CClinicalTrials.gg
Not yet recruitingNCT07739576Updated Aug 18, 2026

Descriptions and Practices of Family Engagement in Emergency Care Setting

An observational study in Emergency Care, sponsored by Mayo Clinic. Not yet recruiting at 3 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-08-18.

Sponsored by Mayo Clinic · Observational

Study type
Observational
Model
Ecologic or community
Time perspective
Cross-sectional
Enrollment
70
Ages
18 Years and older
Sex
All
01

Study summary

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.

02

Conditions studied

  • Emergency Care
03

In context

Lead sponsor

Mayo Clinic is the lead sponsor of 3,218 studies on the registry; 670 are open to participants now.

Of its 445 completed or terminated interventional studies of FDA-regulated products, 313 (70%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
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.

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

Exclusion Criteria:

  • Nurses not caring for patients in the ED
  • Family members who are not present in the ED with the patient.
05

Study design

Observational model
Ecologic or community
Time perspective
Cross-sectional
Enrollment
70 participants (estimated)
Patient registry
No

Groups and cohorts

  • 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.

    Other: Nurse Interview

  • 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.

    Other: Family Interview

Interventions

  • OtherNurse Interview

    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".

  • OtherFamily Interview

    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?"

06

What researchers measure

Primary outcomes

  1. Number of family member participants

    Total number of family members who participated in study interview

    Time frame: Baseline

  2. Number of nursing participants

    Total number of nurses who participated in study interview

    Time frame: Baseline

07

Study locations

3 sites
  • Mayo Clinic Health System Mankato Emergency Department
    Mankato, Minnesota 56001, United States
  • Mayo Clinic Emergency Department
    Rochester, Minnesota 55905, United States
  • Southwestern Vermont Medical Center
    Bennington, Vermont 05201, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07739576
Lead sponsor
Mayo Clinic
Responsible party
Natalie S. McAndrew, PhD, RN (Principal Investigator, Mayo Clinic) — Principal investigator
First posted
Jul 31, 2026
Start date
Sep 1, 2026 (estimated)
Primary completion
Dec 31, 2026 (estimated)
Completion
Dec 31, 2027 (estimated)
Last update
Aug 18, 2026

Study contacts

Natalie McAndrew, PhD,RN,CCRN
Contact
mcandrew.natalie@mayo.edu
414-704-0876
Natalie McAndrew, PhD,RN,CCRN
principal investigator · Mayo Clinic

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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