Using Automated Calls To Improve Compliance With Acute Coronary Syndrome Best Practice Guidelines
NCT ID: NCT01151800
Last Updated: 2010-06-28
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
1608 participants
INTERVENTIONAL
2006-01-31
2010-05-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The study hypothesis is that ACS patients who are contacted by IVR technology will be more likely to receive care as recommended in the BPGs than those followed by usual care.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Using IVR to Maintain ACS Patients on Best Practice Guidelines
NCT01260207
The TEACH (Texting After ACS Discharge) Pilot Randomized Trial
NCT05628337
Improving Quality With Outpatient Decision Support
NCT00225628
Improving Medication Adherence Through Graphically Enhanced Interventions in Acute Coronary Syndromes
NCT00399880
Impact of Health Literacy on Outcomes and Effectiveness of Shared Decision Making Programs in Patients With Chronic Diseases
NCT01083862
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
TREATMENT
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
IVR group
Using IVR to maintain ACS patients on best practice guidelines
Usual care
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Using IVR to maintain ACS patients on best practice guidelines
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Patients who have a land line telephone service at home
* Patients who speak English or French
Exclusion Criteria
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
The Change Foundation
OTHER
Ottawa Heart Institute Research Corporation
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
University of Ottawa Heart Institute
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
University of Ottawa Heart Institute
Ottawa, Ontario, Canada
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
UOHI 2006-128
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.