- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04655014
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
Intervention / Treatment
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.
Sponsor
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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