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Effects of a Short-term Aerobic Interval Exercise Program on Cardiac Fat and Function in Women With Obesity: A Pilot Study

Not Applicable
Withdrawn
Conditions
Obesity
Interventions
Other: Aerobic Interval Training
Registration Number
NCT04802005
Lead Sponsor
Southern Illinois University Edwardsville
Brief Summary

The overall goal of this project is to the study the effects of an aerobic interval training program on cardiac fat, and its relationship to cardiac function using cardiac Magnetic Resonance Imaging.

Detailed Description

Not available

Recruitment & Eligibility

Status
WITHDRAWN
Sex
Female
Target Recruitment
Not specified
Inclusion Criteria
  • females, age 18-40 years old, body mass index (BMI) ≥ 30 kg/m2 and < 39.9 kg/m2, without known metabolic and/or cardiovascular disease
Exclusion Criteria
  • known CV, metabolic or pulmonary diseases or conditions, muscular-skeletal injuries (i.e. spine, knees, hips or shoulders, taking medications that affect endocrine or cardiovascular function, hypertension, being engaged in moderate intensity exercise more than two times per week or moderate-high intensity training of any type and frequency, being pregnant, cigarette smoking, having non-removable pieces or devices incompatible with DXA and CMR assessment

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Aerobic intervalAerobic Interval TrainingAerobic interval will consist of a supervised aerobic interval training sessions 3 times/week. Duration will range between 45-50 min/session depending on the exercise energy expenditure (target expenditure \~450-500kcal/session). Each interval will have a total duration of 5 min, and it will be divided into 2 periods. The first period will consist of 3 minutes of high-intensity activity at 70-85% of predicted HRmax, and for the second period the intensity will be reduced to 60-65% of predicted HRmax for 2 minutes. The training sessions will be carried out outdoors at the trails located on campus. The activity will consist of walking and/or light jogging. The speed/incline will be changed depending on the participants' heart rate and perception using the Borg's rating of perceived exertion (RPE) as needed. The RPE for the first period range will be 13-17 (15-17 at the end of the period) and 10-12 for the second period.
Primary Outcome Measures
NameTimeMethod
Changes in Cardiac Function2 assessment points: at baseline and week 5

Cardiac Function will be measured using cardiac Magnetic Resonance

Changes in Cardiac Adipose Tissue (CAT)2 assessment points: at baseline and week 5

CAT will be measured using cardiac Magnetic Resonance

Secondary Outcome Measures
NameTimeMethod
Changes in Body Composition2 assessment points: at baseline and week 5

Body composition will be measured using dual-energy x-ray absorptiometry

Changes in Blood Pressure2 assessment points: at baseline and week 5

Blood pressure will be measured using pulse wave analysis

Changes in Cardiorespiratory Function2 assessment points: at baseline and week 5

Cardiorespiratory Function will be measured on a treadmill with a metabolic cart

Changes in Muscular Strength2 assessment points: at baseline and week 5

Muscular Strength will be assessed through 1 repetition maximum (1RM).

Trial Locations

Locations (1)

Southern Illinois University Edwardsville

🇺🇸

Edwardsville, Illinois, United States

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