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Quality of life after nutritional orientation for patients with cardiovascular disease

Nutritional orientation for patients in cardiovascular rehabilitation and quality of life

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-3z839h9
Enrollment
Unknown
Registered
2023-10-01
Start date
2021-11-05
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

Cardiac Rehabilitation

Interventions

Individuals randomized in the intervention group (n = 53) will be seen in an outpatient clinic with intervals of 30 days between one appointment and another during a period of 4 months, going through
SP6.680

Sponsors

Universidade Federal de Minas Gerais
Lead Sponsor
Universidade Federal de Minas Gerais
Collaborator

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: The sample of this study will consist of individuals seen at the cardiovascular rehabilitation service of the Jenny Faria outpatient clinic at the Hospital das Clínicas of the Federal University of Minas Gerais. Participants will be recruited upon referral by the physician and/or the physiotherapy team. The study will include patients who are undergoing follow-up with the medical and/or physical therapy team of cardiovascular rehabilitation, aged over 18 years, who have the ability to understand and have a clinical status compatible with the performance of the procedures.

Exclusion criteria

Exclusion criteria: Individuals who are under current nutritional monitoring and who do not demonstrate interest in participating in the study will not be included in the study.

Design outcomes

Primary

MeasureTime frame
It is expected to find an increase in the quality of life score in the period of 3 months of cardiovascular rehabilitation, verified through the SF-36 questionnaire (Medical Outcomes Study 36 - Item Short - Form Health Survey), from the observation of a variation of at least 1 point in each of the 8 domains in the pre- and post-intervention measurements.

Secondary

MeasureTime frame
It is expected to find an increase in cardiopulmonary capacity in the period of 3 months of intervention, verified through the Shuttle Walking Test (SWT). It consists of walking on flat ground, repeatedly covering a distance of 10 meters, around a marking of two cones that are separated by a distance of 9 meters. The single acoustic sounding indicates the time in which the individual must travel the predetermined distance, reach the cone and change direction, returning to the other cone, while the triple acoustic signaling indicates the need to increase speed to cover the distance between the cones. Every minute, the time between the acoustic signals is shortened in such a way that the patient must increase the walking speed to reach the cone at the indicated time. The test comes to an end when the individual is unable to reach the cone twice in a row or when he/she wants to interrupt the test due to symptoms triggered by increasing walking speed. The increase in functional capacity will be verified from a variation to more than at least 1 meter/increment in heart rate and 5 meters in pre- and post-intervention measurements.

Countries

Brazil

Contacts

Public ContactCamila Duarte

Universidade Federal de Minas Gerais

camila.kummel@gmail.com+55(31)34098028

Outcome results

None listed

Source: REBEC (via WHO ICTRP)