[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Çanakkale Onsekiz Mart University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":326},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,12,0,[8,48,76,99,124,148,176,201,231,251,276,299],{"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},"100632966","comparison-of-lateral-internal-sphincterotomy-techniques-for-chronic-anal-fissure-100632966",false,"NCT07520552","Comparison of Lateral Internal Sphincterotomy Techniques for Chronic Anal Fissure","A Prospective Randomized Controlled Trial Comparing Spasm-Controlled, Fissure Apex-Limited, and Dentate Line-Limited Lateral Internal Sphincterotomy Techniques in Chronic Anal Fissure","SPHINX","Inclusion Criteria:\n\n* Age 18 years or older\n* Diagnosis of chronic anal fissure (duration ≥8 weeks)\n* Failure to heal after at least 6 weeks of appropriate medical treatment (topical agents, fiber supplementation, sitz baths)\n* Complete preoperative fecal continence (Wexner Incontinence Score = 0)\n* Primary anal fissure (posterior or anterior midline location)\n* Written informed consent\n\nExclusion Criteria:\n\n* Any degree of preoperative fecal incontinence\n* Secondary anal fissure (associated with Crohn's disease, tuberculosis, HIV, syphilis, or other systemic conditions)\n* Previous anal sphincter surgery\n* History of obstetric sphincter injury\n* Active anorectal infection (abscess or fistula)\n* Pregnancy or breastfeeding\n* Uncorrectable coagulopathy or current anticoagulant use\n* Inability to cooperate with study procedures or attend follow-up visits","ALL","18 Years",{"count":20,"type":21},150,"ESTIMATED","INTERVENTIONAL",[24],"NA","This prospective randomized controlled trial compares three lateral internal sphincterotomy (LIS) techniques in patients with chronic anal fissure refractory to medical treatment: (1) Spasm-Controlled LIS (serial small sphincterotomies using an anal calibrator until 30 mm anal caliber is achieved, under local anesthesia plus sedation), (2) LIS up to the Fissure Apex (spinal or general anesthesia), and (3) LIS up to the Dentate Line (spinal or general anesthesia). The primary outcomes are fissure healing rate and fecal incontinence incidence at 12 months, assessed using the Wexner Incontinence Score. Secondary outcomes include postoperative pain (VAS), recurrence rate, patient satisfaction, and complications. A total of 150 patients (50 per group) will be enrolled and followed for 12 months.",[27],"Chronic Anal Fissure",[29,30,31,32,33,34],"Chronic anal fissure","Lateral internal sphincterotomy","Spasm-controlled sphincterotomy","Fecal incontinence","Dentate line","Fissure apex","RECRUITING","2026-05-12",{"date":38,"type":39},"2026-05-14","ACTUAL",{"date":41,"type":39},"2026-05-06",{"date":43,"type":21},"2028-05-06",{"name":45,"class":46},"Çanakkale Onsekiz Mart University","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":54,"eligibilityCriteria":55,"healthyVolunteers":56,"sex":57,"minAge":58,"maxAge":59,"enrollmentInfo":60,"targetDuration":4,"studyType":22,"phases":62,"briefSummary":63,"conditions":64,"keywords":4,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":73,"leadSponsor":75,"locationsCount":4},"100634528","microgreens-and-mirnas-100634528","NCT07540858","Microgreens and miRNAs","The Effect of Mikrofiliz Application on Serum miRNA Levels Associated With Muscle Damage, Recovery, and the Central Nervous System Following Eccentric Loading","GreenmiRNAs","Inclusion Criteria:Recreationally trained athletes were recruited and randomly allocated to either a microgreen supplementation group or a control group. Inclusion criteria were: (i) being an active athlete, (ii) absence of medical contraindications to exercise (verified by medical clearance), (iii) voluntary participation, and (iv) full adherence to the study protocol.\n\n\\-\n\nExclusion Criteria: Exclusion criteria included: recent musculoskeletal injury (within 6 months), chronic disease or regular medication use, lack of structured training in the previous year, and smoking or alcohol consumption. Participants failing to comply with the protocol, experiencing adverse events, or engaging in high-intensity physical activity during the follow-up period were withdrawn\n\n\\-",true,"MALE","19 Years","24 Years",{"count":61,"type":21},15,[24],"In this study, we investigated the impact of a comprehensive microgreen and wheatgrass juice protocol on the miRNA response following a standardized EIMD model and whether microgreen consumption could modulate key miRNA markers of neuromuscular regeneration and metabolic adaptation, thereby offering a novel nutritional approach to enhancing holistic recovery in athletes.",[65,66,67],"Exercise Training","Microgreens","miRNAs","NOT_YET_RECRUITING","2026-04-15",{"date":71,"type":39},"2026-04-20",{"date":36,"type":21},{"date":74,"type":21},"2026-07-30",{"name":45,"class":46},{"id":77,"slug":78,"hasResults":11,"nctId":79,"briefTitle":80,"officialTitle":81,"acronym":4,"eligibilityCriteria":82,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":83,"targetDuration":4,"studyType":22,"phases":85,"briefSummary":86,"conditions":87,"keywords":89,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":91,"lastUpdatePostDateStruct":92,"startDateStruct":94,"completionDateStruct":96,"leadSponsor":98,"locationsCount":47},"100620572","the-effect-of-breathing-exercises-on-compassion-fatigue-and-work-tress-among-emergency-department-nurses-100620572","NCT07359365","The Effect of Breathing Exercises on Compassion Fatigue and Work Tress Among Emergency Department Nurses","The Effect of Breathing Exercises on Compassion Fatigue and Work Stress Among Emergency Department Nurses: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Currently employed as an emergency department nurse.\n* No diagnosed psychiatric disorders.\n* No prior participation in breathing exercise programs.\n\nExclusion Criteria:\n\n* Presence of respiratory system disease.\n* Physical conditions that prevent participation in breathing exercises.\n* Working outside the emergency department.",{"count":84,"type":21},64,[24],"The purpose of this randomized controlled study is to examine the effect of breathing exercises on compassion fatigue and work stress among emergency department nurses",[88],"Work Stress",[90],"compassion fatigue","2026-03-23",{"date":93,"type":39},"2026-03-27",{"date":95,"type":21},"2026-04-01",{"date":97,"type":21},"2027-01-01",{"name":45,"class":46},{"id":100,"slug":101,"hasResults":11,"nctId":102,"briefTitle":103,"officialTitle":104,"acronym":4,"eligibilityCriteria":105,"healthyVolunteers":11,"sex":17,"minAge":106,"maxAge":4,"enrollmentInfo":107,"targetDuration":4,"studyType":22,"phases":109,"briefSummary":110,"conditions":111,"keywords":113,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":116,"lastUpdatePostDateStruct":117,"startDateStruct":119,"completionDateStruct":121,"leadSponsor":123,"locationsCount":47},"100628483","effect-of-telenursing-on-oral-health-100628483","NCT07462221","Effect of Telenursing on Oral Health","The Effect of Telenursing Interventions on Oral Health in Individuals With COPD","Inclusion Criteria:\n\n* Participants must have been diagnosed with COPD for at least 6 months,\n* receive inpatient treatment in internal medicine and surgical clinics,\n* signed the informed consent form to participate in the study,\n* have internet access and a mobile device with Android\u002FiOS operating system,\n* be able to use a phone,\n* ≥ 40 years old,\n* have no communication barriers,\n* mild (Stage 1), moderate (Stage 2), severe (Stage 3), or very severe (Stage 4) stages according to the GOLD (2023) report.\n\nExclusion Criteria:\n\n* Those diagnosed with COPD less than 6 months ago,\n* Those receiving outpatient treatment,\n* Those hospitalized in the intensive care unit,\n* Those without internet access and a mobile device with Android\u002FiOS operating system,\n* Those who do not have the ability to use a phone,\n* Those under 40 years of age,\n* Those with communication barriers,\n* Those who wish to withdraw from the research\u002Fwithdraw from participation during the research process,","40 Years",{"count":108,"type":21},80,[24],"This research will be conducted using a pre-test and post-test control group experimental design to evaluate the effect of telenursing intervention on oral health in individuals with COPD.",[112],"COPD",[114,115,112],"oral health","tele-nursing","2026-03-05",{"date":118,"type":39},"2026-03-10",{"date":120,"type":21},"2026-03-04",{"date":122,"type":21},"2026-06-30",{"name":45,"class":46},{"id":125,"slug":126,"hasResults":11,"nctId":127,"briefTitle":128,"officialTitle":129,"acronym":4,"eligibilityCriteria":130,"healthyVolunteers":11,"sex":17,"minAge":131,"maxAge":4,"enrollmentInfo":132,"targetDuration":4,"studyType":22,"phases":133,"briefSummary":134,"conditions":135,"keywords":137,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":116,"lastUpdatePostDateStruct":142,"startDateStruct":144,"completionDateStruct":146,"leadSponsor":147,"locationsCount":47},"100622249","the-effect-of-nhaler-training-and-reminders-on-medication-on-adherence-in-elderly-individuals-100622249","NCT07381166","The Effect of İnhaler Training and Reminders on Medication on Adherence in Elderly Individuals","The Effect Of Metered-Dose İnhaler Training And Reminders On Medication Adherence In Elderly Individuals: A Randomized Controlled Study","Inclusion criteria for the study:\n\n* Age ≥ 65 years old\n* Having at least basic literacy,\n* Receiving metered-dose inhaler therapy for at least 6 months,\n* Being hospitalized in the pulmonary ward,\n* Presenting to the pulmonary function test unit,\n* Presenting to the pulmonary outpatient clinic,\n* Signing the informed consent form for participation in the study,\n* Having internet access and a mobile device with Android\u002FiOS operating system,\n* Being able to use a telephone,\n* Having no communication barriers,\n* Being able to use the inhaler without needing assistance,\n* Making an error in at least one of the usage steps according to the MDI usage skills chart.\n\nExclusion criteria for the study:\n\n* Age \\\u003C65\n* Illiteracy\n* Receiving metered-dose inhaler therapy for \\\u003C6 months\n* Outpatient treatment\n* Being hospitalized in the intensive care unit\n* Being hospitalized in wards other than the pulmonary ward (such as surgery, physical therapy)\n* Visiting outpatient clinics other than the pulmonary clinic (such as surgery, physical therapy)\n* Not signing the informed consent form for participation in the study\n* Not having internet access and a mobile device with Android\u002FiOS operating system\n* Not having telephone skills\n* Having communication barriers\n* Requiring assistance while using the inhaler\n* Not making any errors in the usage steps according to the MDI usage skills chart\n* Wanting to withdraw from the study\u002Fwithdrawing from participation during the research process\n* Not completing the questionnaire","65 Years",{"count":84,"type":21},[24],"This study will evaluate the effect of metered-dose inhaler training and reminders on treatment adherence in elderly individuals.",[136],"Elderly (People Aged 65 or More)",[138,139,140,141],"elderly","Metered Dose Inhalers","reminder","adherence to treatment",{"date":143,"type":39},"2026-03-09",{"date":145,"type":39},"2026-01-21",{"date":74,"type":21},{"name":45,"class":46},{"id":149,"slug":150,"hasResults":11,"nctId":151,"briefTitle":152,"officialTitle":153,"acronym":4,"eligibilityCriteria":154,"healthyVolunteers":56,"sex":17,"minAge":155,"maxAge":156,"enrollmentInfo":157,"targetDuration":4,"studyType":22,"phases":159,"briefSummary":160,"conditions":161,"keywords":163,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":169,"lastUpdatePostDateStruct":170,"startDateStruct":171,"completionDateStruct":173,"leadSponsor":175,"locationsCount":47},"100612164","detection-of-residual-caries-on-class-ii-cavity-walls-in-primary-teeth-following-atraumatic-restorative-treatment-art-100612164","NCT07250022","Detection of Residual Caries on Class II Cavity Walls in Primary Teeth Following Atraumatic Restorative Treatment (ART)","Detection of Residual Caries on Class II Cavity Walls in Primary Teeth Following Atraumatic Restorative Treatment (ART): A Comparative Evaluation of Fluorescence-Aided Caries Excavation (FACE), Caries Detection Dye, and Clinical Assessment","Inclusion Criteria:\n\n* Age 4-9 years at enrollment\n* Healthy children who can cooperate with dental examination\n* Multi-surface carious cavities that are asymptomatic (no acute symptoms)\n* Written informed consent from parent\u002Fguardian and assent from the child\n\nExclusion Criteria:\n\n* Acute dental infection present\n* Any systemic disease\u002Fcondition\n* Lack of cooperation during the procedure\n* Refusal to participate \u002F informed consent not obtained from parent\u002Fguardian and\u002For assent not obtained from the child","4 Years","9 Years",{"count":158,"type":21},212,[24],"The primary aim of this study is to compare the diagnostic agreement and effectiveness of three different methods-Fluorescence-Aided Caries Excavation (FACE), caries detection dye, and clinical observation-in detecting residual caries remaining on cavity walls of primary teeth following Atraumatic Restorative Treatment (ART). Through this comparison, the study seeks to identify the method that provides more reliable and accurate results, thereby contributing to clinical practice by guiding clinicians and supporting the development of strategies to enhance the long-term success of ART.",[162],"Primary Dental Caries",[164,165,166,167,168],"dentin caries","dental atraumatic restorative treatment","primary teeth","FACE","residual caries","2026-01-17",{"date":145,"type":39},{"date":172,"type":39},"2025-12-20",{"date":174,"type":21},"2026-02-15",{"name":45,"class":46},{"id":177,"slug":178,"hasResults":11,"nctId":179,"briefTitle":180,"officialTitle":181,"acronym":4,"eligibilityCriteria":182,"healthyVolunteers":56,"sex":17,"minAge":183,"maxAge":184,"enrollmentInfo":185,"targetDuration":4,"studyType":22,"phases":187,"briefSummary":188,"conditions":189,"keywords":4,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":193,"lastUpdatePostDateStruct":194,"startDateStruct":196,"completionDateStruct":198,"leadSponsor":199,"locationsCount":200},"100618024","effects-of-silver-diamine-fluoride-and-intraoral-cryotherapy-on-local-anesthesia-in-mih-affected-molars-100618024","NCT07326241","Effects of Silver Diamine Fluoride and Intraoral Cryotherapy on Local Anesthesia in MIH-Affected Molars","Effects of Silver Diamine Fluoride and Intraoral Cryotherapy on Local Anesthesia Efficacy in Permanent Molars With Molar-Incisor Hypomineralization","Inclusion Criteria:\n\n* Children aged between 6 and 12 years.\n* Systemically healthy children with no medical conditions that could interfere with dental treatment.\n* Presence of at least one permanent first molar affected by molar-incisor hypomineralization (MIH), diagnosed according to the European Academy of Paediatric Dentistry (EAPD) criteria.\n* Teeth with caries lesions classified as ICDAS II codes 2, 3, 4, 5, or 6.\n* Children with an adequate level of cooperation to allow completion of dental treatment under clinical conditions.\n* Children and their parents\u002Flegal guardians who have read, understood, and signed the informed consent form and agreed to participate in the study.\n\nExclusion Criteria:\n\n* Teeth that are not restorable.\n* Children with a known allergy or hypersensitivity to any materials used in the study, including local anesthetics, silver diamine fluoride, or restorative materials.\n* Presence of spontaneous pain, percussion sensitivity, or other signs\u002Fsymptoms of pulpal pathology in the study tooth.\n* Children with systemic diseases or conditions that could affect pain perception, healing, or cooperation during dental treatment.\n* Children who are unable or unwilling to complete the clinical procedure.","6 Years","12 Years",{"count":186,"type":21},75,[24],"Molar-incisor hypomineralization (MIH) is a developmental enamel defect of unclear etiology that affects permanent first molars and often permanent incisors, leading to increased porosity, hypersensitivity, and poor prognosis. The porous structure of MIH-affected enamel facilitates bacterial penetration, which may cause subclinical pulpal inflammation and reduce the effectiveness of local anesthesia during dental procedures. Achieving adequate anesthesia in children with MIH can be challenging, resulting in increased discomfort, anxiety, and behavioral management difficulties.\n\nCryotherapy has been shown to reduce pain by decreasing local inflammation and slowing nerve conduction, while silver diamine fluoride (SDF) has demonstrated efficacy in reducing dentin hypersensitivity through tubule occlusion, antibacterial activity, and remineralization. This study aims to evaluate the effects of intraoral cryotherapy and silver diamine fluoride application on pain perception and the efficacy of local anesthesia during operative dental procedures in MIH-affected permanent first molars.",[190,191,192],"MIH","Molar-Incisor Hypomineralization","Caries Assessment","2025-12-24",{"date":195,"type":39},"2026-01-08",{"date":197,"type":21},"2026-02-01",{"date":95,"type":21},{"name":45,"class":46},2,{"id":202,"slug":203,"hasResults":11,"nctId":204,"briefTitle":205,"officialTitle":206,"acronym":4,"eligibilityCriteria":207,"healthyVolunteers":56,"sex":17,"minAge":208,"maxAge":184,"enrollmentInfo":209,"targetDuration":4,"studyType":22,"phases":211,"briefSummary":212,"conditions":213,"keywords":218,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":224,"lastUpdatePostDateStruct":225,"startDateStruct":226,"completionDateStruct":228,"leadSponsor":230,"locationsCount":47},"100603238","effect-of-ai-supported-child-friendly-communication-on-dental-anxiety-in-pediatric-patients-100603238","NCT07133919","Effect of AI-Supported Child-Friendly Communication on Dental Anxiety in Pediatric Patients","Evaluation of the Effect of Traditional Behavior Management Techniques and AI-Assisted Child-Friendly Communication on Dental Anxiety in Pediatric Dental Anesthesia Applications","Inclusion Criteria:\n\n* Children volunteers and their parents\u002Flegal guardians who have read and signed the informed consent form and agreed to participate in the study\n* Systemically healthy children aged 6-12 years in the mixed dentition period\n* Children requiring restorative dental procedures (including pulpotomy, pulp capping, or composite restorations) on mandibular teeth under inferior alveolar nerve block local anesthesia\n* Children who are attending their first dental visit and demonstrate behavior rated as 2 (negative) or 3 (positive) according to the Frankl Behavior Rating Scale (Categories: 1 - definitely negative; 2 - negative; 3 - positive; 4 - definitely positive) Behaviors will be categorized as positive (+) or negative (-) based on the Frankl Behavior Rating Scale (Wright's modification)\n* Children receiving local anesthesia for the first time\n\nExclusion Criteria:\n\n* Children volunteers and their parents\u002Flegal guardians who read the informed consent form but declined to participate in the study\n* Children with systemic diseases requiring continuous medication\n* Children with mental or cognitive impairments, as well as those with visual or hearing disabilities\n* Children who, after oral prophylaxis at the first visit, exhibit \"definitely negative\" (Frankl 1) or \"definitely positive\" (Frankl 4) behavior according to the Frankl Behavior Rating Scale\n* Children with previous experience of local anesthesia","7 Years",{"count":210,"type":21},60,[24],"This study compares the effects of traditional behavior management techniques and AI-assisted child-friendly communication on dental anxiety, physiological stress, and pain perception during local anesthesia in healthy children aged 6-12. The aim is to evaluate the effectiveness of AI-supported communication tools in reducing anxiety and improving comfort in pediatric dental treatments, potentially enhancing clinical outcomes and advancing technology use in pediatric dentistry.",[214,215,216,217],"Caries, Dental","Local Anesthesia","Inferior Alveolar Nerve Block","Dental Anxiety",[219,220,221,222,223],"dental anesthesia","dental anxiety","pediatric dentistry","pediatric patients","inferior alveolar nerve block","2025-12-22",{"date":193,"type":39},{"date":227,"type":39},"2025-10-15",{"date":229,"type":21},"2026-01",{"name":45,"class":46},{"id":232,"slug":233,"hasResults":11,"nctId":234,"briefTitle":235,"officialTitle":236,"acronym":4,"eligibilityCriteria":237,"healthyVolunteers":56,"sex":17,"minAge":155,"maxAge":156,"enrollmentInfo":238,"targetDuration":4,"studyType":22,"phases":239,"briefSummary":240,"conditions":241,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":243,"lastUpdatePostDateStruct":244,"startDateStruct":246,"completionDateStruct":248,"leadSponsor":250,"locationsCount":47},"100565721","smart-with-different-modifications-in-asymptomatic-deep-carious-lesions-of-primary-molars-100565721","NCT06645860","SMART With Different Modifications in Asymptomatic Deep Carious Lesions of Primary Molars.","Silver Modified Atraumatic Restorative Technique (SMART) With Different Modifications in Asymptomatic Deep Carious Lesions of Primary Molars.","Inclusion Criteria:\n\n1. Patients and parents of the patients who accept to participate and sign the informed consent.\n2. Children between the ages of 4-9\n3. Healthy children without a history of serious systemic conditions necessitating chronic use of medications.\n4. Children whose dental examination reveals at least one untreated asymptomatic cavitated carious lesion (ICDAS II index: code 4,5,6) affecting primary molars.\n5. Absence of former history of spontaneous pain from the offending tooth\u002Fteeth.\n6. Patients with an appropriate level of cooperation to complete treatment under clinical conditions.\n7. Teeth are in a restorable condition.\n8. Natural exfoliation of primary teeth to be treated should not be expected within two years.\n\nExclusion Criteria:\n\n1. Patients and parents of the patients who does not accept to participate and sign the informed consent\n2. Patients with proven allergy to silver compounds or any component of dental materials to be applied.\n3. Patients with special health care needs or any medical conditions.\n4. Primary molar teeth with excessive crown damage that cannot be restored.\n5. Primary molar teeth in which bone loss exceeds 1\u002F3 of the roots.\n6. Primary molar teeth that have previously undergone root canal treatment or pulpotomy treatment.\n7. Presence of internal\u002Fexternal and root resorption in primary teeth to be treated.\n8. Root fracture, ankylosis or mobility in the primary teeth to be treated.",{"count":20,"type":21},[24],"This study aimed to evaluate the clinical success of the 'Silver Modified Atraumatic Restorative Technique '(SMART) with different modifications in asymptomatic deep carious lesions of primary molars.",[242],"Caries; Dentin","2025-08-05",{"date":245,"type":39},"2025-08-08",{"date":247,"type":39},"2025-01-01",{"date":249,"type":21},"2026-01-01",{"name":45,"class":46},{"id":252,"slug":253,"hasResults":11,"nctId":254,"briefTitle":255,"officialTitle":256,"acronym":4,"eligibilityCriteria":257,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":258,"targetDuration":4,"studyType":22,"phases":259,"briefSummary":260,"conditions":261,"keywords":263,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":268,"lastUpdatePostDateStruct":269,"startDateStruct":271,"completionDateStruct":273,"leadSponsor":275,"locationsCount":47},"100595063","effect-of-nutrition-education-on-the-quality-of-life-chronic-disease-adaptation-in-patients-with-thyroid-dysfunction-100595063","NCT07027579","Effect of Nutrition Education on the Quality of Life, Chronic Disease Adaptation in Patients With Thyroid Dysfunction","The Effect of Nutrition Education Program on the Quality of Life and Chronic Disease Adaptation in Patients With Thyroid Dysfunction","Inclusion Criteria:\n\n* Not having any physical or mental disabilities\n* Not having received such training before\n* Volunteering to participate in the study\n* Be 18 years of age or older.\n\nExclusion Criteria:\n\n* Being under 18 years of age.\n* Having cognitive dysfunction.\n* Not volunteering to participate in the study.",{"count":210,"type":21},[24],"This thesis study is designed to examine the effects of nutrition education provided to individuals with thyroid dysfunction on their quality of life and adaptation to the disease. The data will be collected using the Descriptive Characteristics Form, the Nutrition Attitude Scale, the Quality of Life Scale for Thyroid Patients (ThyPRO), and the Chronic Illness Adherence Scale. The Body Mass Index (BMI) of participating patients will be calculated by the researcher based on measured height and weight. Laboratory values including TSH, free T4, and free T3 will be obtained from the patients' medical records on the day of assessment. Data collection will be conducted in two phases. The study population will consist of all patients diagnosed with thyroid dysfunction who present to Dr. Burhan Nalbantoğlu Hospital. Using the G\\*Power 3.1.9.2 software, the required sample size was calculated prior to data collection with a 95% confidence level. For correlation analysis, an alpha value of 0.05, an effect size of 0.455, and a statistical power of 95% were assumed, resulting in a minimum sample size of 56 participants (30 per group). Accounting for potential data loss, a total of 60 patients (30 per group) are planned to be included in the sample.",[262],"Thyroid Disease",[264,265,266,267],"Thyroid Dysfunction","Quality of Life","Chronic Disease Adaptation","Nutrition Education Program","2025-06-11",{"date":270,"type":39},"2025-06-18",{"date":272,"type":21},"2025-07-20",{"date":274,"type":21},"2025-12-30",{"name":45,"class":46},{"id":277,"slug":278,"hasResults":11,"nctId":279,"briefTitle":280,"officialTitle":281,"acronym":4,"eligibilityCriteria":282,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":131,"enrollmentInfo":283,"targetDuration":4,"studyType":22,"phases":284,"briefSummary":285,"conditions":286,"keywords":288,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":292,"lastUpdatePostDateStruct":293,"startDateStruct":295,"completionDateStruct":297,"leadSponsor":298,"locationsCount":200},"100590104","the-effect-of-education-and-tele-follow-up-program-on-diabetes-self-management-and-blood-glucose-regulation-100590104","NCT06963073","The Effect of Education and Tele-Follow-Up Program on Diabetes Self-Management and Blood Glucose Regulation","Effect of Education and Tele-Follow-Up Program Given to New Type 2 Diabetes Patients on Diabetes Self-Management and Blood Glucose Regulation","Inclusion Criteria:\n\n1. Volunteering to participate in the study.\n2. Having recently been diagnosed with Type 2 Diabetes.\n3. Not having cognitive dysfunction.\n4. Not having done diabetes education before.\n\nExclusion Criteria:\n\n1. Being under 18 years of age.\n2. Having cognitive dysfunction.\n3. Not volunteering to participate in the study.",{"count":210,"type":21},[24],"This study is designed as a randomized controlled trial to determine the effects of education and the Tele-Follow-up program on the disease knowledge, self-management, and blood glucose regulation of newly diagnosed Type 2 diabetes patients.",[287],"Diabetes Mellitus, Type 2",[289,290,291],"Diabetes Mellitus","Self-Management","Blood Glucose Regulation","2025-05-06",{"date":294,"type":39},"2025-05-08",{"date":296,"type":21},"2025-06-15",{"date":274,"type":21},{"name":45,"class":46},{"id":300,"slug":301,"hasResults":11,"nctId":302,"briefTitle":303,"officialTitle":304,"acronym":4,"eligibilityCriteria":305,"healthyVolunteers":56,"sex":17,"minAge":18,"maxAge":131,"enrollmentInfo":306,"targetDuration":4,"studyType":22,"phases":308,"briefSummary":309,"conditions":310,"keywords":313,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":318,"lastUpdatePostDateStruct":319,"startDateStruct":321,"completionDateStruct":323,"leadSponsor":325,"locationsCount":47},"100565480","the-effect-of-laughter-yoga-on-nurses-burnout-level-and-stress-100565480","NCT06642727","The Effect of Laughter Yoga on Nurses' Burnout Level and Stress","The Effect of Laughter Yoga on Nurses' Burnout Level and Stress: Randomized Controlled Study","Inclusion Criteria:\n\n* Being a nurse working day and night shifts\n* Not having participated in laughter yoga sessions before\n* Being willing to participate in the study\n\nExclusion Criteria:\n\n* Having a physical condition that prevents participation in laughter yoga sessions (hernia, hemorrhoids, vertigo, respiratory disorders, urinary incontinence, epilepsy)\n* Not being a nurse\n* Working continuously day or continuously night shifts",{"count":307,"type":21},50,[24],"The purpose of this clinical trial is to determine the effect of laughter yoga on the burnout levels and stress of nurses. The main questions of the study are as follows:\n\n1. What is the burnout level of nurses in the control and intervention groups?\n2. What is the stress level of nurses in the control and intervention groups?\n3. Has there been a change in the burnout levels of nurses practicing laughter yoga?\n4. Has there been a change in the stress levels of nurses practicing laughter yoga? To compare whether laughter yoga affects burnout and stress levels, participants will be divided into control and experimental groups. The experimental group will undergo laughter yoga sessions twice a week for one month.",[311,312],"Burnout","Stress",[314,315,316,317],"BURNOUT","stress","nurse","Laughter Yoga","2024-10-11",{"date":320,"type":39},"2024-10-15",{"date":322,"type":21},"2024-11",{"date":324,"type":21},"2027-01",{"name":45,"class":46},""]