NCT03646760Completed
The Improving ATTENDance to Cardiac Rehabilitation Trial
Source: ClinicalTrials.gov · Last updated 29 Jul 2025
Brief summary (registry, in English)
The benefits of cardiac rehabilitation are well known. However, despite center based cardiac rehabilitation (CBCR) representing guideline-based care for patients with cardiovascular disease, most patients do not complete the maximum number of sessions allowed by third party insurance payers. As such, many patients may not be receiving the full clinical benefit ascribed to CR. This study will assess the efficacy of an innovative approach to CR delivery on attendance by combining both center-based and remote- or home-based CR sessions. The intervention group combines center-based CR and remote-/home-based CR and is tailored to the individual needs of each patient, accomplished with the assistance of an easy-to-access telecommunications methodology (telemedicine)
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 282 (actual)
- First submitted
- 14 Aug 2018
- Start date
- 1 Mar 2019
- Primary completion date
- 30 Dec 2023
- Lead sponsor
- Henry Ford Health System
- Diseases
- Heart failure, Coronary artery disease
- NCT number
- NCT03646760
What you commit to
- Study type: Interventional
- Participants enrolled: 282
- From 1 Mar 2019 to the primary completion date, 30 Dec 2023
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Received a left ventricular assist device, receiving continuous inotropic support (e.g., milrinone), or undergoing hemodialysis
Other illness
- Angina at rest or with a low functional capacity (\< 2 METs)
- Advanced cancer, advanced risk for falling, limiting cognitive impairment, or other advanced disorder that limits participation in CR
- Advanced risk for falling will be assessed by 5X sit-to-stand test, with a cut-off score of \>15 seconds
- Cognitive assessment will be completed using the Mini-Cog instrument, with a cut-off score \< 3 used to exclude potential subjects.
- Severe arrhythmia unless adequately treated (e.g., implantable cardiac defibrillator)
Other
- Pregnant or plan to become pregnant in the next year.
- Major cardiovascular procedure or hospitalization planned in the next 6 months
- Less than 12 month life expectancy
- Participation in another clinical trial that interferes with iATTEND participation, follow-up, data collection, exercise capacity or quality of life.
Who the study is looking for
- Has agreed to participate in CR and has experienced a cardiac event (myocardial infraction, coronary revascularization, heart valve surgery, or cardiac transplant in the past 6 months; diagnosed with chronic, stable AHA/ACC stage B or C heart failure or Canadian class 0-2 stable angina pectoris)
- Lives in or plans to remain in the greater Detroit, MI area for the next year
- Age 18-85 years of age
- Agrees to attend at least one CBCR session
- Agrees to scheduling at least 2, up to 3, CR sessions (either CBCR or HYCR)/wk
- Has demonstrated to research staff their ability to access and connect to the internet via smart phone or tablet and already has access to satisfactory home- or community-based exercise equipment
Age in the registry: 18 years to 85 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Henry Ford Health System Coordinator of this site? Confirm its status | Detroit | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.