[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Karadeniz Technical University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":419},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,15,0,[8,48,77,105,127,158,187,216,240,268,293,319,345,370,396],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":28,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100633445","motivational-interviewing-on-loneliness-level-activities-of-daily-living-and-quality-of-life-in-elderly-100633445",false,"NCT07526779","Motivational Interviewing on Loneliness Level, Activities of Daily Living, and Quality of Life in Elderly","The Effect of Motivational Interviewing on Loneliness Level, Activities of Daily Living, and Quality of Life in Elderly Individuals Living Alone: A Randomized Controlled Study","Experimental","Inclusion Criteria:\n\n* being 65 years of age or older,\n* living alone,\n* volunteering to participate in the study,\n* possessing sufficient cognitive ability to communicate,\n* being able to communicate in Turkish.\n\nExclusion Criteria:\n\n* having a diagnosis of severe cognitive impairment or dementia,\n* having significant hearing or communication difficulties,\n* being unable to participate regularly in the research process","ALL","65 Years",{"count":20,"type":21},60,"ESTIMATED","INTERVENTIONAL",[24],"NA","To examine the effects of motivational interviewing on loneliness levels, activities of daily living, and quality of life among older adults living alone",[27],"Motivational Interviewing (MI)",[29,30,31,32,33,34],"Motivational interviewing","elderly","Loneliness Level","Activities of Daily Living","Quality of Life","Living Alone","NOT_YET_RECRUITING","2026-04-06",{"date":38,"type":39},"2026-04-13","ACTUAL",{"date":41,"type":21},"2026-05-01",{"date":43,"type":21},"2026-07-01",{"name":45,"class":46},"Karadeniz Technical University","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":17,"minAge":55,"maxAge":56,"enrollmentInfo":57,"targetDuration":59,"studyType":60,"phases":4,"briefSummary":61,"conditions":62,"keywords":64,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":47},"100575241","anthropometric-predictability-of-full-thickness-peroneus-longus-and-semitendinosus-autograft-size-100575241","NCT06769724","Anthropometric Predictability of Full-Thickness Peroneus Longus and Semitendinosus Autograft Size","Anthropometric Predictability of Full-Thickness Peroneus Longus and Semitendinosus Autograft Size: A Comparative Analysis","Inclusion Criteria:\n\n* Ages between 18-45 years\n* Diagnosed Acl rupture preoperavitely with mri imaging\n* Diagnosed Acl rupture and having symptoms related to acl rupture\n* Eligible for harvesting same side semitendinosus or peroneous longus tendon\n\nExclusion Criteria:\n\n* Previous surgery history on donor side knee or ankle\n* Congenital defect on donor extremity\n* Multiple Ligament Injury History","18 Years","45 Years",{"count":58,"type":21},180,"1 Day","OBSERVATIONAL","The study is aimed to determine correlation between autografts used in anterior cruciate ligaments and anthropometric variables e.g. height, sex, weight, BMI etc..",[63],"Anterior Cruciate Ligaments",[63,65,66,67],"peroneus longus tendon","semitendinosus tendon","anthropometric","RECRUITING","2026-03-17",{"date":71,"type":39},"2026-03-19",{"date":73,"type":39},"2025-01-06",{"date":75,"type":21},"2026-09-06",{"name":45,"class":46},{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":4,"eligibilityCriteria":83,"healthyVolunteers":84,"sex":17,"minAge":55,"maxAge":4,"enrollmentInfo":85,"targetDuration":4,"studyType":22,"phases":86,"briefSummary":87,"conditions":88,"keywords":90,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":4},"100627402","effect-of-standardized-patient-simulation-on-nursing-students-assessment-diagnosis-skills-and-experiences-100627402","NCT07448168","Effect of Standardized Patient Simulation on Nursing Students' Assessment, Diagnosis Skills, and Experiences","The Effect of Teaching With Standardized Patient Simulation on Students' Assessment and Nursing Diagnosis Determination Skills and Determination of Their Experiences","Inclusion Criteria:\n\n* First-year nursing student\n* Successfully completed the Fundamentals of Nursing I course\n* Currently enrolled in the Fundamentals of Nursing II course\n* Aged 18 years or older\n* Voluntary agreement to participate in the study\n\nExclusion Criteria:\n\n* Previously completed the Fundamentals of Nursing II course\n* Withdrawal from the study for any reason\n* Failure to complete the post-test assessment",true,{"count":20,"type":21},[24],"This randomized controlled study aims to determine the effect of teaching delivered through standardized patient simulation on nursing students' assessment and nursing diagnosis determination skills, as well as their learning experiences. First-year nursing students will be randomly assigned to intervention and control groups. The intervention group will receive training based on standardized patient simulation, while the control group will receive traditional instruction. Data will be collected using a sociodemographic information form, case-based assessment tools, and measurement instruments designed to evaluate students' perceptions and experiences related to the educational process. Group comparisons will be conducted to evaluate the effectiveness of the simulation-based teaching method.",[89],"Nurse's Role",[91,92,93,94,95,96],"Nursing assessment","Nursing diagnosis","Nursing process","Nursing students","Simulation training","Standardised patient","2026-03-03",{"date":99,"type":39},"2026-03-04",{"date":101,"type":21},"2026-03-31",{"date":103,"type":21},"2026-05-15",{"name":45,"class":46},{"id":106,"slug":107,"hasResults":11,"nctId":108,"briefTitle":109,"officialTitle":110,"acronym":4,"eligibilityCriteria":111,"healthyVolunteers":84,"sex":17,"minAge":55,"maxAge":112,"enrollmentInfo":113,"targetDuration":4,"studyType":22,"phases":115,"briefSummary":116,"conditions":117,"keywords":4,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":119,"lastUpdatePostDateStruct":120,"startDateStruct":122,"completionDateStruct":124,"leadSponsor":126,"locationsCount":47},"100621178","percussive-massage-therapy-and-muscle-architecture-100621178","NCT07367243","Percussive Massage Therapy and Muscle Architecture","Acute Effects of Percussive Massage Therapy Applied to Healthy Individuals on Gastrocnemius Muscle Architecture: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Aged between 18 and 30 years\n\nExclusion Criteria:\n\n* History of any surgical procedure\n* Hospitalization for any reason within the last two years\n* Hospital admission for treatment purposes within the last six months\n* Use of any medication within the last three months\n* History of congenital, neurological, orthopedic, rheumatologic, or cardiopulmonary pathology or anomaly\n* Presence of any known serious systemic disease\n* Current health-related complaints or symptoms\n* Body mass index (BMI) of 25 kg\u002Fm² or higher","30 Years",{"count":114,"type":21},40,[24],"Percussive massage therapy (PMT) is widely used in therapeutic and athletic settings, but its effects on muscle architecture are not yet fully understood. This study aims to examine the acute effects of PMT applied to the plantar flexor muscles on the muscle architecture of the medial and lateral gastrocnemius muscles in healthy adults aged 18 to 30 years. Participants will be randomly assigned to either a PMT group or a control group. Ultrasonographic assessments will be performed before and after the intervention to evaluate muscle thickness, pennation angle, and fascicle length. The findings of this study may help clarify the acute effects of PMT on muscle structure.",[118],"Muscle Architecture","2026-01-16",{"date":121,"type":39},"2026-01-26",{"date":123,"type":39},"2025-11-17",{"date":125,"type":21},"2026-02-10",{"name":45,"class":46},{"id":128,"slug":129,"hasResults":11,"nctId":130,"briefTitle":131,"officialTitle":132,"acronym":133,"eligibilityCriteria":134,"healthyVolunteers":11,"sex":17,"minAge":55,"maxAge":135,"enrollmentInfo":136,"targetDuration":4,"studyType":60,"phases":4,"briefSummary":138,"conditions":139,"keywords":144,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":150,"lastUpdatePostDateStruct":151,"startDateStruct":153,"completionDateStruct":155,"leadSponsor":157,"locationsCount":47},"100612758","comparison-of-iv-analgesia-thoracic-epidural-analgesia-and-esp-block-for-chronic-pain-after-open-heart-surgery-100612758","NCT07257744","Comparison of IV Analgesia, Thoracic Epidural Analgesia, and ESP Block for Chronic Pain After Open Heart Surgery","A Comparative Evaluation of Intravenous Analgesia, Thoracic Epidural Analgesia, and Erector Spinae Plane Block on Chronic Postoperative Pain Following Open Heart Surgery","TEA-ESPB-IV","Inclusion Criteria:\n\n* Adults aged 18 to 85 years\n* Classified as ASA physical status I-III\n* Scheduled to undergo open heart surgery with median sternotomy\n* BMI \\\u003C 35 kg\u002Fm²\n* Able to understand and provide written informed consent\n* Eligible to receive any of the routine analgesia methods (intravenous analgesia, thoracic epidural analgesia, or erector spinae plane block)\n\nExclusion Criteria:\n\n* Age \\\u003C 18 or \\> 85 years\n* BMI ≥ 35 kg\u002Fm²\n* Coagulation disorders\n* Infection at the intervention site\n* Known allergy to local anesthetics or induction agents\n* Psychiatric disorders limiting cooperation\n* Use of chronic pain medications, antidepressants, corticosteroids, antiepileptics, or routine analgesics\n* Inability to cooperate, communicate, or follow commands\n* Physical or verbal performance impairment\n* Previous open heart surgery","85 Years",{"count":137,"type":21},90,"This prospective observational study aims to compare three routinely used postoperative analgesia techniques in patients undergoing open heart surgery: intravenous analgesia, thoracic epidural analgesia (TEA), and bilateral erector spinae plane block (ESPB). The primary objective is to evaluate the impact of these analgesia modalities on the development of chronic postoperative pain at 3 months. Secondary objectives include assessing postoperative acute pain scores, additional analgesic requirements, extubation time, mobilization time, intensive care unit stay, hospital stay, respiratory complications, and the relationship between acute and chronic pain. No intervention is assigned by protocol, and all analgesia methods are applied as part of routine clinical practice.",[140,141,142,143],"Chronic Postoperative Pain","Open Heart Surgery","Postoperative Analgesia","Analgesia",[141,140,145,146,147,148,149],"Post-Sternotomy Pain","Thoracic Epidural Analgesia (TEA)","Erector Spinae Plane Block (ESPB)","Pain Management","Cardiac Anesthesia","2025-11-27",{"date":152,"type":39},"2025-12-02",{"date":154,"type":39},"2025-02-15",{"date":156,"type":21},"2026-04-20",{"name":45,"class":46},{"id":159,"slug":160,"hasResults":11,"nctId":161,"briefTitle":162,"officialTitle":163,"acronym":164,"eligibilityCriteria":165,"healthyVolunteers":11,"sex":17,"minAge":55,"maxAge":166,"enrollmentInfo":167,"targetDuration":59,"studyType":60,"phases":4,"briefSummary":169,"conditions":170,"keywords":175,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":179,"lastUpdatePostDateStruct":180,"startDateStruct":182,"completionDateStruct":184,"leadSponsor":186,"locationsCount":4},"100611266","analgesic-effectiveness-of-spsipb-versus-thoracic-epidural-and-systemic-opioid-analgesia-after-vats-spsipb-vats-100611266","NCT07238348","Analgesic Effectiveness of SPSIPB Versus Thoracic Epidural and Systemic Opioid Analgesia After VATS (SPSIPB-VATS)","Prospective Evaluation of Analgesic Outcomes of Serratus Posterior Superior Intercostal Plane Block Versus Thoracic Epidural Analgesia and Systemic Opioid Analgesia After Video-Assisted Thoracoscopic Surgery","SPSIPB-VATS","Inclusion Criteria:\n\n* Adults aged 18-75 years\n* Scheduled for elective video-assisted thoracoscopic surgery (VATS)\n* ASA physical status I-III\n* Ability to understand study procedures and provide written informed consent\n* Hemodynamically stable preoperatively\n\nExclusion Criteria:\n\n* Known allergy or contraindication to local anesthetics or study medications\n* Coagulopathy or use of anticoagulants not suitable for regional anesthesia\n* Local infection or skin lesions at the injection site\n* Severe pulmonary disease (e.g., severe COPD, uncontrolled asthma)\n* Chronic opioid use or chronic pain disorders\n* Neurological or psychiatric disorders impairing cooperation\n* Pregnancy or breastfeeding\n* BMI \\> 35 kg\u002Fm²\n* Conversion from VATS to thoracotomy\n* Inability to comply with postoperative assessments","75 Years",{"count":168,"type":21},120,"This prospective observational study aims to compare the postoperative analgesic effectiveness of three commonly used pain management strategies in video-assisted thoracoscopic surgery (VATS): Serratus Posterior Superior Intercostal Plane Block (SPSIPB), Thoracic Epidural Analgesia (TEA), and systemic opioid analgesia. The study evaluates postoperative pain scores, opioid consumption, and the need for rescue analgesics within the first 24 hours after surgery. By analyzing analgesic performance and safety profiles of these techniques, the study seeks to provide evidence to guide optimal postoperative pain management for patients undergoing minimally invasive thoracic procedures.",[171,172,173,174],"Postoperative Pain Management","Video-assisted Thoracoscopic Surgery (VATS)","Thoracic Epidural Analgesia","Serratus Posterior Superior Intercostal Plane Block",[174,173,176,177,178,148],"Systemic Opioid Analgesia","Video-Assisted Thoracoscopic Surgery","Opioid Consumption","2025-11-18",{"date":181,"type":39},"2025-11-20",{"date":183,"type":21},"2025-12-15",{"date":185,"type":21},"2026-08-15",{"name":45,"class":46},{"id":188,"slug":189,"hasResults":11,"nctId":190,"briefTitle":191,"officialTitle":192,"acronym":4,"eligibilityCriteria":193,"healthyVolunteers":11,"sex":17,"minAge":55,"maxAge":194,"enrollmentInfo":195,"targetDuration":4,"studyType":22,"phases":197,"briefSummary":198,"conditions":199,"keywords":203,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":208,"lastUpdatePostDateStruct":209,"startDateStruct":211,"completionDateStruct":213,"leadSponsor":215,"locationsCount":4},"100589143","effect-of-abdominal-massage-on-patients-in-intensive-care-unit-100589143","NCT06950580","Effect of Abdominal Massage on Patients in Intensive Care Unit","Investigation of the Effect of Abdominal Massage on Patients in Intensive Care Unit: Randomised Controlled Trial","Inclusion Criteria:\n\n* Patients aged between 18 to 80 years\n* Patients hospitalized in the intensive care unit for more than 3 days\n* Body Mass Index less than 30 kg\u002Fm²\n* Patients who are not mobilized out of bed\n* Patients without any intervention contraindicating abdominal massage\n\nExclusion Criteria:\n\n* History of abdominal surgery\n* Active gastrointestinal bleeding\n* Patients discharged from ICU within less than 5 days after enrollment","80 Years",{"count":196,"type":21},128,[24],"Bowel motility can be affected by many factors such as immobilization, lack of fiber in the nutritional formula, inadequate fluid intake, and lack of privacy for toileting in patients hospitalized in the intensive care unit. Abdominal massage, which is one of the effective methods to increase intestinal motility, is accepted as an intervention that can be safely applied in patients.\n\nThe aim of our study was to investigate the effect of abdominal massage applied to patients hospitalized in the intensive care unit on sepsis, survival, discharge time from intensive care unit, amount and duration of antibiotic use.\n\nHypotheses H0: Abdominal massage application has no effect on sepsis, survival, discharge time from intensive care unit, amount and duration of antibiotic use in patients hospitalized in intensive care unit.\n\nH1: Abdominal massage application has an effect on sepsis, survival, discharge time from intensive care unit, amount and duration of antibiotic use in patients hospitalized in intensive care unit.\n\nIn this randomized controlled study, the data of patients who received abdominal massage for 5 days during routine physiotherapy applications and those who did not will be recorded. Randomization will be performed in a 1:1 ratio using a computer generated randomization schedule. The effect of abdominal massage on sepsis, survival, discharge time from intensive care, amount and duration of antibiotic use will be examined by using the data of 2 groups with and without abdominal massage in a randomized controlled trial.",[200,201,202],"Intensive Care Unit Patients","Physiotherapy and Rehabilitation","Abdominal Massage",[204,205,206,207],"Intensive care unit patients","Physiotherapy and rehabilitation","Abdominal massage","sepsis","2025-04-25",{"date":210,"type":39},"2025-04-30",{"date":212,"type":21},"2025-05",{"date":214,"type":21},"2026-02",{"name":45,"class":46},{"id":217,"slug":218,"hasResults":11,"nctId":219,"briefTitle":220,"officialTitle":221,"acronym":4,"eligibilityCriteria":222,"healthyVolunteers":11,"sex":17,"minAge":55,"maxAge":194,"enrollmentInfo":223,"targetDuration":4,"studyType":22,"phases":225,"briefSummary":226,"conditions":227,"keywords":229,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":233,"lastUpdatePostDateStruct":234,"startDateStruct":236,"completionDateStruct":237,"leadSponsor":239,"locationsCount":4},"100588811","transcutaneous-diaphragm-stimulation-in-icu-patients-100588811","NCT06946251","Transcutaneous Diaphragm Stimulation in ICU Patients","Evaluation of Patients With Reduced and Preserved Ejection Fraction After Transcutaneous Diaphragm Stimulation","Inclusion Criteria:\n\n* Patients aged between 18 and 80 years\n* Patients expected to require mechanical ventilation for at least 72 hours\n\nExclusion Criteria:\n\n* Presence of known neuromuscular diseases that contraindicate the use of transcutaneous diaphragm stimulation\n* Phrenic nerve injury\n* History of abdominal or thoracic surgery that prevents the application of diaphragm stimulation",{"count":224,"type":21},76,[24],"The aim of this study is to compare the effects of transcutaneous electrical diaphragm stimulation (TEDS) on diaphragm thickness, duration of mechanical ventilation, length of ICU stay, and right\u002Fleft heart functions between patient groups with low and high ejection fraction (EF) levels.\n\nThis randomized controlled trial will record demographic data, diaphragm ultrasound measurements, and echocardiographic findings of patients who receive or do not receive TEDS for five consecutive days.\n\nParticipants will be divided into four groups according to their EF levels and whether or not they receive diaphragm stimulation:\n\nGroup 1: Patients with low EF who receive TEDS Group 2: Patients with high EF who receive TEDS Group 3: Patients with low EF who do not receive TEDS Group 4: Patients with high EF who do not receive TEDS\n\nDiaphragm thickness and echocardiographic assessments will be performed at baseline and at the end of the five-day TEDS intervention.\n\nTEDS Application Protocol\n\nIn the ICU, TEDS is administered by a physiotherapist once daily for 20 minutes, five days a week, as part of the routine treatment protocol. The stimulation is delivered using the LGT-231 model device from the LONGEST brand.\n\nA transcutaneous current with a frequency of 30-50 Hz and a pulse width of 300-400 microseconds is applied to the diaphragm. The stimulation intensity is increased until visible muscle contraction is achieved.\n\nElectrode placement involves:\n\nThe first pair of electrodes placed bilaterally between the 8th and 10th anterior intercostal spaces, lateral to the xiphoid process.\n\nThe second pair placed along the mid-axillary line of the thorax, also between the 8th and 10th intercostal spaces.",[228],"Intensive Care Patients",[230,231,232],"Diaphragm Stimulation","Intensive care unit","Ejection Fraction","2025-04-18",{"date":235,"type":39},"2025-04-27",{"date":212,"type":21},{"date":238,"type":21},"2026-05",{"name":45,"class":46},{"id":241,"slug":242,"hasResults":11,"nctId":243,"briefTitle":244,"officialTitle":245,"acronym":4,"eligibilityCriteria":246,"healthyVolunteers":84,"sex":17,"minAge":55,"maxAge":247,"enrollmentInfo":248,"targetDuration":4,"studyType":22,"phases":250,"briefSummary":251,"conditions":252,"keywords":254,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":260,"lastUpdatePostDateStruct":261,"startDateStruct":263,"completionDateStruct":265,"leadSponsor":267,"locationsCount":47},"100527519","effect-of-progressive-neck-motor-control-exercises-on-temporomandibular-joint-dysfunction-100527519","NCT06148818","Effect of Progressive Neck Motor Control Exercises on Temporomandibular Joint Dysfunction","Investigation of the Effect of Progressive Neck Motor Control Exercises on Craniocervical Pain, Posture, Function and Kinesiophobia in Different Types of Temporomandibular Joint Dysfunction","Inclusion Criteria:\n\n* 18 to 55 years old,\n* Temporomandibular joint-related complaints for at least 3 months,\n* Temporomandibular dysfunction is diagnosed as a result of clinical and radiological evaluation by the dentist,\n* Neck pain of 3 or more according to the numeric pain scale\n\nExclusion Criteria:\n\n* Cognitive problems,\n* The one with the splint,\n* Those who have used painkillers or muscle relaxants for temporomandibular dysfunction complaints in the last 1 week,\n* With any systematic joint or muscle disease (e.g. fibromyalgia, rheumatoid arthritis),\n* Those with serious systemic diseases,\n* Any neurological disorder (e.g. trigeminal neuralgia),\n* Pregnancy or breastfeeding,\n* Treated for Temporomandibular joint or orofacial muscle pain in the last 3 months,\n* Has undergone an operation\u002Ftrauma to the cervical region and\u002For temporomandibular joint,\n* Positive vertebrobasilar artery test","55 Years",{"count":249,"type":21},75,[24],"The primary aim of this study was to investigate the effects of progressive neck motor control exercises on craniocervical pain, posture, function and kinesiophobia in different types of temporomandibular dysfunction. The secondary aim of the study was to examine the differences between the effects of progressive neck motor control exercises on different types of temporomandibular dysfunction.",[253],"Temporomandibular Joint Dysfunction Syndrome",[253,255,256,257,258,259],"Pain","neck motor control exercise","posture","kinesiophobia","function","2025-01-27",{"date":262,"type":39},"2025-01-29",{"date":264,"type":39},"2024-11-04",{"date":266,"type":21},"2025-06-30",{"name":45,"class":46},{"id":269,"slug":270,"hasResults":11,"nctId":271,"briefTitle":272,"officialTitle":273,"acronym":4,"eligibilityCriteria":274,"healthyVolunteers":84,"sex":275,"minAge":55,"maxAge":56,"enrollmentInfo":276,"targetDuration":59,"studyType":60,"phases":4,"briefSummary":278,"conditions":279,"keywords":282,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":73,"lastUpdatePostDateStruct":287,"startDateStruct":289,"completionDateStruct":291,"leadSponsor":292,"locationsCount":47},"100574561","temporomandibular-joint-function-oral-habits-and-pain-complaints-of-pregnant-women-100574561","NCT06760884","Temporomandibular Joint Function, Oral Habits and Pain Complaints of Pregnant Women","Determination of Temporomandibular Joint Function, Oral Habits and Pain Complaints of Pregnant Women: a Cross-Sectional Case-Control Study","Inclusion Criteria (Pregnancy women):\n\n* Being between the ages of 18-45,\n* At least primary school graduate,\n* Able to speak and understand Turkish,\n* Women diagnosed with pregnancy by USG,\n* Singleton pregnancy,\n* Agreeing to participate in the study voluntarily.\n\nExclusion Criteria (Pregnancy women):\n\n* Those with any systemic disease concerning the musculoskeletal system,\n* Women with any type of disability,\n* Having communication problems,\n* Multiple pregnancy,\n* Refusing to participate in the study.\n\nInclusion Criteria (Non-Pregnancy women):\n\n* Being between the ages of 18-45,\n* At least primary school graduate,\n* Able to speak and understand Turkish,\n* Agreeing to participate in the study voluntarily.\n\nExclusion Criteria (Non-Pregnancy women):\n\n* Those with any systemic disease concerning the musculoskeletal system,\n* Women with any type of disability,\n* Having communication problems,\n* Refusing to participate in the study.","FEMALE",{"count":277,"type":21},224,"The aim of this study is to examine the temporomandibular joint functions, oral habits and pain complaints of pregnant women. .",[280,281],"Temporomandibular Disorders (TMD)","Pregnancy",[283,284,285,286],"temporomandibular disorders","pregnancy","oral habits","pain",{"date":288,"type":39},"2025-01-07",{"date":290,"type":39},"2024-12-02",{"date":266,"type":21},{"name":45,"class":46},{"id":294,"slug":295,"hasResults":11,"nctId":296,"briefTitle":297,"officialTitle":298,"acronym":4,"eligibilityCriteria":299,"healthyVolunteers":84,"sex":17,"minAge":55,"maxAge":4,"enrollmentInfo":300,"targetDuration":4,"studyType":22,"phases":302,"briefSummary":303,"conditions":304,"keywords":306,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":311,"lastUpdatePostDateStruct":312,"startDateStruct":314,"completionDateStruct":316,"leadSponsor":318,"locationsCount":47},"100571695","effect-of-informing-family-members-of-patients-during-surgery-100571695","NCT06723600","Effect of Informing Family Members of Patients During Surgery","Effect of Informing Family Members of Patients by Phone Call on Their Anxiety Level During Undergoing Abdominal Cancer Surgery: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Being a first-degree relative who has given consent,\n* Being able to understand and speak Turkish,\n* Being literate,\n* Willing to participate in the study,\n* Using a phone,\n* Being present in the hospital before, during, and after the surgery.\n\nExclusion Criteria:\n\n* Having a hearing or speech impairment,\n* Having a psychiatric disorder or using psychiatric medication.\n\nEndpoint Criteria:\n\n* Inability to reach the participant when called during the surgery,\n* The patient's death during the surgery.",{"count":301,"type":21},104,[24],"Psychological and physiological issues encountered by family members due to the intraoperative process are factors that complicate the support and care systems of the patient. It is stated that family members of patients undergoing surgery, especially those who do not have sufficient information about the surgical process, experience stress, anxiety, and concern. The need for nursing interventions aimed at providing information about the surgical process, reducing the anxiety levels of family members during the surgery, and supporting them is emphasized. In this context, the study aims to evaluate the effect of periodically informing family members of patients undergoing abdominal cancer surgery via phone during the surgery on their anxiety levels.",[305],"Anxiety",[305,307,308,309,310],"Informing","Relatives of the Patient","Phone Call","Satisfaction","2024-12-04",{"date":313,"type":39},"2024-12-09",{"date":315,"type":39},"2024-06-10",{"date":317,"type":21},"2025-05-10",{"name":45,"class":46},{"id":320,"slug":321,"hasResults":11,"nctId":322,"briefTitle":323,"officialTitle":323,"acronym":4,"eligibilityCriteria":324,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":325,"targetDuration":4,"studyType":22,"phases":326,"briefSummary":327,"conditions":328,"keywords":330,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":337,"lastUpdatePostDateStruct":338,"startDateStruct":340,"completionDateStruct":342,"leadSponsor":344,"locationsCount":47},"100562858","the-effect-of-patient-safety-escape-room-on-nursing-students-knowledge-level-and-team-collaboration-100562858","NCT06608628","The Effect of Patient Safety Escape Room on Nursing Students' Knowledge Level and Team Collaboration","Inclusion Criteria:\n\n* Being a first year nursing student,\n* Participating in a theoretical course on Patient Safety,\n* Taking the Nursing Fundamentals-I course for the first time,\n* Volunteering to participate in the research\n\nExclusion Criteria:\n\n* Not attending the theoretical lecture on Patient Safety\n* Nursing Fundamentals course have had it before\n* Having transitioned to nursing through vertical transfer from other health departments,\n* High school in a health-related field, Having an associate degree or bachelor's degree.\n* Incomplete completion or failure to complete the pre-test or post-test,\n* The student's wanting to withdraw from the research at some stage.",{"count":20,"type":21},[24],"The concept of patient safety first emerged more than two decades ago in research by practitioners applying different approaches to improve care in the areas they work in. The main goal in patient safety is to prevent mistakes while providing service, to protect patients from possible harm and to minimize the possibility of making mistakes. For this reason, patient safety is one of the indispensable parts of nursing education. The planned research will be carried out in order to increase the patient safety escape room design and the current knowledge level of student nurses and team cooperation on this subject. The research will be carried out with the first year students of the Faculty of Health Sciences, Nursing Department of a state university, in an experimental design with pre-test and post-test. The data of the research will be collected with the \"General Information Questionnaire\", \"Patient Safety Knowledge Test\", \"Collaboration Scale\" and \"Gamy Experience for Gamification Scale\". It is planned to carry out the study with 60 students. Control Group=30, Experiment Group=30. After the subject of patient safety is explained in the Nursing Fundamentals course, the students who agree to participate in the study will be randomly divided into experimental and control groups.\n\nPatient safety practices will be explained to the control and experimental group students with the demonstration method in the laboratory environment after the lesson. Experimental group students will be taken to patient safety escape rooms prepared by the researcher. Students will be taken to escape rooms in groups of 5 and will be expected to perform the targeted tasks. After the lab and escape room activity, students will fill in the knowledge test and scales again. Since there is a limited number of studies in the literature on the knowledge levels of nursing students on patient safety and team collaboration, and there is no study in which escape room design is used in the field of nursing in Turkey, the research is important in terms of filling this gap in the literature.",[329],"Patient Safety",[331,332,333,334,335,336],"Knowledge","Safety","Patient","Nursing Students","Collaboration","Gamification","2024-09-19",{"date":339,"type":39},"2024-09-23",{"date":341,"type":39},"2024-07-20",{"date":343,"type":21},"2024-12-15",{"name":45,"class":46},{"id":346,"slug":347,"hasResults":11,"nctId":348,"briefTitle":349,"officialTitle":350,"acronym":351,"eligibilityCriteria":352,"healthyVolunteers":11,"sex":17,"minAge":55,"maxAge":4,"enrollmentInfo":353,"targetDuration":4,"studyType":22,"phases":354,"briefSummary":355,"conditions":356,"keywords":358,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":363,"lastUpdatePostDateStruct":364,"startDateStruct":365,"completionDateStruct":367,"leadSponsor":369,"locationsCount":47},"100561280","arteriovenous-fistula-cannulation-pain-and-skin-cooling-device-100561280","NCT06588114","Arteriovenous Fistula Cannulation Pain and Skin Cooling Device","Antistress Ball Applied to Hemodialysis Patients, Valsalva Maneuver and Pain Due to Arteriovenous Fistula Cannulation of Skin Cooling Device and the Effect of Fear of Pain: a Randomized Controlled Trial","HD patients","Inclusion Criteria:\n\n* be 18 years of age or older\n* Volunteering to participate in the study\n* Being a hemodialysis patient and being on hemodialysis for more than three months\n* Having an arteriovenous fistula that has been used for more than a month\n* To be hemodialyzed three times a week\n* To be literate\n* Absence of communication barrier\n* Not having any psychiatric diagnosis\n* Not having cognitive impairment\n\nExclusion Criteria:\n\n* being under the age of 18\n* It takes less than a month for the arteriovenous fistula to be newly opened\n* Having a different type of vascular interference from arteriovenous fistula\n* Having phlebitis, scar tissue, dermatitis, an incision or infection at the site of arteriovenous interference\n* Hemodialysis of the patient more or less than three times a week\n* Having any disease that may affect the perception of pain\n* Illiteracy\n* Having a psychiatric diagnosis\n* Having any discomfort in the hand and arm that allows squeezing the antistress ball\n* There is a communication barrier\n* Having a cognitive impairment",{"count":20,"type":21},[24],"To determine the effect of the antistress ball, valsalva maneuver and skin cooling device, which are one of the nonpharmacological methods applied to hemodialysis patients, on the level of pain and fear of pain due to arteriovenous fistula cannulation.",[357],"Chronic Kidney Disease on Hemodialysis",[359,360,361,362],"Hemodialysis","Arteriovenous fistula","Valsalva","Antistress ball","2024-09-05",{"date":337,"type":39},{"date":366,"type":21},"2024-10-01",{"date":368,"type":21},"2024-12-01",{"name":45,"class":46},{"id":371,"slug":372,"hasResults":11,"nctId":373,"briefTitle":374,"officialTitle":375,"acronym":4,"eligibilityCriteria":376,"healthyVolunteers":84,"sex":17,"minAge":55,"maxAge":377,"enrollmentInfo":378,"targetDuration":4,"studyType":22,"phases":379,"briefSummary":380,"conditions":381,"keywords":383,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":387,"lastUpdatePostDateStruct":388,"startDateStruct":390,"completionDateStruct":392,"leadSponsor":394,"locationsCount":395},"100559812","ir-beam-used-before-peripheral-intravenous-catheter-application-on-vein-visibility-100559812","NCT06569004","IR Beam Used Before Peripheral Intravenous Catheter Application on Vein Visibility","Karadeniz Technical University - Tubitak Student Project","Inclusion Criteria:\n\nAre between the ages of 18-70,\n\n* PIVK will be inserted,\n* Not receiving anticoagulant treatment,\n* Does not have diabetes or peripheral neuropathy,\n* No signs of infiltration or thrombophlebitis in the extremity where IR beam will be used,\n* Dialysis patients without arteriovenous fistula,\n* Does not have any communication problems and whose mental level does not cause any problems in participating in the research,\n* Patients who volunteer to participate in the research will be recruited.\n\nExclusion Criteria:\n\n* Sudden movements during PICK insertion,\n* Missing patient data","70 Years",{"count":20,"type":21},[24],"The study will be conducted in the Oncology and Cardiovascular Surgery (CVS) services of a university hospital. In the research, 30 patients will constitute the control group and 30 patients will constitute the experimental group. A nurse working in the clinics where the study will be conducted will perform the PIVK procedure, and we will randomly select the control and experimental groups and apply light to the area where the PIVK will be applied to the patients in the experimental groups with a flashlight that emits infrared rays for 10 minutes. The nurse will not be aware of whether the radiation application was made to the patient or not. The veins will be evaluated by the nurse performing PIVK. We will fill out the necessary forms in ANNEX 1 (control group) and APPENDIX 2 (experimental group) while the PIVK procedure is applied. After the procedure is completed, the patient's pain, anxiety and satisfaction level during the procedure will be marked. The data will be entered into the SPSS program and evaluated with statistical tests. According to the results, the effect of IR rays used before PIVK application on the patient's pain, anxiety and satisfaction and on the procedure time spent by the nurse for the application will be determined.",[382],"Questionnaire",[384,385,386],"vein","intravenous","nurse","2024-08-21",{"date":389,"type":39},"2024-08-23",{"date":391,"type":21},"2024-09-01",{"date":393,"type":21},"2024-09-30",{"name":45,"class":46},3,{"id":397,"slug":398,"hasResults":11,"nctId":399,"briefTitle":400,"officialTitle":401,"acronym":4,"eligibilityCriteria":402,"healthyVolunteers":84,"sex":17,"minAge":55,"maxAge":403,"enrollmentInfo":404,"targetDuration":4,"studyType":22,"phases":405,"briefSummary":406,"conditions":407,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":411,"lastUpdatePostDateStruct":412,"startDateStruct":414,"completionDateStruct":416,"leadSponsor":418,"locationsCount":47},"100531125","developing-a-simulation-for-parenteral-drug-administration-100531125","NCT06195722","Developing a Simulation for Parenteral Drug Administration","Karadeniz Technical University, Faculty of Health Sciences","Inclusion Criteria:\n\n* Those who have registered for the Fundamentals of Nursing II Course for the first time,\n* Having a computer, tablet or smartphone,\n* Having internet access,\n* Volunteer to participate in the research\n\nExclusion Criteria:\n\n* Having graduated from Health Vocational High School or studied a health-related department,\n* Have any previous experience of basic nursing skills","25 Years",{"count":196,"type":21},[24],"In the current Covid-19 pandemic process, distance education has become widespread and will continue to become widespread in the return to normal. In the distance education process, theoretical courses can be given with methods such as synchronous or asynchronous lectures, questions and answers, and discussion. However, in departments such as the nursing department, where laboratory and clinical practice are given during the term, there are some difficulties in providing the practice with distance education. Since students cannot be in clinical practice, they cannot develop their basic nursing skills. However, it is not possible for students to develop their skills in distance education. In addition, due to the high number of students in face-to-face teaching and the low number of lecturers, the lecturer and students cannot spend enough and effective time in the laboratories. Because there are 50-60 students per lecturer and therefore students are not sufficient in basic nursing skills. In order for students to improve their skills, there are technological methods that allow students to try the application on their own, at the desired place and time, without risking patient safety, in virtual environments, without entering the laboratory. Simulation opportunities can be provided to students by creating environments, models, materials and patients similar to the real hospital environment in virtual environments. It is seen in the literature that similar studies have been carried out outside of our country and are used in nursing education. However, in our country, a similar application was made in the virtual environment only in the thesis study of the director. This thesis study, which is similar to this project study, only includes tracheostomy care skill, which is one of the basic nursing skills. This project will include simulation parenteral drug administration skills in our work. For this reason, it will be the first simulation prepared for parenteral drug applications in our country. Drug administration constitutes an important step in patient safety. Although this section is explained theoretically, students are not given sufficient opportunities to have different drug doses prepared and administered in the laboratory. For this reason, when the student encounters a complex situation in the clinic, the decision-making process is prolonged and the risk of making mistakes increases.",[408,409,410],"Nursing Education","Cognitive Orientation","Injection Site","2024-06-22",{"date":413,"type":39},"2024-06-25",{"date":415,"type":21},"2024-07-01",{"date":417,"type":21},"2025-08-30",{"name":45,"class":46},""]