[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Alanya Alaaddin Keykubat University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":280},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,11,0,[8,47,71,96,124,147,172,192,212,235,256],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":24,"conditions":25,"keywords":29,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100642311","dental-caries-and-oral-hygiene-status-in-children-with-specific-learning-disabilities-100642311",false,"NCT07611981","Dental Caries and Oral Hygiene Status in Children With Specific Learning Disabilities","SLD-OH","Inclusion Criteria:\n\n* Children aged 7-12 years\n* For the study group: diagnosis of specific learning disorder (SLD) confirmed by a psychiatrist\n* For the control group: confirmed healthy with no psychiatric diagnosis by a psychiatrist\n* Written informed consent obtained from the parent or guardian\n\nExclusion Criteria:\n\n* Children with additional psychiatric diagnoses (e.g., autism spectrum disorder, attention-deficit\u002Fhyperactivity disorder, intellectual disability)\n* Children with systemic disease or physical disability that may prevent participation in the study",true,"ALL","7 Years","12 Years",{"count":21,"type":22},70,"ESTIMATED","OBSERVATIONAL","This study aims to evaluate dental caries and oral hygiene status in children aged 7-12 years with specific learning disabilities (SLD) and to compare the findings with healthy children. Clinical oral examinations, including dmft\u002FDMFT, ICDAS II, Plaque Index, and Gingival Index assessments, will be performed. In addition, questionnaire-based evaluations of oral hygiene habits, dietary habits, and parental supervision during toothbrushing will be conducted.",[26,27,28],"Specific Learning Disabilities","Dental Caries","Oral Hygiene",[26,27,30,31,32,33,34],"Oral Health","dmft\u002FDMFT","Pediatric Dentistry","Plaque Index","Gingival Index","RECRUITING","2026-06-15",{"date":38,"type":39},"2026-06-16","ACTUAL",{"date":36,"type":39},{"date":42,"type":22},"2026-10",{"name":44,"class":45},"Alanya Alaaddin Keykubat University","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":55,"targetDuration":4,"studyType":56,"phases":57,"briefSummary":59,"conditions":60,"keywords":62,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":67,"startDateStruct":68,"completionDateStruct":69,"leadSponsor":70,"locationsCount":46},"100642351","plaque-removal-efficiency-in-children-with-specific-learning-disabilities-100642351","NCT07611942","Plaque Removal Efficiency in Children With Specific Learning Disabilities","Quantitative Analysis of Plaque Removal Efficiency in Children With Specific Learning Disabilities","PRE-SLD","Inclusion Criteria:\n\n* Diagnosis of specific learning disabilities confirmed by a child and adolescent psychiatry specialist for the study group\n* Confirmation by a child and adolescent psychiatry specialist that the control group participants are healthy and do not have any psychiatric diagnosis\n* Age between 7 and 12 years\n* Written informed consent obtained from parents or legal guardians\n\nExclusion Criteria:\n\n* Children with additional psychiatric diagnoses such as autism spectrum disorder, attention deficit\u002Fhyperactivity disorder, or intellectual disability\n* Children with systemic health problems or physical disabilities that may interfere with participation in the study",{"count":21,"type":22},"INTERVENTIONAL",[58],"NA","This study aims to evaluate the effectiveness of toothbrushing education on plaque removal in children aged 7-12 years with specific learning disabilities (SLD) and to compare their plaque removal performance with healthy children. Participants will receive standardized toothbrushing education supported by visual and auditory materials. Plaque Index, Gingival Index, and photograph-based quantitative plaque analyses will be evaluated at baseline and after a 2-week follow-up period.",[26,61,28],"Dental Plaque",[26,61,63,64,65,66,32],"Plaque Removal","Quantitative Plaque Analysis","Toothbrushing Education","ImageJ\u002FFIJI",{"date":38,"type":39},{"date":36,"type":39},{"date":42,"type":22},{"name":44,"class":45},{"id":72,"slug":73,"hasResults":11,"nctId":74,"briefTitle":75,"officialTitle":76,"acronym":4,"eligibilityCriteria":77,"healthyVolunteers":16,"sex":17,"minAge":78,"maxAge":79,"enrollmentInfo":80,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":82,"conditions":83,"keywords":85,"overallStatus":87,"whyStopped":4,"lastUpdateSubmitDate":88,"lastUpdatePostDateStruct":89,"startDateStruct":91,"completionDateStruct":93,"leadSponsor":95,"locationsCount":4},"100643277","general-well-being-after-quitting-drug-use-100643277","NCT07641712","General Well-being After Quitting Drug Use","Physical and Physicosocial Well-being After Quitting Drug Use","Inclusion Criteria:\n\n\\- Individuals aged 18-65 who used drugs and asymptomatic individuals in the same age group.\n\nExclusion Criteria:\n\n* Active drug users and those using psychotic drugs","18 Years","65 Years",{"count":81,"type":22},120,"The aim of this study is to investigate physical and physicosocial well-being after quitting drug use.",[84],"Drug Abuse",[86],"well-being","NOT_YET_RECRUITING","2026-06-08",{"date":90,"type":39},"2026-06-11",{"date":92,"type":22},"2026-07-01",{"date":94,"type":22},"2027-02-28",{"name":44,"class":45},{"id":97,"slug":98,"hasResults":11,"nctId":99,"briefTitle":100,"officialTitle":101,"acronym":4,"eligibilityCriteria":102,"healthyVolunteers":16,"sex":17,"minAge":78,"maxAge":103,"enrollmentInfo":104,"targetDuration":4,"studyType":56,"phases":106,"briefSummary":107,"conditions":108,"keywords":111,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":117,"lastUpdatePostDateStruct":118,"startDateStruct":120,"completionDateStruct":122,"leadSponsor":123,"locationsCount":46},"100636307","effect-of-lemon-juice-and-apple-cider-vinegar-on-postprandial-blood-glucose-and-satiety-in-healthy-individuals-100636307","NCT07563985","Effect of Lemon Juice and Apple Cider Vinegar on Postprandial Blood Glucose and Satiety in Healthy Individuals","The Effect of Lemon Juice and Apple Cider Vinegar on Postprandial Blood Glucose and Satiety in Healthy Individuals","Inclusion Criteria:\n\n* Healthy male and female volunteers aged 18-35 years\n* Body Mass Index (BMI) between 18.5 and 25.0 kg\u002Fm²\n* Willingness to provide written informed consent\n* Ability to comply with study procedures and fasting requirements\n* No history of chronic metabolic, gastrointestinal, or endocrine diseases\n\nExclusion Criteria:\n\n* Presence of any chronic disease (e.g., diabetes mellitus, cardiovascular disease, gastrointestinal disorders)\n* Food allergies or intolerances to study foods (white bread, lemon juice, apple cider vinegar)\n* BMI \\\u003C18.5 or \\>25.0 kg\u002Fm²\n* Regular participation in high-intensity physical activity (≥5 days\u002Fweek)\n* Current or recent (past 3 months) smoking or smoking cessation\n* Use of any medication or supplements affecting glucose metabolism\n* History of eating disorders\n* Pregnancy, lactation, or menopause\n* Female participants currently in menstruation period (testing will be postponed during menstruation days)\n* Alcohol consumption within 24 hours prior to testing days\n* Caffeine intake or major dietary changes on the day before testing","35 Years",{"count":105,"type":22},15,[58],"This clinical study aims to examine how acidic drinks (lemon juice and apple cider vinegar) affect blood sugar when consumed with a starchy food. The study focuses on healthy individuals and aims to understand whether these drinks can slow the rise in blood sugar after meals and affect feelings of fullness.\n\nThe main questions this study aims to answer are:\n\nDo lemon juice or apple cider vinegar lower the rise in blood sugar after a meal? Do these drinks increase feelings of fullness? Do different amounts change their effects?\n\nResearchers will compare lemon juice and apple cider vinegar to see which one is more effective.\n\nParticipants will:\n\nConsume white bread in the morning on an empty stomach with one of the following drinks:\n\nWater only Water with lemon juice (50 g or 100 g) Water with apple cider vinegar (10 g or 20 g) Have a one-week break between each test. Have their blood sugar measured at regular intervals for 3 hours after eating. Report their level of fullness using a simple scale.\n\nThis study explores whether simple and practical dietary choices can help manage blood sugar levels. The findings may support new, easy-to-apply nutrition strategies for managing diabetes and weight.",[109,110],"Satiety","Postprandial Glycemia",[112,113,114,115,109,116],"Lemon Juice","Apple Cider Vinegar","Glycemic Response","Starch Hydrolysis","Postprandial Glucose","2026-04-26",{"date":119,"type":39},"2026-05-04",{"date":121,"type":22},"2026-05-01",{"date":92,"type":22},{"name":44,"class":45},{"id":125,"slug":126,"hasResults":11,"nctId":127,"briefTitle":128,"officialTitle":129,"acronym":4,"eligibilityCriteria":130,"healthyVolunteers":11,"sex":17,"minAge":78,"maxAge":4,"enrollmentInfo":131,"targetDuration":4,"studyType":56,"phases":133,"briefSummary":134,"conditions":135,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":138,"lastUpdatePostDateStruct":139,"startDateStruct":141,"completionDateStruct":143,"leadSponsor":145,"locationsCount":146},"100625038","effects-of-graded-motor-imagery-in-individuals-with-footankle-osteoarthritis-100625038","NCT07417436","Effects of Graded Motor Imagery in Individuals With Foot\u002FAnkle Osteoarthritis","Effectiveness of Graded Motor Imagery Training in Individuals With Foot\u002FAnkle Osteoarthritis: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Be 18 years of age or older,\n* Have a diagnosis of foot and\u002For ankle osteoarthritis confirmed by a specialist physician through clinical and\u002For radiological examination\n* Experience pain in the ankle joint most days for at least three months\n* Agree to participate in randomly assigned treatment and follow-up measurements\n* Have sufficient understanding of the Turkish language\n* Have a Standardized Mini Mental Test score of at least 24 points\n\nExclusion Criteria:\n\n* Previous arthrodesis or joint replacement surgery on the affected ankle,\n* Having received physical therapy for ankle osteoarthritis within the last three months\n* Presence of vision or hearing problems that may affect compliance with treatment.\n* Presence of a neuromuscular disease\n* History of intra-articular ankle injections within the last 3 months\n* Initiation of a new disease-specific pharmacological treatment during the study period",{"count":132,"type":22},24,[58],"The aim of our study is to evaluate the effects of graded motor imagery training applied in addition to a structured exercise program in individuals with foot and\u002For ankle osteoarthritis.\n\nThe study population will consist of twenty-four individuals diagnosed with foot\u002Fankle osteoarthritis who applied to the Orthopedics and Traumatology Department of Alanya Alaaddin Keykubat University Education and Research Hospital.\n\nIndividuals who volunteer to participate in the study will be invited to participate through face-to-face interviews. The inclusion and exclusion criteria are as follows:\n\nInclusion criteria:\n\n* Being 18 years of age or older\n* Having a diagnosis of foot\u002Fankle osteoarthritis confirmed by a specialist physician through clinical and\u002For radiological examination\n* Experiencing pain in the ankle joint most days for at least three months\n* Agreeing to participate in randomly assigned treatment and follow-up measurements\n* Having a sufficient level of Turkish language comprehension\n* Having a Standardized Mini Mental Test score of at least 24 points\n\nExclusion criteria:\n\n* Previous arthrodesis or joint replacement surgery on the affected ankle\n* Physical therapy for ankle osteoarthritis within the last three months\n* Vision or hearing problems that would affect compliance with treatment.\n* Presence of a neuromuscular disease\n* History of intra-articular ankle injections within the last 3 months\n* Initiation of a new disease-specific pharmacological treatment during the study period During the study period, participants will receive one of the physical therapy programs. One group will only participate in the structured exercise program, while the other group will receive graded motor imagery training in addition to the exercise program.Both treatment groups will receive a total of 12 treatment sessions over 6 weeks.\n\nThe results of this study may help improve physiotherapy programs for individuals with similar health conditions.",[136,137],"Ankle Osteoarthritis","Foot Osteoarthritis","2026-02-11",{"date":140,"type":39},"2026-02-18",{"date":142,"type":39},"2025-08-28",{"date":144,"type":22},"2026-12-30",{"name":44,"class":45},2,{"id":148,"slug":149,"hasResults":11,"nctId":150,"briefTitle":151,"officialTitle":152,"acronym":4,"eligibilityCriteria":153,"healthyVolunteers":11,"sex":17,"minAge":154,"maxAge":155,"enrollmentInfo":156,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":158,"conditions":159,"keywords":4,"overallStatus":87,"whyStopped":4,"lastUpdateSubmitDate":164,"lastUpdatePostDateStruct":165,"startDateStruct":167,"completionDateStruct":169,"leadSponsor":171,"locationsCount":46},"100566482","craniocervical-dysfunction-index-in-patients-with-temporomandibular-joint-dysfunction-100566482","NCT06655753","Craniocervical Dysfunction Index in Patients With Temporomandibular Joint Dysfunction","Turkish Validity and Reliability of the Craniocervical Dysfunction Index in Patients Temporomandibular Joint Dysfunction","Inclusion Criteria:\n\n* Between the ages of 20-60 years\n* Clinical diagnosis of non-specific neck pain\n* Being able to communicate in Turkish\n* Volunteering to participate in the study\n\nExclusion Criteria:\n\n* Over 60 years of age\n* Those with impairments in cervical mobility that affected the postural assessment","20 Years","60 Years",{"count":157,"type":22},50,"The aims of this study were to perform cultural adaptation of the Craniocervical Dysfunction Index in patients with Temporomandibular Joint Dysfunction, reliability and validity of the index Turkish speaking adults.",[160,161,162,163],"Temporomandibular Joint Dysfunction","Craniocervical Dysfunction","Reliability","Validity","2025-02-07",{"date":166,"type":39},"2025-02-11",{"date":168,"type":22},"2025-03-01",{"date":170,"type":22},"2025-10-01",{"name":44,"class":45},{"id":173,"slug":174,"hasResults":11,"nctId":175,"briefTitle":176,"officialTitle":177,"acronym":4,"eligibilityCriteria":153,"healthyVolunteers":11,"sex":17,"minAge":154,"maxAge":155,"enrollmentInfo":178,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":179,"conditions":180,"keywords":183,"overallStatus":87,"whyStopped":4,"lastUpdateSubmitDate":184,"lastUpdatePostDateStruct":185,"startDateStruct":187,"completionDateStruct":189,"leadSponsor":191,"locationsCount":46},"100565295","craniocervical-dysfunction-index-in-turkish-patients-with-non-specific-neck-pain-100565295","NCT06640322","Craniocervical Dysfunction Index in Turkish Patients With Non-specific Neck Pain","Turkish Validity and Reliability of the Craniocervical Dysfunction Index in Patients With Non-specific Neck Pain",{"count":157,"type":22},"The aims of this study were to perform cultural adaptation of the Craniocervical Dysfunction Index in patients with non-specific neck pain, reliability and validity of the index Turkish speaking adults.",[181,182],"Neck Pain","Craniocervical Disfunction",[181,182,162,163],"2024-10-11",{"date":186,"type":39},"2024-10-15",{"date":188,"type":22},"2025-01",{"date":190,"type":22},"2025-09",{"name":44,"class":45},{"id":193,"slug":194,"hasResults":11,"nctId":195,"briefTitle":196,"officialTitle":197,"acronym":4,"eligibilityCriteria":198,"healthyVolunteers":16,"sex":17,"minAge":78,"maxAge":79,"enrollmentInfo":199,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":201,"conditions":202,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":184,"lastUpdatePostDateStruct":206,"startDateStruct":207,"completionDateStruct":209,"leadSponsor":211,"locationsCount":46},"100520282","turkish-version-of-digital-eye-strain-questionnaire-desq-100520282","NCT06054542","Turkish Version of Digital Eye Strain Questionnaire (DESQ)","Validity and Reliability of the Turkish Version of Digital Eye Strain Questionnaire (DESQ)","Inclusion Criteria:\n\n* Between the ages of 18-65 years\n* People who spend two or more continuous hours a day on their digital devices (computer, tablet, smartphone) or use more than one device\n\nExclusion Criteria:\n\n* History of ophthalmic surgery or active ocular disease\n* Participants who did not understand the instructions or did not sign a consent form were excluded",{"count":200,"type":22},130,"The aims of this study were to perform cultural adaptation of the DESQ and provide information regarding the factor structure, reliability and validity of the instrument in Turkish speaking adults.",[203,162,163,204,205],"Cultural Adaptation","Adults","Eye Strain",{"date":186,"type":39},{"date":208,"type":39},"2023-10-30",{"date":210,"type":22},"2024-12",{"name":44,"class":45},{"id":213,"slug":214,"hasResults":11,"nctId":215,"briefTitle":216,"officialTitle":217,"acronym":218,"eligibilityCriteria":219,"healthyVolunteers":11,"sex":17,"minAge":220,"maxAge":221,"enrollmentInfo":222,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":224,"conditions":225,"keywords":4,"overallStatus":87,"whyStopped":4,"lastUpdateSubmitDate":227,"lastUpdatePostDateStruct":228,"startDateStruct":230,"completionDateStruct":232,"leadSponsor":234,"locationsCount":4},"100564825","the-dubousset-functional-test-in-total-knee-arthloplasty-100564825","NCT06634212","The Dubousset Functional Test in Total Knee Arthloplasty","Validity and Reliability of Dubousset Functional Test in Total Knee Arthloplasty","DFT-TKA","Inclusion Criteria:\n\n* Patients who had Total Knee Arthroplasty\n* Patients aged 50-70 years.\n\nExclusion Criteria:\n\n* Patients who didn't have any Total Kne arthroplasty\n* hose with fractures, pregnancy, a disease that would prevent physical exertion, those with a body mass index (BMI) of 40 kg\u002Fm2 and above, and those with major musculoskeletal or neurological disorders that cause gait disturbance will be excluded from the study.","50 Years","70 Years",{"count":223,"type":22},60,"The aim of this study is to investigate the validity and reliability of Dubousset Functional Test in the patients with Total Knee Prothesis.",[226],"Knee Arthroplasty","2024-10-08",{"date":229,"type":39},"2024-10-09",{"date":231,"type":22},"2024-11-15",{"date":233,"type":22},"2025-07-15",{"name":44,"class":45},{"id":236,"slug":237,"hasResults":11,"nctId":238,"briefTitle":239,"officialTitle":240,"acronym":4,"eligibilityCriteria":241,"healthyVolunteers":11,"sex":17,"minAge":78,"maxAge":79,"enrollmentInfo":242,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":243,"conditions":244,"keywords":246,"overallStatus":87,"whyStopped":4,"lastUpdateSubmitDate":249,"lastUpdatePostDateStruct":250,"startDateStruct":252,"completionDateStruct":253,"leadSponsor":255,"locationsCount":4},"100564366","the-dubousset-functional-test-in-lumbar-spinal-stenosis-100564366","NCT06628245","The Dubousset Functional Test in Lumbar Spinal Stenosis","Validity and Reliability of Dubousset Functional Test in Lumbar Spinal Stenosis","Inclusion Criteria:\n\n* Patients aged 18-65 years, diagnosed with chronic pain (more than three months) due to lumbar spinal stenosis.\n\nExclusion Criteria:\n\n* Those with fractures, pregnancy, a disease that would prevent physical exertion, those with a body mass index (BMI) of 40 kg\u002Fm2 and above, and those with major musculoskeletal or neurological disorders that cause gait disturbance will be excluded from the study.",{"count":223,"type":22},"The aim of this study is to investigate the validity and reliability of Dubousset Functional Test in the patients with lumbar spinal stenosis.",[245],"Lumbar Spinal Stenosis",[245,247,248,162,163],"Functional Status","Dubousset Functional Test","2024-10-03",{"date":251,"type":39},"2024-10-04",{"date":210,"type":22},{"date":254,"type":22},"2025-07",{"name":44,"class":45},{"id":257,"slug":258,"hasResults":11,"nctId":259,"briefTitle":260,"officialTitle":261,"acronym":4,"eligibilityCriteria":262,"healthyVolunteers":16,"sex":17,"minAge":78,"maxAge":263,"enrollmentInfo":264,"targetDuration":4,"studyType":56,"phases":266,"briefSummary":267,"conditions":268,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":273,"lastUpdatePostDateStruct":274,"startDateStruct":276,"completionDateStruct":278,"leadSponsor":279,"locationsCount":46},"100553832","the-relationship-between-pes-planus-diaphragm-postural-control-and-plantar-pressure-100553832","NCT06491212","The Relationship Between Pes Planus, Diaphragm, Postural Control, and Plantar Pressure","Examination of Diaphragm Function, Postural Control, and Plantar Pressure in Individuals With Pes Planus","Inclusion Criteria:\n\nInclusion criteria for individuals with Pes Planus Deformity\n\n* Willing to participate in the study voluntarily\n* Having a Navicular drop test value of 10mm or above\n* Being between the ages of 18-30\n* Having the physical capacity to perform assessments and tests\n* Having a body mass index of 18-25 kg\u002Fm²\n\nExclusion Criteria:\n\n* Exclusion criteria for individuals with Pes Planus Deformity:\n* Termination of voluntariness\n* Those with rigid flatfoot, pes cavus, hallux valgus, hallux rigidus, or calcaneal spur deformity\n* Those with chronic systematic and metabolic diseases (e.g., diabetes mellitus, rheumatoid arthritis, etc.) and musculoskeletal problems (e.g., pes planus) that may affect foot functions and gait\n* Those with any surgical history likely to affect balance, lower extremity strength, and postural control\n* Those with any visual\u002Fvestibular, musculoskeletal, or neurological problems\"\n\nInclusion criteria for healthy participants:\n\n* Willing to participate in the study voluntarily\n* Being between the ages of 18-30\n* Having the physical capacity to perform assessments and tests\n* Having a body mass index of 18-25 kg\u002Fm²\n* Having the ideal height of the medial longitudinal arch of the foot (not having pes planus)\n\nExclusion criteria for healthy participants:\n\n* Termination of voluntariness\n* Those with chronic systematic and metabolic diseases (e.g., diabetes mellitus, rheumatoid arthritis, etc.) and musculoskeletal problems (e.g., pes planus) that may affect foot functions and gait\n* Those with any surgical history likely to affect balance, lower extremity strength, and postural control\n* Those with any visual\u002Fvestibular, musculoskeletal, or neurological problems\"","30 Years",{"count":265,"type":22},34,[58],"Our primary aim is to compare diaphragm function (resting thickness, activity\u002Fresting thickness ratio indicating contractility), postural control, and plantar pressure between individuals with pes planus and healthy controls without pes planus.",[269,270,271,272],"Pes Planus","Diaphragm Issues","Plantar Pressure","Postural Control","2024-06-30",{"date":275,"type":39},"2024-07-09",{"date":277,"type":39},"2024-05-01",{"date":186,"type":22},{"name":44,"class":45},""]