[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100626294":3},{"organization":4,"armGroups":7,"interventions":10,"overallOfficials":12,"centralContacts":17,"locations":23,"responsibleParty":38,"collaborators":10,"id":40,"slug":10,"hasResults":41,"nctId":42,"briefTitle":43,"officialTitle":44,"acronym":45,"eligibilityCriteria":46,"healthyVolunteers":47,"sex":48,"minAge":49,"maxAge":10,"enrollmentInfo":50,"targetDuration":53,"studyType":54,"phases":10,"briefSummary":55,"conditions":56,"keywords":58,"overallStatus":25,"whyStopped":10,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":70,"completionDateStruct":71,"leadSponsor":73,"locationsCount":74},{"fullName":5,"class":6},"Clover Link","INDUSTRY",[8],{"label":9,"type":10,"description":11,"interventionNames":10},"Cohort C - Test-Retest Reliability",null,"Adult volunteers recruited from a health and well-being newsletter subscriber base. Participants complete the 28-item WB6Dim digital self-assessment at baseline (T1) and again 3 days later (T2). A contamination control question at T2 identifies participants who experienced a significant life event during the interval. An optional third assessment (T3) is completed at 9 weeks by participants who voluntarily accessed a well-being program after T2 completion.",[13],{"name":14,"affiliation":15,"role":16},"Frédérique MD, PhD RETORNAZ, MD, PhD","European Hospital, Unit of Care and Research in Internal Medicine and Infectious Diseases.","STUDY_CHAIR",[18],{"name":19,"role":20,"phone":21,"phoneExt":10,"email":22},"quentin ALITTA","CONTACT","+33686505361","quentin.alitta@gmail.com",[24],{"facility":5,"status":25,"city":26,"state":10,"zip":27,"country":28,"cosmosGeoPoint":29,"geoPoint":34,"contacts":35},"RECRUITING","Bandol","83150","France",{"type":30,"coordinates":31},"Point",[32,33],5.74718,43.14247,{"lat":33,"lon":32},[36],{"name":37,"role":20,"phone":21,"phoneExt":10,"email":22},"ALITTA quentin",{"type":39,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100626294",false,"NCT07433764","Test-Retest Reliability of the WB6Dim Digital Well-Being Tool: A 3-Day Interval Study","Psychometric Validation of Test-Retest Reliability of the WB6Dim Digital Self-Assessment Tool for Well-Being Using a 3-Day Interval Protocol and Contamination Control","WB6Dim-TRT","Inclusion Criteria:\n\n* Adults aged 18 years or older\n* Able to read and understand French\n* Access to an internet-connected device\n* Willing to complete the WB6Dim questionnaire at T1 and T2\n* Consent to anonymous data collection for research purposes\n\nExclusion Criteria:\n\n* Under 18 years of age\n* Unable to read or understand French",true,"ALL","18 Years",{"count":51,"type":52},500,"ESTIMATED","9 Weeks","OBSERVATIONAL","This study aims to establish the test-retest reliability of the WB6Dim digital self-assessment tool across its eight well-being dimensions, using a 3-day interval protocol designed to minimize the probability of genuine well-being changes between assessments.\n\nParticipants complete the 28-item WB6Dim questionnaire at baseline (T1) and again 3 days later (T2). A single contamination control question at T2 identifies participants who experienced a significant life event during the interval; these pairs are excluded from primary ICC analyses and retained for exploratory analyses.\n\nAn optional third assessment at 9 weeks (T3) provides preliminary exploratory data on sensitivity to change following access to a well-being program. T3 is not part of the primary design.",[57],"Psychological Well Being",[59,60,61,62,63,64,65],"well-being","Test-retest reliability","Intraclass correlation","Digital self-assessment","WB6Dim","Psychometric validation","Workplace well-being","2026-02-19",{"date":68,"type":69},"2026-02-25","ACTUAL",{"date":66,"type":69},{"date":72,"type":52},"2026-05-09",{"name":5,"class":6},1]