Foundation University College of Physical Therapy
Rawalpindi, Punjab Province, 46000, Pakistan
NCT Number: NCT06609954
Obesity is a global health concern associated with an increased risk of cardio-metabolic diseases and reduced overall health. Exercise is a proven modality for managing obesity, with current focus of researches on identifying more time-efficient modes of exercise training. REHIT and HIIT have proven benefits but comparative effects of REHIT and HIIT in overweight and obese adults is yet to be determined. Hence the objective of this study is to compare the effects of reduced exertion high intensity training (REHIT) versus high intensity interval training (HIIT) on anthropometric measures (weight, waist circumference, hip circumference, waist-to-hip ratio), CUN-BAE adiposity index and cardiorespiratory fitness in overweight and obese adults.
This study is active but is not currently recruiting participants.
18 year–45 year
All sexes
Interventional
Not applicable
Rawalpindi, Punjab Province, 46000, Pakistan
Obesity is a global health concern associated with an increased risk of cardio-metabolic diseases and reduced overall health. Exercise is a proven modality for managing obesity, with current focus of researches on identifying more time-efficient modes of exercise training. REHIT and HIIT have proven benefits but comparative effects of REHIT and HIIT in overweight and obese adults is yet to be determined.The significance of this study is to compare the effects of reduced exertion high intensity training (REHIT) versus high intensity interval training (HIIT) and will also investigate the effectiveness of REHIT as an alternative for overweight and obese individuals who perceive HIIT as too demanding. If found effective, it can also help in providing training protocol for optimizing cardiovascular health in this population, potentially leading to improved outcomes and reduced healthcare burdens. The results of this study will also add data to literature regarding the effects of REHIT and HIIT on anthropometric measures in overweight and obese. Main objective of this study is to compare the effects of reduced exertion high intensity training (REHIT) versus HIIT on anthropometric measures (weight, waist circumference, hip circumference, waist-to-hip ratio), CUN-BAE adiposity index and Cardiorespiratory fitness in overweight and obese individuals. The participants meeting the eligibility criteria will be recruited followed by random allocation to one of the 2 groups, following which they will be required to complete a self-reported demographic form and will be screened using Physical Activity Readiness Questionnaire (PAR-Q). Baseline evaluation will be done using tape measure for anthropometric, assessment of waist circumference and hip circumference, CUN-BAE index for adiposity and Queen's College step test for cardio-respiratory fitness. Experimental group A will perform REHIT while experimental group B will perform HIIT. Participants will also be provided with dietary restriction plan that will be followed during the training protocol. Exercise training would be performed for consecutive 6 weeks, 3 times a week on alternative days for total of 18 sessions.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Participant will perform a 5 min warm-up exercises then do cycling or treadmill running for 20 min at 40%-60% of HRR and then will conclude with 5 min cool down exercises. From week 2 to 6 participants will be instructed to perform training sessions on a cycle ergometer. Each session will consist of a 3-minute warm-up period followed by two 20-second all-out sprints interspersed with 3 minutes of slow pedaling for recovery. Total of 18 sessions of REHIT will be performed thrice a week on alternate days by the participants for consecutive 6 weeks.
Patients in this group will be provided with a caloric restriction plan by a nutritionist that will be followed throughout the training duration. Week 1 will be baseline fitness level and familiarization week. Participant will perform a 5 min warm-up exercises then do cycling or treadmill running for 20 min at 40%-60% of HRR and then will conclude with 5 min cool down exercises. From week 2 to 6 participants will be instructed to perform a warm up of 5 min, then 4 bouts of 4 min of HIIT will be performed at 80%-95% of HRR separated by 3-min active recovery periods of moderate intensity cycling at 60%-70% of the HRR followed by 5 min cool down exercises. Pre and post session vitals will be noted. Total of 18 sessions of either HIIT will be performed thrice a week on alternate days by the participants for consecutive 6 weeks.
Time frame: 6 weeks
Will be measured using a cloth tape measure. Waist circumference will be measured at the level of the smallest circumference above the umbilicus and below the xiphoid appendix.
Time frame: 6 weeks
Measure at the widest point of the hips, with feet together
Time frame: 6 weeks
To determine the waist-to-hip ratio, divide the WC by the HC
Time frame: 6 weeks
Cardiorespiratory Fitness will be assessed via Queens College step test.
Time frame: 6 weeks
Evaluation will be done using CUN-BAE INDEX (Clínica Universidad de Navarra-Body Adiposity Estimator)
Foundation University Islamabad
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT05153252
Behavior, Body Weight
Aurora, Colorado, United States
View Trial DetailsNCT06002685
Allergies, Antibiotic Use
Baltimore, Maryland, United States
View Trial DetailsNCT06151964
Body Weight, Body Weight Changes
Graz, Austria
View Trial DetailsNCT05796141
Body Weight, Nutrition Disorders
Hartford, Connecticut, United States
View Trial Details