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Telemedicine Qualifying Transition Between Tertiary and Primary Health Care in Stable Coronary Artery Disease Patients

Telemedicine in Qualifying Care Transition Between Tertiary and Primary Health Care Among Stable Coronary Artery Disease Patients: a Randomized Non-inferiority Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02489565
Acronym
Tele_DAC
Enrollment
264
Registered
2015-07-03
Start date
2014-05-31
Completion date
2017-11-30
Last updated
2015-07-03

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

Conditions

Coronary Artery Disease

Keywords

Coronary Artery Disease, stable, Telemedicine, Patient Discharge

Brief summary

The purpose of this study is to determine whether the telemedicine use in primary health care is effective in the accompaniment of stable coronary artery disease patients who were discharged from the tertiary health care clinics.

Detailed description

This study is a randomized non-inferiority trial for patients with chronic coronary artery disease from a tertiary hospital with outpatient discharge criteria. The purpose is to compare the use of telemedicine in the quality of care transition between tertiary care and primary care patients (intervention group), with patients who remain in the outpatient clinic of a tertiary hospital (control group).

Interventions

OTHERTelemedicine

Outpatient discharge from tertiary care to primary care with a letter of referral explaining about the study containing phone number from telemedicine and a letter with the patient's history in the hospital. Two months after discharge, the telemedicine's cardiologist initiates contact with the primary care's physician about patient follow-up.

Sponsors

Conselho Nacional de Desenvolvimento Científico e Tecnológico
CollaboratorOTHER_GOV
Ministry of Health, Brazil
CollaboratorOTHER_GOV
Federal University of Rio Grande do Sul
CollaboratorOTHER
Hospital de Clinicas de Porto Alegre
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Masking
NONE

Eligibility

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

Inclusion criteria

* individuals with diagnosis of Coronary Artery Disease (CAD) in Canadian Cardiovascular Society (CCS)'s functional classification of angina Class I or II * patients who did not submit hospitalization for cardiovascular disease in the last year

Exclusion criteria

* patients who were not followed up in the health service to at least one year * unstable patients requiring adjustments of medications or who are performing some diagnostic evaluation at discharge outpatient

Design outcomes

Primary

MeasureTime frameDescription
Number of participants that stay in Canadian Cardiovascular Society (CCS) Functional Classification of Angina I and II as a measure of safetywithin one year after dischargeNot evolve into a higher class than the measure before the intervention

Secondary

MeasureTime frameDescription
blood pressure controlwithin one year after dischargeverified to maintain systemic blood pressure from the observation of a variation of at least 5% in pre and post intervention measurements
Number of participants with instability of the diseasewithin one year after dischargethe need to seek emergency care for cardiovascular disease post intervention.
dyslipidemia controlwithin one year after dischargeverified to maintain dyslipidemia control through laboratory examination, from the observation of a variation of at least 5% in pre and post intervention measurements of Low Density Lipoproteins (LDL) in blood
diabetes controlwithin one year after dischargeverified to maintain diabetes control through laboratory examination, from the observation of a variation of at least 5% in pre and post intervention measurements of fasting glucose in the blood

Other

MeasureTime frameDescription
Access to primary health carewithin six months and one year after dischargemedical consultation in Basic Health Unit held with assessment of current medications and providing prescription.
Number of participants in physical activitywithin one year after dischargemaintenance or start regular physical activity post intervention
Number of participants with control of tobaccowithin one year after dischargeremain without smoking for non smokers; and smoking cessation for smokers

Countries

Brazil

Contacts

Primary ContactCarisi A Polanczyk, PhD
carisi.anne@gmail.com+55 51 33596359
Backup ContactJoanna Lyra, PhD
joannalyra@gmail.com+ 55 51 33596325

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 12, 2026