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Clinical Trials/NCT02435667
NCT02435667
Completed
Not Applicable

Resistance Exercise Training in Heart Failure With Preserved Ejection Fraction (Resist - HFpEF)

Mayo Clinic1 site in 1 country24 target enrollmentJune 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Heart Failure Preserved Ejection Fraction
Sponsor
Mayo Clinic
Enrollment
24
Locations
1
Primary Endpoint
Bone density and strength
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The objective of this proposal is to determine the effect of resistance exercise training on locomotor muscle function, exercise capacity, exertional symptoms, and quality of life in HF patients with preserved ejection fraction (HFpEF).

Detailed Description

In this randomized controlled pilot study of resistance exercise training in patients with HFpEF, the investigators will recruit 24 HFpEF patients who will be randomized to resistance exercise training (RT - n=12) or no resistance exercise training (standard care control group \[CTL\] - n=12). The investigators will have baseline and follow-up measures of clinical characteristics, leg muscle strength, quality of life, lean muscle mass (body composition via DXA including segmental lean mass), maximal cardiopulmonary exercise test (peak VO2, peak work, ventilatory efficiency), constant-load submaximal cardiopulmonary exercise test with speckle tracking echocardiography (exertional dyspnea and fatigue at matched workloads, cardiac output, diastolic function, left ventricular strain, ventilation, gas exchange, and locomotor muscle neural feedback). Participants will be asked to make 4 separate study visits. Those randomized to undergo Resistance Training will be expected to make those visits as well.

Registry
clinicaltrials.gov
Start Date
June 2015
End Date
January 2021
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Thomas P. Olson, M.S., Ph.D.

Principal Investigator

Mayo Clinic

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Bone density and strength

Time Frame: 12 weeks

DEXA scan

Cardiopulmonary Function

Time Frame: 12 weeks

Cardiopulmonary bike exercise

Quality of Life

Time Frame: 12 weeks

Questionnaire

Blood Biomarkers

Time Frame: 12 weeks

Blood draw

Study Sites (1)

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