Skip to main content
Clinical Trials/NCT06647667
NCT06647667
Completed
N/A

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

Cairo University1 site in 1 country60 target enrollmentSeptember 15, 2022
ConditionsHeart Failure

Overview

Phase
N/A
Intervention
Not specified
Conditions
Heart Failure
Sponsor
Cairo University
Enrollment
60
Locations
1
Primary Endpoint
soluble ST2 biomarker level
Status
Completed
Last Updated
last year

Overview

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.

Registry
clinicaltrials.gov
Start Date
September 15, 2022
End Date
October 16, 2023
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
Male

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dina Reda Ali

PhD candidate

Cairo University

Eligibility Criteria

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:
  • Signs of acute heart failure, unstable angina or severe arrhythmia three months prior to enrolment in the study.
  • Pacemakers.
  • Chronic obstructive pulmonary disease.
  • Other disorders counteracting exercise testing conditions that limit lower limb mobility (for example, burns, fractures)
  • Pre-existing neuromuscular diseases (for example Myasthenia Gravis).

Outcomes

Primary Outcomes

soluble ST2 biomarker level

Time Frame: before the start of the trail and at the end of the trail 3 months

sample was taken at the cubited vein at the beginning of the program and also at its end

Secondary Outcomes

  • ejection fraction(before the start of the trail and at the end of the trail 3 months)
  • mannisota of daily living questionnaire score(before the start of the trail and at the end of the trail 3 months)
  • peak exercise response(before the start of the trail and at the end of the trail 3 months)

Study Sites (1)

Loading locations...

Similar Trials