Improving recruitment and retention of family members in ICU clinical trials
Official title: Clinical Trial Recruitment and Retention Strategies for Family Members in the Intensive Care Unit: A Study Within A Trial Randomized Design
Run by Lady Davis Institute · NCT06588101 · Data updated 2026-11-12
This study is trying out different ways to get family members of ICU patients to join and stay in clinical trials to see which methods work best.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 160 (estimated) |
| Sponsor | Lady Davis Institute Academic / other |
| Locations | 1 site (Montreal, Quebec) |
| Status | Recruiting |
| Started | May 1, 2024 |
| Main results expected | April 30, 2026 |
| Study ends | December 31, 2026 |
| Registry record updated | June 4, 2025 |
| Trial ID | NCT06588101 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are family members of patients admitted to an ICU with an expected hospital stay of more than 48 hours.
✕Probably not a fit
Patients who have another family member participating in the trial or those with repeat admissions during the study period may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study evaluates strategies to enhance the recruitment and retention of family members of ICU patients in clinical trials. It will test four specific strategies, two focused on recruitment and two on retention, integrated into three ongoing studies involving these family members. Participants will be randomized using a 2x2 factorial design, with the primary outcomes being the percentage of participants recruited and retained. The goal is to generate high-quality evidence to support family engagement practices in the ICU setting.
Why it matters
Potential benefit: If successful, this study could lead to improved participation of family members in clinical trials, enhancing the quality of evidence for family engagement in ICU care.
How similar studies have gone: While there is a recognized need for improved family engagement in ICU settings, this specific approach to recruitment and retention strategies is novel and has not been extensively tested.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Has family member admitted to an intensive care unit. * Expected hospital stay \> 48 hours * Able to participate in English or French Exclusion Criteria: * Has another family member participating in the trial * Repeat admissions within the study period
Where it's running
-
Jewish General Hospital
Montreal, Quebec, Canada Recruiting
Study contacts
- Principal investigator: Michael J Goldfarb, MD, MSc — Lady Davis Institute, McGill University, Jewish General Hospital
- Study coordinator: Jillian Kifell, MSc
- Email: jillian.kifell.ccomtl@ssss.gouv.qc.ca
- Phone: 5143408222
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.