[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100565894":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":18,"centralContacts":25,"locations":35,"responsibleParty":48,"collaborators":18,"id":51,"slug":18,"hasResults":52,"nctId":53,"briefTitle":54,"officialTitle":54,"acronym":18,"eligibilityCriteria":55,"healthyVolunteers":56,"sex":57,"minAge":58,"maxAge":59,"enrollmentInfo":60,"targetDuration":18,"studyType":63,"phases":64,"briefSummary":66,"conditions":67,"keywords":18,"overallStatus":71,"whyStopped":18,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":81},{"fullName":5,"class":6},"Jinan University Guangzhou","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Mild-heat group","EXPERIMENTAL","Participants will be randomized into groups A and B. When the subject's group cohort undergoes the intervention phase (as opposed to the control phase), they will receive a 7-day, 8-hour intervention with an electric blanket set at +5±1°C above room temperature.",[13],"Device: Electric Blanket",{"label":15,"type":16,"description":17,"interventionNames":18},"Non-mild-heat group","NO_INTERVENTION","Participants will be randomized into groups A and B. There will be no additional sleep temperature intervention while the group is in the control period.",null,[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":18},"DEVICE","Electric Blanket","Participants were randomized to groups A and B. When the subject\\'s group cohort went through the intervention phase (instead of the control phase), they received a 7-day, 8-hour intervention with an electric blanket +5±1°C above room temperature.",[9],[26,31],{"name":27,"role":28,"phone":29,"phoneExt":18,"email":30},"Fangfang Zeng","CONTACT","+86 13822285635","zengffjnu@126.com",{"name":32,"role":28,"phone":33,"phoneExt":18,"email":34},"Jiamin Qiu","+86 178196663352","adniminday@163.com",[36],{"facility":5,"status":18,"city":37,"state":38,"zip":39,"country":40,"countryCode":41,"cosmosGeoPoint":42,"geoPoint":47,"contacts":18},"Guangzhou","Select A State","510632","China","CN",{"type":43,"coordinates":44},"Point",[45,46],113.25,23.11667,{"lat":46,"lon":45},{"type":49,"investigatorFullName":27,"investigatorTitle":50,"investigatorAffiliation":5,"oldNameTitle":18,"oldOrganization":18},"PRINCIPAL_INVESTIGATOR","Associate Professor","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":61,"type":62},40,"ESTIMATED","INTERVENTIONAL",[65],"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.",[68,69,70],"Blood Pressure Check (Hypertension Screening)","Heart Rate","Aldosterone Disorder","NOT_YET_RECRUITING","2024-10-17",{"date":74,"type":75},"2024-10-18","ACTUAL",{"date":77,"type":62},"2024-10-20",{"date":79,"type":62},"2025-01-30",{"name":5,"class":6},1]