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Effect of the PLAN CUIDARTE on the Caregiving Competence of People With Heart Failure

Effect of the PLAN CUIDARTE on the Caregiving Competence of People With Heart Failure: Implementation of the Research Protocol.

Status
Not yet recruiting
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06309875
Acronym
PLANCUIDARTE
Enrollment
84
Registered
2024-03-13
Start date
2024-03-25
Completion date
2024-11-12
Last updated
2024-03-13

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

Conditions

Caregiver Burden, Care Transitions, Discharge Plan, Heart Failure, Nursing

Brief summary

According to the World Health Organization (WHO), by 2021 cardiovascular diseases (CVD) will be a public health problem, among them heart failure (HF), since this is a chronic disease, patients should be competent in their care. Despite the above, according to research conducted in Colombia, 59.7% of people with chronic noncommunicable diseases (NCDs) have a level of care competence considered not optimal; patients report not having sufficient knowledge of the disease or experience feelings of lack of tools for the management of symptoms and the challenges of post-hospitalization. The objective of the research is to determine the effect of the PLAN CUIDARTE on the caregiving competence of people with HF Methodology: Pre-posttest randomized clinical trial, with blinding of the participants, where the intervention PLAN CUIDARTE is applied and the initial and subsequent caregiving competence is evaluated in the comparison group and in the intervention group for pretest - posttest and between-group comparisons.

Detailed description

Eligibility Criteria: Inclusion criteria * Patients over 18 years of age with a diagnosis of HF. * Patients with HF who are hemodynamically stable. * Patients with SPMSQ - PFERFFER of 0 - 4 errors or 5 errors, patient who has not received primary education. * Patient with a PULSES of 6 to 11 Exclusion criteria * Patients with heart failure with heart transplantation scheduled in the next 6 months. * Patients requiring transfer to an intensive or intermediate care unit. Outcome Measures: * Primary: Caring competence. * Secondary: Satisfaction with care

Interventions

OTHERPLAN CUIDARTE

Description Plan Cuidarte

OTHERConventional care

Description Conventional care

Sponsors

Universidad de Caldas
CollaboratorOTHER
Universidad de la Sabana
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Intervention model description

A pre-post test Randomized Clinical Trial (RCT) is proposed with a comparison group, with blinding of the participants with blinding of the participants, with application of a pilot test beforehand. pilot test. The intervention group is established as the group that receives the PLAN CUIDARTE (intervention described later) and as a comparison group the one receiving the conventional discharge plan (described later)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients over 18 years of age who are hospitalized and admitted to the institution with a diagnosis of HF decompensation with a time of diagnosis greater than 6 months. * Patients who are hemodynamically stable, without alteration of the state of consciousness.

Exclusion criteria

* HF patients who are hospitalized for cardiac transplantation, * Who are under palliative management or who, at the time of discharge, have a formal * Who have a designated formal caregiver or are discharged to an institution other than home.

Design outcomes

Primary

MeasureTime frameDescription
Care Competence30 dayscapacity, ability and preparation of the patient or family caregiver to the patient or family caregiver to perform the task of caregiving(4), which is made up of the following five dimensions: knowledge five dimensions: knowledge, uniqueness, instrumental, enjoyment, anticipation and social relationship, uniqueness, instrumental, enjoyment, anticipation and social relationship.

Countries

Colombia

Contacts

Primary ContactAlejandra Fuentes-Ramirez, DR
alejandra.fuentes@unisabana.edu.co+573123722107
Backup ContactGloria Carvajal-Carrascal, DR
gloria.carvajal@unisabana.edu.co+57 3115062590

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026