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EFFECT of PYRAMIDAL TRAINING on EPICARDIAL FAT for CORONARY ARTERY DISEASE PREVENTION

Cairo University (CU) logo

Cairo University (CU)

Status

Not yet enrolling

Conditions

Coronary Artery Disease
Class I Obesity

Treatments

Other: Pyramidal training
Other: Mediterranean diet

Study type

Interventional

Funder types

Other

Identifiers

NCT06799104
P.T.REC/012/005563

Details and patient eligibility

About

To show the effect of pyramidal training for coronary artery disease prevention on:

-Epicardial fat, BMI, Waist circumference (WC), Lipid profile, Quality of life and Mediterranean Diet Adherence.

Full description

Back Ground: Coronary heart disease (CHD) is a type of ischemic heart disease characterized by atherosclerotic plaque accumulation in the coronary arteries.Obesity leads to coronary artery disease (CAD) in part through an inflammatory process that accelerates atherosclerotic plaque formation which may start as early as childhood. Epicardial adipose tissue (EAT) is the Visceral adipose tissue (VAT) of the heart .EAT has unique embryologic, anatomic, and histologic features, including smaller adipocytes and higher prevalence of immune cells when compared to subcutaneous adipose tissue (SAT).

Purpose: To show the effect of pyramidal training for coronary artery disease prevention on:

-Epicardial fat, BMI, Waist circumference (WC), Lipid profile, Quality of life and Mediterranean Diet Adherence.

Methods: This study is Randomize Control Trail that will be carried out on 50 females' patients and will be selected from the Outpatient clinics at Pharos University. Patient will be randomly assigned to two groups.

Experimental group:

This group will include 25 patients who will receive pyramidal aerobic training by treadmill for 40 minutes per session (three sessions per week) for (12 weeks) in addition to Mediterranean diet.

Control group:

This group will include 25 patients who will receive Mediterranean diet for (12 weeks).

Results: Data analysis with Independent t-test will be used to compare the baseline parameters between the intervention and control groups. Repeated measures ANOVA will be used to compare the changes in EATT, anthropometrics and lipid levels at the baseline and after 12 weeks between the two groups.

Keywords: Pyramidal Training, Epicardial Fat, Coronary artery disease.

Enrollment

50 estimated patients

Sex

Female

Ages

30 to 40 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Fifty females' patients with class I obesity (BMI 30 to 34.9 kg/m2, Waist circumference > 88 cm).

    • Their age ranges from 30-40 years old.
    • Dyslipidemia and lipid profile as follow (total cholesterol high: 240 mg/dl, HDL less than 40 mg/dl, LDL high: 160-189 mg/dL and triglycerides high: 200-499 mg/dl).
    • All patients will be clinically and medically stable when attending the study.

Exclusion criteria

  • Patients with conditions will be excluded such as:

    • Musculoskeletal problems.
    • Chronic pulmonary disease.
    • Missed more than two weeks of the program or want to terminate the program.
    • Unstable angina.
    • Acute illness.
    • Uncontrolled cardiac arrhythmia.
    • Decompensated heart failure.
    • Cognitive impairment or mental disorders.
    • Systolic blood pressure higher than 180, and/or diastolic blood pressure over 100mmHg.
    • DVT.
    • Multiple food allergies/intolerances or gastrointestinal difficulties of the prescribed diet.
    • Cancer (have special nutritional and training needs).

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

50 participants in 2 patient groups

Experimental group:
Experimental group
Description:
This group will include 25 patients who will receive pyramidal aerobic training by treadmill for 40 minutes per session (three sessions per week) for (12 weeks) in addition to Mediterranean diet.
Treatment:
Other: Mediterranean diet
Other: Pyramidal training
Control group
Active Comparator group
Description:
This group will include 25 patients who will receive Mediterranean diet for (12 weeks).
Treatment:
Other: Mediterranean diet

Trial contacts and locations

1

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Central trial contact

Rawda M ELkomy, B.Sc.

Data sourced from clinicaltrials.gov

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