Actively Recruiting
Effectiveness of Video Monitoring and Care Transition for Heart Failure Patients (EVIT-HF): Randomized Clinical Trial
Led by Federal University of Uberlandia · Updated on 2026-03-16
368
Participants Needed
1
Research Sites
156 weeks
Total Duration
On this page
Sponsors
F
Federal University of Uberlandia
Lead Sponsor
F
Federal University of Rio Grande do Sul
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this clinical trial is to measure the effectiveness of video monitoring associated with the transition of care for patients with heart failure. The main questions it aims to answer is: Is video monitoring superior to monitoring via audio calls in patients with heart failure? Researchers will compare monitoring by video to a monitoring by audio to see if drug videomonitoring works to improve selfcare in heart failure and other outocomes. Participants will: intervention group receive video calls guided by cardiologist nurses at 7, 30, 60, 180 and 365 days after hospital discharge. the control group will receive audio calls for data collection, at the same time mentioned.
CONDITIONS
Official Title
Effectiveness of Video Monitoring and Care Transition for Heart Failure Patients (EVIT-HF): Randomized Clinical Trial
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 18 years or older
- Admitted for decompensated Heart Failure with Reduced Ejection Fraction (HFrEF)
- Ejection fraction less than 40% confirmed by echocardiogram performed in the last 3 months
- Access to a mobile device with internet access
You will not qualify if you...
- On a heart transplant waiting list
- Had coronary artery bypass surgery in the last 3 months
- Currently in palliative care
- Life expectancy less than 1 year
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Federal University of Uberlândia
Uberlândia, Minas Gerais, Brazil, 38405354
Actively Recruiting
Research Team
O
Omar Almeida de Almeida Neto, PhD
CONTACT
P
Patricia magnabosco, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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