The goal of this clinical trial is to learn if using point-of-care ultrasound (POCUS) can increase participant engagement and changes in behavior among adults with risk factors for pre-symptomatic heart failure presenting to the emergency department. The main questions it aims to answer are: 1. Does POCUS increase understanding of heart failure and the likelihood to improve diet, exercise, and follow up? 2. Does POCUS improve diet, exercise, follow up, and self-efficacy at three months post-intervention? Researchers will compare an educational intervention with versus without POCUS to see if POCUS works to improve outcomes. Participants will: Receive either the educational intervention alone or an educational intervention plus POCUS. They will report the difference in their understanding and likelihood to improve diet, exercise, and follow up immediately post-intervention. They will also report changes in diet, exercise, follow up, and self-efficacy at three months post-intervention.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Enrollment
100
This will include the educational intervention combined with a point-of-care ultrasound
This will include only the educational intervention (without ultrasound)
Rush University Medical Center
Chicago, Illinois, United States
RECRUITINGRate of Primary Care Follow Up
Defined as the presence or absence of a follow up visit with a primary care provider at 3 months
Time frame: 3 Months Post-Intervention
Likelihood to Follow Up with a Primary Care Physician within the 3 Months Post-Intervention
Ordinal scale of 1 (very unlikely) to 7 (very likely)
Time frame: Baseline and Immediately Post-Intervention
Self-perceived knowledge of heart failure
Ordinal scale of 1 (no knowledge) to 7 (extremely knowledgeable)
Time frame: Baseline and Immediately Post-Intervention
Degree of motivation and self-efficacy using a modified High Blood Pressure Self-Care Profile (HBP-SCP) Motivation and Self-Efficacy tool
Time frame: Baseline, Immediately Post-Intervention, and 3 Months Post-Intervention
Likelihood to change their fruit and vegetable intake using the Stages of Change tools for Fruits and Vegetables
Time frame: Baseline, Immediately Post-Intervention, and 3 Months Post-Intervention
Likelihood to change their fat intake using the Stages of Change for Dietary Fat tool
Time frame: Baseline, Immediately Post-Intervention, and 3 Months Post-Intervention
Likelihood to change their exercise using the Stages of Change for Physical Activity
Time frame: Baseline, Immediately Post-Intervention, and 3 Months Post-Intervention
Change in diet quality using the Mediterranean Eating Pattern for Americans tool
Time frame: Baseline and 3 Months Post-Intervention
Change in exercise status using the Exercise Vital Sign tool
Time frame: Baseline and 3 Months Post-Intervention
Satisfaction with the educational intervention
Ordinal scale of 1 (very unsatisfied) to 7 (very satisfied)
Time frame: Immediately Post-Intervention and 3 Months Post-Intervention
New medications or changes in their anti-hypertensive medication use
Time frame: 3 Months Post-Intervention
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.