Those with psychiatric and mental illnesses,\n* Those who have previously attended any training on cervical cancer screening,\n* Pregnant women","30 Years",{"count":378,"type":20},104,[52],"The behaviour of healthcare demand procrastination constitutes an obstacle for individuals to lead a healthy life, and an example of this is the low participation rate of women in pap-smear screening programs compared to the target population. It is known that motivational interviews are frequently used and effective in studies planned to change health behavior. According to the results of the power analysis, at least 104 women, 52 experimental and 52 control, should be included in the study. Data will be collected with the \"Personal Information Form\", \"Healthcare Demand Procrastination Scale\", \"Health Belief Model Scale for Cervical Cancer and Pap Smear Test\" and \"Evaluation Form for Cervical Cancer Screening Participation\". Motivational interviews will be given to the women in the experimental group.",[382,383,384],"Procrastination","Health Behavior","Cancer",[386,387],"Cervical Cancer Screening","Motivational İnterview","2024-07-10",{"date":390,"type":30},"2024-07-11",{"date":392,"type":20},"2024-10-01",{"date":394,"type":20},"2025-05-31",{"name":36,"class":37},{"id":397,"slug":398,"hasResults":11,"nctId":399,"briefTitle":400,"officialTitle":401,"acronym":4,"eligibilityCriteria":402,"healthyVolunteers":45,"sex":46,"minAge":403,"maxAge":404,"enrollmentInfo":405,"targetDuration":4,"studyType":50,"phases":406,"briefSummary":407,"conditions":408,"keywords":4,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":412,"lastUpdatePostDateStruct":413,"startDateStruct":415,"completionDateStruct":417,"leadSponsor":419,"locationsCount":4},"100500523","the-effect-of-continuous-midwife-support-on-various-parameters-related-to-pregnancy-childbirth-and-postpartum-period-100500523","NCT05797363","The Effect of Continuous Midwife Support on Various Parameters Related to Pregnancy, Childbirth and Postpartum Period","The Effect of Continuous Midwife Support During Pregnancy, Childbirth and Postpartum Processes Starting From Preconceptional Period on Various Parameters Related to Pregnancy, Delivery and Postpartum Period: A Randomized Controlled Study\"","Inclusion Criteria:\n\n* She's newly married.\n* Women without children.\n\nExclusion Criteria:\n\n* women's desire to stop working","19 Years","35 Years",{"count":152,"type":20},[52],"There is a need for studies with a high level of evidence regarding the effect of supportive care given during the preconceptional period, pregnancy, childbirth and postpartum processes. With this planned study, it is aimed to evaluate the effect of continuous midwife support during pregnancy, birth and postpartum periods, starting from the preconceptional period, on various parameters related to pregnancy, birth and postpartum period. The research is planned as a randomized controlled experimental study. It consists of two groups, the study group and the control group. 75 women out of 150 women will form the control group and 75 women will form the study group. The women in the working group will be given individual training in line with their needs. Data will be collected by using the checklist and many scales used by the control and study groups in preconceptional counseling recommended by ACOG (American College of Obstetricians and Gynecologists).",[409,410,411],"Pregnant Women","Childbirth","Women's Health","2023-04-02",{"date":414,"type":30},"2023-04-04",{"date":416,"type":20},"2023-04-15",{"date":418,"type":20},"2027-12-30",{"name":36,"class":37},""]