Effects of High Intensity Circuit Training on Physical Fitness, Body Fat Percentage and Waist-Hip Ratio Among Sedentary Females of Sikandarabad

September 30, 2021 updated by: Sana Mehmood, Ziauddin University
Globally, insufficient Physical Activity (PA) and sedentary life style is recognized as major causes of mortality among young and older adults. Approximately, 5 million deaths are attributed due to physical inactivity (PI), which contributes around 6% of global death. The recent evidence shows that 80 million individuals in Pakistan suffered with non-communicable diseases, due to PI that ultimately lead to sedentary behavior. Therefore, the clinical practitioners have been highlighting in improving the physical activity among young adults not only to prevent chronic disease but also to reduce the risk factors. Despite of the fact, a large number of young adults are PI where this proportion remains high among women. WHO reports that generally, PI is found to be more prevalent in women, due to workload of house chores and care giving role in influence of cultural expectations, especially in low socio economic status. Furthermore, several other factors including high cost of fitness programs, access to physical activity facilities, transportation and most importantly time barrier are the major cause of insufficient PA. Addressing the above barriers, different exercise training protocols have been developed to reduce weight in short span of time and then to maintain it. According to American College of Sports Medicine (ACSM), High Intensity Circuit Training (HICT) is a circuit-style workout that uses individual body weight as a resistance therefore eliminating the need of expensive gym equipment such as dumbbells, barbells kettle bells and many more. In addition, HICT can be performed in any environment (at home, parks and in small place) as per the feasibility of the person. However, overweight and obese women are found to adhere easily with short bout of exercises (10 minutes) then same women with long duration of exercises. Therefore, the aim of this study is to provide cost effective and efficient exercise intervention that may not only reduce the disease burden but also motivate young sedentary females for group activity.

Study Overview

Status

Completed

Conditions

Detailed Description

A total 60 healthy sedentary overweight females will be recruited from Sikandrabad. The participants shall be screened by using standardize Physical Activity Readiness Questionnaire (PAR-Q & YOU). After screening, a healthy participant will be allowed to attend the orientation session, where a qualified and trained instructor shall discuss and describe the exercise training protocol. The High Intensity Circuit Training comprises of 7 full body exercises as per recommendation of ACSM, where the participants shall be given total of 18 sessions of their respective protocol, comprising of 20 minutes, 3 times/ week for duration of six weeks. Pre and post assessment will be performed for each participant on all three quantitative outcome measures; Physical Fitness, Body fat percentage and Waist-hip ratio. The training protocol will be terminated on the happening of following event; a) Decrease in oxygen saturation < 90%assessed b) Increase in Heart Rate above the highest limits of Targeted Heart Rate c) if subject feel any discomforts, dizziness, fainting or difficulty in breathing during performance.

Study Type

Interventional

Enrollment (Actual)

60

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 Locations

    • Sindh
      • Karachi, Sindh, Pakistan, 71500
        • Ziauddin University

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

18 years to 35 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria

  • Female Participants with a BMI > 25-29 kg/mm2
  • Aged 18-35 years.
  • Subjects having a sedentary lifestyle, performing only activities of daily living without engaging in any previous exercise training protocol throughout the week, evaluated by Rapid Assessment Disuse Index (RADI) Questionnaire.

Exclusion Criteria

  • History of recent surgeries or trauma that hinders in performing high impact exercises.
  • Severe orthopedic, musculoskeletal, cardiopulmonary, neurovascular, psychiatric, inflammatory, metabolic, or endocrine diseases and taking any prescribed medications.
  • Pregnant females and nursing mothers.

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: Supportive Care
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: High Intensity Circuit Training
The High Intensity Circuit Training comprises of 7 full body exercises as per recommendation of ACSM Where the participants shall be given total of 18 sessions of their respective protocol, comprising of 20 minutes, 3 times/ week for duration of six weeks
The High Intensity Circuit Training comprises of 7 full body exercises as per recommendation of ACSM Where the participants shall be given total of 18 sessions of their respective protocol, comprising of 20 minutes, 3 times/ week for duration of six weeks

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Body Fat Percentage [Pre-treatment]
Time Frame: six weeks
The body fat composition will be obtained by measuring three-site skin fold thickness including triceps, supra-Ilium and thigh by using the skin fold thickness caliper.
six weeks
Body Fat Percentage [Post-treatment]
Time Frame: six weeks
The body fat composition will be obtained by measuring three-site skin fold thickness including triceps, supra-Ilium and thigh by using the skin fold thickness caliper.
six weeks
Waist-Hip ratio [Pre-treatment]
Time Frame: six weeks
Waist-hip ratio will be taken with the help of measuring tape by dividing the circumference of waist in centimeters and circumference of hip in centimeters.
six weeks
Waist-Hip ratio [Post-treatment]
Time Frame: six weeks
Waist-hip ratio will be taken with the help of measuring tape by dividing the circumference of waist in centimeters and circumference of hip in centimeters.
six weeks
Physical Fitness [Pre-treatment]
Time Frame: six weeks
The Modified Harvard step test is used to measure Physical fitness by dividing duration of exercise and pulse count between 1 and 1.5 seconds.
six weeks
Physical Fitness [Post-treatment]
Time Frame: six weeks
The Modified Harvard step test is used to measure Physical fitness by dividing duration of exercise and pulse count between 1 and 1.5 seconds.
six weeks

Collaborators and Investigators

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

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)

January 5, 2021

Primary Completion (Actual)

July 15, 2021

Study Completion (Actual)

September 25, 2021

Study Registration Dates

First Submitted

December 3, 2020

First Submitted That Met QC Criteria

December 3, 2020

First Posted (Actual)

December 4, 2020

Study Record Updates

Last Update Posted (Actual)

October 1, 2021

Last Update Submitted That Met QC Criteria

September 30, 2021

Last Verified

September 1, 2021

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Sana Mehmood

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.

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