Heart Failure Clinical Trials

Find Heart Failure Clinical Trials Near You

Effectiveness of Video Monitoring and Care Transition for Heart Failure Patients (EVIT-HF): Randomized Clinical Trial

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients aged 18 years or older;

• Admitted for decompensated HFrEF

• Ejection fraction less than 40% confirmed by echocardiogram performed in the last 3 months

• Who access to a mobile device with internet access

Locations
Other Locations
Brazil
Federal University of Uberlândia
RECRUITING
Uberlândia
Contact Information
Primary
Omar Almeida de Almeida Neto, PhD
omar.almeida@ufu.br
+5534992132987
Backup
Patricia magnabosco, PhD
magnabosco@ufu.br
+5534914871477
Time Frame
Start Date: 2025-06-01
Estimated Completion Date: 2028-06-01
Participants
Target number of participants: 368
Treatments
Experimental: Videomonitoring Group
Videomonitoring by cardiovascular nursing
No_intervention: Voice call group
Voice call by cardiovascular nurses
Related Therapeutic Areas
Sponsors
Collaborators: Federal University of Rio Grande do Sul, Universidade Federal do Triangulo Mineiro
Leads: Federal University of Uberlandia

This content was sourced from clinicaltrials.gov