[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Yuzuncu Yil University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":495},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,18,0,[8,41,63,88,124,151,179,204,229,256,285,319,344,371,396,424,449,471],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":26,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100053845","investigation-of-the-effect-of-blood-pressure-on-bedsores-100053845",false,"NCT07696416","Investigation of the Effect of Blood Pressure on Bedsores","Investigation of the Effect of Blood Pressure on Bedsores in Adult Internal Medicine Intensive Care Patients","Inclusion Criteria:\n\n* Patients admitted to the intensive care unit,\n* Aged between 18-70 years,\n* Bedridden, immobile patients,\n* Patients who have signed the informed consent form themselves or through a close relative.\n\nExclusion Criteria:\n\n* Patients under 18 years of age,\n* Patients who did not give their consent for the study or whose relatives did not consent, or who wanted to leave while the study was ongoing,\n* Patients who arrived with bedsores","ALL","18 Years","70 Years",{"count":20,"type":21},148,"ESTIMATED","OBSERVATIONAL","The aim of this study is to comprehensively investigate the effect of blood pressure levels on the development of bedsores (pressure ulcers) in adult patients hospitalized in the internal medicine intensive care unit.",[25],"Decubitus Ulcer",[25,27,28],"Blood pressure","İntensive care","RECRUITING","2026-07-10",{"date":32,"type":33},"2026-07-13","ACTUAL",{"date":30,"type":33},{"date":36,"type":21},"2026-11-20",{"name":38,"class":39},"Yuzuncu Yil University","OTHER",1,{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":4,"eligibilityCriteria":47,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":48,"targetDuration":4,"studyType":50,"phases":51,"briefSummary":53,"conditions":54,"keywords":56,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":58,"startDateStruct":59,"completionDateStruct":60,"leadSponsor":62,"locationsCount":40},"100053901","the-effect-of-virtual-reality-application-diagnosed-with-myocardial-infarction-100053901","NCT07696390","The Effect of Virtual Reality Application Diagnosed With Myocardial Infarction","The Effect of Virtual Reality on Vital Signs and Anxiety in Myocardial Infarction Patients Admitted to Cardiology Intensive Care Unit: A Randomized Controlled Study.","Inclusion Criteria:\n\n1. The patient is in intensive care.\n2. The patient has been diagnosed with myocardial infarction.\n3. The patient is between 18 and 70 years old.\n4. The patient is conscious.\n5. The patient is oriented and cooperative.\n6. The patient volunteers to participate in the study.\n7. The patient is open to communication.\n8. The patient agrees to participate in the study.\n9. The patient has no mental, visual, auditory, or speech impairment.\n10. The patient has undergone stent placement.\n11. The patient has STEMI.\n\nExclusion Criteria:\n\n1. The patient has a psychiatric disorder.\n2. The patient has any communication impairment.",{"count":49,"type":21},50,"INTERVENTIONAL",[52],"NA","This study was designed to investigate the effects of VR (virtual reality) glasses on vital signs and anxiety in conscious patients diagnosed with myocardial infarction and admitted to the cardiology intensive care unit.",[55],"Myocardial Infarction",[57],"Myocardial infarction, virtual reality, vital signs, stress",{"date":32,"type":33},{"date":30,"type":33},{"date":61,"type":21},"2026-09-18",{"name":38,"class":39},{"id":64,"slug":65,"hasResults":11,"nctId":66,"briefTitle":67,"officialTitle":68,"acronym":4,"eligibilityCriteria":69,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":70,"targetDuration":4,"studyType":50,"phases":72,"briefSummary":73,"conditions":74,"keywords":77,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":80,"lastUpdatePostDateStruct":81,"startDateStruct":83,"completionDateStruct":85,"leadSponsor":87,"locationsCount":40},"100644924","the-effect-of-a-stress-ball-during-oral-care-procedures-100644924","NCT07676422","The Effect of a Stress Ball During Oral Care Procedures","The Effect of a Stress Ball on Pain, Anxiety, and Stress During Oral Care Procedures: A Randomized Controlled Experimental Study","Inclusion Criteria:\n\n* Being 18 years of age or older,\n* Being conscious and able to communicate,\n* Having an indication for oral care application,\n* Agreeing to participate in the study voluntarily.\n\nExclusion Criteria:\n\n* Being under heavy sedation,\n* Those with limited upper extremity movement,\n* Those with severe neurological disorders,\n* Having any problem with squeezing a ball in their hand (wound, fracture, weakness)\n\nTermination Criteria:\n\n* Those who wish to withdraw from the study,\n* Those who change institutions\u002Fcity,\n* The study will be terminated in the event of the patient's death.",{"count":71,"type":21},52,[52],"This study aims to evaluate the effect of using stress balls during oral care procedures performed on conscious patients in the intensive care unit on patients' pain, anxiety, and stress levels.",[75,76],"Pain","Stress",[78,79],"Stress ball","Oral Care Procedures","2026-06-29",{"date":82,"type":33},"2026-06-30",{"date":84,"type":33},"2026-05-25",{"date":86,"type":21},"2026-08-25",{"name":38,"class":39},{"id":89,"slug":90,"hasResults":11,"nctId":91,"briefTitle":92,"officialTitle":93,"acronym":4,"eligibilityCriteria":94,"healthyVolunteers":95,"sex":16,"minAge":96,"maxAge":4,"enrollmentInfo":97,"targetDuration":4,"studyType":50,"phases":99,"briefSummary":100,"conditions":101,"keywords":108,"overallStatus":115,"whyStopped":4,"lastUpdateSubmitDate":116,"lastUpdatePostDateStruct":117,"startDateStruct":119,"completionDateStruct":121,"leadSponsor":123,"locationsCount":4},"100644577","standardized-patients-in-arterial-pressure-monitoring-training-100644577","NCT07670364","Standardized Patients in Arterial Pressure Monitoring Training","The Effect of Using Standardized Patients in Arterial Blood Pressure Monitoring Training on Cognitive Load, Clinical Skills, and Self-Efficacy: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Being a undergraduate nursing student currently enrolled in the specified nursing department\u002Ffaculty.\n* Volunteering to participate in the study and providing written informed consent.\n* Taking the relevant clinical nursing course for the first time.\n* Having successfully completed the baseline theoretical lectures related to vital signs and basic invasive procedures.\n\nExclusion Criteria:\n\n* Having prior formal clinical experience or advanced training regarding invasive arterial blood pressure monitoring or line stabilization.\n* Having a known physical or visual impairment that would prevent the participant from performing psychomotor simulation tasks.\n* Repeating the academic year or the clinical course due to prior failure. --Withdrawing from the study voluntarily or failing to attend the mandatory 45-minute baseline theoretical training session.",true,"20 Years",{"count":98,"type":21},74,[52],"This study aims to evaluate and compare the effects of using standardized patients versus static manikins in nursing education for arterial blood pressure monitoring and stabilization training. The primary objective is to investigate the impact of these two different simulation methods on students' cognitive load, clinical skills, and self-efficacy levels.\n\nArterial pressure monitoring is a critical, invasive intervention commonly performed in intensive care units and operating rooms, requiring a high degree of precision. While traditional technical skill assessments usually focus solely on procedural success scores or completion speed, this study utilizes the framework of Cognitive Load Theory to examine the mental toll (intrinsic, extrinsic, and germane load) and psychological readiness (self-efficacy) experienced by nursing students during the procedure.\n\nThe study will be conducted as a randomized controlled experimental trial with 3rd-year nursing students who have successfully completed their Medical-Surgical Nursing course. Participants will be randomly assigned to either the experimental group or the control group:\n\nThe Experimental Group will receive theoretical and practical training, followed by performing the arterial pressure monitoring line stabilization on a \"Standardized Patient\" (an experienced healthcare professional acting a scenario with a moving limb to mimic real clinical chaos without any actual invasive intervention).\n\nThe Control Group will receive the same training but will perform the stabilization procedure on a traditional static medical manikin.\n\nData will be collected using a Descriptive Information and Performance Recording Form (to measure procedural time and error rates), the Cognitive Load Scale, and the Self-Efficacy Scale for Clinical Skills. Measurements will be taken at baseline (pre-test) and immediately after the intervention (post-test). The findings of this study are expected to provide evidence-based guidance for developing \"mind-friendly\" nursing curricula and safer, more realistic simulation protocols that enhance student self-efficacy while ensuring patient safety before entering actual clinical environments.",[102,103,104,105,106,107],"Arterial Pressure","Blood Pressure Determination","Simulation Training","Education, Nursing","Cognitive Load","Self Efficacy",[109,110,106,111,112,113,114],"Standardized Patient","Arterial Pressure Monitoring","Clinical Skills","Self-Efficacy","Nursing Education","Simulation-Based Training","NOT_YET_RECRUITING","2026-06-24",{"date":118,"type":33},"2026-06-26",{"date":120,"type":21},"2026-10-15",{"date":122,"type":21},"2026-12-30",{"name":38,"class":39},{"id":125,"slug":126,"hasResults":11,"nctId":127,"briefTitle":128,"officialTitle":129,"acronym":4,"eligibilityCriteria":130,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":131,"enrollmentInfo":132,"targetDuration":4,"studyType":50,"phases":134,"briefSummary":135,"conditions":136,"keywords":138,"overallStatus":115,"whyStopped":4,"lastUpdateSubmitDate":143,"lastUpdatePostDateStruct":144,"startDateStruct":146,"completionDateStruct":148,"leadSponsor":150,"locationsCount":40},"100642901","effect-of-emg-biofeedback-and-multimodal-exercise-on-temporomandibular-joint-dysfunction-100642901","NCT07577687","Effect of Emg-Biofeedback and Multimodal Exercise on Temporomandibular Joint Dysfunction","The Effect of Emg-Biofeedback Based Relaxation Training Added to a Multimodal Exercise Program on Pain and Function in Patients With Temporomandibular Joint Dysfunction","Inclusion Criteria:\n\n* Having been diagnosed with TMD, meaning having been diagnosed with Group 1 (1a: myofascial pain - 1b: referral myofascial pain) within Axis 1 according to the RDC\u002FTMD diagnostic system.\n* Having experienced TMJ pain for at least 3 months\n* Having a sufficient cognitive level to follow simple instructions and take tests.\n\nExclusion Criteria:\n\n* Having a malignant condition in the TMJ and\u002For cervical spine and having undergone surgery,\n* Having neurological or psychiatric disorders, pregnancy,\n* Having a history of BTA (Botulinum toxin injection) within the last year,\n* Having received physical therapy related to TMJ less than 6 months ago,\n* Being under orthodontic treatment,\n* Having uncontrolled diabetes,\n* Having inflammatory rheumatic diseases (rheumatoid arthritis, etc.)","65 Years",{"count":133,"type":21},40,[52],"Temporomandibular joint dysfunction (TMD) is a multifactorial musculoskeletal disorder affecting the masticatory muscles, temporomandibular joint, and related structures, characterized by pain and functional limitations. In TMD, myofascial pain is particularly prominent, leading to decreased mandibular range of motion, impaired masticatory function, and reduced quality of life. Current literature shows that conservative treatment approaches, especially multimodal physiotherapy programs, are effective in reducing TMD symptoms. However, evidence regarding the clinical effectiveness of adding EMG-Biofeedback-based relaxation training, aimed at increasing awareness of muscle activity, to multimodal treatment programs is limited. The aim of this randomized controlled trial is to investigate the effect of EMG-Biofeedback-based relaxation training, added to a multimodal exercise program, on pain levels and functional parameters in individuals diagnosed with temporomandibular joint dysfunction. Participants will be divided into two groups using a simple randomization method. The control group will receive multimodal physiotherapy consisting of manual therapy and a home exercise program, while the experimental group will receive EMG-Biofeedback-based relaxation training in addition to the same program. Assessments will be conducted before the intervention and at the end of the 4-week intervention.\n\nPain intensity will be measured with a Visual Analog Scale (VAS), pressure pain threshold with a digital algometer, mandibular joint range of motion with a linear scale, and cervical joint range of motion with a digital goniometer. Functional status will be assessed using the Fonseca Anamnestic Index, Neck Disability Index, and Oral Health Impact Profile-14. The obtained data will be compared using appropriate statistical analysis methods. This study is expected to provide scientific evidence regarding the clinical effectiveness of adding EMG-Biofeedback-based relaxation training to multimodal exercise programs in the conservative treatment of TMD and to contribute to filling the methodological gap mentioned in the literature.",[137],"Temporomandibular Joint Disease",[139,140,141,142],"Muscle Relaxation","Biofeedback","Exercise Therapy","Manual Therapy","2026-06-04",{"date":145,"type":33},"2026-06-09",{"date":147,"type":21},"2026-06-18",{"date":149,"type":21},"2026-12-15",{"name":38,"class":39},{"id":152,"slug":153,"hasResults":11,"nctId":154,"briefTitle":155,"officialTitle":156,"acronym":157,"eligibilityCriteria":158,"healthyVolunteers":95,"sex":16,"minAge":159,"maxAge":160,"enrollmentInfo":161,"targetDuration":4,"studyType":50,"phases":162,"briefSummary":163,"conditions":164,"keywords":166,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":171,"lastUpdatePostDateStruct":172,"startDateStruct":174,"completionDateStruct":176,"leadSponsor":178,"locationsCount":40},"100635419","orofacial-muscle-pressure-and-maxillary-transverse-development-100635419","NCT07552441","Orofacial Muscle Pressure and Maxillary Transverse Development","Investigation of the Effect of Lip, Cheek, and Tongue Muscle Pressure on Maxillary Transverse Development","OMPTD","Inclusion Criteria:Participants aged between 12 and 25 years.Diagnosed as Skeletal Class I (ANB angle: $0\\^\\\\circ$ to $4\\^\\\\circ$).Experimental Group: Clinical and radiographic diagnosis of maxillary transversal constriction.Control Group: Normal maxillary transversal width with no crossbite or constriction.Permanent dentition (excluding third molars).Good oral hygiene and no active periodontal disease.Ability to understand and follow instructions for the IOPI measurement protocol.\n\n\\-\n\nExclusion Criteria:Previous orthodontic or orthognathic surgical treatment.\n\nHistory of craniofacial anomalies or syndromes (e.g., cleft lip and palate).\n\nNeuromuscular disorders or systemic diseases affecting muscle function.\n\nHistory of trauma to the jaw or facial region.\n\nCongenitally missing teeth (hypodontia) or extensive prosthetic restorations.\n\nMacroglossia or severe tongue-tie (ankyloglossia).\n\nUse of medications that may influence muscle tone (e.g., muscle relaxants).\n\nPresence of large tonsils or adenoids that significantly obstruct the airway.\n\n\\-","12 Years","25 Years",{"count":133,"type":21},[52],"Study Title: Investigation of the Effects of Tongue, Lip, and Cheek Pressures on the Development of Upper Jaw Narrowness\n\nIntroduction and Hypothesis The structure of our face and the alignment of our teeth are influenced not only by our genetics but also by the surrounding soft tissues, such as the lips, cheeks, and tongue. These muscles exert constant pressure on our teeth and jawbones. According to the \"Equilibrium Theory,\" teeth stay in their proper positions when the inward pressure from the lips and cheeks is balanced by the outward pressure from the tongue.\n\nThe hypothesis of this study is that individuals with a narrow upper jaw (maxillary constriction) may have different muscle pressure patterns compared to those with normal jaw widths. We believe that identifying these pressure differences will help dentists and orthodontists better understand why jaw narrowness occurs and how to achieve more stable results after treatment.\n\nWhat is Being Measured? To measure these delicate pressures, we use a specialized, high-tech device called the Iowa Oral Performance Instrument (IOPI). This device uses a small, air-filled balloon (bulb) that the patient presses with their tongue or lips. It allows us to measure muscle strength and endurance in \"kilopascals\" (a unit of pressure) without any pain or discomfort.\n\nStudy Procedure\n\nThis study will involve patients aged 12 to 25 who are seeking orthodontic treatment at Van Yüzüncü Yıl University. We will divide the participants into two groups:\n\nPatients with a narrow upper jaw.\n\nPatients with a normal upper jaw width (the control group).\n\nBefore any orthodontic braces are applied, we will measure:\n\nTongue Pressure: How hard the tongue can push against the roof of the mouth.\n\nLip Pressure: The strength of the upper and lower lips.\n\nCheek (Buccal) Pressure: The pressure exerted by the cheeks during rest and function.\n\nImportance of the Study While many studies have looked at how these muscles affect the forward or backward position of teeth, there is very little research on how they affect the width of the jaw. By comparing these two groups, we hope to discover whether \"weak\" or \"overactive\" muscles contribute to a narrow palate. This information could lead to new treatment methods that focus not just on moving teeth, but also on training the oral muscles to ensure that the beautiful smiles created by orthodontists last a lifetime.",[165],"Maxillary Transversal Deficiency (Maxillary Constriction) and Perioral Muscle Pressures (Tongue, Lip, and Cheek)",[167,168,169,170],"Maxillary transversal deficiency","Perioral muscle pressure","Tongue and lip strength","Iowa Oral Performance Instrument (IOPI)","2026-04-20",{"date":173,"type":33},"2026-04-27",{"date":175,"type":21},"2026-05-01",{"date":177,"type":21},"2026-12-01",{"name":38,"class":39},{"id":180,"slug":181,"hasResults":11,"nctId":182,"briefTitle":183,"officialTitle":184,"acronym":4,"eligibilityCriteria":185,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":186,"enrollmentInfo":187,"targetDuration":4,"studyType":50,"phases":188,"briefSummary":189,"conditions":190,"keywords":194,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":196,"lastUpdatePostDateStruct":197,"startDateStruct":198,"completionDateStruct":200,"leadSponsor":202,"locationsCount":203},"100634475","the-effect-of-stress-ball-on-nausea-anxiety-and-fatigue-in-patients-with-stomach-cancer-100634475","NCT07540169","The Effect of Stress Ball on Nausea, Anxiety, and Fatigue in Patients With Stomach Cancer","The Effect of Stress Balls on Nausea, Anxiety, and Fatigue in Patients With Stomach Cancer","Inclusion Criteria:\n\n* Between the ages of 18-80\n* Those who agree to participate in the study\n* Those without motor skill loss\n* Patients diagnosed with stomach cancer\n* Patients with hand-arm orientation skills\n\nExclusion Criteria:\n\n* Patients with loss of motor skills\n* Patients who wish to withdraw from the study","80 Years",{"count":71,"type":21},[52],"In this study, we will observe the effects of the Stress Ball.",[191,192,193],"Stomach Cancer","Chemotherapy-induced Nausea and Vomiting","Fatigue",[195],"Stress Ball","2026-04-16",{"date":171,"type":33},{"date":199,"type":33},"2025-10-15",{"date":201,"type":21},"2026-05-24",{"name":38,"class":39},2,{"id":205,"slug":206,"hasResults":11,"nctId":207,"briefTitle":208,"officialTitle":209,"acronym":4,"eligibilityCriteria":210,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":131,"enrollmentInfo":211,"targetDuration":4,"studyType":50,"phases":212,"briefSummary":213,"conditions":214,"keywords":216,"overallStatus":115,"whyStopped":4,"lastUpdateSubmitDate":222,"lastUpdatePostDateStruct":223,"startDateStruct":225,"completionDateStruct":226,"leadSponsor":228,"locationsCount":40},"100633331","mulligans-mobilization-in-rotator-cuff-pathology-100633331","NCT07525297","Mulligan's Mobilization in Rotator Cuff Pathology","The Effect of Adding Thoracic Mobilization to Mulligan's Mobilization With Movement in Individuals With Rotator Cuff Pathology","Inclusion Criteria:\n\n* Having been diagnosed with unilateral rotator cuff pathology (impingement syndrome, tendinopathy, or partial tear) by a specialist physician through clinical examination and\u002For radiological imaging (USG\u002FMR);\n* Being between 18 and 65 years of age;\n* Having shoulder pain that has persisted for at least 3 months;\n* Having a positive result on at least two of the Neer, Hawkins-Kennedy, and Empty Can tests;\n* Having a pain intensity of at least 3\u002F10 on the Pain Numerical Rating Scale (NPRS) during rest or activity;\n* Having sufficient cognitive ability to follow simple instructions and administer the tests;\n* Having a Mini Mental State Test score ≥24;\n* Having the ability to provide signed informed consent and agreeing to participate in the study voluntarily.\n\nExclusion Criteria:\n\n* Having undergone previous surgery on the shoulder or thoracic region;\n* Having full-thickness rotator cuff tears requiring surgical indication;\n* Having adhesive capsulitis, shoulder instability, labrum tears, or calcific tendinitis;\n* Having cervical radiculopathy or neurological diseases affecting the upper extremity;\n* Having uncontrolled diabetes, inflammatory rheumatic diseases (rheumatoid arthritis, etc.), or malignancy;\n* Having severe osteoporosis, unstable vertebral fractures, or active infection in the thoracic region;\n\nhaving received steroid (cortisone) or PRP injections to the shoulder region within the last 3 months.",{"count":133,"type":21},[52],"Rotator cuff pathology is defined as the degeneration or tear of one or more of the muscles or tendons of the rotator cuff, namely the supraspinatus, infraspinatus, teres minor, and subscapularis. Shoulder girdle biomechanics are not solely comprised of the glenohumeral joint but are built upon a kinetic chain involving the synchronized movement of the scapula, clavicle, and thoracic spine. In this context, the concept described in the literature as the \"Regional Dependence\" model argues that functional impairment in a distal segment like the shoulder may stem from or exacerbate limitations in a more proximal region like the thoracic spine. Conventional treatment approaches that focus solely on the shoulder joint may have limited clinical outcomes due to neglecting the fundamental link in the kinetic chain. Maintained natural apophyseal glides (SNAGs), a cornerstone of Mulligan's Concept in spinal rehabilitation, are a dynamic manual therapy technique aimed at correcting microscopic misalignments in facet joints during active movement. The aim of this randomized controlled trial is to investigate the effects of thoracic mobilization added to the Mulligan movement shoulder mobilization technique on pain intensity, range of motion, proprioception, and upper extremity functionality in individuals with rotator cuff pathology, and to evaluate the superiority of this combined approach over shoulder mobilization alone. Assessments will be performed before treatment and at the end of the 3-week intervention. Rest and activity pain intensity will be assessed using the Pain Numerical Rating Scale (PMR), shoulder range of motion using a digital goniometer, thoracic kyphosis degrees using a smartphone with the 'Angle Meter' software installed and calibrated gyroscope and accelerometer sensors, functionality using the Shoulder Pain and Disability Index (SPAI), and proprioception using a laser pointer and target device. The obtained data will be compared using appropriate statistical analysis methods. This study is expected to provide scientific evidence regarding the clinical effectiveness of thoracic mobilization technique added to shoulder mobilization technique applied in conjunction with conventional treatment in individuals with rotator cuff pathology, and to contribute to filling the methodological gap mentioned in the literature.",[215],"Rotator Cuff Injuries",[217,218,219,220,221],"Rotator cuff injuries","Manual therapy","Exercise","Shoulder joint","Thoracic Vertebrae","2026-04-06",{"date":224,"type":33},"2026-04-13",{"date":171,"type":21},{"date":227,"type":21},"2026-10-20",{"name":38,"class":39},{"id":230,"slug":231,"hasResults":11,"nctId":232,"briefTitle":233,"officialTitle":234,"acronym":4,"eligibilityCriteria":235,"healthyVolunteers":11,"sex":236,"minAge":17,"maxAge":131,"enrollmentInfo":237,"targetDuration":239,"studyType":22,"phases":4,"briefSummary":240,"conditions":241,"keywords":243,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":249,"lastUpdatePostDateStruct":250,"startDateStruct":251,"completionDateStruct":253,"leadSponsor":255,"locationsCount":40},"100633185","joint-health-balance-and-quality-of-life-in-adults-with-hemophilia-a-100633185","NCT07523399","Joint Health, Balance and Quality of Life in Adults With Hemophilia A","Quality of Life in Adults With Hemophilia A: Associations With Joint Health, Pain, Dynamic Balance, and Falls","Inclusion Criteria:\n\n* Diagnosis of severe hemophilia A\n* Age ≥18 years\n* A minimum single-joint score of 3 points for the knee or ankle according to the Hemophilia Joint Health Score (HJHS)\n\nExclusion Criteria:\n\n* Use of walking aids (e.g., crutches)\n* Presence of neurological or psychiatric disorders, chronic inflammatory disease, -Regular use of medications that could affect balance,\n* History of major lower extremity surgery within the previous six months.","MALE",{"count":238,"type":21},36,"2 Weeks","Hemophilia is a hereditary bleeding disorder characterized by recurrent bleeding episodes, particularly into joints and muscles, leading to chronic musculoskeletal complications. Repeated joint bleeding may result in hemophilic arthropathy, which is associated with progressive joint damage, chronic pain, reduced mobility, and functional limitations. Advances in prophylactic treatment have significantly improved life expectancy in individuals with hemophilia; however, long-term musculoskeletal complications continue to affect daily functioning and overall well-being. Therefore, the evaluation of health-related quality of life (QoL) has become increasingly important in adults with hemophilia, as it reflects the broader impact of the disease beyond clinical severity.\n\nJoint health is considered one of the major determinants of physical functioning in people with hemophilia. Hemophilic arthropathy may lead to chronic pain, muscle weakness, reduced range of motion, and impaired physical performance. In addition to structural joint changes, impairments in neuromuscular function, including reduced proprioception, muscle strength, and postural control, may also contribute to activity limitations. Balance impairments may increase the risk of falls, which may be particularly relevant for individuals with hemophilia because fall-related trauma can lead to bleeding episodes and further joint deterioration. Although previous studies have investigated the relationship between joint health, pain, and functional limitations, the combined contribution of joint health, pain severity, dynamic balance performance, and fall history to QoL in adults with hemophilia has not been sufficiently clarified.\n\nThis prospective cross-sectional study aims to evaluate QoL in adults with hemophilia and to investigate the associations of joint health, pain severity, dynamic balance performance, and fall history with QoL outcomes. The study includes 36 adults diagnosed with severe hemophilia A who are followed at the Adult Hematology Unit of Van Yuzuncu Yil University. Participants aged 18 years and older who met the inclusion criteria were recruited consecutively. Individuals using walking aids, having neurological or psychiatric disorders, chronic inflammatory diseases, recent lower extremity surgery, or regular medication use that could affect balance were excluded.\n\nJoint health is assessed using the Hemophilia Joint Health Score (HJHS), a clinician-administered tool evaluating joint impairment in the knees and ankles. Dynamic balance is assessed using a computerized stabilometric platform (Pro-kin Tecnobody Stabilometric Analysis System) with the Limits of Stability (LoS) test, which evaluates the ability to voluntarily control the center of pressure within the base of support. Pain intensity is measured using the Numeric Pain Rating Scale (NPRS), an 11-point scale ranging from 0 to 10. Fall history is determined based on the self-reported number of falls within the previous 12 months. QoL is assessed using the Turkish version of the Haemophilia-Specific Quality of Life Questionnaire for adults (Haem-A-QoL), a validated patient-reported outcome measure evaluating multiple domains of physical, emotional, and social well-being. Higher scores indicate poorer QoL.\n\nThe findings of this study are expected to improve the understanding of factors associated with QoL in adults with hemophilia and may help identify potentially modifiable clinical targets for rehabilitation interventions.",[242],"Hemophilia A",[244,242,245,246,247,248],"Quality of life","Arthropathy","Postural balance","Falls","Musculoskeletal Pain","2026-04-04",{"date":224,"type":33},{"date":252,"type":33},"2026-02-21",{"date":254,"type":21},"2026-05-21",{"name":38,"class":39},{"id":257,"slug":258,"hasResults":11,"nctId":259,"briefTitle":260,"officialTitle":261,"acronym":4,"eligibilityCriteria":262,"healthyVolunteers":11,"sex":16,"minAge":263,"maxAge":131,"enrollmentInfo":264,"targetDuration":4,"studyType":50,"phases":265,"briefSummary":266,"conditions":267,"keywords":270,"overallStatus":115,"whyStopped":4,"lastUpdateSubmitDate":277,"lastUpdatePostDateStruct":278,"startDateStruct":280,"completionDateStruct":282,"leadSponsor":284,"locationsCount":4},"100624995","the-effects-of-dual-task-exercises-on-parameters-after-total-knee-arthroplasty-100624995","NCT07416877","The Effects of Dual-Task Exercises on Parameters After Total Knee Arthroplasty","The Effects of Dual-Task Exercises on Pain, Balance, Function, and Reaction Time After Total Knee Arthroplasty","Inclusion Criteria:\n\n* Mini Mental State Test score ≥24; ability to provide signed informed consent and voluntary agreement to participate in the study.\n* Underwent primary unilateral total knee replacement surgery.\n* Being between 50 and 65 years old\n\nExclusion Criteria:\n\n* Having undergone revision or bilateral knee replacement surgery,\n* Having experienced postoperative complications,\n* Having undergone lower extremity surgery,\n* Having a neurological disease.","50 Years",{"count":133,"type":21},[52],"Introduction: Total knee arthroplasty (TKA) is a widely used surgical treatment method worldwide for advanced pain and functional loss resulting from osteoarthritis and other degenerative knee pathologies. The aim of TKA is to reduce pain, restore joint function, and improve quality of life. Although many patients experience a significant reduction in pain after surgery, balance problems, risk of falls, and functional limitations may persist in the postoperative period.In addition, loss of performance may occur in daily tasks requiring motor-cognitive interaction (e.g., talking while walking, changing direction while carrying objects).The dual-task paradigm describes exercises and assessments that require the simultaneous execution of both motor and cognitive tasks; in rehabilitation, it aims to improve daily living functions by targeting the simultaneous functioning of motor and cognitive systems.In the literature, studies on dual-task assessment and training in individuals with knee osteoarthritis and TKA are limited, and the findings are heterogeneous. Studies in elderly and osteoarthritic populations have reported that both single-task and dual-task training improve balance performance, but dual-task training does not always show a clear superiority compared to single-task training. These studies have generally focused on balance and gait parameters; evidence on how other clinically important variables such as pain, reaction time, and fear of movement (kinesiophobia) change with dual-task interventions is insufficient and inconsistent.\n\nMethod: The effect size of the WOMAC Osteoarthritis Index assessment parameter in the reference article is 1.02. It was calculated that a minimum of 20 individuals in total, 10 in each group, were required for a study with 80% power, using a type I error of α=0.05 and a type II error of β=0.20.After obtaining informed consent from all participants, their sociodemographic information will be recorded. Subsequently, their cognitive status will be assessed using the Mini Mental State Test (MMSE).Pain will be assessed using the Numerical Pain Rating Scale (NPRS). Functional mobility will be assessed using the Timed Up and Go (TUG). Dynamic balance will be assessed using the Functional Reach Test. Static balance will be assessed using the Berg Balance Scale (BBS). Functionality will be assessed using the WOMAC Osteoarthritis Index. Kinesiophobia will be assessed using the Tampa Kinesiophobia Scale (TKS). Lower extremity reaction time will be assessed using the Fitlight Trainer (FITLIGHT Sports Corp., Ontario, Canada), a wireless system consisting of 8 sensors.Interventions: After participants were randomly divided into two groups, those in the control group would perform a physiotherapy program consisting of strengthening and balance exercises at home, provided by us, and would not participate in any other exercise program during the study period. Exercises would be taught to the control group in person by a physiotherapist at the time of the initial assessment, and follow-up sessions would be video-recorded. The intervention group's program would be a dual-task exercise program, in addition to the exercises provided in the home exercise program. Interventions would last for 8 weeks, 2 days a week, and the program would be updated weekly.",[268,269],"Total Knee Arthroplasty","Dual Task Exercises",[271,272,273,274,275,276],"Total knee arthroplasty","dual task exercises","exercise","reaction time","functionality","kinesiophobia","2026-02-11",{"date":279,"type":33},"2026-02-18",{"date":281,"type":21},"2026-02-15",{"date":283,"type":21},"2026-09-15",{"name":38,"class":39},{"id":286,"slug":287,"hasResults":11,"nctId":288,"briefTitle":289,"officialTitle":290,"acronym":4,"eligibilityCriteria":291,"healthyVolunteers":11,"sex":16,"minAge":292,"maxAge":293,"enrollmentInfo":294,"targetDuration":4,"studyType":50,"phases":295,"briefSummary":296,"conditions":297,"keywords":304,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":311,"lastUpdatePostDateStruct":312,"startDateStruct":314,"completionDateStruct":316,"leadSponsor":318,"locationsCount":40},"100617754","the-effect-of-massage-on-sleep-quality-stress-comfort-and-vital-signs-in-preterm-infants-100617754","NCT07322731","The Effect of Massage on Sleep Quality, Stress, Comfort, and Vital Signs in Preterm Infants","The Effect of Massage on Sleep Quality, Stress, Comfort, and Vital Signs in Preterm Infants: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Preterm infants born between 35-37 weeks gestational age.\n* Admitted to the neonatal intensive care unit (NICU).\n* Medically stable and cleared for massage therapy by neonatologist.\n* Parental\u002Fguardian consent obtained.\n\nExclusion Criteria:\n\n* Infants with congenital anomalies or major medical complications.\n* Infants requiring mechanical ventilation or intensive respiratory support.\n* Infants with known neurological disorders.\n* Parental\u002Fguardian refusal or inability to participate.","35 Months","37 Months",{"count":133,"type":21},[52],"This randomized controlled trial investigates the effects of massage therapy on sleep quality, stress, comfort, and vital signs in preterm infants (gestational age 35-37 weeks) admitted to the Neonatal Intensive Care Unit (NICU) at Van YYU Training and Research Hospital. Infants in the intervention group will receive a 15-minute massage three times a day for three consecutive days, while the control group will receive standard care. Data will be collected using the Premature Infant Comfort Scale, Neonatal Stress Scale, actigraphy for sleep monitoring, and vital sign measurements. The study aims to determine whether massage therapy can improve the overall well-being and development of preterm infants in NICU settings.",[298,299,300,301,302,303],"Premature Infants","Sleep Quality","İnfant Stress","İnfant Comfort","Vital Signs","NICU",[305,306,303,307,308,309,310],"Preterm infants","neonatal massage","sleep quality","stress reduction","comfort","vital signs","2025-12-22",{"date":313,"type":33},"2026-01-07",{"date":315,"type":33},"2025-08-15",{"date":317,"type":21},"2026-06-15",{"name":38,"class":39},{"id":320,"slug":321,"hasResults":11,"nctId":322,"briefTitle":323,"officialTitle":324,"acronym":325,"eligibilityCriteria":326,"healthyVolunteers":95,"sex":327,"minAge":17,"maxAge":4,"enrollmentInfo":328,"targetDuration":4,"studyType":50,"phases":330,"briefSummary":331,"conditions":332,"keywords":334,"overallStatus":115,"whyStopped":4,"lastUpdateSubmitDate":336,"lastUpdatePostDateStruct":337,"startDateStruct":339,"completionDateStruct":341,"leadSponsor":343,"locationsCount":40},"100611070","vr-episiotomy-simulation-impact-on-midwifery-students-skills-and-self-efficacy-veses-100611070","NCT07235800","VR Episiotomy Simulation: Impact on Midwifery Students' Skills and Self-Efficacy (VESES)","The Effect of Virtual Reality-Based Episiotomy Simulation on Midwifery Students' Skills and Self-Efficacy Levels","VESES","Inclusion Criteria:\n\n* Able to speak and understand Turkish\n\nHave not received previous episiotomy training\n\nNo medical conditions preventing the use of virtual reality (e.g., epilepsy)\n\nEnrolled as a third-year midwifery student at Van Yüzüncü Yıl University Faculty of Health Sciences\n\nExclusion Criteria:\n\n* Individuals who do not speak or understand Turkish\n\nThose who have previously received episiotomy training\n\nParticipants with medical conditions contraindicating the use of virtual reality (e.g., epilepsy)\n\nNot enrolled as a third-year midwifery student at Van Yüzüncü Yıl University Faculty of Health Sciences","FEMALE",{"count":329,"type":21},87,[52],"This study aims to develop and evaluate a virtual reality (VR)-based episiotomy training simulation for midwifery students. Episiotomy is a surgical procedure performed during childbirth, and incorrect application may lead to serious psychological and physiological consequences. While traditional training methods often use animal tissues or synthetic materials, recent advances in technology have introduced simulation-based learning. VR technology has shown potential to enhance learning outcomes, confidence, and satisfaction among healthcare students. Despite its growing use in medical education, there is currently no VR training model specifically designed for teaching episiotomy skills. This study will design a VR episiotomy simulation, assess its effectiveness in skill acquisition and learning, and propose it as a new educational method in midwifery training.",[333],"Use of Virtual Reality Simulation in Midwifery Training",[335],"Midwifery Virtual Reality Simulation Episiotomy Learning Process","2025-11-14",{"date":338,"type":33},"2025-11-19",{"date":340,"type":21},"2025-12-21",{"date":342,"type":21},"2026-04",{"name":38,"class":39},{"id":345,"slug":346,"hasResults":11,"nctId":347,"briefTitle":348,"officialTitle":349,"acronym":4,"eligibilityCriteria":350,"healthyVolunteers":11,"sex":16,"minAge":351,"maxAge":159,"enrollmentInfo":352,"targetDuration":4,"studyType":50,"phases":353,"briefSummary":354,"conditions":355,"keywords":358,"overallStatus":115,"whyStopped":4,"lastUpdateSubmitDate":363,"lastUpdatePostDateStruct":364,"startDateStruct":366,"completionDateStruct":368,"leadSponsor":370,"locationsCount":40},"100604121","69--5000-the-effect-of-mandala-painting-on-pain-stress-and-sleep-quality-in-children-hospitalized-in-the-burn-unit-a-randomized-controlled-study-100604121","NCT07145398","69 \u002F 5.000 THE EFFECT OF MANDALA PAINTING ON PAIN, STRESS, AND SLEEP QUALITY IN CHILDREN HOSPITALIZED IN THE BURN UNIT: A RANDOMIZED CONTROLLED STUDY","THE EFFECT OF MANDALA PAINTING ON PAIN, STRESS, AND SLEEP QUALITY IN CHILDREN HOSPITALIZED IN THE BURN UNIT: A RANDOMIZED CONTROLLED STUDY","Inclusion Criteria:\n\n* Both the parent and the child are willing to participate in the study.\n* Child is between 6 and 12 years of age.\n* Burn degree is 1st or 2nd degree.\n* The child does not have an acute psychiatric diagnosis (e.g., severe anxiety disorder, psychotic conditions).\n* The child has basic fine motor skills (e.g., ability to hold a pencil, ability to color).\n* The child does not have any chronic illness.\n* The child has newly initiated burn treatment.\n\nExclusion Criteria:\n\n* Parent or child is not willing to participate in the study.\n* Burn degree is 3rd or 4th degree.\n* The child has any chronic illness.\n* The child has a developmental disorder.\n* The child has visual perception impairments (e.g., color blindness, severe visual loss).","6 Years",{"count":133,"type":21},[52],"The mandala coloring method allows patients to focus their attention on a circle and use colors with repetitive movements. This state of focus and relaxation can have positive effects on anxiety and other negative moods. There are a limited number of studies in the literature on the use of mandala coloring in children. Therefore, the study was designed to investigate the effects of mandala coloring on pain, stress, and sleep quality in children hospitalized in the burn unit.",[356,357],"Pediatric Burns","Pediatric Burn",[359,360,361,362,307],"pediatric burn","mandala painting","paın","stress","2025-08-27",{"date":365,"type":33},"2025-08-28",{"date":367,"type":21},"2025-08-25",{"date":369,"type":21},"2026-06-05",{"name":38,"class":39},{"id":372,"slug":373,"hasResults":11,"nctId":374,"briefTitle":375,"officialTitle":376,"acronym":4,"eligibilityCriteria":377,"healthyVolunteers":95,"sex":16,"minAge":17,"maxAge":131,"enrollmentInfo":378,"targetDuration":4,"studyType":50,"phases":380,"briefSummary":381,"conditions":382,"keywords":384,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":389,"lastUpdatePostDateStruct":390,"startDateStruct":391,"completionDateStruct":393,"leadSponsor":395,"locationsCount":40},"100604014","prevention-of-emergence-agitation-in-rhinoplasty-with-subanesthetic-propofol-and-single-dose-dexmedetomidine-a-prospective-double-blind-clinical-study-100604014","NCT07144007","Prevention of Emergence Agitation in Rhinoplasty With Subanesthetic Propofol and Single-Dose Dexmedetomidine: A Prospective Double-Blind Clinical Study","Van Yuzuncu Yil University Faculty of Medicine Ethics Committee","Inclusion Criteria:\n\n* Patients scheduled for rhinoplasty\n* Between 18-65 years\n* ASA I-II group\n\nExclusion Criteria:\n\n* Those who are outside the age range of 18-65\n* Those who are ASA III and above\n* Those with renal,hepatic, cardiac and respiratory diseases\n* Those with a known allergy to the medication to be used\n* Those who underwent urinary catheterization",{"count":379,"type":21},80,[52],"To compare of prevention of emergence agitation in rhinoplasty with subanesthetic propofol and single dose dexmedetomidine",[383],"Emergence Agitation",[385,386,387,388],"emergence agitaion","Propofol","Dexmedetomidine","Rhinoplasty","2025-08-26",{"date":363,"type":33},{"date":392,"type":33},"2025-04-15",{"date":394,"type":21},"2026-02-01",{"name":38,"class":39},{"id":397,"slug":398,"hasResults":11,"nctId":399,"briefTitle":400,"officialTitle":401,"acronym":4,"eligibilityCriteria":402,"healthyVolunteers":95,"sex":327,"minAge":17,"maxAge":403,"enrollmentInfo":404,"targetDuration":4,"studyType":50,"phases":406,"briefSummary":407,"conditions":408,"keywords":410,"overallStatus":115,"whyStopped":4,"lastUpdateSubmitDate":416,"lastUpdatePostDateStruct":417,"startDateStruct":419,"completionDateStruct":421,"leadSponsor":423,"locationsCount":4},"100591866","the-efficacy-of-intrathecal-morphine-versus-intrathecal-morphine-dexamethasone-combination-in-cesarean-delivery-100591866","NCT06985992","The Efficacy of Intrathecal Morphine Versus Intrathecal Morphine-Dexamethasone Combination in Cesarean Delivery","The Efficacy of Intrathecal Morphine Versus Intrathecal Morphine-Dexamethasone Combination in Cesarean Delivery: A Prospective Randomized Double-Blind Clinical Trial","Inclusion Criteria:\n\n* Patients scheduled for caesarean sections\n* Between 18-40 years\n* ASA II group\n* Those who will undergo spinal anesthesia\n* Those between 35-40 weeks of pregnancy\n* 1st and 2nd caesarean sections\n\nExclusion Criteria:\n\n* Those who prefer general anesthesia\n* Those who are outside the age range of 18-40\n* Those who are ASA III and above\n* Those with HT, DM, cardiac and respiratory diseases\n* Preeclampsia, eclampsia, HELLP\n* Those with a history of drug use that affects the cardiovascular system\n* Placenta Previa, Placenta Acreta, Placenta Acreta Those with a history of antiemetic or antidepressant drug use","40 Years",{"count":405,"type":21},120,[52],"The Efficacy of Intrathecal Morphine Versus Intrathecal Morphine+Dexamethasone Combination added to bupivacaine in elective cesarean section under spinal anesthesia",[409],"Caesarean Section",[411,412,413,414,415],"Caesarean section","morphine","dexamethasone","nausea-vomiting","postoperative complications","2025-05-22",{"date":418,"type":33},"2025-05-29",{"date":420,"type":21},"2025-07-01",{"date":422,"type":21},"2025-11-01",{"name":38,"class":39},{"id":425,"slug":426,"hasResults":11,"nctId":427,"briefTitle":428,"officialTitle":376,"acronym":4,"eligibilityCriteria":429,"healthyVolunteers":95,"sex":327,"minAge":17,"maxAge":403,"enrollmentInfo":430,"targetDuration":4,"studyType":50,"phases":431,"briefSummary":432,"conditions":433,"keywords":435,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":441,"lastUpdatePostDateStruct":442,"startDateStruct":444,"completionDateStruct":446,"leadSponsor":448,"locationsCount":40},"100589588","to-compare-the-effects-of-oxytocin-and-carbetocin-on-intraoperative-hemodynamic-changes-in-cesarean-section-surgeries-100589588","NCT06956365","To Compare the Effects of Oxytocin and Carbetocin on Intraoperative Hemodynamic Changes in Cesarean Section Surgeries.","Inclusion Criteria:\n\n* Patients scheduled for caesarean sections\n* Between 18-40 years\n* ASA I-II group\n* Those who will undergo general anesthesia\n* Those between 35-40 weeks of pregnancy\n* 1st and 2nd caesarean sections\n\nExclusion Criteria:\n\n* Those who prefer spinal or epidural anesthesia\n* Those who are outside the age range of 18-40\n* Those who are ASA III and above\n* Those with HT, DM, cardiac and respiratory diseases\n* Preeclampsia, eclampsia, HELLP\n* Those with a history of drug use that affects the cardiovascular system\n* Placenta Previa, Placenta Acreta, Placenta Acreta",{"count":379,"type":21},[52],"To compare the effects of oxytocin and carbetocin, used as uterotonics in elective caesarean section surgeries, in terms of intraoperative hemodynamic changes.",[434],"Cesarean Section",[436,437,438,439,440],"Cesarean section","Oxytocin","Carbetocin","Uterotonic","Intraoperative bleeding","2025-04-24",{"date":443,"type":33},"2025-05-04",{"date":445,"type":33},"2024-05-14",{"date":447,"type":21},"2025-07-30",{"name":38,"class":39},{"id":450,"slug":451,"hasResults":11,"nctId":452,"briefTitle":453,"officialTitle":453,"acronym":4,"eligibilityCriteria":454,"healthyVolunteers":95,"sex":327,"minAge":455,"maxAge":456,"enrollmentInfo":457,"targetDuration":4,"studyType":50,"phases":459,"briefSummary":460,"conditions":461,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":463,"lastUpdatePostDateStruct":464,"startDateStruct":466,"completionDateStruct":468,"leadSponsor":470,"locationsCount":40},"100571410","web-based-newborn-care-education-for-primiparous-pregnant-women-100571410","NCT06719895","Web-Based Newborn Care Education for Primiparous Pregnant Women","Inclusion Criteria:\n\n* Aged between 15 and 19 years\n* Being 19 years old and above\n* Being literate\n* Being primigravida\n* Having a single baby (not twins or more)\n* Being a volunteer to participate in the study\n* Having no health problems for the mother and the baby\n* Having a computer, tablet or smart phone and the ability to use it\n* Having regular internet access\n\nExclusion Criteria:\n\n* The mother being 18 years of age or younger\n* Being multigravida and\u002For multiparous\n* Having a health problem related to the mother or the baby\n* Not having a smart phone or wireless internet during the study period\n* Not filling out the survey forms incompletely and not watching videos about hygienic care of the newborn","19 Years","35 Years",{"count":458,"type":21},100,[52],"For pregnant women expecting their first baby, readiness during pregnancy is an important factor in successfully performing hygienic care for their babies. This study was planned to determine the effect of web-based education on the readiness levels of primiparous pregnant women for newborn hygienic care practices. In this study, the aim was to support pregnant women and mothers after birth in newborn care and to develop their application skills with the web-based education program given to primiparous pregnant women.",[462],"Web Based Education","2024-12-05",{"date":465,"type":33},"2024-12-06",{"date":467,"type":33},"2024-11-19",{"date":469,"type":21},"2025-01-10",{"name":38,"class":39},{"id":472,"slug":473,"hasResults":11,"nctId":474,"briefTitle":475,"officialTitle":476,"acronym":4,"eligibilityCriteria":477,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":478,"targetDuration":479,"studyType":22,"phases":4,"briefSummary":480,"conditions":481,"keywords":483,"overallStatus":115,"whyStopped":4,"lastUpdateSubmitDate":487,"lastUpdatePostDateStruct":488,"startDateStruct":490,"completionDateStruct":492,"leadSponsor":494,"locationsCount":4},"100564013","34salivary-melatonin-and-cortisol-levels-in-individuals-with-bruxism34-100564013","NCT06623643",""Salivary Melatonin and Cortisol Levels in Individuals with Bruxism"","The Investigation of Melatonin and Cortisol Levels in the Saliva of Individuals with Bruxism","Inclusion Criteria:\n\n\\- Individuals without any known hormonal diseases, not using antidepressants or medications that could alter saliva content, without degenerative diseases affecting the salivary glands, without cysts or tumors affecting the temporomandibular region, and not undergoing insomnia treatment will be included in the study\n\nExclusion Criteria:\n\n* Individuals with systemic diseases that affect or may potentially affect saliva content, or those using medications that cause these effects, will not be included in the study",{"count":458,"type":21},"1 Day","The effects of the hormones melatonin and cortisol, which play a highly effective role in regulating the sleep-wake cycle, on teeth grinding will be scientifically evaluated. Based on the research results, more effective methods for treating patients suffering from bruxism may be identified.",[482],"Bruxism",[484,485,486],"melatonin","saliva","cortizol","2024-10-02",{"date":489,"type":33},"2024-10-04",{"date":491,"type":21},"2024-10-30",{"date":493,"type":21},"2025-02-28",{"name":38,"class":39},""]