Clinical Trial Recruitment and Retention Strategies for Family Members in the ICU

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorLady Davis Institute

About this trial

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 criteria

Qualifiers

Has family member admitted to an intensive care unit.

Expected hospital stay > 48 hours

Able to participate in English or French

Disqualifiers

Has another family member participating in the trial

Repeat admissions within the study period

Trial design

Treatments tested in this trial

  • Written informed consent with infographic
  • Compensation

Treatment groups

160 Participants
are divided into 4 treatment groups

Sponsors and collaborators

Lady Davis Institute

Lead sponsor

Canadian Institutes of Health Research (CIHR)

Collaborator