Skip to content

The Family-ICU Trial

Health Care Delivery | Critical Care, Intensive Care | Physician Rounds | Family-centered Care | Family...

Family inclusion in adult intensive care unit (ICU) rounds is recommended by critical care professional societies, yet widespread uptake of this practice is limited. A key barrier cited by ICU clinicians is insufficient evidence to support this practice. There is a need for robust evidence to support family participation in adult ICU rounds and influence change to routine clinical care. The primary purpose of this study is to assess whether family participation in adult ICU rounds improves family engagement in care. The secondary objectives are to assess family satisfaction, and anxiety and depression, to explore user experiences of family participation in ICU rounds, and to evaluate strategies to improve family member recruitment and retention rates. This is a stepped-wedge cluster randomized trial (n=194) at 6 Canadian ICUs. The stepped wedge cluster randomized trial is a pragmatic study design that overcomes methodological limitations in evaluating a healthcare service delivery intervention. In the stepped-wedge cluster design, there is random and sequential crossover of clusters from control (phase 1) to intervention (phase 2) until all clusters are exposed. The stepped-wedge design also allows each site to function as its own control. The stepped-wedge design is more powerful than a parallel design when substantial cluster level effects are present.

null

Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    18 and up

Participation 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

Study Location

McGill University Health Centre
McGill University Health Centre
Montreal, Quebec
Canada

Contact Study Team

Primary Contact

Jillian Kifell, MSc

[email protected]
5143408222
Backup Contact

Michael J Goldfarb, MD, MSc

Jewish General Hospital
Jewish General Hospital
Montreal, Quebec
Canada

Contact Study Team

Backup Contact

Michael J Goldfarb, MD, MSc

Primary Contact

Jillian Kifell, MSc

[email protected]
5143408222
Study Sponsored By
Lady Davis Institute
Participants Required
More Information
Study ID: NCT06586541