RECRUITING

Integration of Telemedicine and Home-Based Cardiac Rehabilitation: Feasibility, Efficacy, and Adherence

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Integration of Telemedicine and Home-Based Cardiac Rehabilitation: Feasibility, Efficacy, and Adherence

Quick Facts

Study Start:2023-06-01
Study Completion:2024-11-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05972070

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Over the age of 18
  2. 2. NYHA Functional Class I, II,
  3. 3. 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)
  4. 4. Candidate for traditional center-based cardiac rehabilitation
  1. 1. Under the age of 18
  2. 2. Adults lacking capacity to consent.
  3. 3. NYHA Functional Class III, IV
  4. 4. Acute coronary syndrome
  5. 5. Systolic heart failure (LV EF \<40%)
  6. 6. Status post cardiac surgery for structural heart disease or heart transplant
  7. 7. Percutaneous coronary angioplasty
  8. 8. Adults lacking capacity to consent.
  9. 9. Pregnant women

Contacts and Locations

Study Contact

LaToya T. King
CONTACT
2035184735
Latoya.King@romtech.com

Study Locations (Sites)

ROMTech
Brookfield, Connecticut, 06804
United States

Collaborators and Investigators

Sponsor: ROM Technologies, INC

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-06-01
Study Completion Date2024-11-30

Study Record Updates

Study Start Date2023-06-01
Study Completion Date2024-11-30

Terms related to this study

Keywords Provided by Researchers

  • Cardiac rehabilitation
  • Home based cardiac rehabilitation
  • Telemedicine and Home-Based Cardiac Rehabilitation

Additional Relevant MeSH Terms

  • Myocardial Infarction
  • Percutaneous Transluminal Coronary Angioplasty
  • Coronary Artery Bypass
  • Stable Angina
  • Heart Failure
  • Valve Disease, Heart
  • Cardiac Rehabilitation
  • Stent