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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06077552
Other study ID # P.T.REC/012/004666
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 1, 2023
Est. completion date January 30, 2025

Study information

Verified date February 2024
Source Cairo University
Contact marwa elsayed, PhD
Phone 0201156033818
Email marwadd999@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


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: 1. Level one: will be set as a 20% walking of Karvonen formula. 2. Level two: will be set as a 30% running of Karvonen formula. 3. Level three: will be set as a 50%running of Karvonen formula. 4. Level four: will be set as a 70% running of Karvonen formula. 5. Level five: will be set as a 80% running of Karvonen formula The whole program will be 40 minutes with warm up and cool down 5 minutes of stretch exercise for each. Participants will be asked to get on the treadmill and start the program, the therapist is monitoring the heart rate by using a pulse oximeter, and when the participants reach targeted percent of Karvonen formula, the therapist set the treadmill by increasing the speed to enter or start the up next level till reaching the highest level then start the decremental phase of the pyramidal training. The therapist shifts between the level by time or targeted percent of Karvonen formula which comes first.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date January 30, 2025
Est. primary completion date December 30, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 30 Years to 40 Years
Eligibility Inclusion Criteria: - 1) Fifty women with central obesity. 2) Waist circumference > 88 cm. 3) Their age will be ranged from 30-40years old. 4) Body mass index (BMI) from 30 to 34.9 kg/m2. 5) High normal or abnormal lipid profile (total cholesterol > 200 mg/dl, HDL< 35 mg/dl, or triglycerides >150 mg/dl) and atherogenic index of plasma (AIP) ranges 0.11-0.21 6) HOMA-IR > 2.9 7) They are clinically and medically stable. 8) All participants are sedentary activity level according to physical activity index. Exclusion Criteria: - 1) Participants with musculoskeletal problems (e.g., Sever osteoarthritis or difficulties in ambulation). 2) Participants with uncontrolled pulmonary disease. (e.g., Exaggerated chronic obstructive pulmonary disease, acute asthma). 3) Any participants who missed more than two weeks of the program or want to terminate the program. 4) Participants with unstable angina, uncontrolled cardiac arrhythmia, decompensated heart failure. 5) The participants have hearing impairment or mental disorders. 6) Implanted pacemaker. 7) Diabetes and hypertension.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
pyramidal training by treadmill
pyramidal training by treadmill for 40 minutes per session three sessions per week for eight weeks in addition to the diet health advises

Locations

Country Name City State
Egypt Faculty of Physical Therapy Cairo Dokki

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary atherogenic index of plasma blood analysis 8 weeks
Secondary Waist circumference tape measurement 8 weeks
Secondary Body mass index measurement weight on height 8 weeks
Secondary lipid profile blood analysis 8 weeks
Secondary insulin resistance homeostatic model assessment for insulin resistance 8 weeks
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