Home-Based High-Intensity Interval Training for Obese Individuals with Elevated Cardiovascular Disease Risk
This study aims to evaluate your adherence and compliance to a home-based high-intensity interval training program, as well as observe the change in your aerobic fitness, if you are an obese individual with an elevated risk of cardiovascular disease.
Training mode
Body Weight+5
+ Nutrition Disorders
+ Nutritional and Metabolic Diseases
Basic Science Study
Summary
Study start date: March 9, 2015
Actual date on which the first participant was enrolled.This study focuses on a 12-week home-based exercise program designed for obese individuals who have an increased risk of cardiovascular disease. The goal is to create a workout plan that's suitable for people with low fitness and mobility levels, as current high-intensity interval training (HIT) programs often require special equipment and supervision. The study involves obese adults who have at least three additional risk factors for cardiovascular disease. The importance of this research lies in its potential to make exercise more accessible, thereby addressing a significant public health challenge. Participants in this study are divided into three groups. One group follows the home-based HIT program (Home-HIT), another group engages in a lab-supervised HIT program (Lab-HIT), and the third group performs moderate-intensity continuous training at home (Home-MICT). The Home-HIT group performs simple bodyweight exercises that don't require any equipment. The exercises are monitored using a heart rate monitor and a mobile app to ensure they're done correctly. The study measures changes in various health markers, such as aerobic fitness, insulin sensitivity, body composition, and heart health. It also assesses the participants' ability to stick to the exercise program and meet the target heart rates.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.32 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Basic Science Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 55 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.3 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
ExperimentalGroup III
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Liverpool John Moores University
Liverpool, United KingdomOpen Liverpool John Moores University in Google Maps