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SMART to Optimize an Intervention to Maintain Health Improvements After Cardiac Rehabilitation
An Application of SMART Methodology to Optimize an Intervention to Maintain Improvements in Health Behaviors in Under-resourced Patients After Phase II Cardiac Rehabilitation
Who can join
Ages 18 and older · All sexes
Full eligibility criteria
Inclusion Criteria: * ≥18 years of age or older * Have completed at least 6 CR sessions * Must enroll within 6 weeks of their final CR session * BMI ≥27 * Own an internet-connected device * Home internet access * English proficiency * Able to walk ≥1 block without stopping Lastly, the participant MUST belong to ≥1 of the following groups or identities: * Identifies as a woman * Identifies as LGBTQIA+ * Identifies as a racial or ethnic minority * Insecure transportation for medical appointments * Self-reported trouble paying for healthcare needs (e.g., copays) * Receive income-based subsidized benefits (e.g., state-funded health insurance for low-income residents) * Reside in a small town or rural area per 2010 United States Department of Agriculture Rural-Urban Commuting Area zip code or the Distressed Communities Index * Low educational attainment (≤high school diploma) * Low household income (less than twice the Federal Poverty Level) or meeting federal poverty guidelines per the National Committee on Vital and Health Statistics and the Department of Health and Human Services) Exclusion Criteria: * New York Heart Association Class IV heart failure * Heart transplant in the last 5 months * Left ventricular assist device in the last 4 months * Physician diagnosis of dementia * Physician prescription for 24 hours of oxygen therapy daily * Coronary artery bypass surgery in the last 3 months * Current dialysis * Chronic gait or balance disturbances that would make unsupervised exercise unsafe * Current pregnancy * Report of conditions that the investigators believe would render them potentially unlikely to follow the protocol including terminal illness, active substance dependence, or other significant psychiatric problems that require inpatient hospitalization
About the study
The study is sponsored by the National Heart, Lung, and Blood Institute, which is part of the National Institutes of Health. The study expects to enroll 400 subjects. The research team will recruit research participants that are finishing or will finish cardiac rehabilitation soon. Participants belong to one or more groups of people who are less often studied in cardiac rehabilitation research, may have less access to a formal cardiac rehabilitation maintenance program, or they may especially benefit from additional support after cardiac rehabilitation ends. The main purposes of this study are to evaluate which treatments work the best after cardiac rehabilitation, which order to deliver the treatments in, and which treatments are as minimally burdensome as possible while still working well. This study will make two comparisons (one comparison between a set of low-intensity interventions and another between a set of higher-intensity interventions) to determine which produces the best behavioral adherence immediately after Phase II (outpatient) cardiac rehabilitation
What is being tested
- Text Messaging (behavioral)
- Fully Automated Online Program (behavioral)
- Low-Intensity Cardiac Rehabilitation Maintenance Program (behavioral)
- High Intensity Cardiac Rehabilitation Maintenance Program (behavioral)
Sponsor: The Miriam Hospital · Participants: 400 · Started: Apr 1, 2026
Contact the study team
- Carly M Goldstein, PhD, FAACVPR · Phone: 401-793-8960
- Kristen Walaska, BS · Phone: 401-793-8022
Official record on ClinicalTrials.gov — NCT06886789
Locations in the U.S.
| Rhode Island | Weight Control and Diabetes Research Center of The Miriam Hospital, Providence |
Conditions
From ClinicalTrials.gov, data retrieved Sep 29, 2026. Each study sets its own eligibility; the study team decides who can join.