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Isometric Exercise Training in Participants With Heart Failure With Preserved Ejection Fraction

S

St George's, University of London

Status

Not yet enrolling

Conditions

Heart Failure With Preserved Ejection Fraction

Treatments

Other: Isometric exercise training

Study type

Interventional

Funder types

Other

Identifiers

NCT05551663
2021.0214

Details and patient eligibility

About

Heart failure with a preserved ejection fraction (HFpEF) is a major cause of morbidity and mortality. Hypertension remains one of the major modifiable risk factors in HFpEF development and progression. The role of aerobic exercise training for blood pressure (BP) reduction is well established, with positive cardiac, vascular, and neurohumoral adaptations all cited as potential mechanisms for improving arterial haemodynamics. However, recent evidence has shown that a specific type of resistance exercise alone, known as isometric exercise (IE), produces greater mean BP reductions than what has traditionally been seen with both aerobic and dynamic resistance exercise training programmes. Indeed, short duration IE training causes significant improvements in both cardiac structure and function, in addition to inducing significant reductions in resting BP in normotensive, pre-hypertensive and hypertensive individuals. This study aims to compare the acute and chronic effects of an IE training intervention on diastolic function parameters in patients who have been diagnosed with HFpEF compared to a control group.

Enrollment

48 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients diagnosed with HFpEF.
  • Patients under the care of a St George's Heart Failure cardiology consultant.
  • Patients willing and able to provide informed consent.
  • Male and female, aged 18 years or above.
  • Medically optimised patients.

Exclusion criteria

  • Recent myocardial infarction or electrocardiographic changes, complete heart block, unstable angina.
  • Inability or unwilling to provide informed consent.
  • Male and female, aged 17 years or younger.
  • Patients with HFrEF.
  • Patients with musculoskeletal injury that could conceivably be affected by their involvement.
  • Resting BP values of ≥180/110 mmHg.
  • Patients unable to understand verbal and written English.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

48 participants in 2 patient groups

Isometric exercise training
Experimental group
Treatment:
Other: Isometric exercise training
Control group
No Intervention group

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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