To determine the change in sedentary time and number of steps/day for older patients with
heart failure at risk for mobility disability who receive a program to decrease sedentary
behavior versus a standard program to increase exercise.
Behavioral: Reducing Sedentary Behavior
Behavioral: Physical Activity Group
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Locations near you
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Full eligibility criteria for NCT02911493
Ages eligible for Study
65 Years to 100 Years
Genders eligible for Study
Accepts Healthy Volunteers
Age ≥ 65,
SPPB score of > 4 and ≤ 10 of 12,
and deemed (by 1° cardiologist) to be at maximal tolerated dose of heart failure medication (ACE-inhibitor (ACE-I)/angiotensin receptor blocker and beta blocker
(BB) for patients with HF with reduced ejection fraction (HFrEF), and
blood pressure controlled for HF with preserved ejection fraction (HFpEF) according to the American Heart Failure Association HF guidelines.
Patients requiring medication titration such as ACE-I or BB, (will return to their cardiologist and be eligible after 3 months of stable medication.)
Oxygen dependent lung disease,
Orthopedic or neurologic disease that severely limits mobility,
Active cancer diagnosis except non-melanoma skin cancer,
Geriatric Depression Scale (GDS) score of ≥ 9 ,
Limited life-expectancy of <6 months,
Known dementia or disease that effects ability to learn/follow directions, or
Failed MiniCog test.
All locations for NCT02911493
United States (1)
University of Colorado University
Aurora, Colorado, United States, 80045
View full eligibility
Tris trial is registered with FDA with number: NCT02911493. The sponsor of the trial is University of Colorado, Denver and it is looking for 50 volunteers for the current phase.
Official trial title: Reducing Sedentary Time in Patients With Heart Failure
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