Building Strength Through Rehabilitation for Heart Failure Patients (BISTRO-STUDY)



Status:Recruiting
Conditions:Cardiology
Therapuetic Areas:Cardiology / Vascular Diseases
Healthy:No
Age Range:18 - Any
Updated:9/9/2018
Start Date:September 6, 2018
End Date:December 2019
Contact:Christine Haedtke, PhD
Email:chaedtke@iu.edu
Phone:317-274-5358

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Building Strength Through Rehabilitation for Heart Failure Patients

In the U.S., 5.7 million people have heart failure (HF), 915,000 new cases are diagnosed each
year, and both incidence and prevalence are increasing due to the aging of the population and
to better survival from ischemic heart disease. A hallmark of HF, is poor functional status
that, characteristically, deteriorates as the condition progresses, negatively affecting
patients' quality of life. Poor functional status is associated with increased risk of
hospitalization for exacerbations of HF and with increased mortality. Optimization of drug
therapy and appropriate use of resynchronization therapy can improve functional status, as
can patient engagement in exercise. Although exercise is recommended as a component of HF
management, adherence is consistently low. This is particularly troubling because exercise
has great potential as a low-risk, low-cost intervention to improve functional status and
quality of life while decreasing HF symptoms and hospitalizations in patients with HF. Low
adherence is due in part to inadequate strength and inability to tolerate or sustain even low
levels of activity. In this study, we propose to use neuromuscular electrical stimulation
(NMES) to assist patient initiation of quadriceps strengthening in order to progressively
increase low exercise tolerance. NMES has been shown to improve muscle strength, exercise
capacity and quality of life, in samples less than 20 of male patients with HF. Larger sample
studies are needed to demonstrate efficacy of this practice to jump start patients' abilities
to benefit from formalized exercise program. The purpose of this double blinded, randomized,
controlled, longitudinal study is to determine if NMES will increase muscle mass and
strength, decrease sedentary time, and improve HF symptoms and exercise capacity, thus
improving quality of life in patients with HF. It is hypothesized that with this increase in
muscle mass, patients will improve overall exercise tolerance and capacity. In addition,
after the intervention patients will be better able to tolerate an exercise program thus
improving adherence to exercise recommendations. After 6 weeks of intervention, patients will
be encouraged to participate in a formalized exercise program.


Inclusion Criteria:

- Adult patients who have recently been hospitalized for heart failure

- live at home

- are receiving guideline recommended pharmacologic therapy

- do not regularly exercise (10 minutes or more a day of exercise most days of the week
for the past week).

Exclusion Criteria:

- Patients, who have undertaken cardiac rehab within the 12 months prior to enrollment

- Cognitive or other impairment which prevents accurate application of intervention or
inability to provide informed consent

- End Stage Renal Disease or receiving mechanical ventilation

- Receiving non-approved FDA-investigational agents or devices,

- Has received a heart transplant, a destination Ventricular Assist Device (LVAD),
pacemaker, or implantable cardiac device

- previously used NMES (Neuromuscular electrical stimulation) or TENS (Transcutaneous
electrical nerve stimulation)

- Uncontrolled arrhythmia's or 3 degree AV heart block

- are unable to correctly apply and operate the device even after instruction

- Those with wounds over area of proper placement of electrodes

- Those who are unable to speak and write English.
We found this trial at
1
site
425 University Blvd.
Indianapolis, Indiana 46202
(317) 274-4591
Phone: 317-274-5358
Indiana University INDIANA UNIVERSITY is a major multi-campus public research institution, grounded in the liberal...
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Indianapolis, IN
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