Improving family engagement in critical care settings
Official title: Increasing Family Engagement in Critical Care: The NGAGE Trial (The NGAGE Trial)
Run by Lady Davis Institute · NCT06586528 · Data updated 2026-11-12
This study is testing a new tool to see if it helps families of ICU patients feel more involved and satisfied with their loved one's care.
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 | March 26, 2025 |
| Main results expected | July 2026 |
| Study ends | September 2027 |
| Registry record updated | May 18, 2025 |
| Trial ID | NCT06586528 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 expected to stay in the ICU for at least 48 hours.
✕Probably not a fit
Patients who do not wish to involve their family members in their 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 effectiveness of the NGAGE tool in enhancing family engagement among relatives of ICU patients. It is a stepped wedge cluster randomized trial conducted across six adult ICUs in Canada, involving 194 family members. The NGAGE tool includes modules for learning, engaging, and reporting, allowing family members to communicate their desired involvement in patient care to the healthcare team. The study aims to improve communication, care satisfaction, psychological well-being, and quality of life for family members during the critical care experience.
Why it matters
Potential benefit: If successful, this could significantly enhance the involvement and satisfaction of family members in the care of ICU patients.
How similar studies have gone: Other studies have shown positive outcomes with family engagement tools in critical care settings, indicating a promising approach.
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 * Able to participate in English or French 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
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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: Jillian Kifell, MSc
- Email: jillian.kifell.ccomtl@ssss.gouv.qc.ca
- Phone: 5143408222
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Involving families in ICU rounds to improve care engagement
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.
-
Family-centred care in UK inpatient wards
This study tests how family involvement in adult internal medicine wards is understood and experienced by patients, their families, and nurses at Milton Keynes University Hospital.
-
Deciphering why some patients stay a long time in the ICU using detailed clinical profiling
This study will try to identify clinical patterns in adults who stay in the ICU five days or longer to better understand persistent critical illness.
-
Delphi consensus to guide mechanical insufflation-exsufflation use in the ICU
A panel of ICU and lung specialists will use a structured survey process to agree on best practices for using mechanical insufflation-exsufflation to help airway clearance in critically ill patients.
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Behavioral health collaborative care for family members of ICU survivors in the Post-ICU clinic pilot
This pilot tests a telehealth-based behavioral health program using the NeuroFlow app for family members of ICU survivors to try to reduce anxiety, depression, and PTSD symptoms.
-
Family-integrated newborn care for preterm and low-birth-weight babies
This project will try training and integrating parents into hospital care for preterm and low-birth-weight newborns in Tigray to see if it shortens hospital stays and improves outcomes.
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.