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Implementation Intention to reduce salt intake on Heart Failure

Implementation Intention strategies to reduce sodium intake among Heart Failure patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-7mty35
Enrollment
Unknown
Registered
2020-03-20
Start date
2012-06-12
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 an experimental study, with the establishment of groups: Collaborative (n=15) and Individual (n=15) Intervention and Collaborative (n=15) and Individual (n=15) Control. The intervention was Im
Behavioural
F01.145.113.547

Sponsors

Faculdade de Enfermagem, Universidade Estadual de Campinas
Lead Sponsor
Faculdade de Enfermagem, Universidade Estadual de Campinas
Collaborator

Eligibility

Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: There were included Heart Failure patients and their social referee. For patiets the inclusion criteria were: Age over 18 years old and inferior to 85 years old; Being in clinical follow-up for at least 6 months. For social referee: Wife/ husbund, daughters/ sons, parents, house workers or any other person who was reponsible to prepare the patients meal at home; Age over 18 years old and inferior to 85 years old; Available to go with patient to the health clinic in all phases of the study.

Exclusion criteria

Exclusion criteria: Patients were excluded: With diagnosis of Hert Failure functional class IV; With recently history of being hospitalized (less than 01 month) before the study; With no condition of effective verbal communication; With diagnosis of mental disorders (described in medical report); Whose social referee who prepares meals at home could not be present at all consultations. For socials referee: With no condition of effective verbal communication; Wiht diagnosis of mental disorders (described in medical report); Who did not agree in participating of the study.

Design outcomes

Primary

MeasureTime frame
End-point: The patients who received the intervention showed a significant decrease on salt intake by self-reported methods. The results are: T0:Individual intervention group (mean) = 12.2g salt/day; Collaborative intervention group (mean) = 11.4g salt/day; Individual control group (mean) = 9.8g salt/day; Collaborative control group = 14.9g salt/day. T3:Individual intervention group (mean) = 5.0g salt/day; Collaborative intervention group (mean) = 4.8g salt/day; Individual control group (mean) = 10.4g salt/day; Collaborative control group = 14.2g salt/day.

Secondary

MeasureTime frame
Secondary end-point: the patients who received the intervention showed a significant decrease on habit. The results are: T0: Individual intervention group (mean) = 3.0; Collaborative intervention group (mean) = 4.0; Individual control group (mean) = 4.0; Collaborative control group = 3.6. T3: Individual intervention group (mean) = 1.2; Collaborative intervention group (mean) = 1.2; Individual control group (mean) = 4.1; Collaborative control group = 4.1. ;Secondary end-point: the patients who received the intervention showed a significant increase in self-efficacy. The results are: T0: Individual intervention group (mean) = 4.1; Collaborative intervention group (mean) = 4.3; Individual control group (mean) = 3.4; Collaborative control group = 3.5. T3:Individual intervention group (mean) = 5.0; Collaborative intervention group (mean) = 4.9; Individual control group (mean) = 3.2; Collaborative control group = 2.7.

Countries

Brazil

Contacts

Public ContactAndressa;Andressa Nunciaroni;Nunciaroni

Escola de Enfermagem Alfredo Pinto - UNIRIO;Faculdade de Enfermagem, Universidade Estadual de Campinas

andressateoli@gmail.com;andressateoli@gmail.com19997906048;+55-19-997906048

Outcome results

None listed

Source: REBEC (via WHO ICTRP)