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Clinical Trials in Mexico / NCT07283406
Enrolling by invitation Not applicable

Effect of High-intensity Interval Training on Cardiometabolic Health and Physical Fitness in Young Adults With Obesity

NCT07283406 · tracked via the Priya Life Science Mexico tracker
Sponsor
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)

Trial sites (1)

FacilityCityRegionStatus
Centro Universitario de Tlajomulco, Universidad de Guadalajara Guadalajara Jalisco

More Centro Universitario de Tlajomulco, Universidad de Guadalajara trials in Mexico

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07283406 on ClinicalTrials.gov ↗ ← All trials in Mexico