Education Program for Cardiac Patients

NCT ID: NCT01341093

Last Updated: 2014-05-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-08-31

Study Completion Date

2013-10-31

Brief Summary

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The purpose of this study is to elaborate an educative program that includes telephone follow-up and assess its impact on the perceived health status of patients submitted to percutaneous coronary intervention.

Detailed Description

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Conditions

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Percutaneous Coronary Intervention Coronary Artery Disease

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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usual care

Group Type ACTIVE_COMPARATOR

Usual care

Intervention Type BEHAVIORAL

Patients will receive orientations about the surgery and the rehabilitation by health professionals, especially in the discharge. And will have return for evaluation scheduled by health professionals.

educational program+telephone follow up

Group Type EXPERIMENTAL

educational program+telephone follow up

Intervention Type BEHAVIORAL

Patients will participate in the educational program with telephone follow-up, the education program will initiate in preoperative period and will continue for six months.

Interventions

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educational program+telephone follow up

Patients will participate in the educational program with telephone follow-up, the education program will initiate in preoperative period and will continue for six months.

Intervention Type BEHAVIORAL

Usual care

Patients will receive orientations about the surgery and the rehabilitation by health professionals, especially in the discharge. And will have return for evaluation scheduled by health professionals.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Adult patients (18 years or more) of both sexes
* Being submitted to the first coronary artery bypass graft surgery between April 2011 and July 2012
* Having a properly functioning residential phone line

Exclusion Criteria

* No cognitive condition to participate (assessed through the Mini-Mental State Examination - MMSE)

* Illiterate participants who did not reach the minimum score 13 on the MMSE
* Participants with one to seven years of education who did not reach the minimum score 18 on the MMSE
* Participants with eight or more years of education who did not reach the minimum of 26 points on the MMSE
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Sao Paulo

OTHER

Sponsor Role lead

Responsible Party

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Rejane Kiyomi Furuya

Ph.D

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Rejane K. Furuya, PhDCandidate

Role: PRINCIPAL_INVESTIGATOR

University of São Paulo at Ribeirão Preto College of Nursing

Lidia A. Rossi, PhD

Role: STUDY_CHAIR

University of São Paulo at Ribeirão Preto College of Nursing

Locations

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Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo

Ribeirão Preto, São Paulo, Brazil

Site Status

Countries

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Brazil

References

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Furuya RK, Arantes EC, Dessotte CA, Ciol MA, Hoffman JM, Schmidt A, Dantas RA, Rossi LA. A randomized controlled trial of an educational programme to improve self-care in Brazilian patients following percutaneous coronary intervention. J Adv Nurs. 2015 Apr;71(4):895-908. doi: 10.1111/jan.12568. Epub 2014 Nov 17.

Reference Type DERIVED
PMID: 25400127 (View on PubMed)

Other Identifiers

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2010/19761-3

Identifier Type: -

Identifier Source: org_study_id

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