[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100496198":3},{"organization":4,"armGroups":7,"interventions":25,"overallOfficials":33,"centralContacts":34,"locations":43,"responsibleParty":60,"collaborators":33,"id":64,"slug":65,"hasResults":66,"nctId":67,"briefTitle":68,"officialTitle":68,"acronym":33,"eligibilityCriteria":69,"healthyVolunteers":66,"sex":70,"minAge":71,"maxAge":33,"enrollmentInfo":72,"targetDuration":33,"studyType":75,"phases":76,"briefSummary":78,"conditions":79,"keywords":33,"overallStatus":46,"whyStopped":33,"lastUpdateSubmitDate":86,"lastUpdatePostDateStruct":87,"startDateStruct":90,"completionDateStruct":92,"leadSponsor":94,"locationsCount":95},{"fullName":5,"class":6},"Scripps Translational Science Institute","OTHER",[8,13,17,21],{"label":9,"type":6,"description":10,"interventionNames":11},"Control: study provided wearables","Following consent and the completion of the baseline assessments the control group will receive basic education on symptom management. At the 3 month timepoint they will be prompted to order their device and receive enhanced education that will provide information on how wearable devices can be used to monitor and manage symptoms.",[12],"Device: Wearable device",{"label":14,"type":6,"description":15,"interventionNames":16},"Treatment: study provided wearables","Following consent and the completion of the baseline assessments the treatment group will be prompted to order their device and receive basic education on symptom management along with the enhanced education on wearable devices.",[12],{"label":18,"type":6,"description":19,"interventionNames":20},"Control: self provided wearables","Following consent and the completion of the baseline assessments the control group will receive basic education on symptom management. At the 3 month timepoint they will be receive enhanced education that will provide information on how wearable devices can be used to monitor and manage symptoms.",[12],{"label":22,"type":6,"description":23,"interventionNames":24},"Treatment: self provided wearables","Following consent and the completion of the baseline assessments the treatment group will receive basic education on symptom management along with the enhanced education on wearable devices.",[12],[26],{"type":27,"name":28,"description":29,"armGroupLabels":30,"otherNames":31},"DEVICE","Wearable device","The treatment group will receive their wearable device and the enhanced education at the start of the study. Their outcomes will be compared with the control group who will receive at 3 months.",[18,9,22,14],[32],"Educational materials",null,[35,40],{"name":36,"role":37,"phone":38,"phoneExt":33,"email":39},"Andrea Goosen","CONTACT","0000000000","agoosen@scripps.edu",{"name":41,"role":37,"phone":33,"phoneExt":33,"email":42},"Romina Foster-Bonds","rfoster@scripps.edu",[44],{"facility":45,"status":46,"city":47,"state":48,"zip":49,"country":50,"countryCode":51,"cosmosGeoPoint":52,"geoPoint":57,"contacts":58},"Scripps Research","RECRUITING","La Jolla","California","92037","United States","US",{"type":53,"coordinates":54},"Point",[55,56],-117.2742,32.84727,{"lat":56,"lon":55},[59],{"name":36,"role":37,"phone":33,"phoneExt":33,"email":33},{"type":61,"investigatorFullName":62,"investigatorTitle":63,"investigatorAffiliation":5,"oldNameTitle":33,"oldOrganization":33},"PRINCIPAL_INVESTIGATOR","Julia Moore Vogel","Director","100496198","the-long-covid-19-wearable-device-study-100496198",false,"NCT05741112","The Long COVID-19 Wearable Device Study","Inclusion Criteria:\n\n* Is at least 18 years old.\n* Has a self\u002Fand or physician diagnosis of:\n* Long COVID (based on the WHO working definition),\n* ME\u002FCFS (myalgic encephalomyelitis \u002F chronic fatigue syndrome, self-diagnosis based on IOM criteria), and\u002For\n* POTS (Postural Orthostatic Tachycardia Syndrome).\n* Is interested in tools to manage ME\u002FCFS, POTS, and\u002For Long COVID symptoms.\n* Owns a wearable device they are willing to use for this study or does not own a device and agrees to utilize a study-provided one.\n* Agrees to wear the device throughout the study period, share the data with the study, and sync data at least weekly.\n* Has access to a smartphone or tablet to enable syncing wearable data and viewing device feedback.\n* Agrees to disclose involvement in other ME\u002FCFS, POTS, and\u002For Long COVID interventions such as medical treatment, self-management, and other interventional studies.\n* Agrees to complete at least 75% of the study surveys.\n\nExclusion Criteria:\n\n* As long as they meet inclusion there is no exclusion","ALL","18 Years",{"count":73,"type":74},100500,"ESTIMATED","INTERVENTIONAL",[77],"NA","To further characterize Long COVID-19 by collecting data from individuals who already own wearable devices or are provided with a wearable device along with basic and enhanced educational materials to determine if both can improve Long COVID-19 symptom management and post-exertional malaise.",[80,81,82,83,84,85],"Long COVID","Postural Orthostatic Tachycardia Syndrome","Dysautonomia","Myalgic Encephalomyelitis","Chronic Fatigue Syndrome","Long Covid19","2025-05-09",{"date":88,"type":89},"2025-05-11","ACTUAL",{"date":91,"type":89},"2023-11-16",{"date":93,"type":74},"2025-12-01",{"name":5,"class":6},1]