Effect of Upper Limb Ergometer on the AIP in Post Menopausal Obese Women.

Cairo University (CU)

Status: Completed

Conditions: Post Menopausal Obese Women

Treatments: Device: Electronic Upper limb( body) ergometer

Study type: Interventional

Funder types: Other

Identifiers

NCT04676074

Rana Hesham

Details and patient eligibility

About

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.

Full description

Control group (A):

1. Each participant will sign a consent form after receiving a detailed explanation about the procedure.

2. A blood sample will been taken by a nurse in a heparinized tube and delivered to lab within six hours.

3. BMI will been measured body weight(Kg) and height (m2)

   a. BMI= body weight (Kg)/ height (m2).

4. Waist circumference will be measured.

5. After one month blood analysis evaluation will be done to record the response to the routine medication.

Training Procedure for group (B):

1. Each participant will sign a consent form after receiving a detailed explanation about the procedure.

2. A blood sample will been taken by a nurse in a heparinized tube and delivered to lab within six hours.

3. BMI will been measured body weight(Kg) and height (m2)

   a. BMI= body weight (Kg)/ height (m2).

4. Waist circumference will be measured.

5. The maximum heart rate will be determined from Tanaka formula (208- 0.7 *age of the participant)

   • Then the exercise load will be determined according heart rate reserve of the participants ( maximum heart rate - resting heart rate).

6. 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.

7. Increase the speed and intensity for 10-30 seconds before dropping it back for 2-5 minutes and Repeat according to the intensity.

8. Finally, a five minutes of cooling down with no resistance had performed.

9. After one month blood analysis evaluation will be done to record the response to the routine medication.

Enrollment: 40 patients

Sex: Female

Ages: 45 to 60 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• female aged 45-60 years old.
• class 1 and 2 obesity.
• post menopausal.
• diagnosed as controlled diabetic.
• diagnosed as controlled hypertensive.

Exclusion criteria

• uncontrolled diabetic.
• uncontrolled hypertensive.
• class 3 and morbid obesity.
• mentally unstable person.
• Any shoulder, hand and elbow orthopedic or neural disorders.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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40 participants in 2 patient groups

control group

No Intervention group

Description:

the participant will not do any exercise program but just they will take the routine medication.

study group

Experimental group

Description:

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.

Treatment:

Device: Electronic Upper limb( body) ergometer