[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Eastern Mediterranean University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":385},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,13,0,[8,52,87,110,140,167,200,225,248,275,301,327,356],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":32,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":40,"lastUpdatePostDateStruct":41,"startDateStruct":44,"completionDateStruct":46,"leadSponsor":48,"locationsCount":51},"100054226","effects-of-different-myofascial-release-techniques-on-function-in-chronic-non-specific-neck-pain-100054226",false,"NCT07694882","Effects of Different Myofascial Release Techniques on Function in Chronic Non-Specific Neck Pain","Investigation of the Effects of Different Myofascial Release Techniques on Functional Outcomes in Individuals With Chronic Non-Specific Neck Pain","MFR \u002F CNNP","Inclusion Criteria:\n\n* Neck pain persisting for at least 3 months and diagnosed as chronic non-specific neck pain by a specialist physician\n* Aged between 18 and 45 years\n* Perceived pain affecting daily living activities (VAS at least 3)\n* Presence of myofascial trigger points in the upper-quarter muscles\n\nExclusion Criteria:\n\n* Specific serious cervical spine pathology (radiculopathy, myelopathy, severe nerve root compression, spondylosis, and similar)\n* History of rheumatologic, neurologic, or systemic disease (for example, acute inflammation, multiple sclerosis, Parkinson's disease, rheumatoid arthritis, fibromyalgia, or cancer)\n* History of trauma, fracture, or surgery involving the neck, shoulder, or upper extremity\n* Pregnancy or breastfeeding\n* Any diagnosed psychiatric disorder (for example, major depression or anxiety disorder) or regular use of psychopharmacological medication\n* Use of systemic analgesics, NSAIDs, or muscle relaxants within the last 7 days for pain control\n* Any physiotherapy, manual therapy, or injection treatment to the neck region within the last 3 months","ALL","18 Years","45 Years",{"count":21,"type":22},84,"ESTIMATED","INTERVENTIONAL",[25],"NA","This single-center, three-arm randomized controlled trial compares the effects of different myofascial release techniques, combined with a structured exercise program, on functional outcomes in individuals with chronic non-specific neck pain (CNNP).\n\nEligible participants (aged 18 to 45 years, neck pain for at least 3 months, pain intensity VAS at least 3, and myofascial trigger points in the upper-quarter muscles) are allocated by simple randomization into three groups:\n\n* Conventional Therapy Group: hot pack, conventional TENS, and a structured exercise program.\n* Manual Myofascial Release Group: conventional therapy plus therapist-applied manual myofascial release.\n* Self-Myofascial Release Group: conventional therapy plus supervised self-applied myofascial release using a duo-ball, balls, and a massage stick\u002Fcane.\n\nAll interventions are delivered 3 days per week for 6 weeks. The primary outcome is pain intensity. Secondary outcomes include pressure pain threshold and tolerance, cervical range of motion, muscle stiffness, craniovertebral angle, cervical proprioception, muscle strength and endurance, disability, neck awareness, multidimensional biopsychosocial status, sleep quality, quality of life, and kinesiophobia. The aim is to determine whether manual or self-applied myofascial release, added to exercise, produces greater functional improvement in people with chronic non-specific neck pain.",[28,29,30,31],"Chronic Neck Pain","Non-specific Neck Pain","Myofascial Trigger Points","Myofascial Pain Syndrome - Neck",[33,34,35,36,37,38],"chronic non-specific neck pain","myofascial release","manual therapy","trigger points","therapeutic exercise","physiotherapy","NOT_YET_RECRUITING","2026-07-10",{"date":42,"type":43},"2026-07-13","ACTUAL",{"date":45,"type":22},"2026-07-15",{"date":47,"type":22},"2026-12-31",{"name":49,"class":50},"Eastern Mediterranean University","OTHER",1,{"id":53,"slug":54,"hasResults":11,"nctId":55,"briefTitle":56,"officialTitle":57,"acronym":4,"eligibilityCriteria":58,"healthyVolunteers":59,"sex":17,"minAge":60,"maxAge":61,"enrollmentInfo":62,"targetDuration":4,"studyType":23,"phases":64,"briefSummary":65,"conditions":66,"keywords":68,"overallStatus":78,"whyStopped":4,"lastUpdateSubmitDate":79,"lastUpdatePostDateStruct":80,"startDateStruct":82,"completionDateStruct":84,"leadSponsor":86,"locationsCount":51},"100588009","comparison-of-the-effects-of-bimanual-finger-and-vr-exercises-in-pwmci-100588009","NCT06935812","Comparison of the Effects of Bimanual, Finger and VR Exercises in PwMCI","Comparison of the Effects of Bimanual, Finger and Virtual Reality Exercises in Individuals With Mild Cognitive Impairment - Randomized Controlled Study","Inclusion Criteria:\n\n* Participants who are between 50-75 years of age\n* Individuals diagnosed with MCI by a geriatrician according to DSM-5 criteria,\n* Who has the Montreal Cognitive Assessment score between 13-26,\n* Who has the Quick Mild Cognitive Impairment screen score between 48-67,\n* Who has Instrumental Activities of Daily Living Scale score ≥6\u002F8,\n* Who says yes to \"Do you have a memory problem?\" question,\n* Who can walk independently without using any walking aids\n\nExclusion Criteria:\n\n* Participants who have any musculoskeletal disorders that may cause balance and gait disorders,\n* Who have central or peripheral neurological diseases (eg. stroke, Parkinson's disease or polyneuropathies),\n* Who are using psychiatric drugs that may affect psychiatric disease and\u002For cognitive performance (Using nonsteroidal anti-inflammatory drugs more than three times a week, which may affect cognitive functions, using gingko biloba and antioxidant supplements (for example, coenzyme Q10 and alpha-lipoic acid)),\n* Who has daltonism and\n* Who attends any exercise program last 6 months will not be included in this study.",true,"50 Years","75 Years",{"count":63,"type":22},106,[25],"Mild Cognitive Impairment (MCI) is defined as an impairment in a single cognitive function, usually memory, other than normal cognitive decline with age, that does not fulfil dementia criteria. Finger movements have been shown to stimulate the sensory-motor and cognitive parts of the cerebral cortex, as well as the supplementary motor area, Broca's area, premotor cortex, and prefrontal cortex, all of which contribute to movement skills. Asymmetrical hand and finger movements done concurrently were proven to improve cognitive processes and cerebral blood flow more than movements performed with one hand.",[67],"Mild Cognitive Impairment",[69,70,71,72,73,74,75,76,77],"Finger Exercise","Bimanual Exercise","Virtual Reality","Processing Speed","Cognitive Functions","Walking Speed","Gross Motor Skills","Fine Motor Skills","Dual Task","RECRUITING","2026-05-17",{"date":81,"type":43},"2026-05-19",{"date":83,"type":43},"2025-04-29",{"date":85,"type":22},"2026-09-24",{"name":49,"class":50},{"id":88,"slug":89,"hasResults":11,"nctId":90,"briefTitle":91,"officialTitle":92,"acronym":4,"eligibilityCriteria":93,"healthyVolunteers":59,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":94,"targetDuration":4,"studyType":23,"phases":96,"briefSummary":97,"conditions":98,"keywords":4,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":102,"lastUpdatePostDateStruct":103,"startDateStruct":105,"completionDateStruct":107,"leadSponsor":109,"locationsCount":51},"100635037","the-effect-of-aging-simulation-suits-on-nursing-students-attitudes-toward-older-adults-and-their-levels-of-compassion-100635037","NCT07547475","The Effect of Aging Simulation Suits on Nursing Students' Attitudes Toward Older Adults and Their Levels of Compassion","\"The Effect of an Aging Simulation Suit on Nursing Students' Attitudes Toward Older Adults and Their Levels of Compassion Competence: A Randomized Controlled Pretest-Posttest Study\"","Inclusion Criteria:\n\n* Being a third-year nursing student\n* Being enrolled in the HMSR 312 Geriatric Nursing course\n* Volunteering to participate in the study\n\nExclusion Criteria:\n\n* Having a physical condition that would prevent the use of an aging simulation suit\n* Having advanced orthopedic, neurological, or balance problems",{"count":95,"type":22},102,[25],"With the increasing elderly population, nursing students' attitudes toward older adults and their levels of compassion competence have become increasingly important. While traditional educational methods may be insufficient in developing these skills, experiential learning approaches offer more effective outcomes. In particular, aging simulation applications enable students to understand the physical and emotional challenges experienced by older individuals, thereby enhancing their levels of empathy and compassion. The literature reports that simulation-based education has positive effects on attitudes and awareness. Therefore, the integration of aging simulation suits into nursing education is of great importance.",[99,100,101],"Ethics","Aging","Compassion","2026-04-16",{"date":104,"type":43},"2026-04-23",{"date":106,"type":22},"2026-04-25",{"date":108,"type":22},"2026-06-25",{"name":49,"class":50},{"id":111,"slug":112,"hasResults":11,"nctId":113,"briefTitle":114,"officialTitle":115,"acronym":4,"eligibilityCriteria":116,"healthyVolunteers":59,"sex":117,"minAge":18,"maxAge":118,"enrollmentInfo":119,"targetDuration":4,"studyType":23,"phases":121,"briefSummary":122,"conditions":123,"keywords":128,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":133,"lastUpdatePostDateStruct":134,"startDateStruct":136,"completionDateStruct":137,"leadSponsor":139,"locationsCount":4},"100628469","effect-of-virtual-reality-on-pain-and-anxiety-during-pap-smear-testing-100628469","NCT07462039","Effect of Virtual Reality on Pain and Anxiety During Pap Smear Testing","The Effect of Virtual Reality Transition on Pain and Anxiety Experienced During Pap Smear Testing","Inclusion Criteria:\n\n* Women aged 18-65 years\n* Scheduled for a Pap smear procedure\n* Able to communicate in Turkish\n* Able to understand and complete the study questionnaires\n* Willing to provide written informed consent\n* No visual or hearing impairment preventing the use of a VR headset\n\nExclusion Criteria:\n\n* History of severe motion sickness or vertigo\n* Diagnosed psychiatric disorder affecting anxiety assessment\n* Use of anxiolytic or sedative medication within 24 hours prior to the procedure\n* Presence of acute pelvic pain or active vaginal infection\n* Previous participation in this study\n* Any condition preventing safe use of a VR headset","FEMALE","65 Years",{"count":120,"type":22},60,[25],"This randomized controlled pretest-posttest experimental study aims to evaluate the effect of virtual reality (VR) on pain and anxiety levels experienced during Pap smear sampling. Although cervical cancer is largely preventable through regular screening, many women avoid Pap smear testing due to anxiety, fear of pain, and discomfort during gynecological examinations. Innovative, non-invasive interventions are needed to improve women's screening experiences and participation rates.\n\nThe study will be conducted in a gynecology outpatient clinic with 60 women aged 18-65 years who meet the inclusion criteria and provide informed consent. Participants will be randomly assigned to either the intervention group (VR headset during the procedure) or the control group (standard care). Women in the intervention group will watch a 360° relaxing nature video during the Pap smear procedure. Data will be collected using a Personal Information Form, the State Anxiety Inventory, and the Visual Analog Scale (VAS). The findings may support integrating VR into clinical practice to enhance patient comfort during screening procedures.",[124,125,126,127],"Nurse's Role","Pain Management","Cervical Cancer Screening","Anxiety",[129,130,131,132,126],"virtual reality","pap smear","pain","anxiety","2026-03-09",{"date":135,"type":43},"2026-03-10",{"date":135,"type":22},{"date":138,"type":22},"2026-05-10",{"name":49,"class":50},{"id":141,"slug":142,"hasResults":11,"nctId":143,"briefTitle":144,"officialTitle":145,"acronym":4,"eligibilityCriteria":146,"healthyVolunteers":59,"sex":17,"minAge":147,"maxAge":148,"enrollmentInfo":149,"targetDuration":4,"studyType":23,"phases":151,"briefSummary":152,"conditions":153,"keywords":155,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":159,"lastUpdatePostDateStruct":160,"startDateStruct":162,"completionDateStruct":164,"leadSponsor":166,"locationsCount":4},"100620212","the-effect-of-the-developed-psychological-resilience-program-on-phubbing-behaviors-and-communication-skills-100620212","NCT07354685","The Effect of the Developed Psychological Resilience Program on Phubbing Behaviors and Communication Skills","The Effect of a Psychological Resilience Program for Phubbing on Nursing Students' Communication Skills and Phubbing Behaviors: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Undergraduate nursing students aged 18 - 30 years old\n* Voluntary participation\n* Ability to understand and complete self-report questionnaires.\n\nExclusion Criteria:\n\n* Presence of a diagnosed severe psychiatric disorder\n* Current participation in another psychological intervention program.","18 Months","30 Months",{"count":150,"type":22},90,[25],"The goal of this study is to determine whether a psychological resilience-based intervention program developed to prevent sociotelism is effective in nursing students. The study also aims to evaluate the feasibility and acceptability of the program.\n\nThe main questions this study aims to answer are:\n\nDoes the psychological resilience development program reduce sociotelism behaviors among nursing students?\n\nDoes the program improve nursing students' communication skills?\n\nResearchers will compare nursing students who participate in the psychological resilience development program with those in a control group who do not receive the intervention, in order to determine whether the program is effective in reducing sociotelism behaviors and enhancing communication skills.",[154],"Phubbing",[154,156,157,158],"Nursing Students","Communication Skills","psychological resilience","2026-01-12",{"date":161,"type":43},"2026-01-21",{"date":163,"type":22},"2026-04",{"date":165,"type":22},"2026-07",{"name":49,"class":50},{"id":168,"slug":169,"hasResults":11,"nctId":170,"briefTitle":171,"officialTitle":172,"acronym":173,"eligibilityCriteria":174,"healthyVolunteers":59,"sex":175,"minAge":176,"maxAge":177,"enrollmentInfo":178,"targetDuration":4,"studyType":180,"phases":4,"briefSummary":181,"conditions":182,"keywords":185,"overallStatus":78,"whyStopped":4,"lastUpdateSubmitDate":192,"lastUpdatePostDateStruct":193,"startDateStruct":195,"completionDateStruct":197,"leadSponsor":199,"locationsCount":51},"100618217","dynamic-q-angle-and-core-endurance-in-adolescent-athletes-with-patellofemoral-pain-syndrome-100618217","NCT07328750","Dynamic Q Angle and Core Endurance in Adolescent Athletes With Patellofemoral Pain Syndrome","Dynamic Q Angle And Core Endurance In Adolescent Athletes With Patellofemoral Pain Syndrome: A Sex-Based Comparative Retrospective Study","PFPS-QCORE","Inclusion Criteria:\n\n1. Male adolescent elite athletes aged 15-17 years\n2. Licensed and actively training and competing in their respective sports branch\n3. Minimum 3 years of continuous training experience\n4. Ability to complete all clinical and biomechanical assessments\n5. Written informed consent (parental consent for minors)\n\nExclusion Criteria:\n\n1. Acute musculoskeletal injury within the past 3 months\n2. Chronic lower extremity or spinal pathology\n3. History of orthopedic surgery within the past 6 months\n4. Neurological, metabolic, or systemic condition affecting movement or balance\n5. Inability to comply with the testing protocol or incomplete data","MALE","15 Years","17 Years",{"count":179,"type":22},85,"OBSERVATIONAL","This cross-sectional observational study aims to compare trunk mobility, lower extremity flexibility, and functional balance performance across different sports branches in adolescent elite male athletes. Trunk mobility will be assessed using a digital inclinometer in flexion, extension, and rotational movements; hamstring flexibility will be evaluated using the Straight Leg Raise test; and functional balance will be measured using the normalized Y-Balance Test. The study seeks to identify sport-specific biomechanical characteristics and potential indicators related to injury risk and performance adaptations in adolescent competitive athletes.",[183,184],"Postural Balance","Athletic Performance",[186,187,188,189,190,191],"Y-Balance Test","Trunk Mobility","Digital Inclinometer","Sports-Specific Biomechanics","Elite Male Athletes","Adolescent Sports Performance","2026-01-08",{"date":194,"type":43},"2026-01-09",{"date":196,"type":43},"2025-12-01",{"date":198,"type":22},"2026-02-20",{"name":49,"class":50},{"id":201,"slug":202,"hasResults":11,"nctId":203,"briefTitle":204,"officialTitle":205,"acronym":4,"eligibilityCriteria":206,"healthyVolunteers":59,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":207,"targetDuration":4,"studyType":23,"phases":208,"briefSummary":209,"conditions":210,"keywords":213,"overallStatus":78,"whyStopped":4,"lastUpdateSubmitDate":217,"lastUpdatePostDateStruct":218,"startDateStruct":220,"completionDateStruct":222,"leadSponsor":224,"locationsCount":51},"100598125","effect-of-aromatherapy-on-anxiety-in-colonoscopy-patients-100598125","NCT07067424","Effect of Aromatherapy on Anxiety in Colonoscopy Patients","The Effect of Lavender and Bergamot Aromatherapy Before Colonoscopy on Anxiety, Vital Signs, and Feelings of Embarrassment\"","Inclusion Criteria:\n\n* Patients over 18 years of age\n* Patients undergoing a colonoscopy\n* Patients capable of reading and understanding the study instructions\n\nExclusion Criteria:\n\n* Patients who refused to participate in the study\n* Patients who reported an allergy to any of the lavender or bergamot extracts used in the study",{"count":95,"type":22},[25],"The aim of this study is to investigate the effects of aromatherapy with lavender and bergamot essential oils on anxiety, vital signs, and feelings of embarrassment before colonoscopy. The findings of this study are expected to contribute both to filling a gap in the literature and to the planning of evidence-based nursing interventions aimed at minimizing pre-colonoscopy anxiety and embarrassment in patients.",[127,211,212],"Colonoscopy","Aromatherapy",[214,215,127,211,216],"Lavender","Bergamot","Embarrassment","2025-07-15",{"date":219,"type":43},"2025-07-16",{"date":221,"type":43},"2025-01-01",{"date":223,"type":22},"2025-11-30",{"name":49,"class":50},{"id":226,"slug":227,"hasResults":11,"nctId":228,"briefTitle":229,"officialTitle":230,"acronym":4,"eligibilityCriteria":231,"healthyVolunteers":59,"sex":17,"minAge":232,"maxAge":233,"enrollmentInfo":234,"targetDuration":4,"studyType":23,"phases":236,"briefSummary":237,"conditions":238,"keywords":4,"overallStatus":78,"whyStopped":4,"lastUpdateSubmitDate":240,"lastUpdatePostDateStruct":241,"startDateStruct":243,"completionDateStruct":245,"leadSponsor":247,"locationsCount":51},"100590942","hiit-in-sedentary-obese-adults-effects-on-metabolic-risk-body-composition-and-fabp4-100590942","NCT06973980","HIIT in Sedentary Obese Adults: Effects on Metabolic Risk, Body Composition, and FABP4","The Effect of High-Intensity Interval Training on Cardiometabolic Risk Factors, Body Composition, and Plasma FABP4 Levels in Sedentary Obese Adults.","Inclusion Criteria:\n\n* Aged between 20 and 35 years,\n* BMI between 30 and 35 kg\u002Fm²,\n* Waist circumference of 90-100 cm for women, 105-110 cm for men,\n* Sedentary lifestyle (\\\u003C600 MET-min\u002Fweek),\n* Referred by a physician (with a statement confirming no contraindication to exercise).\"\n\nExclusion Criteria:\n\n* BMI \\> 35,\n* Pregnancy,\n* Cardiovascular Diseases: Individuals with serious cardiovascular issues, such as uncontrolled hypertension, heart failure, coronary artery disease, or a heart attack within the last 6 months, which could pose a risk during exercise.\n* Respiratory Diseases: Individuals with chronic respiratory conditions, such as uncontrolled or severe asthma or COPD, who cannot tolerate exercise due to their condition.\n* Neurological Disorders: Individuals with neurological issues that limit exercise capacity, such as Parkinson's disease, stroke, or multiple sclerosis.\n* Musculoskeletal Issues: Individuals with chronic musculoskeletal problems, particularly knee or hip osteoarthritis, that may increase the risk of pain or injury during exercise.\n* Metabolic or Endocrine Disorders: Individuals with uncontrolled metabolic issues, such as diabetes or thyroid disorders, that could cause blood sugar or hormonal fluctuations during exercise.\n* Acute Infections or Illness: Individuals with acute infections, fever, or recently undergone surgical procedures.\n* Any health condition that may prevent participation in exercise.\"","20 Years","35 Years",{"count":235,"type":22},28,[25],"It is aimed to investigate the responses of Fatty Acid Binding Protein 4 (FABP4), which has been discovered as a novel biomarker of obesity and metabolic diseases, to regular exercise training.\n\nThe aim of this study is to investigate the effects of high-intensity interval training (HIIT) on cardiometabolic risk factors, body composition, and plasma FABP4 levels in sedentary obese adults.",[239],"High-Intensity Interval Training","2025-05-14",{"date":242,"type":43},"2025-05-15",{"date":244,"type":43},"2025-03-01",{"date":246,"type":22},"2025-09-01",{"name":49,"class":50},{"id":249,"slug":250,"hasResults":11,"nctId":251,"briefTitle":252,"officialTitle":253,"acronym":4,"eligibilityCriteria":254,"healthyVolunteers":59,"sex":117,"minAge":18,"maxAge":19,"enrollmentInfo":255,"targetDuration":4,"studyType":23,"phases":257,"briefSummary":258,"conditions":259,"keywords":263,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":268,"startDateStruct":270,"completionDateStruct":271,"leadSponsor":273,"locationsCount":274},"100589332","effects-of-acupressure-applied-before-cesarean-delivery-on-anxiety-physiological-parameters-and-fetal-heart-rate-100589332","NCT06953037","Effects of Acupressure Applied Before Cesarean Delivery on Anxiety, Physiological Parameters and Fetal Heart Rate","Effects of Acupressure Applied Before Cesarean Delivery on Anxiety, Physiological Parameters and Fetal Heart Rate: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Agree to participate in the study,\n* Be between the ages of 18-45,\n* Have a caesarean section between 37-40 weeks,\n* Not have a risky pregnancy,\n* Have spinal anesthesia,\n\nExclusion Criteria:\n\n* Not having anxiety 1 hour before the cesarean section,\n* Having a risky pregnancy,\n* Having a chronic disease,\n* Having a severe systemic disease,\n* Not receiving spinal anesthesia,\n* Having a body mass index over 25,\n* Having previous acupressure experience,",{"count":256,"type":22},64,[25],"Cesarean section is the most commonly preferred surgical method in cases where vaginal birth is not possible or complications that may endanger the health of the mother and baby occur. Cesarean section rates are increasing worldwide. According to the latest data (2010-2018) from 154 countries covering 94.5% of live births in the world, 21.1% of women have cesarean section births and it is estimated that this rate will increase to 28.5% by 2030. According to the Centers for Disease Control and Prevention (CDC), the cesarean section rate in the USA, which was 32.1% in 2022, increased to 32.4% in 2023. When the cesarean section rates of the Turkey Demographic Health Survey (TDHS) are examined, the rate, which was 7% in 1993, increased to 52% in 2018, an increase of 45% is observed. In the TRNC, this rate was 11.1% in 1981, but in 2017 this rate increased by an average of 7 times, reaching 72.5%. Pregnant women tend to have cesarean sections because they are affected by the risks that will occur during birth, negative birth stories told among the public, and painful birth scenes seen on social media. Studies have shown that despite the high rates of cesarean sections in pregnant women's birth methods, a significant increase in women's anxiety levels is observed. While waiting for the surgery, pre-operative anxiety, fear of the procedure, etc. are more common than other feelings and symptoms.Studies have also shown that anxiety increases in patient rooms, the night before surgery, and when moving to the operating table. In a study conducted by Lopez, the most important causes of preoperative anxiety were listed as fear of the hospital environment (35%), fear of surgery (33%), fear of anesthesia (45%), and unawareness of the surgery (45%). Concerns about the success of the operation (29.3%), fear of postoperative prognosis (19.5%), and surgical complications (11.4%) are the most common causes of preoperative anxiety. High levels of anxiety experienced before surgery cause increased heart rate, blood pressure, and oxygen consumption during surgery.\n\nControlling and managing preoperative anxiety is one of the most important goals of nursing care worldwide, as in cesarean cases. Mothers need to relax mentally and physically after cesarean sections so that they can care for their babies after birth. A common way to control preoperative anxiety is to use sedatives, but these medications can cause side effects. Therefore, acupressure, which is a non-invasive, low-cost, uncomplicated and non-pharmacological method due to fewer complications, can be used to reduce preoperative anxiety. Acupressure is the application of pressure to stimulate acupoints and meridian lines using an object or fingers, without the use of needles. Acupressure is a simple treatment approach and can be applied by nurses or patients who have received the necessary training, because it is simple and does not require any equipment.",[260,261,262],"Caesarean Section","Pregnant Women","Anxiety Disorder",[264,265,132,266,267],"pregnant women","caesarean section","fetal heart rate","accupressure",{"date":269,"type":43},"2025-05-01",{"date":242,"type":22},{"date":272,"type":22},"2025-07-05",{"name":49,"class":50},2,{"id":276,"slug":277,"hasResults":11,"nctId":278,"briefTitle":279,"officialTitle":280,"acronym":4,"eligibilityCriteria":281,"healthyVolunteers":59,"sex":17,"minAge":282,"maxAge":18,"enrollmentInfo":283,"targetDuration":285,"studyType":180,"phases":4,"briefSummary":286,"conditions":287,"keywords":4,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":293,"lastUpdatePostDateStruct":294,"startDateStruct":296,"completionDateStruct":298,"leadSponsor":300,"locationsCount":51},"100582587","psychometric-properties-of-the-turkish-version-of-the-modified-mini-mental-state-examination-100582587","NCT06865248","Psychometric Properties of the Turkish Version of the Modified Mini Mental State Examination","Investigation of Psychometric Properties of the Turkish Version of the Modified Mini Mental State Examination in Typically Developing Children and Children With Neurodevelopmental Disorders","Inclusion Criteria:\n\n* Between the ages of 5-18,\n* Children diagnosed with neurodevelopmental disorders (Attention Deficit and Hyperactivity Disorder, Specific Learning Disorder, Autism Spectrum Disorder, Motor Disorders (Spastic SP)\n* Children who can understand and apply Turkish commands\n\nExclusion Criteria:\n\nThose with have serious hearing and speech problems","5 Years",{"count":284,"type":22},397,"7 Days","One of the most commonly used screening tests for the mental status of adults is the Standardized Mini Mental State Examination (MMSE). The MMSE is designed to screen for cognitive dysfunction, assess the severity of impairments, and identify changes over time. In the country of the researchers, the Turkish adaptation of the MMSE for children has not been done and the validity and reliability of the Turkish version has not been demonstrated. This paper aims to investigate the pschiatric features of the MMSE for Turkish pediatric population.",[288,289,290,291,292],"Children","Neurologic Disorder","Cerebral Palsy","Down Syndrome","Healthy","2025-03-11",{"date":295,"type":43},"2025-03-13",{"date":297,"type":22},"2025-04",{"date":299,"type":22},"2025-06",{"name":49,"class":50},{"id":302,"slug":303,"hasResults":11,"nctId":304,"briefTitle":305,"officialTitle":306,"acronym":4,"eligibilityCriteria":307,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":308,"targetDuration":4,"studyType":23,"phases":310,"briefSummary":311,"conditions":312,"keywords":316,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":320,"lastUpdatePostDateStruct":321,"startDateStruct":323,"completionDateStruct":324,"leadSponsor":326,"locationsCount":4},"100571588","different-same-day-colonoscopic-bowel-preparation-procedures-on-patient-compliance-tolerability-and-bowel-cleansing-100571588","NCT06722209","Different Same-day Colonoscopic Bowel Preparation Procedures on Patient Compliance, Tolerability, and Bowel Cleansing","Investigation of the Effect of Different Same-day Colonoscopic Bowel Preparation Procedures on Patient Compliance, Tolerability, and Bowel Cleansing: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Drinking at least 75 per cent of the solution\n* Have the ability to read and understand research instructions\n* Patients who agreed to participate in the study\n\nExclusion Criteria:\n\n* Patients with active lower intestinal bleeding\n* KKY\n* Liver failure,\n* Patients with end-stage acute renal failure",{"count":309,"type":22},128,[25],"The aim of this study was to investigate the effect of different bowel preparation protocols applied on the same day on patients' compliance, tolerance and bowel cleansing before colonoscopy.\n\nHypotheses of the Study : Same-day administration of bowel preparation before colonoscopy; H1.1: There is a significant difference between the bowel preparation protocol with polyethylene glycol (Protocol I) and the protocol with sodium phosphate (Protocol II) in bowel preparation score scores H1.2: There is a significant difference between the compliance levels of the patients who underwent a bowel preparation protocol containing polyethylene glycol (Protocol I) and a protocol containing sodium phosphate (Protocol II) H1.3: There is a significant difference between the tolerance of the patients who underwent a bowel preparation protocol containing polyethylene glycol (Protocol I) and a protocol containing sodium phosphate (Protocol II)\n\nIn patients in Protocol I and II groups, data will be collected one day before the procedure with the Descriptive Characteristics Form and the procedure will be explained face to face. After the procedure, bowel preparation score during colonoscopy and compliance and tolerance to the bowel preparation protocol will be evaluated from the patients in both groups.",[211,313,314,315],"Colonoscopy Diagnostic Techniques and Procedures","Colonoscopy Preparation","Colonoscopy Preparation Outcome",[211,317,318,319],"Bowel preparation","Colorectal cancer","Patients compliance","2025-02-25",{"date":322,"type":43},"2025-02-26",{"date":244,"type":22},{"date":325,"type":22},"2025-12-10",{"name":49,"class":50},{"id":328,"slug":329,"hasResults":11,"nctId":330,"briefTitle":331,"officialTitle":332,"acronym":4,"eligibilityCriteria":333,"healthyVolunteers":11,"sex":175,"minAge":334,"maxAge":335,"enrollmentInfo":336,"targetDuration":4,"studyType":23,"phases":338,"briefSummary":339,"conditions":340,"keywords":342,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":349,"lastUpdatePostDateStruct":350,"startDateStruct":352,"completionDateStruct":353,"leadSponsor":355,"locationsCount":51},"100564892","investigation-of-the-effectiveness-of-telerehabilitation-training-in-pectus-excavatum-deformity-100564892","NCT06635083","Investigation of the Effectiveness of Telerehabilitation Training in Pectus Excavatum Deformity","Comparison of the Effects of Vacuum Bell Therapy and Additional Telerehabilitation on Physical Fitness, Respiratory Functions, Posture and Psychosocial Factors in Children with Pectus Excavatum : a Single-Blind Randomized Controlled Trial","Inclusion Criteria:\n\n* Children aged 10-14\n* Boys\n* Those who have undergone Vacuum Bell treatment for the first time\n\nExclusion Criteria:\n\n* Those with complex type pectus deformity\n* Those who have undergone any surgical treatment due to pectus excavatum\n* Those with chronic systemic disease (cardiovascular, gastrointestinal, metabolic)\n* Those with diagnosed serious psychiatric disease\n* Those with scoliosis over 20 degrees\n* Those with other musculoskeletal anomalies and connective tissue disorders (Marfan syndrome, Turner syndrome, neurofibromatosis tuberous sclerosis)\n* Those with neurological disease\n* Those with hearing or vision impairment that cannot be corrected with hearing aids or glasses\n* Those who do not have internet access or do not own a tablet\u002Fcomputer","10 Years","14 Years",{"count":337,"type":22},62,[25],"The aim of this study is to investigate the effectiveness of telerehabilitation-based exercise training in addition to Vacuum Bell therapy on physical fitness, respiratory functions, posture and psychosocial factors in boys aged between 10-14 years diagnosed with pectus excavatum.",[341],"Pectus Excavatum",[343,344,345,346,347,348],"Telerehabilitation","Posture","Congenital Abnormalities","Quality of Life","Physical Fitness","Respiratory Function Tests","2024-10-08",{"date":351,"type":43},"2024-10-10",{"date":351,"type":22},{"date":354,"type":22},"2025-04-30",{"name":49,"class":50},{"id":357,"slug":358,"hasResults":11,"nctId":359,"briefTitle":360,"officialTitle":361,"acronym":362,"eligibilityCriteria":363,"healthyVolunteers":59,"sex":117,"minAge":18,"maxAge":4,"enrollmentInfo":364,"targetDuration":4,"studyType":23,"phases":366,"briefSummary":367,"conditions":368,"keywords":372,"overallStatus":78,"whyStopped":4,"lastUpdateSubmitDate":377,"lastUpdatePostDateStruct":378,"startDateStruct":380,"completionDateStruct":382,"leadSponsor":384,"locationsCount":51},"100508505","development-of-my-breastfeeding-guide-mobile-nursing-application-100508505","NCT05901298","Development of 'My Breastfeeding Guide' Mobile Nursing Application","Development of 'My Breastfeeding Guide' Mobile Nursing Application and Its Effect on Breastfeeding Process, Self-Efficacy, Infant Nutrition and Attachment","Nursing","Inclusion Criteria:\n\n* Women aged 18 and over,\n* Women who are in the last trimester of pregnancy (32nd gestational week and above),\n* Women with singleton pregnancy,\n* Women who do not have any health problems that may prevent breastfeeding,\n* Women with smartphones with Android and iOS operating systems,\n* Women who can access the Internet,\n* There will be women who do not have literacy problems, mental disabilities and communication problems.\n\nExclusion Criteria:\n\n* Women under 18 years of age,\n* Women who are under the last trimester of pregnancy (32nd week of pregnancy),\n* Women who do not speak Turkish,\n* Women who own a smartphone with an operating system other than Android and iOS.",{"count":365,"type":22},88,[25],"The research was planned to develop the \"My Breastfeeding Guide\" mobile nursing application, which was developed based on Dennis' Breastfeeding Self-Efficacy Theory and Pender's Health Promotion Model, and to determine its effect on the postpartum breastfeeding process, breastfeeding self-efficacy, infant feeding and attachment. The research is in randomized controlled experimental and longitudinal (prospective) design. The research will be carried out with pregnant women who applied to Famagusta State Hospital Obstetrics and Gynecology Polyclinic and a pregnant polyclinic of a private hospital in Famagusta. Pregnant women who applied to Famagusta State Hospital Gynecology and Obstetrics Polyclinic and private hospital's pregnancy polyclinic and met the inclusion criteria of the study will constitute the population of the research. The research will be designed in two groups as the mobile nursing practice group (intervention) and standard care group (control) developed based on Dennis's Breastfeeding Self-Efficacy Theory and Pender's Health Promotion Model. By calculating the sample size in the research, 44 people in the intervention group and 44 people in the control group will reach a total of 88 people. Pregnant Identification Form, Maternal Information Form, Breastfeeding Self-Efficacy Short Form Scale (Postnatal Form), Antenatal Self-Efficacy Short Form Scale, Infant Nutrition Attitude Scale, Breastfeeding Rating Scale, Maternal Attachment Scale and Breastfeeding Self-assessment Form will be used to collect data. Statistical analyzes of the data obtained from the research will be made using the Statistical Package for the Social Science (SPSS) 20.0 package program. While evaluating the research data, frequency, percentage, mean, standard deviation, median, variance analysis from descriptive statistical methods will be used. For homogeneity test between intervention and control groups, the Chi-square test for categorical variables, Mann Whitney test for numerical variables, and sociodemographic variables (age, education status, employment status of himself and his spouse, income level, etc.) and whether the groups are similar in terms of some characteristics. U test will be used. The conformity of the scale scores to the normal distribution will be evaluated with the Shapiro-Wilk test. The results will be evaluated at the 95% confidence level, and the significance at the p\\\u003C0.05 level.",[369,370,371],"Self Efficacy","Breast Feeding","Attachment",[373,374,375,376],"Breastfeeding","Nurse","Mobile application","Self-efficiency","2024-09-11",{"date":379,"type":43},"2024-09-19",{"date":381,"type":43},"2023-12-15",{"date":383,"type":22},"2024-12-15",{"name":49,"class":50},""]