Expired Study
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Detroit, Michigan 48202


Purpose:

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)


Criteria:

Inclusion Criteria: 1. 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) 2. Lives in or plans to remain in the greater Detroit, MI area for the next year 3. Age 18-85 years of age 4. Agrees to attend at least one CBCR session 5. Agrees to scheduling at least 2, up to 3, CR sessions (either CBCR or HYCR)/wk 6. 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 Exclusion Criteria: 1. Received a left ventricular assist device, receiving continuous inotropic support (e.g., milrinone), or undergoing hemodialysis 2. Angina at rest or with a low functional capacity (< 2 METs) 3. Advanced cancer, advanced risk for falling, limiting cognitive impairment, or other advanced disorder that limits participation in CR 1. Advanced risk for falling will be assessed by 5X sit-to-stand test, with a cut-off score of >15 seconds 2. Cognitive assessment will be completed using the Mini-Cog instrument, with a cut-off score < 3 used to exclude potential subjects. 4. Severe arrhythmia unless adequately treated (e.g., implantable cardiac defibrillator) 5. Pregnant or plan to become pregnant in the next year. 6. Major cardiovascular procedure or hospitalization planned in the next 6 months 7. Less than 12 month life expectancy 8. Participation in another clinical trial that interferes with iATTEND participation, follow-up, data collection, exercise capacity or quality of life.


NCT ID:

NCT03646760


Primary Contact:

Principal Investigator
Steven Keteyian, PhD
Henry Ford Health System

Crystal Payter
Phone: 313-972-1815
Email: cpayter1@hfhs.org


Backup Contact:

Email: msaval1@hfhs.org
Matt Saval
Phone: 313-972-4018


Location Contact:

Detroit, Michigan 48202
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: February 04, 2019

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