Providence, RINCT06886789Now EnrollingIRB Ready

Cardiovascular Diseases Clinical Trial in Providence, RI

Access cutting-edge cardiovascular diseases treatment through this clinical trial at a research site in Providence. Study-provided care at no cost to qualified participants.

Sponsored by The Miriam Hospital

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Expert Care in Providence

Access cardiovascular diseases specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related cardiovascular diseases treatment provided free

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Check if you qualify for this cardiovascular diseases clinical trial in Providence, RI

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Providence

    Convenient for RI residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Providence site if eligible
  4. 4Begin participation

About This Cardiovascular Diseases Study in Providence

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

Sponsor: The Miriam Hospital

Who Can Participate

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
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

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Providence?

Yes, this clinical trial (NCT06886789) has an active research site in Providence, RI that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Cardiovascular Diseases Treatment Options in Providence, RI

If you're searching for cardiovascular diseases treatment options in Providence, RI, this clinical trial (NCT06886789) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Providence research site is actively enrolling participants for this clinical trial. You'll receive care from experienced cardiovascular diseases specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all cardiovascular diseases clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Providence, RI