Cardiovascular risk
Conditions
Interventions
Clinical trial, parallel, randomized-controlled of two arms, triple blind (patients, research team and statistician). With an intervention group with 23 patients (the instrument built for data collect
E01.370.370
Sponsors
Universidade da Integração Internacional da Lusofonia Afro-Brasileira
Universidade da Integração Internacional da Lusofonia Afro-Brasileira
Eligibility
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Having the nursing diagnosis risk of impaired cardiovascular function; being aged =18 years and < 60 years; both genders; being enrolled in Comprehensive Health Care Center
Exclusion criteria
Exclusion criteria: Reporting a diagnosis of cardiovascular disease; presenting impediments to obtaining anthropometric measurements (pregnant women, wheelchair users) or requiring instruments adapted for the execution of interventions (physically, hearing, and visually impaired), not yet developed by other researchers; being in temporary or permanently impaired mental conditions that make it impossible for them to be aware of and cooperate with the research
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to reduce at least three nursing diagnosis indicators through the method of comparing present and absent factors after the intervention is applied, improving 100% the quality of care and reducing risk factors. We will observe the reduction of factors and the need for risk diagnoses with the use of the software. We expect to find the reduction of harmful life habits such as smoking, obesity and alcoholism verified by the intention-to-treat method from a variation of at least 5% between the pre and post-intervention measurements. | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to decrease serum levels of total cholesterol, HDL-c, LDL-cholesterol, non-HDL-cholesterol and triglycerides, markers of uric acid, urea, creatinine, AST, ALT, albumin and the ultrasensitive CRP, observing the reduction, equivalence or increase of the markers. Improving in 100% the biochemical levels and reducing bad markers. This reduction will be achieved by the specific method of each test and by comparing the tests before and after the intervention. It is hoped to find a reduction in bad markers by the intention-to-treat method from a variation of at least 5% between the pre- and post-intervention measurements. | — |
Countries
Brazil
Contacts
Public ContactJoão Neto
Universidade da Integração Internacional da Lusofonia Afro-Brasileira
Outcome results
None listed