RECRUITING

Improving Cardiac Rehabilitation Exercise Using Target Heart Rate Trial

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 goal of this clinical trial is to compare two types of exercise prescriptions in cardiac rehabilitation eligible older adults (60 years or older) with heart disease. The investigators found in a single site pilot trial (insert NCTxxx) that one exercise prescription was better and are now repeating this study in a larger population at two sites (Baystate Medical Center, Springfield MA and Henry Ford Health System, Detroit MI). The main questions the investigators aim to answer are: 1. Compare two different exercise prescriptions in cardiac rehabilitation on exercise outcomes 1. Graded exercise test +Target heart rate range prescription \[GXT-THRR\] 2. Rating of perceived exertion (RPE) 2. What is the role of psychological feedback on fitness outcomes during cardiac rehabilitation and physical activity outside of cardiac rehabilitation. 3. What are the long-term clinical outcomes between the two exercise prescriptions Participants will be asked to: * Complete surveys about physical activity, exercise anxiety, exercise efficacy, and fears about exercising * Perform fitness measures (6-minute walk test, balance tests, stand to sit tests, a 400 meter walk, and handgrip strength) * Attend at least 18 sessions of cardiac rehabilitation after they are randomized to their exercise prescription group * Wear a heart rate monitor and a physical activity monitor per study protocol Participants will be randomized (flip of a coin) to either receive a graded exercise test and psychoeducational feedback or lifestyle education (nutrition for cardiac). The graded exercise test will be used to create a personalized exercise prescription with the target heart rate range calculated from the test and the lifestyle education group will use their ratings of perceived exertion for their exercise prescription.

Official Title

Improving Outcomes From Cardiac Rehabilitation Among Older Adults Through Exercise Testing and Individualized Exercise Intensity Prescriptions

Quick Facts

Study Start:2023-08-10
Study Completion:2027-06-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05925634

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:60 Years to 99 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patients who are eligible for cardiac rehabilitation by having had a cardiac event such as a myocardial infarction (heart attack), heart failure, percutaneous coronary intervention or angioplasty with stent, coronary artery bypass graft, or heart valve surgery in the past 6 months.
  2. * Lives in, or plans to reside in, the Springfield, MA, or greater Detroit, MI, area for the next year.
  3. * Recruited from a Phase 2 Cardiac Rehabilitation Center at either Baystate Medical Center or Henry Ford Health System.
  4. * Age ≥ 60 years
  5. * Agrees to attend at least 18 sessions of cardiac rehabilitation after randomization
  6. * Agrees to attend cardiac rehabilitation at least twice a week
  1. * Permanent atrial fibrillation
  2. * Heart transplant
  3. * Left-ventricular assist devices
  4. * Stable angina
  5. * High-risk un-revascularized coronary artery disease
  6. * Symptomatic peripheral artery disease
  7. * Aortic and/or mitral stenosis
  8. * Any condition where exercise testing or training might be unsafe or limited

Contacts and Locations

Study Contact

Quinn R Pack, MD
CONTACT
413-794-5856
quinn.pack@baystatehealth.org
Karen L Riska, PhD
CONTACT
413-794-0303
karen.riska@baystatehealth.org

Principal Investigator

Quinn R Pack, MD
PRINCIPAL_INVESTIGATOR
Baystate Medical Center

Study Locations (Sites)

Baystate Medical Center
Springfield, Massachusetts, 01199
United States
Henry Ford Health System
Detroit, Michigan, 48202
United States

Collaborators and Investigators

Sponsor: Baystate Medical Center

  • Quinn R Pack, MD, PRINCIPAL_INVESTIGATOR, Baystate Medical Center

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 Date2023-08-10
Study Completion Date2027-06-30

Study Record Updates

Study Start Date2023-08-10
Study Completion Date2027-06-30

Terms related to this study

Additional Relevant MeSH Terms

  • Myocardial Infarction
  • Coronary Artery Bypass
  • Percutaneous Coronary Intervention
  • Heart Failure
  • Cardiac Valve Surgery