High Intensity Interval Training Versus Low-intensity Continuous Training on Physical Fitness Among Overweight Adult

June 13, 2021 updated by: Heba Yasser, Horus University

Effect of High Intensity Interval Training Versus Low Intensity Continuous Training on Physical Fitness Among Overweight Adult

The purpose of the study is to compare the effect of high intensity interval training and low intensity training on physical fitness among adult overweight.

Study Overview

Detailed Description

Excess body weight has been shown to negatively influence musculoskeletal health and may limit physical function. Thus, there is a need for effective interventions to reduce body weight in those individuals who may already be overweight or obese. Physical activity can be an important component of lifestyle interventions for weight loss. Thus, it is important for clinicians, health care providers, and health-fitness professionals to recognize the influence of physical activity on body weight and to understand recommendations that can affect physical activity behavior. Several studies reported that HIIT can improve cardiorespiratory fitness (increase vo2 max) in adults with varied body weight and health status.

High intensity interval training induced improvements in insulin sensitivity, blood pressure, and body composition more consistently occur in adults with overweight, with or without high risk of cardiovascular disease and diabetes especially if these participate in prolonged exercise program up to 12 or more weeks.

Low intensity exercise has been shown to have a range of physiological and biochemical effects during a subsequent bout of exercise Low intensity exercise would result in muscle acetyl group accumulation and thereby would accelerate mitochondrial ATP production (and reduce ATP production from nonoxidative routes) during a subsequent bout of moderate intensity exercise. In accordance with these changes, we also hypothesized that the vo2 on-kinetics during moderate intensity exercise would be accelerated when preceded by low intensity exercise .

The significant behind this study came up with the importance to declare the effect of high intensity interval training on improving physical fitness and body composition which be more suitable for overweight active people that don't have time to practice prolonged exercise during the week and this study also will investigates the effect of low intensity exercise on physical fitness and body composition to declare where is going to be beneficial for overweight sedentary subjects and compare it is effect with pervious.

This study will be designed to provide a guideline about the effect of high intensity interval training& low intensity training exercise on physical fitness in the overweight adult patient.

Study Type

Interventional

Enrollment (Anticipated)

30

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Damieta, Egypt, 34518
        • Recruiting
        • Outpatient clinic - Faculty of Physical Therapy - Horus University
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years to 30 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Body mass index (BMI) will be ≥ 25 -29.9 kg/m².
  2. Age will be ranging from 20 to 30 years.
  3. Waist circumference >88cm2 in men and >102cm2 in women.
  4. Content of body fat will be assisted by electrical bioimpedence≥33%.
  5. Stable body weight in the month prior to the trial.
  6. Follow instructions for healthy life style.

Exclusion Criteria:

  1. Patients with musculoskeletal deformities and disorders.
  2. Patients with other neuromuscular disorders.
  3. Patients with foot deformities and ulcers.
  4. Patients with lower limb operations.
  5. Smoking cigarettes, thyroid diseases.
  6. History of coronary artery disease Asthma, chronic obstructive pulmonary diseases.
  7. poorly controlled hypertension (mean systolic blood pressure (SBP) > 140 mm Hg and/or mean diastolic blood pressure (DBP) > 90 mm Hg) during the month prior to the trial.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: High-intensity Interval Training
Group 2: the included 15 subjects will participate in High intensity Interval training exercise running on treadmill for 12 weeks, 3 times / week.

Consisting of the following program:

  • Warming up period for 10 minutes at 60-70% of HR max.
  • Training phase 4x4 min intervals at 85-90% of HRmax with a 3 min active recovery at 70% of HRmax between each interval.
  • Duration of HIIT 4 minute
  • Number of interval per session 4
  • Duration of rest interval 3 minute 3-10 min cool-down period, giving a total of 60 min.
Active Comparator: Low-intensity Continuous Training
Group 1: the included 15 subjects will participate in low intensity continuous exercise on treadmill for 12 weeks, 3 times / week

Consisting of the following program:

  • Warming up period for 10 minutes.
  • Training phase for 60-minute walking on a treadmill at intensity 40-50% HRR (1- 6) weeks then 60-70% HRR (7-12) weeks.
  • cooling down period for 10 minutes.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Assessing the change in body Weight
Time Frame: Baseline and 2 months post-intervention
Assessment via using body weight scale with height (m) scale to be able to calculate body mass index (Kg) to all subjects before starting the study BMI= Weight (KG) /Height2 (M2)
Baseline and 2 months post-intervention
Assessing the change in Waist hip ratio
Time Frame: Baseline and 2 months post-intervention
Assessment via using was measured to the nearest 0.1 cm by using a flexible steel tape at the level of umbilicus, and hip circumference (HC) was measured at the widest level over the greater trochanters.
Baseline and 2 months post-intervention
Assessing the change in body fat
Time Frame: Baseline and 2 months post-intervention
Assessment through bioelectrical impedance analysis by using a Body Composition Analyzer (TANITA Corporation, Japan).
Baseline and 2 months post-intervention
Assessing the change Cardiorespiratory fitness
Time Frame: Baseline and 2 months post-intervention
Assessment via using Shuttle run test The 20-m shuttle run (20MSR) test, also called the ''Course Navette'', "PACER", or "Multistage fitness test", is probably the most widely used field test for estimating cardiorespiratory fitness.
Baseline and 2 months post-intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Heba Yasser, Demonstrator, Horus University in Egypt

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 1, 2021

Primary Completion (Anticipated)

June 30, 2021

Study Completion (Anticipated)

July 15, 2021

Study Registration Dates

First Submitted

June 13, 2021

First Submitted That Met QC Criteria

June 13, 2021

First Posted (Actual)

June 21, 2021

Study Record Updates

Last Update Posted (Actual)

June 21, 2021

Last Update Submitted That Met QC Criteria

June 13, 2021

Last Verified

June 1, 2021

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Hebayasser_MSc

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Overweight

Clinical Trials on High-intensity Interval Training

Subscribe