Involving families in ICU rounds to improve care engagement
Family Participation in Intensive Care Unit Rounds (The Family-ICU Trial)
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
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 194 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Lady Davis Institute Academic / other |
| Locations | 2 sites (Montreal, Quebec and 1 other locations) |
| Trial ID | NCT06586541 on ClinicalTrials.gov |
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.
Who should consider this trial
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.
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.
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 performed: Previous studies have shown positive outcomes with family engagement in critical care settings, suggesting this approach may be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult family members (age ≥ 18 years) of ICU patients * Expected ICU stay ≥ 48 hours * Family members wishing to participate in rounds virtually must have the technological capability and understanding to participate virtually (must have a phone or computer with internet and audio/video capabilities) 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 this trial is running
Montreal, Quebec and 1 other locations
- Jewish General Hospital — Montreal, Quebec, Canada (Recruiting)
- McGill University Health Centre — Montreal, Quebec, Canada (Not_yet_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
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.