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The study will be conducted on fifty women with central obesity. Their ages will be from 30-40 years old. They will be selected from Al Hayat specialized Hospital in Cairo, Egypt and The participants will be randomly assigned into two equal groups:
Group (A): study group, 25 participants will receive pyramidal training by treadmill for 40 minutes per session three sessions per week for eight weeks in addition to the diet health advices.
Group (B): Control group, 25 participants will receive diet health advices. The subjects will be selected from El Haya specialized Hospital, Cairo.
Full description
The study will be conducted on fifty women with central obesity. Their ages will be from 30-40 years old. They will be selected from Al Hayat specialized Hospital in Cairo, Egypt and The participants will be randomly assigned into two equal groups:
Group (A): study group, 25 participants will receive pyramidal training by treadmill for 40 minutes per session three sessions per week for eight weeks in addition to the diet health advices.
Group (B): Control group, 25 participants will receive diet health advices. The subjects will be selected from El Haya specialized Hospital, Cairo. Before starting the procedure the participants target heart rate (THR) will be calculated from Karvonen formula as follow: target heart rate (THR) = maximum heart rate (HRmax) - resting heart rate × intensity + resting heart rate(RHR)(Yabe et al.,2021).
The formula 208-0.7•age yield more precise estimates of HRmax over a wide age range (Nes et al., 2013).
After calculating THR, the study group participants will be on a pyramidal training program of incremental and decremental levels as follow:
The course of the program will be 2 sets of pyramidal training with 10 minutes for rest between them. each set will be 5 levels of incremental and 5 levels of decremental aerobic exercise and each level 2 minutes on a treadmill. All these levels will be ranked according to a percentage from the THR; the ranking will be as follow:
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Exclusion criteria
Participants with musculoskeletal problems (e.g., Sever osteoarthritis or difficulties in ambulation).
Participants with uncontrolled pulmonary disease. (e.g., Exaggerated chronic obstructive pulmonary disease, acute asthma).
Any participants who missed more than two weeks of the program or want to terminate the program.
Participants with unstable angina, uncontrolled cardiac arrhythmia, decompensated heart failure.
The participants have hearing impairment or mental disorders. 6) Implanted pacemaker. 7) Diabetes and hypertension.
Primary purpose
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Interventional model
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60 participants in 2 patient groups
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Central trial contact
marwa elsayed, PhD
Data sourced from clinicaltrials.gov
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