[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Ordu University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":442},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,16,0,[8,39,76,107,138,164,194,217,241,268,292,316,343,367,392,417],{"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":4,"briefSummary":22,"conditions":23,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":4},"100053638","groningen-meander-walking-test-in-older-adults-with-balance-problems-100053638",false,"NCT07692373","Groningen Meander Walking Test in Older Adults With Balance Problems","Test-Retest Reliability and Construct Validity of the Groningen Meander Walking Test in Older Adults With Self-Reported Balance Problems and\u002For a History of Falls","Inclusion Criteria:\n\nAged 65 years or older Self-reported balance problems during activities of daily living and\u002For a history of at least one fall within the previous 12 months Able to walk independently with or without a single walking aid Able to understand and follow verbal instructions Willing to provide written informed consent\n\nExclusion Criteria:\n\nPresence of neurological, vestibular, visual, orthopedic, systemic, or medical conditions that may substantially affect gait or balance Acute lower-extremity injury or recent lower-extremity surgery Severe pain preventing completion of the walking or balance tests Cognitive impairment that may limit the ability to understand or follow test instructions Inability to walk independently without personal assistance Use of a rollator","ALL","65 Years",{"count":19,"type":20},70,"ESTIMATED","OBSERVATIONAL","This observational cross-sectional psychometric study aims to examine the test-retest reliability and construct validity of the Groningen Meander Walking Test in older adults with self-reported balance problems and\u002For a history of falls. Participants aged 65 years or older will be recruited from the Orthopedics and Traumatology outpatient clinic of Ordu University Training and Research Hospital. The Groningen Meander Walking Test will be performed twice during the first session and repeated in a second session to assess within-day and between-day reliability. Construct validity will be evaluated using the Timed Up and Go Test, Figure-of-Eight Walking Test, Berg Balance Scale, and Falls Efficacy Scale-International. The study will also explore the ability of the Groningen Meander Walking Test to discriminate between participants with low and increased fall risk according to the Berg Balance Scale.",[24,25,26],"Fall","Gait Disorders in Old Age","Older People","NOT_YET_RECRUITING","2026-07-09",{"date":30,"type":31},"2026-07-13","ACTUAL",{"date":33,"type":20},"2026-07-15",{"date":35,"type":20},"2026-09-01",{"name":37,"class":38},"Ordu University","OTHER",{"id":40,"slug":41,"hasResults":11,"nctId":42,"briefTitle":43,"officialTitle":43,"acronym":4,"eligibilityCriteria":44,"healthyVolunteers":45,"sex":46,"minAge":47,"maxAge":48,"enrollmentInfo":49,"targetDuration":4,"studyType":51,"phases":52,"briefSummary":54,"conditions":55,"keywords":57,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":75},"100637396","the-effect-of-value-clarification-based-on-meleiss-transition-theory-on-menopausal-symptoms-depression-anxiety-stress-and-quality-of-life-in-perimenopausal-women-100637396","NCT07584109","The Effect of Value Clarification Based on Meleis's Transition Theory on Menopausal Symptoms, Depression, Anxiety, Stress, and Quality of Life in Perimenopausal Women","Inclusion Criteria:\n\n* Women who agree to participate in the study,\n* Have at least a primary school education,\n* Understand, read, and write Turkish,\n* Have no communication barriers,\n* Are between 45-55 years of age,\n* Have started experiencing menstrual cycle irregularities or have not menstruated,\n* Have experienced at least one menopausal symptom in the last 6 months (hot flashes, irritability, sleep problems, urogenital complaints, etc.),\n* Are in the perimenopausal period according to the Straw Classification of Reproductive Aging in Women criteria,\n* Women who have entered menopause naturally will be included in the study.\n\nExclusion Criteria:\n\n* Women who:\n* Use any complementary or alternative treatment methods (such as Reiki, phytoestrogens, acupressure),\n* Use hypnotic or sedative medications,\n* Have a diagnosed psychiatric illness,\n* Have a gynecological problem causing menstrual irregularities,\n* Have entered menopause as a result of any surgical operation such as a hysterectomy,\n* Are receiving hormone replacement therapy will be excluded from the study.",true,"FEMALE","45 Years","55 Years",{"count":50,"type":20},88,"INTERVENTIONAL",[53],"NA","Menopause is a life stage influenced not only by hormonal factors but also by psychological, social, and cultural factors. Symptoms such as hot flashes, sleep problems, and mood changes may occur, and their severity depends on how a woman perceives and copes with this period.\n\nThe study aims to examine the effects of the \"Value Clarification\" method based on Meleis Transition Theory on menopausal symptoms, depression, anxiety, stress, and quality of life in women during menopause.",[56],"Menopausal Women",[58,59,60,61,62,63,64,65,66],"Menopause","Meleis Transition Theory","Value Clarification","depression","stress","anxiety","menopausal symptoms","quality of life","nursing","2026-05-06",{"date":69,"type":31},"2026-05-13",{"date":71,"type":20},"2026-05-04",{"date":73,"type":20},"2026-11-04",{"name":37,"class":38},1,{"id":77,"slug":78,"hasResults":11,"nctId":79,"briefTitle":80,"officialTitle":81,"acronym":4,"eligibilityCriteria":82,"healthyVolunteers":11,"sex":16,"minAge":83,"maxAge":84,"enrollmentInfo":85,"targetDuration":87,"studyType":21,"phases":4,"briefSummary":88,"conditions":89,"keywords":93,"overallStatus":99,"whyStopped":4,"lastUpdateSubmitDate":100,"lastUpdatePostDateStruct":101,"startDateStruct":102,"completionDateStruct":104,"leadSponsor":106,"locationsCount":75},"100635778","fascial-plane-blocks-and-quality-of-recovery-in-cardiac-surgery-100635778","NCT07557108","Fascial Plane Blocks and Quality of Recovery in Cardiac Surgery","Pecto-Intercostal Fascial Plane Block-Based Multimodal Analgesia to Improve Quality of Recovery After Median Sternotomy: A Randomized Non-Inferiority Trial Comparing Retro-Intercostal Fascial Plane Block and Rectus Sheath Block","Inclusion Criteria:\n\n* Patients who have provided written informed consent\n* Open-heart surgery performed under elective conditions via median sternotomy with cardiopulmonary bypass (on-pump)\n* American Society of Anesthesiologists (ASA) physical status class II or III\n* Aged 18-70 years\n\nExclusion Criteria:\n\n* Off-pump surgical procedure\n* Emergency or repeat cardiac surgery\n* Known allergy to induction agents or local anesthetics\n* Body mass index (BMI) \\>35 kg\u002Fm²\n* Coagulopathy\n* Infection at the surgical site\n* Left ventricular ejection fraction (LVEF) \\\u003C40%\n* Renal insufficiency (estimated glomerular filtration rate \\\u003C60 mL\u002Fmin\u002F1.73 m²) or hepatic insufficiency \\[Presence of major systemic diseases such as acute decompensated cirrhosis characterized by bilirubin \\>12 mg\u002FdL, INR \\>2.5, or hepatic encephalopathy, in accordance with the European Association for the Study of the Liver-Chronic Liver Failure Consortium criteria\\]\n* Psychiatric disorders\n* History of chronic pain or regular use of analgesics (corticosteroids, analgesics, anticonvulsants)\n* Cognitive impairments that could interfere with the assessment of postoperative pain\n* Patients with impaired physical and verbal performance","18 Years","70 Years",{"count":86,"type":20},123,"1 Year","In this randomized trial, the investigators will test the hypothesis that combining regional analgesia techniques-which have the potential to improve the quality of postoperative recovery following median sternotomy-with PIFB will accelerate recovery. Additionally, it is anticipated that RIFB, an alternative fascial plane block, will demonstrate non-inferior (at least as effective as) performance compared to RSB, thereby providing flexibility and ease of application in clinical practice.",[90,91,92],"Cardiovascular Surgical Procedures","Pain, Postoperative","Cardiovascular Diseases",[90,94,95,96,97,98],"Anesthesia, Conduction","Acute Postoperative Pain","Pain Management","Enhanced Recovery After Surgery","Anesthesia, Regional","RECRUITING","2026-04-28",{"date":71,"type":31},{"date":103,"type":31},"2026-04-05",{"date":105,"type":20},"2026-12-20",{"name":37,"class":38},{"id":108,"slug":109,"hasResults":11,"nctId":110,"briefTitle":111,"officialTitle":112,"acronym":113,"eligibilityCriteria":114,"healthyVolunteers":45,"sex":46,"minAge":83,"maxAge":115,"enrollmentInfo":116,"targetDuration":4,"studyType":51,"phases":118,"briefSummary":119,"conditions":120,"keywords":124,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":130,"lastUpdatePostDateStruct":131,"startDateStruct":133,"completionDateStruct":135,"leadSponsor":137,"locationsCount":75},"100635170","hbm-based-solution-focused-birth-program-on-fear-of-childbirth-in-primigravidas-100635170","NCT07549204","HBM-Based Solution-Focused Birth Program on Fear of Childbirth in Primigravidas","The Effect of a Health Belief Model-Based Solution-Focused Childbirth Preparation Program on Fear of Childbirth, Belief in Normal Birth, Pregnancy Stress, and Mode of Delivery in Primigravid Women","Primigravida","Inclusion Criteria:\n\n* Being 18 years of age or older\n* Having at least a primary school level of education\n* Being able to understand and speak Turkish\n* Having a singleton pregnancy\n* Being a primigravida\n* Being between 28 and 32 weeks of gestation at the time of the intervention.\n\nExclusion Criteria:\n\n* Having a high-risk pregnancy (e.g., preeclampsia, diabetes, cardiovascular disease, placenta previa, oligohydramnios)\n* Having a chronic and\u002For psychiatric disorder\n* Having conceived through infertility treatment","49 Years",{"count":117,"type":20},72,[53],"Pregnancy is a period characterized by significant physiological and psychosocial changes, during which women adapt to new roles. While some women experience this period with excitement and hope, others may experience anxiety, uncertainty, and fear. Fear of childbirth (tokophobia) is a common condition that can negatively affect women's quality of life, birth preferences, and childbirth experiences. High levels of fear of childbirth have been associated with increased cesarean section rates, negative birth perceptions, and postpartum psychological problems.\n\nThis randomized controlled trial aims to evaluate the effect of a solution-focused childbirth preparation education program based on the Health Belief Model on fear of childbirth and belief in normal birth among primigravida women. Secondary outcomes include pregnancy-related stress and mode of delivery.\n\nParticipants will be randomly assigned to either an intervention group receiving structured education or a control group receiving routine prenatal care. Data will be collected before and after the intervention using validated measurement tools, and delivery outcomes will be recorded after birth. The findings are expected to contribute to improving maternal psychological well-being and promoting positive childbirth experiences.",[121,122,123],"Fear","Stress (Psychology)","Pregnancy",[123,121,125,126,127,128,129],"Health Belief Model","Solution-Focused Approach","Antenatal Education","Mode of Delivery","Randomized Controlled Trial","2026-04-17",{"date":132,"type":31},"2026-04-24",{"date":134,"type":20},"2026-05-15",{"date":136,"type":20},"2026-12-15",{"name":37,"class":38},{"id":139,"slug":140,"hasResults":11,"nctId":141,"briefTitle":142,"officialTitle":143,"acronym":144,"eligibilityCriteria":145,"healthyVolunteers":11,"sex":16,"minAge":146,"maxAge":83,"enrollmentInfo":147,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":149,"conditions":150,"keywords":152,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":156,"lastUpdatePostDateStruct":157,"startDateStruct":159,"completionDateStruct":161,"leadSponsor":163,"locationsCount":75},"100633514","hypoglycemia-fear-affect-autonomic-function-physical-activity-and-exercise-capacity-in-type-i-diabetes-100633514","NCT07527676","Hypoglycemia Fear Affect Autonomic Function, Physical Activity, and Exercise Capacity in Type I Diabetes","Does Fear of Hypoglycemia Affect Autonomic Function, Physical Activity, and Exercise Capacity in Children and Adolescents With Type I Diabetes?","HypoFear-T1DM","Inclusion Criteria:\n\n* being aged 10-18 years,\n* having been diagnosed with T1DM at least one year ago,\n* having an HbA1c of ≤7% in the last three months,\n* being literate in Turkish,\n* voluntarily participating in the study.\n\nExclusion Criteria:\n\n* visual, auditory or cognitive problems that would prevent participation, orthopaedic or neurological problems (e.g. walking or running difficulties) that would prevent participation,\n* BMI \\\u003C18.5 kg\u002Fm², any complications related to T1DM,\n* being in the insulin\u002Fsensor dose adjustment\u002Fadjustment phase or having a history of diabetic ketoacidosis in the last month.","10 Years",{"count":148,"type":20},67,"This cross-sectional study aims to investigate whether fear of hypoglycemia affects autonomic function, physical activity levels, and exercise capacity in children and adolescents with T1DM.\n\nThe main question it aims to answer is:\n\nDoes Fear of Hypoglycemia Affect Autonomic Function, Physical Activity, and Exercise Capacity in Children and Adolescents with Type I Diabetes? Participants will answer questionnaires about fear of Hypoglycemia and physical activity. Heart rate (HR), heart rate variability (HRV), blood pressure (BP), and peripheral oxygen saturation (SpO₂) will evaluate for autonomic function.",[151],"Type 1 Diabetes Mellitus",[153,154,155],"Hypoglycemia","physical activity","heart rate","2026-04-09",{"date":158,"type":31},"2026-04-14",{"date":160,"type":20},"2026-05-02",{"date":162,"type":20},"2026-07-30",{"name":37,"class":38},{"id":165,"slug":166,"hasResults":11,"nctId":167,"briefTitle":168,"officialTitle":169,"acronym":4,"eligibilityCriteria":170,"healthyVolunteers":45,"sex":16,"minAge":171,"maxAge":172,"enrollmentInfo":173,"targetDuration":4,"studyType":51,"phases":175,"briefSummary":176,"conditions":177,"keywords":180,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":186,"lastUpdatePostDateStruct":187,"startDateStruct":189,"completionDateStruct":191,"leadSponsor":193,"locationsCount":4},"100631760","the-effect-of-gardening-activities-on-the-quality-of-life-of-students-with-mild-intellectual-disability-100631760","NCT07504874","The Effect of Gardening Activities on the Quality of Life of Students With Mild Intellectual Disability","The Effect of Gardening Activities on the Quality of Life of Mildly Intellectually Disabled Secondary School Students: A Mixed-Method Study","Inclusion Criteria:\n\n* Students studying at a special education secondary school,\n* Who are open to communication and collaboration,\n* Who have no physical or mental disabilities that would prevent them from participating in gardening activities,\n* And whose parents have provided written informed consent for their participation will be included in the research.\n\nExclusion Criteria:\n\n* Students who do not attend the educational program regularly will be excluded from the research.","11 Years","14 Years",{"count":174,"type":20},30,[53],"This study will be conducted to determine the effect of gardening activities applied to mildly intellectually disabled secondary school students on their quality of life and to examine their views on these activities in depth.",[178,179],"Intellectual Disability","Quality of Life",[181,182,183,184,185],"Intellectual disability","Gardening activities","Quality of life","Nursing","Mixed method","2026-04-02",{"date":188,"type":31},"2026-04-08",{"date":190,"type":20},"2026-05-01",{"date":192,"type":20},"2026-12-01",{"name":37,"class":38},{"id":195,"slug":196,"hasResults":11,"nctId":197,"briefTitle":198,"officialTitle":199,"acronym":4,"eligibilityCriteria":200,"healthyVolunteers":45,"sex":46,"minAge":83,"maxAge":47,"enrollmentInfo":201,"targetDuration":4,"studyType":51,"phases":202,"briefSummary":203,"conditions":204,"keywords":208,"overallStatus":99,"whyStopped":4,"lastUpdateSubmitDate":210,"lastUpdatePostDateStruct":211,"startDateStruct":212,"completionDateStruct":214,"leadSponsor":216,"locationsCount":75},"100632735","sexual-health-education-during-pregnancy-100632735","NCT07517549","Sexual Health Education During Pregnancy","The Effect Of Sexual Counseling Based On the Extended Plissit Model On Sexual Function, Marital Adjustment, Sexual Quality Of Life, Depression, Anxiety, And Stress During Pregnancy And Postpartum","Eligibility criteria;\n\n* Volunteers to participate in the research,\n* primary school graduate,\n* Pregnant between 16-20 weeks\n* Having a single pregnancy,\n* Able to understand and speak Turkish,\n* Living with his wife for the past four weeks,\n* No threat of abortion or premature birth,\n\nExclusion Criteria:\n\n* Someone who has been diagnosed with a chronic illness,\n* People with diagnosed physical and mental health issues,\n* Someone who has been diagnosed with a psychological disorder,\n* Having a high-risk pregnancy,\n* Having an IVF pregnancy,\n* Low threat,\n* Anyone who has been diagnosed with any sexually transmitted disease, either themselves or in their partner,\n* Those using medications that may negatively affect sexual function,\n* including antipsychotics, antihypertensives, phenobarbital, and opioids.",{"count":19,"type":20},[53],"This experimental, randomized controlled, single-blind study includes intervention and control groups. Pregnant women between 16 and 20 weeks of gestation who meet the inclusion criteria and agree to participate will be included in the study. Pregnant women will be randomly assigned to groups. Pre-test data will be collected from both groups. The intervention group will receive sexual counseling training in two sessions, face-to-face and in groups, until week 22. Second test data will be collected after week 37 (before delivery), and final test data will be collected three months after delivery. This study is expected to have a significant impact on women's lives, as this topic is considered taboo in our country, leading to a lack of open discussion and the prevalence of misconceptions and false beliefs (sexual myths).",[205,206,207],"Sexuality","Depression","Pregnancy Related",[205,123,209],"Anxiety","2026-04-01",{"date":188,"type":31},{"date":213,"type":31},"2026-03-15",{"date":215,"type":20},"2026-11-30",{"name":37,"class":38},{"id":218,"slug":219,"hasResults":11,"nctId":220,"briefTitle":221,"officialTitle":222,"acronym":4,"eligibilityCriteria":223,"healthyVolunteers":45,"sex":16,"minAge":83,"maxAge":4,"enrollmentInfo":224,"targetDuration":4,"studyType":51,"phases":226,"briefSummary":227,"conditions":228,"keywords":230,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":235,"lastUpdatePostDateStruct":236,"startDateStruct":238,"completionDateStruct":239,"leadSponsor":240,"locationsCount":4},"100631417","the-effect-of-gardening-on-psychological-well-being-and-care-among-nursing-home-care-staff-100631417","NCT07500402","THE EFFECT OF GARDENING ON PSYCHOLOGICAL WELL-BEING AND CARE AMONG NURSING HOME CARE STAFF","THE EFFECT OF GARDENING ACTIVITIES APPLIED TO CARE STAFF IN NURSING HOMES ON PSYCHOLOGICAL WELL-BEING AND CARE: A MIXED METHODS STUDY","Inclusion Criteria:\n\n* Care staff working in active care services at a nursing home, Who have been working at a nursing home for at least one year (Maunder et al., 2022), Who are open to communication and collaboration, And who are willing to participate in the study will be included in the research.\n\nExclusion Criteria:\n\n* Those on leave, on sick leave, or undergoing a job reassignment during the research process Care staff with any physical or mental disabilities that could prevent them from participating in gardening activities will not be included in the study.",{"count":225,"type":20},41,[53],"This study will be conducted to evaluate the effects of horticultural activities applied to nursing home care staff on their psychological well-being and caregiving, and to examine in depth the care staff's views on horticultural activities.",[229],"Horticultural Activities Among Caregivers",[231,232,233,234],"Caregiver","psychological well-being","horticultural activity","Care","2026-03-24",{"date":237,"type":31},"2026-03-30",{"date":190,"type":20},{"date":192,"type":20},{"name":37,"class":38},{"id":242,"slug":243,"hasResults":11,"nctId":244,"briefTitle":245,"officialTitle":246,"acronym":4,"eligibilityCriteria":247,"healthyVolunteers":11,"sex":46,"minAge":83,"maxAge":4,"enrollmentInfo":248,"targetDuration":4,"studyType":51,"phases":250,"briefSummary":251,"conditions":252,"keywords":254,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":260,"lastUpdatePostDateStruct":261,"startDateStruct":263,"completionDateStruct":265,"leadSponsor":267,"locationsCount":4},"100621910","primary-dysmenorrhea-and-comfort-theory-100621910","NCT07376759","Primary Dysmenorrhea and Comfort Theory","Effects of Comfort Theory-Based Education on Dysmenorrhea, Menstrual Symptoms, Premenstrual Syndrome and General Well-Being Levels in University Students With Primary Dysmenorrhea","Inclusion Criteria:\n\n* Female students aged 18 and over\n* Single\n* Having a menstrual pain intensity of 3 or higher according to the Visual Analog Scale\n* Having had a regular menstrual cycle for the last 6 months\n* Volunteering to participate in the study\n\nExclusion Criteria:\n\n* Women diagnosed with a psychiatric illness\n* Women diagnosed with a gynecological illness\n* Women diagnosed with a chronic illness\n* Women using a pharmacological or non-pharmacological method for primary dysmenorrhea\n* Women using hormonal birth control methods",{"count":249,"type":20},80,[53],"Dysmenorrhea is defined as lower abdominal pain experienced during menstruation. It is divided into two types: primary dysmenorrhea and secondary dysmenorrhea. In young women, the majority of dysmenorrhea cases are primary dysmenorrhea. Primary dysmenorrhea has a physical, psychological, and social impact on young women. Pharmacological and non-pharmacological methods are used to treat primary dysmenorrhea. Education is important in increasing the effectiveness of primary dysmenorrhea treatment. An effective education process takes place in accordance with nursing theories and models. There are a limited number of studies on the effect of comfort theory-based education in the management of primary dysmenorrhea. In this research, planned as a randomized controlled trial, the intervention group will receive comfort theory-based education, while the control group will receive no intervention. This study aims to contribute to the literature by investigating the effect of comfort theory-based education on dysmenorrhea, menstrual symptoms, premenstrual syndrome, and general well-being in university students with primary dysmenorrhea.",[253],"Primary Dysmenorrhea",[255,256,257,258,259,66],"primary dysmenorrhea","comfort theory","menstrual symptoms","premenstrual syndrome","general wellbeing","2026-01-21",{"date":262,"type":31},"2026-01-29",{"date":264,"type":20},"2026-02",{"date":266,"type":20},"2026-06",{"name":37,"class":38},{"id":269,"slug":270,"hasResults":11,"nctId":271,"briefTitle":272,"officialTitle":272,"acronym":4,"eligibilityCriteria":273,"healthyVolunteers":11,"sex":16,"minAge":83,"maxAge":4,"enrollmentInfo":274,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":276,"conditions":277,"keywords":282,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":284,"lastUpdatePostDateStruct":285,"startDateStruct":287,"completionDateStruct":289,"leadSponsor":291,"locationsCount":4},"100621096","can-the-face-index-an-anthropometric-measurement-predict-difficult-laryngoscopy-and-intubation-100621096","NCT07366177","Can the \"Face Index\"; an Anthropometric Measurement, Predict Difficult Laryngoscopy and Intubation?","Inclusion Criteria:\n\nAll adult patients over the age of 18 who have given written consent to undergo elective and\u002For emergency surgery under general anesthesia and be intubated in the operating rooms of our hospital's main building and annex building\n\nExclusion Criteria:\n\nPatients with a prior history of difficult airway\u002Fdifficult intubation, those who have undergone facial, neck, or airway surgery, those with deformities or scars in the facial and neck area due to burns or injuries, those with previous or recent tracheostomy, those with facial deformities due to any cause (congenital or acquired pathologies), and those with communication problems and who are uncooperative during measurements will be excluded from the study. Children and pregnant patients will not be included.",{"count":275,"type":20},1000,"Patient safety is the cornerstone of anesthetic practice, and maintaining adequate respiration represents its most critical initial step. In situations where spontaneous breathing cannot be sustained-such as during general anesthesia-the airway must be mechanically secured. While simple face masks may be sufficient in some cases, endotracheal intubation remains the most reliable method for airway control in conditions associated with respiratory depression.\n\nAirway management may be challenging due to various patient-related anatomical factors, including facial and mandibular structure, obesity, limited mouth opening, facial hair, sunken cheeks, wide facial morphology, and a short or muscular neck. These challenges are collectively described as difficult ventilation and difficult intubation (cannot ventilate-cannot intubate), which may occur unexpectedly or be anticipated. A difficult airway is defined as difficulty encountered by a trained anesthesiologist in face mask ventilation, tracheal intubation, or both.\n\nSeveral predictors of difficult airway are widely accepted, such as thyromental and sternomental distances, neck circumference, Mallampati classification, upper lip bite test, mouth opening, and interincisor distance. Thorough preoperative airway evaluation is mandatory, as difficult mask ventilation and failed intubation remain major contributors to anesthesia-related morbidity and mortality. Although numerous studies have examined these predictors, research focusing on facial morphology and anthropometric indices-particularly the face index-is extremely limited.\n\nFacial morphology varies considerably among individuals and can be evaluated anthropometrically using simple, noninvasive tools such as a digital caliper. Anthropometric analysis is commonly applied in forensic medicine and reconstructive surgery but has rarely been incorporated into airway assessment.\n\nThis study aims to introduce face index analysis as a novel predictor of difficult airway alongside conventional methods. By evaluating measurements such as trichion-gnathion distance, total facial index, upper facial index, and nasal index, the study investigates whether airway difficulty can be predicted using a single index value. All measurements are standard, noninvasive, and routinely performed during preoperative assessment.",[278,279,280,281],"Anesthesia Intubation Complication","Laryngoscopy","Intubation; Difficult or Failed","Anesthesia Morbidity",[283],"Difficult airway, face index, anesthesia","2026-01-18",{"date":286,"type":31},"2026-01-26",{"date":288,"type":20},"2026-03",{"date":290,"type":20},"2027-03",{"name":37,"class":38},{"id":293,"slug":294,"hasResults":11,"nctId":295,"briefTitle":296,"officialTitle":297,"acronym":4,"eligibilityCriteria":298,"healthyVolunteers":45,"sex":16,"minAge":83,"maxAge":4,"enrollmentInfo":299,"targetDuration":4,"studyType":51,"phases":301,"briefSummary":302,"conditions":303,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":308,"lastUpdatePostDateStruct":309,"startDateStruct":311,"completionDateStruct":313,"leadSponsor":315,"locationsCount":4},"100596527","prevention-of-phlebitis-infiltration-and-extravasation-with-infusion-monitoring-system-100596527","NCT07046624","Prevention of Phlebitis, Infiltration and Extravasation With Infusion Monitoring System","Development of an Infusion Monitoring System to Prevent Phlebitis, Infiltration and Extravasation and Its Application in the Intensive Care Unit","Inclusion Criteria:\n\n* 18 years of age and older\n* Receiving medication via peripheral intravenous catheter,\n* Monitored daily for signs of phlebitis, infiltration and extravasation,\n* Patients who can speak\n\nExclusion Criteria:\n\n* Unconscious patients",{"count":300,"type":20},102,[53],"Peripheral venous catheter complications are conditions that are frequently seen in intensive care clinics and require nursing care. The most common complications are phlebitis, infiltration and extravasation. Nurses should take the necessary precautions to prevent these complications from developing.. Therefore, this planned thesis study aims to establish an infusion monitoring system and evaluate its effectiveness in early detection of complications related to peripheral intravenous catheters. The research is planned as a randomized controlled experimental study. The study will be conducted in Ordu State Hospital General Intensive Care Unit 1 and General Intensive Care Unit 3 clinics. The universe of the study will consist of patients receiving inpatient treatment in General Intensive Care Unit 1 and General Intensive Care Unit 3 clinics. The sample size will be determined by g-power analysis after a two-month preliminary follow-up. Data will be collected with the \"Clinical Follow-up Form\", \"Patient Information Form\", and \"Complication Follow-up Form\". The clinics included in the study will be divided into two groups as experimental and control groups. First, the frequency of complications will be determined in the experimental and control groups. Then, while the control group continues its routine protocol and applications, an infusion follow-up system will be developed in the experimental group and will be used by nurses in patient care. In the final stage, the frequency of peripheral venous catheter complications will be determined again. Data will be evaluated using the SPSS 22.0 package program at a significance level of p\\\u003C0.05 and a confidence interval of 95%.",[304,305,306,307],"Extravasation","Intensive Care Units (ICUs)","Phlebitis","Infiltration","2025-11-14",{"date":310,"type":31},"2025-11-17",{"date":312,"type":20},"2025-11-08",{"date":314,"type":20},"2026-07-08",{"name":37,"class":38},{"id":317,"slug":318,"hasResults":11,"nctId":319,"briefTitle":320,"officialTitle":321,"acronym":4,"eligibilityCriteria":322,"healthyVolunteers":45,"sex":46,"minAge":323,"maxAge":17,"enrollmentInfo":324,"targetDuration":4,"studyType":51,"phases":325,"briefSummary":326,"conditions":327,"keywords":331,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":335,"lastUpdatePostDateStruct":336,"startDateStruct":338,"completionDateStruct":340,"leadSponsor":342,"locationsCount":4},"100587503","effects-of-health-education-on-knowledge-attitude-and-screening-for-cervical-cancer-in-women-100587503","NCT06929234","Effects of Health Education on Knowledge, Attitude and Screening for Cervical Cancer in Women","Effects of Peer-Supported Health Education on Knowledge, Attitude and Screening for Cervical Cancer in Women: A Mixed Method Randomized Controlled Pilot Study","Inclusion Criteria:\n\n* Women enrolled at the Training Center,\n* Women between the ages of 30 and 65,\n* Women who are married,\n* Women who have not been screened for cervical cancer in accordance with the year interval,\n* Women who are open to communication and collaboration,\n* Women who volunteer to participate in the study will be included in the research.\n\nExclusion Criteria:\n\n* Women who have had a total hysterectomy,\n* Pregnant women,\n* Women diagnosed with cervical cancer,\n* Women who are screened on time will be excluded from the research.","30 Years",{"count":174,"type":20},[53],"Women's knowledge, attitudes and behaviors about cancer are very important in the prevention of cervical cancer. In addition to medical interventions, psychosocial support and education programs are of great importance in the fight against cancer. Peer support helps individuals going through the same disease process to exchange information and emotional support by sharing their experiences with each other. In addition, the information obtained through peer support provides more permanent learning in individuals due to the transfer of information based on similar experiences and the creation of more trust and empathy compared to traditional education methods. Peer-supported education programs for women diagnosed with cervical cancer not only provide theoretical knowledge but also support the applicability of this knowledge in daily life. The trainings address topics such as risk factors of cervical cancer, the importance of HPV vaccination, the necessity of regular screening tests and healthy lifestyle behaviors, including attitudes towards cervical cancer prevention and cancer-related information. It is very important that this information is not limited to individual learning and that it is discussed within the group and supported by experiences through peer support, in order to increase the level of knowledge.",[328,329,330],"Peer Support","Health Education","Cervical Cancers",[328,332,333,334],"Cervical Cancer","Health","Education","2025-04-12",{"date":337,"type":31},"2025-04-16",{"date":339,"type":20},"2025-05-01",{"date":341,"type":20},"2025-10-01",{"name":37,"class":38},{"id":344,"slug":345,"hasResults":11,"nctId":346,"briefTitle":347,"officialTitle":348,"acronym":4,"eligibilityCriteria":349,"healthyVolunteers":45,"sex":46,"minAge":4,"maxAge":4,"enrollmentInfo":350,"targetDuration":4,"studyType":51,"phases":352,"briefSummary":353,"conditions":354,"keywords":358,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":359,"lastUpdatePostDateStruct":360,"startDateStruct":362,"completionDateStruct":364,"leadSponsor":366,"locationsCount":4},"100584354","effectiveness-of-menstruation-education-to-secondary-school-students-100584354","NCT06888245","Effectiveness of Menstruation Education to Secondary School Students","Evaluation of the Effectiveness of Menstruation Education Given to Secondary School Students With and Without Animation","Inclusion Criteria:\n\n* Secondary school student\n* Open to communication and collaboration,\n* Female students who agreed to participate in the study and whose parents gave their consent were included in the study.\n\nExclusion Criteria:\n\n* Special education students from the research,\n* Female students who do not want to continue the research will be excluded.",{"count":351,"type":20},90,[53],"Supporting adolescents with education about the menstruation process is important in terms of managing the process physically and mentally healthy and gaining lifelong positive health behaviors. Various narrative techniques including visuals, slides and animations are utilized in menstruation education for adolescents. Within the scope of these narrative techniques, technological tools are frequently used for learning purposes in adolescence. In technology-supported education, training that includes visual materials such as animations and multimedia software is very important. Presentations supported by various visuals and texts can be effective in trainings on mentoring. Presentations can appeal to students' visual senses and attract their attention. Animation is one of the technology-based applications that are frequently used in the education of adolescents and support education. The presentation can be animated or non-animated.",[355,334,356,357],"Menstruation","Student","Animation",[355,356,334,357],"2025-03-15",{"date":361,"type":31},"2025-03-21",{"date":363,"type":20},"2025-04-01",{"date":365,"type":20},"2025-08-01",{"name":37,"class":38},{"id":368,"slug":369,"hasResults":11,"nctId":370,"briefTitle":371,"officialTitle":372,"acronym":4,"eligibilityCriteria":373,"healthyVolunteers":45,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":374,"targetDuration":4,"studyType":51,"phases":376,"briefSummary":377,"conditions":378,"keywords":382,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":385,"lastUpdatePostDateStruct":386,"startDateStruct":388,"completionDateStruct":390,"leadSponsor":391,"locationsCount":4},"100580959","biopsychosocial-effects-of-gardening-activities-100580959","NCT06844084","Biopsychosocial Effects of Gardening Activities","Biopsychosocial Effects of Gardening Activities on Elderly People in Nursing Homes","Inclusion Criteria:\n\n* Elderly people who have been living in a nursing home for at least 6 months,\n* Elderly people with a mini mental test score of 24 and above,\n* Elderly people who do not have vision or hearing loss that may prevent gardening activities,\n* Elderly people who are open to communication and cooperation and who volunteer to participate in the study will be included in the study.\n\nExclusion Criteria:\n\n* Elderly people with physical (such as stroke, Parkinson's) and psychiatric diseases (such as mental retardation) that may prevent gardening activities,\n* Elderly people with chronic diseases in the exacerbation process (heart failure, chronic renal failure, etc.) will be excluded from the study.",{"count":375,"type":20},42,[53],"Due to the increasing number of elderly population worldwide, elderly care is becoming increasingly important and the number of elderly in institutional care is increasing. In this context, the implementation of easily applicable, cost-effective and accessible physical activity programmes for the elderly in nursing homes is important for the physical, mental and social health of the elderly. Gardening activities are a non-pharmacological intervention that has recently increased in popularity in the elderly and can be easily applied. It is known that gardening activities in the elderly affect some biochemical parameters along with mental health effects and reduce stress, especially by reducing cortisol levels. By providing physical mobility in the elderly with gardening activities, there may be an increase in irisin level and BDNF level, which is an indicator of improvement in cognitive functions, and a decrease in cortisol level, which is an indicator of stress. With the project, the effects of gardening activities on the elderly will be examined comprehensively in a biopsychosocial manner. In this project, the effects of gardening activities on anxiety, depression, life satisfaction, psychological well-being and biochemical parameters will be examined in the elderly living in a nursing home. In the project, gardening activities will be applied to the elderly in the experimental group once a week for 60 minutes for 16 weeks (4 months). With the project, it is aimed to strengthen the elderly biopsychosocially by making them do gardening activities.",[379,209,206,380,381],"Cognition","Life Satisfaction","Psychological Well Being",[383,384,381,209,206,380],"Elderly","Gardening Activity","2025-02-19",{"date":387,"type":31},"2025-02-25",{"date":389,"type":20},"2025-03-03",{"date":365,"type":20},{"name":37,"class":38},{"id":393,"slug":394,"hasResults":11,"nctId":395,"briefTitle":396,"officialTitle":397,"acronym":4,"eligibilityCriteria":398,"healthyVolunteers":45,"sex":46,"minAge":83,"maxAge":4,"enrollmentInfo":399,"targetDuration":4,"studyType":51,"phases":400,"briefSummary":401,"conditions":402,"keywords":404,"overallStatus":99,"whyStopped":4,"lastUpdateSubmitDate":409,"lastUpdatePostDateStruct":410,"startDateStruct":412,"completionDateStruct":414,"leadSponsor":416,"locationsCount":75},"100568916","the-effect-of-two-methods-applied-to-mothers-on-insufficient-milk-perception-breastfeeding-motivation-fatigue-anxiety-100568916","NCT06687447","The Effect of Two Methods Applied to Mothers on Insufficient Milk Perception, Breastfeeding Motivation, Fatigue, Anxiety","The Effect of Oxytocin Massage and Reflexology Applied to Primiparous Mothers After Cesarean Section on Insufficient Milk Perception, Breastfeeding Motivation, Fatigue, Anxiety and Uterus Involution","Inclusion Criteria:\n\n* Mothers who gave birth at the age of 18 and over\n* The one who is married\n* At least primary school graduate,\n* Primiparous mothers who gave birth by cesarean section,\n* Having a single, healthy newborn at full term,\n* Those who did not experience any problems during pregnancy and the early postpartum period,\n* The tissue integrity in the area to be applied is complete and healthy,\n* Breastfeeding her baby after birth,\n* The baby is healthy, has no problems with the sucking reflex and does not have any congenital anomalies,\n* Women who agree to participate in the research will be included in the study.\n\nExclusion Criteria:\n\n* Those who gave birth by cesarean section before the 37th week of pregnancy,\n* Women who gave birth by cesarean section with combined anesthesia,\n* Discharged before 36 hours after birth,\n* Having chronic diseases such as heart disease, diabetes, hypertension,\n* Those with infectious diseases, infections, open wounds, masses, fractures, dislocations, deformities, varicose veins, burns, eczema, hematomas, thrombophlebitis, deep vein thrombosis on the foot skin,\n* Experiencing any postpartum complications,\n* Their baby is not with their mother for any reason,\n* Those who have received a psychiatric diagnosis such as anxiety and depression,\n* Women who want to leave the research at any stage of the research",{"count":351,"type":20},[53],"Although the World Health Organization predicts the caesarean section rate to be 10-15%, the caesarean section rate in Turkey is 52%, more than three times the international standard. It is very important to eliminate the physical and psychosocial problems experienced by women during this period, to encourage breastfeeding, and at the same time to protect and improve maternal health. Maintaining the mother's well-being after cesarean section and supporting pharmacological treatment with non-pharmacological practices have an important place in nursing care. Therefore, this study will examine the effects of oxytocin massage and reflexology applied to mothers in the post-cesarean period on the perception of insufficient milk, breastfeeding motivation, fatigue, anxiety and uterine involution.",[403],"Caesarean Section",[405,406,407,63,408],"reflexology","oxytocin massage","fatigue","milk production","2024-11-12",{"date":411,"type":31},"2024-11-13",{"date":413,"type":31},"2023-12-06",{"date":415,"type":20},"2025-07-06",{"name":37,"class":38},{"id":418,"slug":419,"hasResults":11,"nctId":420,"briefTitle":421,"officialTitle":422,"acronym":4,"eligibilityCriteria":423,"healthyVolunteers":45,"sex":46,"minAge":323,"maxAge":17,"enrollmentInfo":424,"targetDuration":4,"studyType":51,"phases":426,"briefSummary":427,"conditions":428,"keywords":429,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":434,"lastUpdatePostDateStruct":435,"startDateStruct":437,"completionDateStruct":439,"leadSponsor":441,"locationsCount":4},"100555241","the-effect-of-motivational-interviewing-based-on-the-com-b-model-100555241","NCT06509529","The Effect of Motivational Interviewing Based on the COM-B Model","The Effect of Motivational Interviewing Based on the COM-B Model on Women's Cervical Cancer Health Beliefs and Participation in Screening: A Single-Blind Randomized Controlled Study","Inclusion Criteria:\n\n* Registered at Altınordu Central Family Health Center,\n* A woman,\n* Between 30-65 years of age,\n* The one who is married,\n* Have not had a Pap Smear test in the last 5 years,\n* Has a smart phone\n* Has an internet connection,\n* Open to communication and collaboration,\n* Women who volunteer to participate in the study will be included in the study.\n\nExclusion Criteria:\n\n* Who had total hysterectomy surgery,\n* The pregnant one,\n* Those diagnosed with cervical cancer and\n* Women with a psychiatric diagnosis will be excluded from the study.",{"count":425,"type":20},68,[53],"This research will be conducted to determine the effect of motivational interviewing based on the COM-B model on women's cervical cancer health beliefs and participation in screening.",[332],[332,430,431,432,184,433],"Motivational Interviewing","Early Diagnosis and Screening","Health Beliefs","COM-B Model","2024-07-14",{"date":436,"type":31},"2024-07-19",{"date":438,"type":20},"2024-08-15",{"date":440,"type":20},"2025-01-30",{"name":37,"class":38},""]