Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
60 participants
INTERVENTIONAL
2011-08-31
2013-10-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Education Program for Burn Patients
NCT01379495
Satisfaction Degree in a Nurse Educational Program to Heart Transplant Patient
NCT02938676
Implementation of Practice Standards for ECG Monitoring
NCT01269736
Nursing Health Education to Improve Functionality and Quality of Life After Ischemic Stroke
NCT07343284
Telenursing in Coronary Artery Disease
NCT07110779
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
usual care
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.
educational program+telephone follow up
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.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
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.
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.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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
* 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
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Sao Paulo
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Rejane Kiyomi Furuya
Ph.D
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
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
Explore where the study is taking place and check the recruitment status at each participating site.
Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo
Ribeirão Preto, São Paulo, Brazil
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
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.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2010/19761-3
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.