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High Interval Versus Moderate Intensity Continuous Training on Soluble st2 Biomarkers in Chronic Heart Failure

High Interval Versus Moderate Intensity Continuous Training on Soluble st2 Biomarkers in Chronic Heart Failure

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06647667
Enrollment
60
Registered
2024-10-18
Start date
2022-09-15
Completion date
2023-10-16
Last updated
2024-10-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure

Keywords

sST2 biomarker, Minnesota Questionare, HIITS

Brief summary

This study was designed to compare between the effect of high intensity interval training (HIIT) and moderate intensity continuous training (MICT) on soluble ST2 biomarkers among chronic heart failure patients, also measure the improvement in the quality of life with different modes of exercise and with of it is more benifitial for the heart failure patient

Detailed description

The data concerned with the study including soluble ST2 biomarker levels, ejection fraction and MLHFQ was measured before and after twelve weeks of treatment.In this study a total sixty male patients with chronic heart failure NYHA class (I &II) were selected from the outpatient clinic, El-Demerdash hospital, Ain-shams University. Their age ranged from 50-60 years. Patients were randomly assigned into two groups, group A receiving HIIT along with prescribed medical treatment and group B receiving MCT along with prescribed medical treatment.

Interventions

OTHERHIITS

Frequency: HIIT will be in 2 supervised sessions per week for 12 weeks on the treadmill. session duration from 30-40 min including the waming up and cooling down Intensity: HIIT included 4 minute intervals aiming 60-85% of heart rate reserve

OTHERMICT

Frequency: Moderate continuous training is scheduled 2 times per week for 12 weeks. Intensity: exercise had been applied on the treadmill with 40%-59% of heart rate reserve) session duration from 30-40 min including the warming up and cooling down

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

1. Patients will receive high intensity interval training (HIIT) 2. Patients will receive moderate intensity continuous training (MICT)

Eligibility

Sex/Gender
MALE
Age
50 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* The patients selection was according to the following criteria: * Patients diagnosed with chronic heart failure (New York heart association class I& II) with systolic left ventricular dysfunction. * Their left ventricular ejection fraction (LVEF) \<40%. * Medical treatment was optimized at least three months prior to study entry. * All patients didn't participate in any rehabilitation programs prior to the study.

Exclusion criteria

* Patients who had met one of the following criteria were excluded from the study: 1. Signs of acute heart failure, unstable angina or severe arrhythmia three months prior to enrolment in the study. 2. Pacemakers. 3. Chronic obstructive pulmonary disease. 4. Other disorders counteracting exercise testing conditions that limit lower limb mobility (for example, burns, fractures) 5. Pre-existing neuromuscular diseases (for example Myasthenia Gravis).

Design outcomes

Primary

MeasureTime frameDescription
soluble ST2 biomarker levelbefore the start of the trail and at the end of the trail 3 monthssample was taken at the cubited vein at the beginning of the program and also at its end

Secondary

MeasureTime frameDescription
ejection fractionbefore the start of the trail and at the end of the trail 3 monthsLeft ventricular systolic dysfunction was assessed using the ejection fraction by 2D simpson method
mannisota of daily living questionnaire scorebefore the start of the trail and at the end of the trail 3 monthsThe twenty one item questionnaire was usedfrom 0 (none) to 5 (very much). It provides a total score (range 0-105, from best to worst HRQoL), as well as scores for two dimensions, physical (8 items, range 0-40) and emotional (5 items, range 0-25). The other eight items (of the total of 21) are only considered for the calculation of the total score.
peak exercise responsebefore the start of the trail and at the end of the trail 3 monthsmonitoring the peak exercise response

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026