[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100617235":3},{"organization":4,"armGroups":7,"interventions":10,"overallOfficials":10,"centralContacts":15,"locations":22,"responsibleParty":57,"collaborators":59,"id":68,"slug":69,"hasResults":70,"nctId":71,"briefTitle":72,"officialTitle":72,"acronym":73,"eligibilityCriteria":74,"healthyVolunteers":75,"sex":76,"minAge":77,"maxAge":78,"enrollmentInfo":79,"targetDuration":10,"studyType":82,"phases":10,"briefSummary":83,"conditions":84,"keywords":86,"overallStatus":90,"whyStopped":10,"lastUpdateSubmitDate":91,"lastUpdatePostDateStruct":92,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"locationsCount":100},{"fullName":5,"class":6},"BioSensics","INDUSTRY",[8,12],{"label":9,"type":10,"description":11,"interventionNames":10},"Hungtinton's Disease",null,"Participants with clinical diagnosis of HD",{"label":13,"type":10,"description":14,"interventionNames":10},"Age-matched healthy adults","Age-matched healthy adults. Clinically assessed to be in good health, with no evidence of neurological disorders that could cause involuntary movements or gait disturbances.",[16],{"name":17,"role":18,"phone":19,"phoneExt":20,"email":21},"Ana Enriquez","CONTACT","888-589-6213","502","ana.enriquez@biosensics.com",[23,42],{"facility":24,"status":10,"city":25,"state":26,"zip":27,"country":28,"countryCode":29,"cosmosGeoPoint":30,"geoPoint":35,"contacts":36},"University of Rochester Medical Center","Rochester","New York","14642","United States","US",{"type":31,"coordinates":32},"Point",[33,34],-77.61556,43.15478,{"lat":34,"lon":33},[37,40],{"name":38,"role":18,"phone":10,"phoneExt":10,"email":39},"Jamie Adams, MD","Jamie_Adams@urmc.rochester.edu",{"name":38,"role":41,"phone":10,"phoneExt":10,"email":10},"PRINCIPAL_INVESTIGATOR",{"facility":43,"status":10,"city":44,"state":45,"zip":46,"country":28,"countryCode":29,"cosmosGeoPoint":47,"geoPoint":51,"contacts":52},"Vanderbilt University Medical Center","Nashville","Tennessee","37212",{"type":31,"coordinates":48},[49,50],-86.78444,36.16589,{"lat":50,"lon":49},[53,55],{"name":54,"role":18,"phone":10,"phoneExt":10,"email":10},"Daniel Claassen, MD",{"name":56,"role":41,"phone":10,"phoneExt":10,"email":10},"Daniel Claassen",{"type":58,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR",[60,63,66],{"name":61,"class":62},"National Center for Advancing Translational Sciences (NCATS)","NIH",{"name":64,"class":65},"University of Rochester - CHeT\u002FCTCC","UNKNOWN",{"name":43,"class":67},"OTHER","100617235","multi-modal-digital-monitoring-of-disease-symptoms-huntingtons-disease-100617235",false,"NCT07315984","Multi-Modal Digital Monitoring of Disease Symptoms Huntington's Disease","BioDigit HD-02","Inclusion Criteria:\n\n* Male or female, aged 25-65 years\n* For HD participants: Genetically diagnosed with HD\n* Fluent in English (able to speak and read).\n* Ambulatory without the need for a walking aid.\n* Able to independently perform all study activities safely, as determined by the investigator.\n* Willing and able to provide informed consent and comply with all study procedures.\n\nFor control participants:\n\n* Male or female, aged 25-65 years\n* Clinically assessed to be in good health, with no evidence of neurological disorders that could cause involuntary movements or gait disturbances\n\nExclusion Criteria:\n\n* Diagnosis of juvenile-onset HD.\n* Individuals who are non-ambulatory.\n* Individuals with a neurological, medical, or psychiatric condition that, in the investigator's judgment, would interfere with safe participation in study activities.\n* Montreal Cognitive Assessment (MoCA) score of 18 or lower\n* Pregnant individuals, due to potential changes in gait and physical activity during pregnancy.\n* Cannot be enrolled into a blinded intervention trial at baseline.",true,"ALL","25 Years","65 Years",{"count":80,"type":81},75,"ESTIMATED","OBSERVATIONAL","The objective of the study is to validate the use of wearable sensors and digital health technologies for monitoring disease activity in Huntington's Disease (HD). Healthy subjects, as well as subjects with documented diagnosis of HD will be screened and recruited at University of Rochester Medical Center and Vanderbilt University Medical Center to participate in this 12-month observational study. There will be a total of 5 visits every approximately 3 months.\n\nIn each study visit, participants will complete several Patient Reported Outcomes (PROs), Clinical Reported Outcomes, complete a series of Digital Assessments (Speech, Cognitive, Motor, and Finger Tapping). Participants will be provided with a pendant, wrist, and ankle sensors to monitor their daily physical activities for 7 days after each study visit. Participants will also be provided with a tablet to complete digital assessments (Speech, Cognitive, Motor, and Finger Tapping) on monthly basis at home.",[85],"Huntington Disease",[87,88,89],"huntington disease","wearable sensors","digital health","NOT_YET_RECRUITING","2025-12-31",{"date":93,"type":94},"2026-01-05","ACTUAL",{"date":96,"type":81},"2026-01-31",{"date":98,"type":81},"2028-12-31",{"name":5,"class":6},2]