CClinicalTrials.gg
Status unknownNCT05551663Updated Oct 26, 2022

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

An interventional study of Isometric exercise training in Heart Failure With Preserved Ejection Fraction, sponsored by St George's, University of London. Status unknown. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2022-10-26.

Sponsored by St George's, University of London · Not applicable, Interventional, and Prevention

The sponsor has not verified this record recently (last verified Oct 2022), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
48
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

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.

02

Conditions studied

  • Heart Failure With Preserved Ejection Fraction

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Keywords

  • Heart Failure
  • Isometric Exercise Training
03

In context

Heart Failure

5,697 studies on the registry are indexed under Heart Failure; 1,219 are open to participants now.

This study's planned enrollment of 48 is below the median of 72 across 3,733 interventional studies indexed under Heart Failure.

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Lead sponsor

St George's, University of London is the lead sponsor of 105 studies on the registry; 11 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

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

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.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Investigator)
Enrollment
48 participants (estimated)

Study arms

  • Experimental
    Isometric exercise training

    Other: Isometric exercise training

  • No intervention
    Control group

Interventions

  • OtherIsometric exercise training

    Participants randomised to the intervention will perform a 4-week programme of isometric exercise training.

06

What researchers measure

Primary outcomes

  1. Diastolic function

    Whether an isometric exercise training (IET) programme statistically significantly improves diastolic function parameters in patients who have been diagnosed with HFpEF. These parameters will be measured quantitatively using transthoracic echocardiography and using measures of transmitral filling velocity (early \[E\] and late \[A\] left ventricular filling velocities), the E/A ratio and tissue Doppler velocities (mitral annulus velocities in diastole \[E'\]) and the E/E' ratio.

    Time frame: 1-year

Secondary outcomes

  1. Blood pressure

    Isometric exercise training has been shown to reduce systolic and diastolic blood pressure (mmHg). Our secondary outcome measure is to record any statistically significant changes in blood pressure following a programme of isometric exercise training compared to a control group.

    Time frame: 1-year

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 26, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05551663
Lead sponsor
St George's, University of London
Responsible party
Sponsor
First posted
Sep 23, 2022
Start date
Nov 2022 (estimated)
Primary completion
Sep 2023 (estimated)
Completion
Dec 2023 (estimated)
Last update
Oct 26, 2022

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Oct 2022. You cannot join it, but the record below documents what was studied.

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