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Participants had randomly divided into two equal groups. Group (A) which is the control group receive normal routine medication. Group (B) will receive normal routine medication with the treatment program of moderate intensity upper limb ergometer for 15 minute with frequency three times per week for four weeks.
Control group (A):
Each participant will sign a consent form after receiving a detailed explanation about the procedure.
A blood sample will been taken by a nurse in a heparinized tube and delivered to lab within six hours.
BMI will been measured body weight(Kg) and height (m2)
a. BMI= body weight (Kg)/ height (m2).
Waist circumference will be measured.
After one month blood analysis evaluation will be done to record the response to the routine medication.
Training Procedure for group (B):
Each participant will sign a consent form after receiving a detailed explanation about the procedure.
A blood sample will been taken by a nurse in a heparinized tube and delivered to lab within six hours.
BMI will been measured body weight(Kg) and height (m2)
a. BMI= body weight (Kg)/ height (m2).
Waist circumference will be measured.
The maximum heart rate will be determined from Tanaka formula (208- 0.7 *age of the participant)
Start with sitting resting without any effort for 5 min then Start at a low speed and intensity for 5 minutes to warm up the body.
Increase the speed and intensity for 10-30 seconds before dropping it back for 2-5 minutes and Repeat according to the intensity.
Finally, a five minutes of cooling down with no resistance had performed.
After one month blood analysis evaluation will be done to record the response to the routine medication.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| control group | No Intervention | the participant will not do any exercise program but just they will take the routine medication. | |
| study group | Experimental | will receive normal routine medication with the treatment program of moderate intensity upper limb ergometer for 15 minute with frequency three times per week for four weeks. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Electronic Upper limb( body) ergometer | Device | Electronic pedal for the upper limb using for training the upper body. Intensity, speed and resistance can be adjusted. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Effect of the upper body ergometer on arthrogenic index ( triglyceride/ high density lipoprotein) | Effect of the upper body ergometer on arthrogenic index ( triglyceride/ high density lipoprotein) | after one month of the trial application |
| Measure | Description | Time Frame |
|---|---|---|
| Effect of the upper body ergometer on total body weight kg. | Effect of the upper body ergometer on total body weight kg. | after one month of the trial application |
| Effect of the upper body ergometer on estimated maximum heart rate(beat/min). |
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Inclusion Criteria:
Exclusion Criteria:
Post Menopausal Obese Women
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| Name | Affiliation | Role |
|---|---|---|
| Rana H El Banna, PHD | Faculty of physical therapy at Cairo University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Outpatient clinic faculty of physical therapy at Cairo University | Giza | 12613 | Egypt |
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Participants had randomly divided into two equal groups. Group (A) which is the control group receive normal routine medication. Group (B) will receive normal routine medication with the treatment program of moderate intensity upper limb ergometer for 15 minute with frequency three times per week for four weeks.
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Participant
Effect of the upper body ergometer on estimated maximum heart rate(beat/min).
| after one month of the trial application |