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Effects of Aerobic and Resistance Training on Abdominal Fat Loss

Effects of Aerobic and Resistance Training on Abdominal Fat Loss

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03700827
Enrollment
18
Registered
2018-10-09
Start date
2017-10-01
Completion date
2020-05-01
Last updated
2021-10-04

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

Conditions

Obesity, Abdominal

Keywords

Abdominal Fat, Visceral Adipose Tissue, Subcutaneous Adipose Tissue, Exercise, Intervention

Brief summary

Study the effects of different exercise modes on total and regional adiposity variation in subcutaneous and visceral adipose tissue (VAT and SAT). The investigators hypothesize that total abdominal will improve for all the exercise groups compared to the control group. When comparing intervention groups: 1) no differences on the degree of improvement in total abdominal fat depots (VAT and SAT) 2) different degree of change when comparing specific sections at VAT and SAT are expected.

Interventions

OTHERResistance Training

High-intensity Resistance Training Group

OTHERAerobic Training

Aerobic Interval Training Group

Sponsors

Washington University School of Medicine
CollaboratorOTHER
Southern Illinois University Edwardsville
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* 30 - 39.9 kg/m2 BMI * White/Caucasian * Female * Sedentary

Exclusion criteria

* Known cardiovascular, pulmonary, metabolic disease * Pregnant females * Any excluded criteria with MRI scans (i.e. certain metal implants, recent tattoos) * Diabetic * Hypertension * Cigarette smoking * MRI related contraindications (metal, no removable devices, etc.)

Design outcomes

Primary

MeasureTime frameDescription
Changes in Visceral Abdominal Tissue (VAT)2 assessment periods: at baseline and week 4Changes in VAT will be measured using Magnetic Resonance Imaging

Secondary

MeasureTime frameDescription
Changes in Muscular Strength2 assessment periods: at baseline and week 4Changes in muscular strength will be assessed by one-repetition maximum test on leg press and bench press
Changes in Cardiorespiratory Function2 assessment periods: at baseline and week 4Changes in cardiorespiratory will measured on a treadmill with a metabolic cart
Changes in fat mass (kg)2 assessment periods: at baseline and week 4Changes in fat mass will be measured using dual-energy x-ray absorptiometry
Changes in relative body fat (%BF)2 assessment periods: at baseline and week 4Changes in body composition (relative body fat, lean body mass and fat mass) will be measured using dual-energy x-ray absorptiometry
Changes in relative lean body mass (kg)2 assessment periods: at baseline and week 4Changes in lean body mass will be measured using dual-energy x-ray absorptiometry
Changes in Lipid profile (TG, Total Cholesterol, HDL2 HDL3, LDL)2 assessment periods: at baseline and week 4Samples will be processed to obtain serum and plasma, and stored at -80°c until analysis
Changes in Subcutaneous Abdominal Tissue (SAT)2 assessment periods: at baseline and week 4Changes in SAT will be measured using Magnetic Resonance Imaging
Changes in concentration of Fibrinogen2 assessment periods: at baseline and week 4Will be performed using a Luminex MAGPIX System with xPONENT 4.2
Changes in concentration of C-reactive protein (CRP)2 assessment periods: at baseline and week 4Will be performed using a Luminex MAGPIX System with xPONENT 4.2
Changes in concentration of IL-62 assessment periods: at baseline and week 4Will be performed using a Luminex MAGPIX System with xPONENT 4.2
Changes in concentration of IL-102 assessment periods: at baseline and week 4Will be performed using a Luminex MAGPIX System with xPONENT 4.2
Changes in concentration of TNF-alpha2 assessment periods: at baseline and week 4Will be performed using a Luminex MAGPIX System with xPONENT 4.2
Changes in concentration of Troponin2 assessment periods: at baseline and week 4Will be performed using a Luminex MAGPIX System with xPONENT 4.2

Countries

United States

Outcome results

None listed

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