Descriptions and Practices of Family Engagement in Emergency Care Setting

August 14, 2026 updated by: Natalie S. McAndrew, PhD, RN, Mayo Clinic

Descriptions and Practices of Family Engagement in Emergency Care Setting: An International, Multisite Qualitative- Descriptive Study

The purpose of this study is to explore and describe nurses' perceptions of their levels and practices of family engagement in Emergency Departments and the experiences of family members in delivery of Emergency Department care.

Study Overview

Status

Not yet recruiting

Conditions

Study Type

Observational

Enrollment (Estimated)

70

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Minnesota
      • Mankato, Minnesota, United States, 56001
        • Mayo Clinic Health System Mankato Emergency Department
      • Rochester, Minnesota, United States, 55905
        • Mayo Clinic Emergency Department
    • Vermont
      • Bennington, Vermont, United States, 05201
        • Southwestern Vermont Medical Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Research team members and nurse researchers who are members of the International Family Nursing Association (IFNA) Research Committee will recruit ED nurses and family members in collaboration with local research or clinical staff.

Description

Inclusion Criteria:

  • Nurses: Registered professional nurses, including those with a diploma, associate's degree, and baccalaureate degrees, who are in charge of the plan of care for the ED patient.

    • Nurses who have been working in that particular ED environment for at least 6 months.
    • Nurses involved in providing direct patient care (not managers).
    • Nurses who are employed by the institution of the research study, not agency staff.
  • Family Members: a family member who expressed a sense of belonging to a patient admitted to the ED, or a person that a communicating patient had defined as family or being significant to the patient.

    • Family members who are present with a patient who is being seen in the ED for acute or chronic illness (1 family member to participate per patient).
    • Age 18 years or older
    • Able to speak and read in English (for the United States sample)

Exclusion Criteria:

  • Nurses not caring for patients in the ED
  • Family members who are not present in the ED with the patient.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Emergency Department Nurses
Registered professional nurses, including those with a diploma, associate's degree, and baccalaureate degrees, who are in charge of the plan of care for the ED patient.
Nurses who consent to participate in the study will be asked to partake in an interview that will include questions such as "Please describe how you work with families", "What do you do to engage families?", or "What promotes or hinders family engagement in your ED".
Family Members of Emergency Department Patients
A family member who expressed a sense of belonging to a patient admitted to the ED, or a person that a communicating patient had defined as family or being significant to the patient.
Family members who consent to participate in the study will be asked to partake in an interview and will be asked "What has it been like to be in the ED with your family member?"

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of family member participants
Time Frame: Baseline
Total number of family members who participated in study interview
Baseline
Number of nursing participants
Time Frame: Baseline
Total number of nurses who participated in study interview
Baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Investigators

  • Principal Investigator: Natalie McAndrew, PhD,RN,CCRN, Mayo Clinic

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

September 1, 2026

Primary Completion (Estimated)

December 31, 2026

Study Completion (Estimated)

December 31, 2027

Study Registration Dates

First Submitted

July 28, 2026

First Submitted That Met QC Criteria

July 28, 2026

First Posted (Actual)

July 31, 2026

Study Record Updates

Last Update Posted (Actual)

August 18, 2026

Last Update Submitted That Met QC Criteria

August 14, 2026

Last Verified

August 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • 25-012667

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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