[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100561279":3},{"organization":4,"armGroups":7,"interventions":28,"overallOfficials":37,"centralContacts":42,"locations":49,"responsibleParty":66,"collaborators":69,"id":73,"slug":74,"hasResults":75,"nctId":76,"briefTitle":77,"officialTitle":78,"acronym":79,"eligibilityCriteria":80,"healthyVolunteers":75,"sex":81,"minAge":82,"maxAge":19,"enrollmentInfo":83,"targetDuration":19,"studyType":86,"phases":87,"briefSummary":89,"conditions":90,"keywords":19,"overallStatus":52,"whyStopped":19,"lastUpdateSubmitDate":99,"lastUpdatePostDateStruct":100,"startDateStruct":103,"completionDateStruct":105,"leadSponsor":107,"locationsCount":108},{"fullName":5,"class":6},"Lady Davis Institute","OTHER",[8,15,20,24],{"label":9,"type":10,"description":11,"interventionNames":12},"Both recruitment strategies","EXPERIMENTAL","Consent form with Infographic + Large compensation",[13,14],"Other: Written informed consent with infographic","Other: Compensation",{"label":16,"type":17,"description":18,"interventionNames":19},"Neither recruitment strategy","NO_INTERVENTION","Consent form + No compensation",null,{"label":21,"type":10,"description":22,"interventionNames":23},"One recruitment strategy - Infographic","Consent form with Infographic + No compensation",[13],{"label":25,"type":10,"description":26,"interventionNames":27},"One recruitment strategy - Compensation","Consent form + Large compensation",[14],[29,33],{"type":6,"name":30,"description":31,"armGroupLabels":32,"otherNames":19},"Written informed consent with infographic","Potential participants are provided a visual infographic depicting the key elements of the written consent form in addition to the standard written consent form.",[9,21],{"type":6,"name":34,"description":35,"armGroupLabels":36,"otherNames":19},"Compensation","Potential participants are provided an e-gift card to Amazon or Second Cup as a reward for completing the enrollment questionnaire.",[9,25],[38],{"name":39,"affiliation":40,"role":41},"Michael J Goldfarb, MD, MSc","Lady Davis Institute, McGill University, Jewish General Hospital","PRINCIPAL_INVESTIGATOR",[43],{"name":44,"role":45,"phone":46,"phoneExt":47,"email":48},"Jillian Kifell, MSc","CONTACT","5143408222","25806","jillian.kifell.ccomtl@ssss.gouv.qc.ca",[50],{"facility":51,"status":52,"city":53,"state":54,"zip":19,"country":55,"countryCode":56,"cosmosGeoPoint":57,"geoPoint":62,"contacts":63},"Jewish General Hospital","RECRUITING","Montreal","Quebec","Canada","CA",{"type":58,"coordinates":59},"Point",[60,61],-73.58781,45.50884,{"lat":61,"lon":60},[64,65],{"name":44,"role":45,"phone":46,"phoneExt":47,"email":48},{"name":39,"role":41,"phone":19,"phoneExt":19,"email":19},{"type":41,"investigatorFullName":67,"investigatorTitle":68,"investigatorAffiliation":5,"oldNameTitle":19,"oldOrganization":19},"Michael Goldfarb","Attending Staff, Division of Cardiology",[70],{"name":71,"class":72},"Canadian Institutes of Health Research (CIHR)","OTHER_GOV","100561279","clinical-trial-recruitment-and-retention-strategies-for-family-members-in-the-icu-100561279",false,"NCT06588101","Clinical Trial Recruitment and Retention Strategies for Family Members in the ICU","Clinical Trial Recruitment and Retention Strategies for Family Members in the Intensive Care Unit: A Study Within A Trial Randomized Design","SWAT","Inclusion Criteria:\n\n* Has family member admitted to an intensive care unit.\n* Expected hospital stay \\> 48 hours\n* Able to participate in English or French\n\nExclusion Criteria:\n\n* Has another family member participating in the trial\n* Repeat admissions within the study period","ALL","18 Years",{"count":84,"type":85},160,"ESTIMATED","INTERVENTIONAL",[88],"NA","There is a need to identify strategies that improve the conduct of clinical trials involving family members of intensive care unit (ICU) patients. The purpose of the present study is to evaluate recruitment and retention strategies for clinical trials involving family members of ICU patients. 4 strategies (2 recruitment and 2 retention) will be tested. Investigators will integrate the strategies into three existing studies that involve family members of ICU patients. Participants will be randomized using a 2x2 factorial design. The co-primary outcomes are recruitment percentage (participants enrolled\u002Fparticipants approached) and retention percentage (participants completing follow-up\u002Fparticipants enrolled).",[91,92,93,94,95,96,97,98],"Family Members","Recruitment","Clinical Study","Retention","Recruitment of Participants","Study Enrollment","Retention of Participants","Compensation Incentives","2025-05-29",{"date":101,"type":102},"2025-06-04","ACTUAL",{"date":104,"type":102},"2024-05-01",{"date":106,"type":85},"2026-12-31",{"name":5,"class":6},1]