[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Jinan University Guangzhou\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":70},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,43],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100565894","effects-of-sleep-body-temperature-on-body-composition-100565894",false,"NCT06648109","Effects of Sleep Body Temperature on Body Composition","Inclusion Criteria:\n\n\\- Participants aged 18-30 years, inclusive of both male and female genders.\n\nExclusion Criteria:\n\n* Individuals suffering from serious diseases such as heart, liver, kidney, brain, hematopoietic, immune, thyroid, malignant tumors, etc.;\n* Those with familial hereditary hypertension (both parents are hypertensive) or those diagnosed with hypertension;\n* Individuals with cognitive or mental impairments that prevent the completion of the questionnaire;\n* Persons with physical disabilities that hinder normal walking;\n* Persons who have experienced a weight change of \\>3.0 kg within 1 month or \\>10 kg within 6 months prior to screening (as per the study in Nutrients. 2020 Oct 21;12(10):3221);\n* Individuals required to take antibiotics from one week before the trial starts until its conclusion;\n* Those with habitual diarrhea or who have experienced diarrhea from one week before the trial starts until its end;\n* Subjects who have participated in other ambient temperature-related trials within the last 6 months;\n* Individuals with extreme sleep schedules (i.e., not falling asleep between 21:00 and 2:00 a.m. the following morning, or waking up before 5:00 a.m.);\n* Those with sleep latency (the time it takes to fall asleep after going to bed) greater than one hour;\n* Pittsburgh Sleep Quality Index (PSQI) scores greater than 16;\n* Participants who do not sign the informed consent form or are deemed unsuitable by the investigator for any other reason.",true,"ALL","18 Years","30 Years",{"count":20,"type":21},40,"ESTIMATED","INTERVENTIONAL",[24],"NA","This will be a crossover controlled trial designed to recruit 40 participants, who will be divided into two groups of 20 subjects each. The participants will be randomly assigned to either Group A or Group B. Group A will receive the sleep electric blanket intervention for a period of 7 days, while Group B will serve as the control group without any additional intervention. After the intervention period, there will be a washout period of 7 days to ensure that any effects of the intervention have subsided before the crossover.\n\nFollowing the washout period, the groups will switch roles: Group B will then receive the sleep electric blanket intervention, and Group A will become the control group. This second phase will also last for 7 days, preceded and followed by the same assessment procedures as the initial phase. This design will allow for a comparison of the intervention's effects against a control period within the same group of participants, enhancing the study's internal validity.",[27,28,29],"Blood Pressure Check (Hypertension Screening)","Heart Rate","Aldosterone Disorder","NOT_YET_RECRUITING","2024-10-17",{"date":33,"type":34},"2024-10-18","ACTUAL",{"date":36,"type":21},"2024-10-20",{"date":38,"type":21},"2025-01-30",{"name":40,"class":41},"Jinan University Guangzhou","OTHER",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":49,"eligibilityCriteria":50,"healthyVolunteers":15,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":51,"targetDuration":18,"studyType":53,"phases":4,"briefSummary":54,"conditions":55,"keywords":60,"overallStatus":61,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":42},"100537225","chinese-obesity-and-metabolic-surgery-database-comes-database-100537225","NCT06275061","Chinese Obesity and MEtabolic Surgery Database (COMES Database)","Chinese Obesity and MEtabolic Surgery Database","COMES","Inclusion Criteria:\n\n* Patients diagnosed as obesity undergoing metabolic and bariatric surgery.\n\nExclusion Criteria:\n\n* Patients treated by non-surgical modalities.",{"count":52,"type":21},1000000,"OBSERVATIONAL","The purpose of the Chinese Obesity and MEtabolic Surgery Database (COMES Database) is to collect data and examine the long-term effects of metabolic and bariatric surgery on obesity and metabolic disorders in the Chinese population.",[56,57,58,59],"Obesity","Metabolic Surgery","Bariatric Surgery","Weight Loss",[56,57,58,59],"RECRUITING","2024-02-21",{"date":64,"type":34},"2024-02-23",{"date":66,"type":34},"2020-05-01",{"date":68,"type":21},"2040-12-31",{"name":40,"class":41},""]