[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100491257":3},{"organization":4,"armGroups":7,"interventions":8,"overallOfficials":12,"centralContacts":17,"locations":25,"responsibleParty":43,"collaborators":7,"id":45,"slug":46,"hasResults":47,"nctId":48,"briefTitle":49,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":47,"sex":52,"minAge":53,"maxAge":54,"enrollmentInfo":55,"targetDuration":7,"studyType":58,"phases":7,"briefSummary":59,"conditions":60,"keywords":7,"overallStatus":28,"whyStopped":7,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":71},{"fullName":5,"class":6},"The Leeds Teaching Hospitals NHS Trust","OTHER",null,[9],{"type":6,"name":10,"description":11,"armGroupLabels":7,"otherNames":7},"No intervenetion","Observational inception cohort, with remote follow-up via participants and data record linkage",[13],{"name":14,"affiliation":15,"role":16},"Helena Marzo-Ortega, MD\u002FPhD","Leeds Teaching Hospital Trust","PRINCIPAL_INVESTIGATOR",[18,22],{"name":14,"role":19,"phone":20,"phoneExt":7,"email":21},"CONTACT","+44 113 3924848","h.marzo-ortega@leeds.ac.uk",{"name":23,"role":19,"phone":7,"phoneExt":7,"email":24},"Sayyora Alieva","sayyorakhon.alieva@nhs.net",[26],{"facility":27,"status":28,"city":29,"state":7,"zip":30,"country":31,"countryCode":32,"cosmosGeoPoint":33,"geoPoint":38,"contacts":39},"Chapel Allerton Hospital","RECRUITING","Leeds","LS7 4SA","United Kingdom","UK",{"type":34,"coordinates":35},"Point",[36,37],-1.54785,53.79648,{"lat":37,"lon":36},[40,41],{"name":23,"role":19,"phone":7,"phoneExt":7,"email":24},{"name":42,"role":19,"phone":7,"phoneExt":7,"email":21},"Helena Marzo-Ortega, PhD",{"type":44,"investigatorFullName":7,"investigatorTitle":7,"investigatorAffiliation":7,"oldNameTitle":7,"oldOrganization":7},"SPONSOR","100491257","british-axial-spondyloarthritis-inception-cohort-100491257",false,"NCT05676775","British Axial Spondyloarthritis Inception Cohort","BAxSIC","Inclusion Criteria:\n\n1. Aged ≥16 years.\n2. A physician diagnosis of axSpA (including ankylosing spondylitis) within the last 6 months prior to baseline.\n3. Willing and able to give informed consent to participate in the study.\n\nExclusion Criteria:\n\n1. Age \\\u003C16 years.\n2. Unable to communicate in English or are deemed, in any other way, to be unable to give informed consent","ALL","16 Years","50 Years",{"count":56,"type":57},500,"ESTIMATED","OBSERVATIONAL","The British Axial Spondyloarthritis Cohort (BAxSIC) study has been established under the auspices of the British Society for Spondyloarthritis (BRITSpA) in collaboration with the National Axial Spondyloarthritis Society (NASS) to provide real-world data to evaluate the impact of delay in diagnosis (from symptom onset to diagnosis) on work participation and functional outcomes and the natural history and impact of newly-diagnosed axial Spondyloarthritis, including disease activity, pain, fatigue, functional and work outcomes, comorbidities, therapies in the United Kingdom (UK). The study is a prospective cohort, enrolling patients attending rheumatology clinics in the UK who are newly diagnosed with axial Spondyloarthritis and naïve to biologic therapy.\n\nThe study will run for an initial 3 year period commencing January 2023. Financial support was provided as a Research Grant from Pfizer Limited, UCB and Novartis.",[61],"Axial Spondyloarthritis","2023-07-14",{"date":64,"type":65},"2023-07-18","ACTUAL",{"date":67,"type":65},"2023-06-09",{"date":69,"type":57},"2029-01-09",{"name":5,"class":6},1]