Involving families in ICU rounds to improve care engagement
Official title: Family Participation in Intensive Care Unit Rounds (The Family-ICU Trial)
Run by Lady Davis Institute · NCT06586541 · Data updated 2026-11-12
This study tests if including families in rounds at adult ICUs can help them feel more involved and satisfied with the care their loved ones receive.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 194 (estimated) |
| Sponsor | Lady Davis Institute Academic / other |
| Locations | 2 sites (Montreal, Quebec and 1 other locations) |
| Status | Recruiting |
| Started | November 18, 2024 |
| Main results expected | February 2028 |
| Study ends | July 2029 |
| Registry record updated | August 14, 2026 |
| Trial ID | NCT06586541 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adult family members of ICU patients who are willing to participate in rounds and have the necessary technology to do so.
✕Probably not a fit
Patients who do not wish to involve their family in care or those with repeat admissions during the study period may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This trial evaluates the impact of family participation in adult ICU rounds on family engagement in care. It addresses the limited uptake of family inclusion in ICU practices by providing robust evidence to support this approach. The study employs a stepped-wedge cluster randomized design across six Canadian ICUs, involving 194 participants. Key outcomes include family satisfaction, anxiety, and depression, as well as strategies for improving family recruitment and retention.
Why it matters
Potential benefit: If successful, this study could enhance family engagement and satisfaction in the care of ICU patients.
How similar studies have gone: Previous studies have shown positive outcomes with family engagement in critical care settings, suggesting this approach may be effective.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult family members (age ≥ 18 years) of ICU patients * Expected ICU stay ≥ 48 hours Exclusion Criteria: * Family members who do not wish to participate in care * Repeat admissions within the study period * Another family member has already participated in the study
Where it's running
-
Jewish General Hospital
Montreal, Quebec, Canada Recruiting -
McGill University Health Centre
Montreal, Quebec, Canada Recruiting
Study contacts
- Principal investigator: Michael J Goldfarb, MD, MSc — Lady Davis Institute, McGill University, Jewish General Hospital
- Study coordinator: Kabisan Vilvaratnam
- Email: kabisan.vilvaratnam.ccomtl@ssss.gouv.qc.ca
- Phone: 5143408222
Similar studies
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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.