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Palliative care and heart failure: Comfort through nursing

Palliative care in heart failure: the comfort as an outcome of nursing care.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-4rwr8k
Enrollment
Unknown
Registered
2017-03-27
Start date
2012-10-30
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

A single group of 26 patients with advanced heart failure and criteria for palliative care received a nursing follow-up through monthly outpatient visits. In these consultations, the nurse evaluated t
Performed interventions such as: promotion of body mechanics
Maintenance of the family process
Facilitating learning
Stimuli to religious rituals
Counseling, strengthening of self-esteem
Among others to increase patient comfort and
Assessed monthly if the interventions generated improvements in the patients comfort status. Patient follow-up lasted 6 months.
Other

Sponsors

Instituto Nacional de Cardiologia
Lead Sponsor
Serviço de Insuficiência Cardíaca e Transplante
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Volunteers with chronic heart failure of any etiology having been diagnosed for more than 1 year and optimizing drug therapy at the time of study entry; or Volunteers with chronic heart failure of any etiology with diagnosis less than 1 year, associated with 2 or more hospitalizations due to decompensated HF, or 1 hospitalization in the last year with venous amines use; Being in New York Heart Association (NYHA) III or IV Functional Class at time of enrollment; Have left ventricular ejection fraction (EF) 18 years; Be regularly followed at the HF clinic of the research institution;

Exclusion criteria

Exclusion criteria: Volunteers who have any other clinical condition that implies a life expectancy less than 6 months after the start of the study;

Design outcomes

Primary

MeasureTime frame
Increase of at least 30% of the patient's total comfort status in relation to the beginning of the study.

Secondary

MeasureTime frame
Are not expected

Countries

Brazil

Contacts

Public ContactLiana Trotte

Escola de Enfermagem Anna Nery - Universidade Federal do Rio de Janeiro

liana.correatrotte@gmail.com+5521981512741

Outcome results

None listed

Source: REBEC (via WHO ICTRP)