- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05854732
Comparison Of Uninclined And Inclined Treadmill Training In Obese Adults.
Comparison of Uninclined and Inclined Treadmill Training on, Total Body Fat, Lipid Profile and Quality of Life In Obese Adults.
The goal of this clinical trial is to compare the effects of inclined and uninclined treadmill training on total body fat, lipid profile and quality of life in obese adults. The main question it aims to answer is :
Will there be difference between the effectiveness of inclined and uninclined treadmill training on total body fat, lipid profile and quality of life in obese adults.
Participants will be divided into group A and Group B. Group A participants will be considered as a control group with no inclination of the treadmill and speed of 5.0 mph. Whereas Group B participants will be considered as an interventional group with fixed speed of 5.0 mph and increased inclination of 1% after every one minute.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Obesity is defined as an excessive or abnormal fat accumulation, with body mass index i.e. BMI ≥ 30kg/m2 presenting multiple conditions related to health. Globally which is associated with high rate of mortality and morbidity and low levels of quality of life in adults. Trainings that include moderate and high intensity exercises are believed to be crucial preventive and anti-obesity treatment strategy now a day. Physical activity is a modifiable factor for obesity. Regular physical activity (PA) is an important component of overall well-being of humans and is well known to improve cardiorespiratory fitness, lipid profile, quality of life which are all negatively correlated with the risks of multiple chronic disease. Treadmill exercises are one of the most commonly known exercise therapy models. It can be modified with inclination like 10 degrees which lies in high intensity activity with HR of 80-90%., uninclined treadmill lies in category of moderate intensity physical activity with HR of 55-60%.Advance studies states that HIIT treadmill with variations in inclination is a good way to decrease body fat mass percentage in obese/overweight individuals. In this study Measurements of the anthropometrics of body like bodyweight, BMI (body mass index), WHR (waist and hip ratio), and body fat mass were calculated pre and post the intervention which shows that there was significant decrease in body fat mass percentage according to study.
Literature was reviewed regarding treadmill training effect on total body fat, and lipid profile in different groups of population. The purpose of this study will be to assess the effect of uninclined and inclined treadmill training on obese adults and its effect on calorie burn. This study will help to determine whether which treadmill training is effective to get more benefits on health in less time and on lipid profile and total body fat in obese adults.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Jawad Naweed, MS-SPT
- Phone Number: +923235292523
- Email: jawad.naweed@riphah.edu.pk
Study Locations
-
-
Federal
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Islamabad, Federal, Pakistan, 44080
- Yusra Medical and Dental College
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Participants falling in this category would be recruited into the study.
- Males & females
- Body Mass Index (BMI)> 30 kg / m2 (10).
- Age: 18-25
- Physically independent
- Body fat percentage > 25%
Exclusion Criteria:
Participant failing to fall in this category would be excluded of the study.
- Pregnancy
- Nutrition
- Steroid injections in last 6 months
- Psychomotor dysfunction
- Any infection.
- Any neurological and musculoskeletal problems.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Inclined Treadmill Training Group
The Inclined Treadmill Training Group will be considered as an Experimental group with fixed speed of 5.0 mph and increased inclination of 1% after every one minute. The FITT program for the participants will be:
|
Research subjects will be included in the study according to the inclusion criteria and would be randomized into 2 groups, namely inclined treadmill training group and uninclined treadmill training group and will receive intervention for 6 weeks.
The participants will be considered as a experimental group with fixed speed of 5.0 mph and increased inclination of 1% after every one minute.
FIIT FORMULA will be considered while providing intervention for 5 days per week to the subjects of each group.
The FITT program for the participants will be starting with Warmup of 5 mints with Frequency of 5days/week for 6 weeks with fixed speed of 5.0 mph and increased inclination of 1% after every one minute for 30 minutes ending with Cool down for 5 minutes.
|
Active Comparator: Uninclined Treadmill Training Group
The uninclined Treadmill Training Group will be considered as active comparator with no inclination of the treadmill and speed of 5.0 mph. The FIIT program for the participants will be:
|
Research subjects will be included in the study according to the inclusion criteria and would be randomized into 2 groups, namely inclined treadmill training group and uninclined treadmill training group and will receive intervention for 6 weeks.
The participants will be considered as a active comparator with fixed speed of 5.0 mph and fixed inclination.
FIIT FORMULA will be considered while providing intervention for 5 days per week to the subjects of each group.
The FITT program for the participants will be starting with Warmup of 5 mints with Frequency of 5days/week for 6 weeks with fixed speed of 5.0 mph and fixed inclination for 30 minutes ending with Cool down for 5 minutes.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Total Body Fat
Time Frame: 6 Weeks
|
To estimate the overall amount of body fat, the skinfold thickness is measured using a skinfold caliper.
This approach is predicated on the idea that subcutaneous fat is measured by the thickness of the skinfold and that body fat is distributed evenly throughout the body.
Four skinfolds are measured in order to determine how much body fat is present overall that includes Biceps muscle fold, Thoracic skinfold, Skinfold on the sub scapula and iliac crest skinfold.
|
6 Weeks
|
Body Mass Index
Time Frame: 6 Weeks
|
A scale or balance is a tool used to determine mass or weight.
|
6 Weeks
|
Lipid Profile Level (cholesterol and triglycerides)
Time Frame: 6 weeks
|
The lipid profile test that is used to check amount of cholesterol and triglycerides in blood.
|
6 weeks
|
Quality of Life Questionnaire
Time Frame: 6 Weeks
|
The WHOQOL, a tool that measures subjective dimensions of quality of life, was created by the World Health Organization (WHO).
One of the most well-known tools for comparing quality of life across cultures is the WHOQOL-BREF, which is accessible in more than 40 languages.Each individual question on the WHOQOL-BREF is graded on a response scale, which is defined as a five-point ordinal scale, with scores ranging from 1 to 5. The scores are then linearly translated to a scale from 0 to 100.
The mobility, everyday activities, functional ability, energy, pain, and sleep are all part of the physical health domain that are included in the WHOQOL.
|
6 Weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Jawad Naweed, MS-SPT, Riphah International University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/01409 FARYAL SHAKOOR
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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