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
Lady Davis Institute
160 participants
May 1, 2024
INTERVENTIONAL
Conditions
Summary
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/participants approached) and retention percentage (participants completing follow-up/participants enrolled).
Eligibility
Inclusion Criteria3
- Has family member admitted to an intensive care unit.
- Expected hospital stay \> 48 hours
- Able to participate in English or French
Exclusion Criteria2
- Has another family member participating in the trial
- Repeat admissions within the study period
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Interventions
Potential participants are provided a visual infographic depicting the key elements of the written consent form in addition to the standard written consent form.
Potential participants are provided an e-gift card to Amazon or Second Cup as a reward for completing the enrollment questionnaire.
Locations(1)
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NCT06588101