Resistance Training in HFpEF
NCT02435667 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24
Last updated 2021-02-03
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).
Conditions
- Heart Failure Preserved Ejection Fraction
Interventions
- OTHER
-
Resistance Exercise Training
1. Aerobic Exercise a. Each participant will engage in 5 minutes of aerobic based exercise on an arm/leg ergometer (NuStep Cross Trainer) at an intensity of 12-14 on the Borg Rating of Perceived Exertion Scale as a warm-up prior to the exercise session and again as a cool-down at the end of the exercise session. 2. Resistance Exercise - 2 sets of 8-12 repetitions - beginning at 60% of the initial 1 RM. a) Leg Extension, b) Bicep Curl, c) Leg Press, d) Chest Press, e) Leg Curl, f)Seated Row (horizontal or pulldown), g) Calf Raises 3. Core Strengthening Exercises a. 5-10 minutes of stability ball and balance exercises
- RADIATION
-
DEXA bone scan
A DEXA scan that provides bone density measures.
- OTHER
-
Cardiopulmonary Max Exercise Test
Pedaling on a cycle ergometer to volitional fatigue.
- OTHER
-
Quality of Life Questionnaire
A 10 minute questionnaire that measures quality of life.
- OTHER
-
Submaximal Exercise Test
Two short submaximal constant-load exercise sessions at 20 Watts. Each session will include 6 minutes of cycling (baseline). Following baseline, the sessions will be randomized to continued constant-load cycling for an additional 9 minutes (for echocardiographic measures) or randomized sub-systolic inflation of bilateral thigh pressure tourniquets to 40 and 80 mmHg for 3 minutes with 3 minutes of deflation between inflations to stimulate locomotor muscle neural feedback.
- OTHER
-
Blood Draw
A blood draw amounting to 1 teaspoon of blood drawn.
Sponsors & Collaborators
- lead OTHER
Principal Investigators
-
Thomas Olson, MS, PhD · Mayo Clinic
Study Design
- Allocation
- RANDOMIZED
- Purpose
- SUPPORTIVE_CARE
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-06-30
- Primary Completion
- 2021-01-31
- Completion
- 2021-01-31
Countries
- United States
Study Locations
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