Actively Recruiting

Phase Not Applicable
Age: 65Years +
All Genders
NCT06951620

Optimizing Aerobic Fitness in Older Adults

Led by University of Vermont Medical Center · Updated on 2025-06-08

114

Participants Needed

1

Research Sites

219 weeks

Total Duration

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Sponsors

U

University of Vermont Medical Center

Lead Sponsor

N

National Institute on Aging (NIA)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Hospitalization and treatment for cardiovascular disease is one of the main contributors to disability in older adults. Moderate intensity continuous aerobic and resistance training have been the cornerstone of cardiac rehabilitation (CR) for decades to remediate hospital-acquired functional deficits, but some groups receive less or minimal functional benefit from this training. The proposed studies seek to optimize recovery of aerobic fitness and physical function among older cardiac patients using a novel high intensity training regimen with the long-term goal of reducing subsequent disability and improving clinical outcomes.

CONDITIONS

Official Title

Optimizing Aerobic Fitness in Older Adults

Who Can Participate

Age: 65Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Over 65 years old
  • Able to walk (ambulatory)
  • Enrolled in cardiac rehabilitation at the study center after a recent heart attack or percutaneous intervention (angioplasty, stent placement, or valve replacement)
Not Eligible

You will not qualify if you...

  • Have an active cancer except for non-melanoma skin cancer or low grade prostate cancer under surveillance
  • Not willing to follow the assigned exercise program
  • Have a submaximal performance on entry exercise test, defined as respiratory exchange ratio less than 1.0

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

UVMMC Cardiac Rehabilitation

South Burlington, Vermont, United States, 05403

Actively Recruiting

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Research Team

P

Patrick Savage, Research Coordinator

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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