Integration of Telemedicine and Home-Based Cardiac Rehabilitation: Feasibility, Efficacy, and Adherence
Recruiting · NCT05972070 · Observational (researchers observe without assigning treatment) · Lead sponsor: ROM Technologies, INC
View the official record on ClinicalTrials.gov →Interventions studied
ROMTech Portable Connect
What this trial is about
The aim of this study is to evaluate feasibility, efficacy, and adherence of home-based cardiac rehabilitation with the integration of telemedicine. Several components will be assessed such as quality-of-life, nutritional counseling, maximum metabolic activity (MET's), diabetic management, tobacco cessation, lipid, blood pressure, and psychosocial management. These tasks will be accomplished through concurrent conversations between patients and their therapist's utilizing telemedicine with observed exercise training.
Who can take part
Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)
Inclusion criteria
- Over the age of 18
- NYHA Functional Class I, II,
- Recent (within 60 days) status post coronary artery revascularization for atherosclerotic coronary artery disease (coronary artery bypass grafting or percutaneous coronary revascularization with stent implantation)
- Candidate for traditional center-based cardiac rehabilitation
Exclusion criteria
- Under the age of 18
- Adults lacking capacity to consent.
- NYHA Functional Class III, IV
- Acute coronary syndrome
- Systolic heart failure (LV EF \<40%)
- Status post cardiac surgery for structural heart disease or heart transplant
- Percutaneous coronary angioplasty
- Adults lacking capacity to consent.
- Pregnant women
Where it is running
1 location listed across 1 US state.
- ROMTech - Brookfield, Connecticut, United States