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Clinical monitoring of patients with heart failure

Effectiveness of clinical monitoring in the Transition of patients with Heart Failure between health care networks: Randomized Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-9fkncwv
Enrollment
Unknown
Registered
2024-02-26
Start date
2024-03-01
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure

Interventions

This is a two-arm, double-blind, randomized controlled clinical study. Group intervention/experimental: 70 patients with heart failure (IC), hospitalized, certified at the time of hospital discharge,

Sponsors

Universidade Federal de Uberlândia
Lead Sponsor
Universidade Federal de Uberlândia
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Adults more than 18 years old; with decompensated heart failure with a minimum left ventricular ejection fraction lower than 40 percent; possibility of access to cell phones to receive video calls

Exclusion criteria

Exclusion criteria: Patients on the heart transplant waiting list; who have undergone surgical or percutaneous treatment (coronary or valve) in the last 3 months and with heart failure considered terminal or in palliative care confirmed in medical records; patients with other serious clinical comorbidities with life expectancy less than 1 year confirmed in medical records

Design outcomes

Primary

MeasureTime frame
Self-Care: It is expected to find an average difference of at least 10 points in self-care scores the difference between self-care scores in 180 days will be calculated, subtracted from the baseline score

Secondary

MeasureTime frame
It is expected to find an average difference of at least 10 points in knowledge for heart failure. The difference between knowledge scores in 180 days will be calculated, subtracted from the baseline score;It is expected to find an average difference of at least 10 points in quality of life. The difference between quality of life scores in 180 days will be calculated, subtracted from the baseline score

Countries

Brazil

Contacts

Public ContactOmar de Almeida Neto

Universidade Federal de Uberlândia

omar.almeida@ufu.br+55(34)32282000

Outcome results

None listed

Source: REBEC (via WHO ICTRP)