[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Trakya University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":331},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,12,0,[8,43,77,106,130,151,174,201,226,257,285,309],{"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":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100619779","early-effects-of-orthognathic-surgery-on-periodontal-phenotype-a-6-month-prospective-clinical-and-radiographic-evaluation-100619779",false,"NCT07349056","Early Effects of Orthognathic Surgery on Periodontal Phenotype: A 6-Month Prospective Clinical and Radiographic Evaluation","Evaluation of Periodontal Phenotype Following Orthognathic Surgery: A Two-Center, 6-Month Prospective Clinical and CBCT Study","Inclusion Criteria:\n\n* Adults aged ≥18 years.\n* Presence of a Class III molar relationship of any severity at baseline.\n* Presence of a Class II molar relationship of any severity at baseline.\n* Presence of transverse arch discrepancies.\n* Presence of vertical maxillary excess.\n* Presence of maxillary and\u002For mandibular asymmetry.\n* Presence of anterior open bite.\n* Full permanent dentition up to the first molars, with no supernumerary teeth and no agenesis (congenital absence) of teeth up to the first molars.\n* No previous orthodontic treatment.\n* No history of tooth extraction other than second or third molars.\n* Availability of complete baseline and end-of-follow-up periodontal parameters and phenotype records suitable for evaluation.\n* Healthy periodontium with no signs of gingival hypertrophy.\n* No systemic disease history or medication use that could affect gingival\u002Fperiodontal conditions.\n\nExclusion Criteria:\n\n* Patients planned for orthodontic camouflage treatment with fixed appliances for Class II\u002FClass III correction instead of orthognathic surgery.\n* History of interproximal enamel reduction (interproximal stripping).\n* Presence of dental implants.\n* Age \\\u003C 18 years.\n* Pregnant or breastfeeding individuals.\n* Any systemic condition contraindicates orthognathic surgery.\n* Psychiatric disorders.\n* Syndromic conditions.\n* History of previous orthognathic surgery.\n* Refusal to sign the informed consent form.\n* Individuals belonging to a vulnerable population.","ALL","18 Years","65 Years",{"count":20,"type":21},100,"ESTIMATED","OBSERVATIONAL","The goal of this observational study is to learn how the health and thickness of the gums and supporting bone around the teeth change over 6 months in adults having jaw surgery to correct the bite. The main questions it aims to answer are:\n\n* Do gum and tooth-support measurements change from before surgery to 1, 3, and 6 months after surgery?\n* Do CT scan-based measurements of the tooth-supporting bone change over the same time period?\n\nParticipants will:\n\n* Have a gum check-up (periodontal examination) before surgery and at 1, 3, and 6 months after surgery.\n* Have CT scan-based measurements (CBCT) taken at the same time points for study assessment.",[25,26,27,28,29],"Gingival Biotype","Gingival Phenotype","Buccal Bone Thickness","Recession, Gingival","Dental Surgery","RECRUITING","2026-06-05",{"date":33,"type":34},"2026-06-08","ACTUAL",{"date":36,"type":34},"2026-02-23",{"date":38,"type":21},"2027-02-23",{"name":40,"class":41},"Trakya University","OTHER",2,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":50,"targetDuration":4,"studyType":52,"phases":53,"briefSummary":55,"conditions":56,"keywords":61,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":4},"100638234","hyperangulated-vs-standard-videolaryngoscopy-vs-direct-laryngoscopy-for-double-lumen-endobronchial-tube-intubation-100638234","NCT07614529","Hyperangulated vs Standard Videolaryngoscopy vs Direct Laryngoscopy for Double-Lumen Endobronchial Tube Intubation","Evaluation of Efficacy and Safety of Hyperangulated and Standard Curvature Blade Video Laryngoscopy Versus Direct Laryngoscopy for Double-Lumen Endobronchial Tube Intubation","Inclusion Criteria:\n\n* Age 18 years or older\n* Written informed consent obtained prior to surgery\n* ASA physical status class I, II, or III\n* Scheduled for elective thoracic surgery requiring one-lung ventilation and double-lumen endobronchial intubation\n\nExclusion Criteria:\n\n* Age under 18 years\n* Refusal or inability to provide informed consent\n* ASA physical status class IV or above\n* Emergency surgery\n* Anticipated difficult airway, defined by any of the following: Mallampati score 4, thyromental distance less than 6.5 cm, restricted mouth opening, or BMI greater than 30 kg\u002Fm²\n* History of upper airway surgery\n* Significant upper airway obstruction or stridor\n* Pregnancy",{"count":51,"type":21},180,"INTERVENTIONAL",[54],"NA","This is a prospective, randomized, single-center, three-arm, open-label, low-risk medical device clinical study conducted at the Department of Anesthesiology and Reanimation, Trakya University Medical Faculty.\n\nThe study aims to compare the efficacy, safety, and clinical usability of three laryngoscopy methods for double-lumen endotracheal tube (DLT) intubation in patients undergoing elective thoracic surgery requiring one-lung ventilation: (i) C-MAC hyperangulated (D-blade) videolaryngoscopy, (ii) C-MAC Macintosh blade videolaryngoscopy, and (iii) direct Macintosh laryngoscopy.\n\nThe primary outcome is the total time to successful DLT placement (in seconds), defined as the interval from the end of mask ventilation to fiberoptic bronchoscopic confirmation of correct tube position. Secondary outcomes include glottic visualization quality (POGO score and Cormack-Lehane grade), intubation difficulty (Intubation Difficulty Scale), number of intubation attempts, need for auxiliary maneuvers, intubation-related complications, malposition rate, and postoperative airway symptoms (sore throat, dysphonia) assessed at 1, 6, and 24 hours postoperatively.\n\nEligible patients are adults (≥18 years), ASA class I-III, scheduled for elective thoracic surgery requiring one-lung ventilation. Patients with anticipated difficult airway, emergency surgery, pregnancy, or prior upper airway surgery are excluded. A total of 180 patients will be enrolled and randomized 1:1:1 into three groups (60 per group) using computer-generated block randomization.",[57,58,59,60],"Endobronchial Intubation","Double Lumen Tube Intubation","Thoracic Surgery","One Lung Ventillation (OLV)",[62,63,64,65,66,67],"double-lumen endotracheal tube","videolaryngoscopy","direct laryngoscopy","C-MAC","thoracic anesthesia","one-lung ventilation","NOT_YET_RECRUITING","2026-05-28",{"date":71,"type":34},"2026-05-29",{"date":73,"type":21},"2026-05-15",{"date":75,"type":21},"2029-01-15",{"name":40,"class":41},{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":4,"eligibilityCriteria":83,"healthyVolunteers":11,"sex":16,"minAge":84,"maxAge":4,"enrollmentInfo":85,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":87,"conditions":88,"keywords":92,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":105},"100629939","frailty-and-nottingham-hip-fracture-score-for-predicting-90-day-mortality-after-hip-fracture-surgery-100629939","NCT07481188","Frailty and Nottingham Hip Fracture Score for Predicting 90-Day Mortality After Hip Fracture Surgery","Incremental Prognostic Value of Frailty Beyond the Nottingham Hip Fracture Score for Predicting 90-Day Mortality After Hip Fracture Surgery: A Prospective Cohort Study","Inclusion Criteria:\n\n* Age 60 years or older\n* Admission for acute proximal femoral fracture (femoral neck, intertrochanteric, or subtrochanteric fracture)\n* Surgical treatment for hip fracture\n* Ability to obtain clinical data required for NHFS and frailty assessment\n\nExclusion Criteria:\n\n* Pathological fractures\n* Periprosthetic fractures\n* Hip fractures resulting from high-energy trauma or polytrauma\n* Non-operative treatment\n* Second hip fracture occurring in the same patient during the study period","60 Years",{"count":86,"type":21},200,"Hip fractures are serious injuries that occur mostly in older adults. Many people experience health problems or may die in the months after surgery. Doctors try to identify patients who have a higher risk of poor outcomes as early as possible.\n\nDoctors often use the Nottingham Hip Fracture Score (NHFS) to estimate the risk of death after hip fracture surgery. This score uses information such as age and other health conditions. However, it does not fully reflect how physically vulnerable a person may be.\n\nAnother important concept is frailty. Frailty describes how strong or weak a person's overall health and physical reserve are. In this study, frailty will be measured using the Clinical Frailty Scale (CFS). This scale evaluates a person's level of independence and physical function before the fracture.\n\nThe purpose of this study is to determine whether measuring frailty can improve the prediction of death after hip fracture surgery.\n\nOlder adults with hip fractures who undergo surgery will be invited to participate in the study. Researchers plan to include about 200 participants or all eligible patients enrolled within one year, whichever occurs first. Health information that is already collected during routine hospital care will be recorded. Frailty will be assessed when participants are admitted to the hospital.\n\nParticipants will be followed for 30 days and 90 days after surgery to determine survival status. Researchers will review hospital records and may contact participants or their relatives by phone if needed.\n\nThe results of this study may help doctors better identify patients at higher risk and improve care planning after hip fracture surgery.",[89,90,91],"Hip Fracture","Proximal Femur Fracture","Frailty",[93,94,91,95,96],"Hip fracture","Proximal femur fracture","Geriatric fracture","Mortality prediction","2026-03-25",{"date":99,"type":34},"2026-03-31",{"date":101,"type":34},"2026-03-15",{"date":103,"type":21},"2027-03-15",{"name":40,"class":41},1,{"id":107,"slug":108,"hasResults":11,"nctId":109,"briefTitle":110,"officialTitle":111,"acronym":4,"eligibilityCriteria":112,"healthyVolunteers":113,"sex":16,"minAge":17,"maxAge":114,"enrollmentInfo":115,"targetDuration":4,"studyType":52,"phases":117,"briefSummary":118,"conditions":119,"keywords":4,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":122,"lastUpdatePostDateStruct":123,"startDateStruct":125,"completionDateStruct":127,"leadSponsor":129,"locationsCount":105},"100628680","the-effects-of-kinesio-taping-on-heel-rise-endurance-and-gastrocnemius-muscle-oxygenation-in-healthy-young-adults-100628680","NCT07464795","The Effects of Kinesio Taping on Heel-Rise Endurance and Gastrocnemius Muscle Oxygenation in Healthy Young Adults","Acute Effects of Kinesio Taping on Heel-Rise Endurance and Gastrocnemius Muscle Oxygenation: A Randomized Controlled Crossover Trial","Inclusion Criteria:\n\n* Young adults aged 18-25 years\n* Cumberland Ankle Instability Tool score of ≥28\n\nExclusion Criteria:\n\n* Sedentary (\\\u003C150 min\u002Fweek moderate or \\\u003C75 min\u002Fweek vigorous physical activity)\n* Elite athletes\n* History of ankle sprain\n* Lower extremity fracture\n* Surgical intervention\n* Neurological or vestibular disorders",true,"25 Years",{"count":116,"type":21},34,[54],"acilitative kinesio taping (KT) is commonly used by athletes to support muscle performance and delay fatigue. However, evidence regarding its effects on muscle endurance and oxygenation remains inconsistent. This study aims to investigate the acute effects of facilitative KT applied to the gastrocnemius muscle on heel-rise endurance performance and local muscle oxygenation in healthy young adults.\n\nIn this randomized crossover trial, participants will complete two experimental sessions: one with facilitative kinesio taping and one with sham taping. After taping application, participants will perform a single-leg heel-rise test to task failure. Muscle oxygenation will be continuously monitored using a portable near-infrared spectroscopy device. The findings of this study may contribute to understanding whether kinesio taping has immediate physiological and performance-related effects on calf muscle endurance.",[120,121],"Endurance Calf Test","KINESIOTAPING","2026-03-06",{"date":124,"type":34},"2026-03-11",{"date":126,"type":21},"2026-04-01",{"date":128,"type":21},"2026-10-01",{"name":40,"class":41},{"id":131,"slug":132,"hasResults":11,"nctId":133,"briefTitle":134,"officialTitle":135,"acronym":4,"eligibilityCriteria":136,"healthyVolunteers":113,"sex":16,"minAge":137,"maxAge":138,"enrollmentInfo":139,"targetDuration":4,"studyType":52,"phases":141,"briefSummary":142,"conditions":143,"keywords":4,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":145,"startDateStruct":147,"completionDateStruct":148,"leadSponsor":150,"locationsCount":4},"100627061","pinwheel-and-bubble-blowing-for-pain-and-emotional-responses-in-children-100627061","NCT07443735","Pinwheel and Bubble Blowing for Pain and Emotional Responses in Children","The Effects of Pinwheel and Bubble Blowing on Pain and Emotional Responses in Children During Venous Blood Sampling","Inclusion Criteria:\n\n* Children aged 3-6 years\n* Willingness to undergo intravenous blood collection\n* Children's ability to apply distraction techniques during blood collection\n* No communication problems in children\n* No mental or neurological disability in the child\n* Venous blood collection performed in a single session\n* Parents and children must be willing to participate in the study\n\nExclusion Criteria:\n\n* Children not being between the ages of 3 and 6\n* Absence of intravenous blood collection request\n* Communication problems in children\n* Presence of mental or neurological disability in the child\n* Complaints that disrupt the child's comfort, such as pain, nausea, vomiting, etc., due to other reasons\n* Use of analgesic or sedative medication within 6 hours prior to the study\n* Absence of healthy skin integrity\n* Repeated attempts\n* Unexpected events occurring during blood collection\n* Parents or children not volunteering to participate in the study","3 Years","6 Years",{"count":140,"type":21},75,[54],"Venous blood sampling is one of the most frequently performed invasive procedures in children during diagnostic and treatment processes and may lead to pain, fear, and negative emotional responses. Such negative experiences in childhood may contribute to the development of anxiety toward healthcare services and reduced cooperation with healthcare professionals during treatment. Therefore, the use of non-pharmacological interventions aimed at reducing pain levels and emotional responses during procedures is of great importance in pediatric care.\n\nThe aim of this study is to determine the effects of pinwheel and bubble blowing techniques applied during venous blood sampling on pain levels and emotional states in children. This study will be conducted as a prospective, randomized controlled trial in the Blood Sampling Unit of the Pediatric Outpatient Clinic of a university hospital located in Edirne. A total of 66 children aged 3-6 years who will undergo venous blood sampling will be included in the study (pinwheel group: 22, bubble blowing group: 22, control group: 22).\n\nStudy data will be collected using the Child and Family Information Form, the Wong-Baker Faces Pain Rating Scale, and the Children's Emotional Indicators Scale. During venous blood sampling, pinwheel or bubble blowing techniques will be applied to the children in the experimental groups, while routine procedures will be performed for the children in the control group. The collected data will be analyzed using appropriate statistical methods. The results of this study are expected to contribute to the dissemination of evidence-based non-pharmacological practices aimed at reducing pain and emotional stress in pediatric nursing care.",[144],"Pain and Emotional Responses in Children During Venous Blood Sampling",{"date":146,"type":34},"2026-03-02",{"date":126,"type":21},{"date":149,"type":21},"2027-04-30",{"name":40,"class":41},{"id":152,"slug":153,"hasResults":11,"nctId":154,"briefTitle":155,"officialTitle":156,"acronym":4,"eligibilityCriteria":157,"healthyVolunteers":113,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":158,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":160,"conditions":161,"keywords":4,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":167,"lastUpdatePostDateStruct":168,"startDateStruct":169,"completionDateStruct":171,"leadSponsor":173,"locationsCount":105},"100625365","3d-volumetric-plaque-assessment-on-teeth-composite-restorations-and-ceramic-veneers-using-an-intraoral-scanner-100625365","NCT07421687","3D Volumetric Plaque Assessment on Teeth, Composite Restorations, and Ceramic Veneers Using an Intraoral Scanner","Differences in Plaque Accumulation on Natural Teeth, Composite Restorations, and Ceramic Veneers Assessed by Intraoral Scanner-Based 3D Volumetric Analysis","Inclusion Criteria:\n\n* 18 years or older. \n* Able and willing to provide written informed consent. \n* Generally healthy and not using regular systemic medications. \n* Have at least 6 teeth in each quadrant of the mouth. \n* Have low plaque levels at baseline (plaque index \\\u003C10%). \n* Do not have periodontal pockets deeper than 4 mm. \n* In the upper front teeth (maxillary anterior) on the outer (vestibular) surfaces, participants must fit one of these predefined surface types: Natural tooth surface (no restoration ), direct composite restoration, or Indirect ceramic veneer restoration. \n* No cavitated tooth decay on the surfaces to be assessed and no obvious surface defects that would clearly increase plaque retention.\n\nExclusion Criteria:\n\n* Diagnosis of gingivitis or periodontitis. \n* Regular use of mouthwash as part of daily oral hygiene. \n* Use of antibiotics within the last 6 months. \n* Smoking. \n* Pregnant or breastfeeding. \n* Presence of dental implants or removable dentures. \n* Any systemic disease or medical treatment that could affect oral health or healing (examples include diabetes, cancer, disorders affecting bone metabolism, immunosuppressive therapy, chemotherapy, radiotherapy, or other conditions\u002Fmedications affecting wound healing). \n* Having a pacemaker or an implantable defibrillator. \n* History of allergy or intolerance to study-related materials (e.g., ingredients of the plaque-disclosing agent or the lip\u002Fcheek retractor material). \n* Defective fillings\u002Frestorations on the assessed surfaces that could increase plaque retention. \n* Malocclusion or spacing between teeth (diastema). \n* Gum recession affecting more than one-third of the root length. \n* Wearing fixed orthodontic appliances (braces). \n* Any physical, mental, or psychiatric condition that could interfere with understanding the study or completing the procedures",{"count":159,"type":21},45,"The goal of this observational study is to evaluate and compare a 3D intraoral scanner-based, computer-assisted approach for assessing dental biofilm\u002Fplaque accumulation on natural teeth and restorative surfaces with a conventional clinical plaque index (Turesky modified Quigley-Hein Plaque Index, TMQHPI) in systemically healthy adults. The main questions it aims to answer are:\n\n* How well does the plaque-covered surface measurement derived from 3D intraoral scanner data agree with TMQHPI scores after plaque disclosure?\n* How sensitively do the two methods detect changes in plaque levels after supervised toothbrushing?\n* Do plaque accumulation patterns differ between natural tooth surfaces and restorative materials (direct composite restorations and indirect ceramic veneers), and where are plaque-retentive areas most frequently located?\n\nParticipants (≥18 years) will receive routine professional mechanical plaque removal as part of standard clinical care. They will then be asked to avoid mechanical and\u002For chemical plaque control for 4 days. At the follow-up visit, participants will undergo:\n\n1. An intraoral scan and standardized photographs of the full dental arch,\n2. Plaque disclosure followed by repeat scanning\u002Fphotography and TMQHPI scoring by a periodontist,\n3. Supervised toothbrushing using the modified Bass technique for 2 minutes, followed by a final scan and photographs. Digital models will be used to quantify plaque-covered surface measures and to generate 3D maps of plaque-retentive areas.",[162,163,164,165,166],"Dental Plaque Accumulation","Oral Hygiene, Oral Health","Dental Materials","Dental Plaque Imaging Methods","Dental Plaque Index","2026-02-19",{"date":36,"type":34},{"date":170,"type":21},"2026-03-16",{"date":172,"type":21},"2027-03-24",{"name":40,"class":41},{"id":175,"slug":176,"hasResults":11,"nctId":177,"briefTitle":178,"officialTitle":179,"acronym":4,"eligibilityCriteria":180,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":181,"targetDuration":4,"studyType":52,"phases":183,"briefSummary":184,"conditions":185,"keywords":188,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":193,"lastUpdatePostDateStruct":194,"startDateStruct":196,"completionDateStruct":198,"leadSponsor":200,"locationsCount":105},"100621126","effect-of-foot-bath-on-pain-sleep-and-comfort-levels-after-abdominal-surgery-100621126","NCT07366567","Effect of Foot Bath on Pain, Sleep, and Comfort Levels After Abdominal Surgery","Effect of Foot Bath on Pain, Sleep, and Comfort Levels After Abdominal Surgery: A Randomized Controlled Trial","Inclusion Criteria:\n\n* who are hospitalized in the General Surgery Clinic,\n* are on day 0 of surgery,\n* volunteer to participate in the study,\n* have no neuropsychiatric diagnosis and are not taking antipsychotic medications,\n* are over 18 years of age,\n* accept random selection,\n* and undergo abdominal surgery.\n* For the experimental group, all patients with no infectious diseases (shingles, fungal infections, eczema, warts, calluses), local infections (abscesses, etc.), open lesions\u002Fwounds, scar tissue, edema, hematomas, thrombophlebitis, deep vein thrombosis, lymphangitis, coagulation disorders, varicose veins, osteoporosis, osteomyelitis, hepatitis, degenerative joint diseases, neuropathy due to diabetes, toe deformities, recent fractures, dislocations, or ruptures of muscle fibers, tendons, or ligaments will be included in the sample.\n\nExclusion Criteria:\n\n* patients who underwent multiple simultaneous surgeries along with abdominal surgery,\n* those with postoperative complications such as delirium,\n* those who underwent reoperation,\n* those with a pain score \\>7 because it could affect sleep levels,\n* and those who received narcotic analgesics on postoperative day 0 due to pain will be excluded from the sample.",{"count":182,"type":21},96,[54],"The aim of this study was to investigate the effects of foot bath application on pain level, comfort and sleep quality in the postoperative period.\n\nH1: Foot baths have a postoperative pain-reducing effect. H2: Foot baths have a postoperative comfort-enhancing effect. H3: Foot baths have a postoperative sleep-improving effect.",[186,187],"Pain, Postoperative","Sleep",[189,190,191,192],"pain","foot bath","sleep quality","comfort","2026-01-16",{"date":195,"type":34},"2026-01-26",{"date":197,"type":21},"2025-12-29",{"date":199,"type":21},"2026-12-30",{"name":40,"class":41},{"id":202,"slug":203,"hasResults":11,"nctId":204,"briefTitle":205,"officialTitle":206,"acronym":4,"eligibilityCriteria":207,"healthyVolunteers":113,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":208,"targetDuration":209,"studyType":22,"phases":4,"briefSummary":210,"conditions":211,"keywords":217,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":218,"lastUpdatePostDateStruct":219,"startDateStruct":221,"completionDateStruct":223,"leadSponsor":225,"locationsCount":4},"100611430","assessing-the-turkish-ddivat-for-visual-acuity-measurement-100611430","NCT07240480","Assessing the Turkish DDIVAT for Visual Acuity Measurement","Validation of the Turkish Version of the DDIVAT Visual Acuity Measuring Device in a Turkish-speaking Population","Inclusion Criteria:\n\n* Adults aged 18 years or older\n\nTurkish-speaking individuals able to understand the study purpose\n\nWillingness to participate and provide written informed consent\n\nParticipants with or without refractive errors (e.g., myopia, hyperopia, astigmatism)\n\nExclusion Criteria:\n\n* Age below 18 years\n\nIndividuals unable to complete visual acuity testing\n\nPresence of severe ocular pathology (e.g., corneal opacity, retinal detachment) that prevents accurate measurement\n\nCognitive or communication difficulties preventing informed consent",{"count":86,"type":21},"1 Day","The goal of this observational methodological study is to validate the Turkish version of the DDIVAT visual acuity measuring device in a Turkish-speaking adult population.\n\nThe main questions it aims to answer are:\n\nDoes the Turkish version of the DDIVAT provide reliable and valid visual acuity measurements in Turkish speakers?\n\nAre the results of the DDIVAT comparable to those obtained with the standard Snellen chart used in clinical practice?\n\nResearchers will compare DDIVAT visual acuity test results with Snellen chart results to see if both methods produce consistent measurements.\n\nParticipants will:\n\nBe adults aged 18 years or older, including both patients and healthy volunteers.\n\nUndergo visual acuity testing using the DDIVAT system displayed on a smart TV connected to the university server.\n\nHave their visual acuity re-measured using the standard Snellen optotype under the same conditions.\n\nNo medication or invasive procedure will be used. The study carries no risk to participants.",[212,213,214,215,216],"Visual Acuity","Refractive Errors","Myopia","Hyperopia","Astigmatism",[212,213],"2025-11-26",{"date":220,"type":34},"2025-12-04",{"date":222,"type":21},"2025-12-01",{"date":224,"type":21},"2026-05-31",{"name":40,"class":41},{"id":227,"slug":228,"hasResults":11,"nctId":229,"briefTitle":230,"officialTitle":231,"acronym":4,"eligibilityCriteria":232,"healthyVolunteers":113,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":233,"targetDuration":235,"studyType":22,"phases":4,"briefSummary":236,"conditions":237,"keywords":245,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":249,"lastUpdatePostDateStruct":250,"startDateStruct":252,"completionDateStruct":254,"leadSponsor":256,"locationsCount":4},"100591815","3-dimensional-evaluation-of-body-perception-100591815","NCT06985329","3-Dimensional Evaluation of Body Perception","Evaluation of Neurocognitive Skills, VisuoSpatial Perception and Perspective Perception in Amputees","Inclusion criteria for the amputee group:\n\n* Acquired amputees\n* Aged 18-65 years\n* Using a prosthesis for at least six months\n* At least a primary school graduate\n* Individuals who can adapt to prolonged, attention-demanding activities will be included.\n* Standardised Mini Mental State Examination score of \\>24.\n\nFollowing the recruitment of the amputee group, a healthy control group will be recruited to match it in terms of age, gender and educational status.\n\nInclusion criteria for the healthy control group:\n\n* Age range: 18-65 years\n* At least a primary school graduate\n* Individuals who can adapt to prolonged, attention-demanding activities will be included.\n* Standardised Mini Mental State Examination score of \\>24.\n\nExclusion criteria for the amputee group:\n\n* Individuals with congenital amputation\n* Those with phantom limb pain and\u002For sensation\n* Those with an open wound on the stump\n* Bilateral amputation\n* Any neurological or psychiatric diagnosis\n* Those using sedative medication and\u002For its derivatives\n* Have vision and related problems\n* Individuals who are illiterate\n* Individuals participating in treatments targeting body representation (e.g. imagery-based treatments or progressive motor visualisation) will not be included in the study.\n\nExclusion criteria for the Healthy Control Group:\n\n* Having any neurological or psychiatric diagnosis\n* Using sedative medication and\u002For its derivatives\n* People with vision and related problems\n* Illiterate individuals will not be included in the study.",{"count":234,"type":21},60,"15 Days","The goal of this observational study is to evaluate the changing body perception of amputees aged 18-65 years using prostheses through different personal perspectives of the right-left distinction. In addition, we aimed to examine the relationship between possible changes in body perception and visual spatial perception and neurocognitive performances. The main questions that this study aimed to answer are as follows:\n\n1. Is there a difference between the amputee group and the control group in terms of parameters related to body perception?\n2. Is there a difference between the amputee group and the control group in terms of neurocognitive skills?\n3. Is there any difference between the amputee group and the control group in terms of visual spatial perception abilities?\n\nTo examine whether changes in body perception in amputees affect neurocognitive performance, visuospatial perception and perspective perception and the relationship between them will be compared with a healthy control group.\n\nThe assessments to be applied to both groups can be summarised as follows:\n\n* Demographic information such as age, gender, and education level will be recorded.\n* Mini-mental state test will be used to assess the cognitive level.\n* Edinburgh Handedness Scale will be used to determine the dominant side.\n* Right-left discrimination and personal perspective perception will be assessed using a desktop programme.\n* The clock drawing test and Benton line orientation test will be used to visual spatial perception.\n* A computer based program called The Central Nervous System (CNS) Vital Signs Neurocognitive Test Battery will be used to asesses neurocognitive abilities.",[238,239,240,241,242,243,244],"Body Image","Cognition","Decision Making","Visuospatial\u002FPerceptual Abilities","Neurocognitive Function","Executive Function (Cognition)","Amputation",[238,239,246,244,247,240,248],"Neuropsychological Test","Executive Function","Visuospatial Skills","2025-05-14",{"date":251,"type":34},"2025-05-22",{"date":253,"type":21},"2025-06",{"date":255,"type":21},"2026-06-15",{"name":40,"class":41},{"id":258,"slug":259,"hasResults":11,"nctId":260,"briefTitle":261,"officialTitle":262,"acronym":4,"eligibilityCriteria":263,"healthyVolunteers":113,"sex":16,"minAge":264,"maxAge":265,"enrollmentInfo":266,"targetDuration":4,"studyType":52,"phases":268,"briefSummary":269,"conditions":270,"keywords":273,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":277,"lastUpdatePostDateStruct":278,"startDateStruct":280,"completionDateStruct":282,"leadSponsor":284,"locationsCount":105},"100575049","effects-of-reformer-pilates-on-adolescents-posture-and-trunk-endurance-100575049","NCT06767228","Effects of Reformer Pilates on Adolescents' Posture and Trunk Endurance","The Effects of Reformer Pilates Exercises on Trunk Endurance, Posture, and Body Awareness in Adolescents","Inclusion Criteria:\n\n* Aged between 10-19 years.\n* Voluntary participation with signed informed consent.\n* Ability to read and write in Turkish.\n\nExclusion Criteria:\n\n* History of orthopedic injury within the last 3 months.\n* Obesity (BMI \\> 30 kg\u002Fm²).\n* Being under follow-up for a scoliosis diagnosis.","10 Years","19 Years",{"count":267,"type":21},26,[54],"This study aims to investigate the effects of reformer pilates exercises on posture, core endurance, and body awareness in adolescents. The hypothesis is that reformer pilates will improve these outcomes compared to a control group receiving only informational support. Participants will be randomized into two groups and assessed over six weeks.",[271,272],"Adolescent","Healthy",[271,274,275,276],"Exercise therapy","Posture","Body awareness","2025-04-08",{"date":279,"type":34},"2025-04-11",{"date":281,"type":34},"2025-03-01",{"date":283,"type":21},"2025-10-07",{"name":40,"class":41},{"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":52,"phases":296,"briefSummary":297,"conditions":298,"keywords":300,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":302,"lastUpdatePostDateStruct":303,"startDateStruct":304,"completionDateStruct":306,"leadSponsor":308,"locationsCount":105},"100585972","animated-video-and-booklet-education-for-improving-asthma-control-and-medication-compliance-in-children-100585972","NCT06909318","Animated Video and Booklet Education for Improving Asthma Control and Medication Compliance in Children","The Effect of Animated Video and Booklet Education on Asthma Control and Medication Compliance in Children With Asthma: A Randomized Controlled Study","Inclusion Criteria:\n\n* Children aged between 7 and 11 years\n* Diagnosed with asthma by a pediatric allergy specialist\n* Mild or moderate asthma severity according to GINA criteria\n* No communication difficulties\n* Have not received any asthma-related education outside of routine clinical care during the study period\n* No known mental or neurological disabilities\n* No serious chronic illness other than asthma (e.g., cardiac, neurological conditions)\n* At least one parent owns a smartphone or tablet\n* Child and parent volunteer to participate and provide informed consent\n\nExclusion Criteria:\n\n* Children younger than 7 or older than 11\n* Severe persistent asthma according to GINA criteria\n* Communication difficulties\n* Prior asthma education outside of routine clinical care\n* Children with cognitive or neurological impairments\n* Children who frequently require emergency care due to asthma exacerbations\n* Families without access to communication tools (e.g., no internet, smartphone, or unable to communicate)\n* Lack of consent from either the child or parent","7 Years","11 Years",{"count":295,"type":21},66,[54],"Asthma is a chronic inflammatory disease that causes wheezing, coughing, and shortness of breath, and it is a significant cause of morbidity and mortality in the pediatric population. The World Health Organization (WHO) estimated that 262 million people were affected by asthma in 2019, with 461,000 asthma-related deaths annually. In Turkey, the prevalence of asthma in children aged 6-12 ranges from 2% to 16%. Inadequate asthma control in children is often associated with poor medication adherence, lack of knowledge, misbeliefs, and ineffective communication with healthcare professionals. Education is therefore a crucial element of successful asthma management.\n\nRecently, the use of digital tools such as animated videos has become increasingly popular in pediatric education due to their engaging and interactive nature. Studies have shown that visual and interactive materials can improve knowledge, satisfaction, and adherence in children with chronic illnesses.\n\nThis randomized controlled study aims to evaluate the effect of an educational intervention using an animated video and booklet on asthma control and medication compliance in children aged 7-11 diagnosed with asthma. It is expected that this child-friendly, visually enriched educational approach will enhance asthma management and support medication adherence in children.",[299],"Asthma Bronchiale",[301],"pediatric","2025-04-07",{"date":277,"type":34},{"date":305,"type":21},"2025-05-15",{"date":307,"type":21},"2025-10-15",{"name":40,"class":41},{"id":310,"slug":311,"hasResults":11,"nctId":312,"briefTitle":313,"officialTitle":314,"acronym":4,"eligibilityCriteria":315,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":316,"enrollmentInfo":317,"targetDuration":4,"studyType":52,"phases":319,"briefSummary":320,"conditions":321,"keywords":4,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":323,"lastUpdatePostDateStruct":324,"startDateStruct":326,"completionDateStruct":328,"leadSponsor":330,"locationsCount":105},"100574560","the-effect-of-cold-steam-application-on-nausea-and-vomiting-100574560","NCT06760871","The Effect of Cold Steam Application on Nausea and Vomiting","The Effect of Cold Steam Application on Nausea and Vomiting After Laparoscopic Abdominal Surgery: Randomized Controlled Trial","Inclusion Criteria:\n\n* Undergoing abdominal surgery under general anaesthesia,\n* Admitted to the general surgery ward after surgery,\n* Who volunteered to participate in the research,\n* No mental disability,\n* 18 years of age,\n* Literate,\n* Accepting random selection,\n* without Turkish communication problems,\n* No preoperative oncological treatment,\n* undergoing elective surgery,\n* Postoperatively without a nasogastric catheter,\n* with an operation time \\\u003C4 hours,\n* Laparoscopic surgery performed,\n* No postoperative nausea and vomiting or mild\u002Fmoderate nausea,\n* Patients with ASA score 1, 2 or 3 were determined as inclusion criteria.\n\nExclusion Criteria:\n\n* Severe nausea or active vomiting prior to administration,\n* Migraine, vertigo, etc. who may experience nausea and vomiting due to vestibular disease, pregnancy,\n* COPD, asthma, etc. with respiratory problems,\n* Not accepting the application of cold steam,\n* Not accepting random selection,\n* Those with a history of chemotherapy or radiotherapy before surgery,\n* Patients who underwent sudden movement changes (bed change, patient transfer, etc.) during the data collection period (0 to 2nd hour),","110 Years",{"count":318,"type":21},88,[54],"The aim of this study was to determine the effect of cold vapour applied to patients undergoing laparoscopic abdominal surgery primarily on nausea and vomiting and secondarily on antiemetic requirement, patient satisfaction and thirst.\n\nH1: Cold steam application after surgical intervention has a decreasing effect on postoperative nausea.\n\nH2: Cold steam application after surgical intervention has a decreasing effect on postoperative vomiting.\n\nH3: Cold steam application after surgical intervention reduces the need for antiemetic drugs.\n\nH4: Cold steam application after surgical intervention has a satisfactory effect on reducing nausea and vomiting.",[322],"Nausea and Vomiting, Postoperative","2025-01-06",{"date":325,"type":34},"2025-01-07",{"date":327,"type":21},"2025-01-15",{"date":329,"type":21},"2025-12-30",{"name":40,"class":41},""]