- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07739576
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
Intervention / Treatment
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
- Name: Natalie McAndrew, PhD,RN,CCRN
- Phone Number: 414-704-0876
- Email: mcandrew.natalie@mayo.edu
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
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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.