Centro Universitario de Tlajomulco, Universidad de Guadalajara
Phase
Not applicable
Started
2026-01-03
Last updated
2025-12-15
Condition(s) studied
Obesity & Overweight
Investigational drug(s) / intervention(s)
High-intensity interval training interventionModerate-intensity continuous training interventionEducational sessions
High-intensity interval training intervention: The HIIT group will undergo training for 12 weeks, with a frequency of three sessions per week, completing a total of 36 sessions. Each session will include a 5-minute warm-up and a 5-minute cool-down at 50-60% of maximum heart rate (HRmax). The training protocol will consist of 2-minute high-intensity intervals performed at 90-95% HRmax, corresponding to a Borg rating of perceived exertion (RPE) of 17-18, alternated with 2-minute recovery periods at 70% HRmax (RPE 12-14). A total of five intervals will be completed per session, resulting in an overall high-intensity workload of 18 minutes. All training sessions will be conducted on a stationary cycle ergometer
Moderate-intensity continuous training intervention: The MICT group will perform moderate-intensity continuous training at 60-70% HRmax, corresponding to an RPE of 12-14, for 35-45 minutes on a stationary cycleergometer. Heart rate and physical activity levels will be continuously monitored in both groups using a chest-strap heart rate sensor (Polar H9, Polar Electro, Finland).
Educational sessions: In addition, four educational sessions will be conducted to provide dietary recommendations to all participants. These sessions will aim to promote balanced eating habits and to discourage the excessive consumption of ultra-processed foods or alcohol, as these factors could interfere with the intervention outcomes.
Study summary
The objective of the present project is to compare the effects of two types of training on cardiovascular health components and physical fitness in young adults with obesity.
Eligibility
Sex
ALL
Min age
18 Years
Max age
35 Years
Healthy volunteers
No
Inclusion Criteria:
* Young adults
* BMI ≥ 30 kg/m\^2" and \< 40 kg/m\^2
* Signed informed consent form
Exclusion Criteria:
* Participants who smoke
* Clinical diagnosis of hypothyroidism
* Clinical diagnosis of type 1 diabetes mellitus
* Clinical diagnosis of type 2 diabetes mellitus
* Clinical diagnosis of grade 3 obesity
* Clinical diagnosis of hypertension
* Clinical diagnosis of acute myocardial infarction or angina pectoris
* Use of nitrates and calcium channel blockers within 4 days prior to the start of the study
* Use of beta-blockers or hypoglycemic agents within 7 days prior to the intervention
* Pregnant women
* Breastfeeding women
* Men consuming more than 40 g of alcohol per day or women consuming more than 20 g per day
* Postural and biomechanical disorders (knee, foot, and spine)
Primary outcome measure(s)
Maximum oxygen uptake (VO₂max) — Baseline and after 12 weeks VO₂max (ml/min/kg): Change from Baseline at 12 weeks, measured using a submaximal exercise test based on the Åstrand-Ryhming protocol
Weight — Baseline and after 12 weeks Weight (kg): Changes in weight from baseline to 12 weeks of intervention.
Height — Baseline and after 12 weeks Height (cm): Changes in height from baseline to 12 weeks of intervention.
Body mass index (BMI) — Baseline and after 12 weeks BMI (kg/m2): Change from Baseline at 12 weeks, calculated by: weight (kg)/ height (m\^2)
Body fat percentage — Baseline and after 12 weeks Body fat percentage (%): Changes in body fat assessed by bioelectrical impedance analysis (BIA)
Muscle mass percentage — Baseline and after 12 weeks Muscle mass percentage (%): Changes in muscle mass measured using bioelectrical impedance analysis (BIA)
Waist circumference — Baseline and after 12 weeks Waist circumference (cm): Changes in waist circumference will be measured using a Lufkin measuring tape (USA) following the guidelines of the International Society for the Advancement of Kinanthropometry (ISAK)
Waist-to-hip ratio — Baseline and after 12 weeks Waist-to-hip ratio: Changes in waist-to-hip ratio will be calculated by dividing the waist measurement by the hip measurement
Glucose — Baseline and after 12 weeks Glucose (mg/dl): Changes from baseline to 12 weeks of intervention
Triglycerides — Baseline and after 12 weeks Triglycerides (mg/dl): Changes from baseline to 12 weeks of intervention
Total cholesterol — Baseline and after 12 weeks Total cholesterol (mg/dl): Changes from baseline to 12 weeks of intervention
HDL cholesterol — Baseline and after 12 weeks HDL cholesterol (mg/dl): Changes from baseline to 12 weeks of intervention
LDL cholesterol — Baseline and after 12 weeks LDL cholesterol (mg/dl): Changes from baseline to 12 weeks of intervention
C-reactive protein (CRP) — Baseline and after 12 weeks CRP (mg/dl): Changes from baseline to 12 weeks of intervention
Systolic blood pressure (SBP) — Baseline and after 12 weeks SBP (mmHg): Changes from baseline to 12 weeks of intervention
Diastolic blood pressure (DBP) — Baseline and after 12 weeks DBP (mmHg): Changes from baseline to 12 weeks of intervention
Trial sites (1)
Facility
City
Region
Status
Centro Universitario de Tlajomulco, Universidad de Guadalajara
Guadalajara
Jalisco
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