Response Of Metabolic Syndrome Severity Score To High Intenisty Interval Training In Women With Central Obesity.

Soma Adel Gaber Abd El-Ghany

Status: Enrolling

Conditions: Metabolic Syndrom

Treatments: Dietary Supplement: Caloric restricted diet; Device: High intensity interval training

Study type: Interventional

Funder types: Other

Identifiers

NCT06509464

Cairo soma 46

Details and patient eligibility

About

This study will be conducted to investigate any significant effect of high intensity interval training on metabolic syndrome severity score in women with central obesity.

Full description

RESPONSE OF METABOLIC SYNDROME SEVERITY SCORE TO HIGH INTENISTY INTERVAL TRAINING IN WOMEN WITH CENTRAL OBESITY

forty eight women with age ranges from 25 to 45 years old will be selected from nutrition-outpatient clinic; they will participate in the study for 6 weeks, and randomly be assigned into two equal groups.

Study group A (n =24) will receive low volume High-intensity interval training (HIIT) three times /week for 6 weeks , study group B (n =24) will receive caloric restriction diet

For evaluation Physical efficiency index using Modified Harvard Step test It is a powerful indicator for aerobic fitness. The Fitness Index score is determined according to the following equation

Fitness Index (long form) = (100 x test duration in seconds) divided by (2 x sum of heart beats in the recovery periods).

Metabolic syndrome severity score Metabolic syndrome severity score will be calculated through MetS Calculator (MetSCalc).

-3Laboratory investigation before & after treatment: for fasting blood glucose level and Lipid profile (total cholesterol, LDL, HDL, TAGs).

4- The 45-item Diet Satisfaction Questionnaire (DSat-45)

B) For treatment

1- Grand II Treadmill: (AC999- for maximum weight 150 Kg-

Enrollment: 48 estimated patients

Sex: Female

Ages: 25 to 45 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 1. 48 Women subjects with age ranges from 25to 45 years.

2. Waist height ratio ranges from 49-58 (overweight and seriously overweight).

Exclusion criteria

• 1. Uncontrolled Diabetes 2. Uncontrolled hypertension 3. Cognitive impaired patients 4. Severe Anemic women 5. Subjects with physical or musculoskeletal disabilities 6. Pregnancy 7. Recent cardiothoracic surgery

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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48 participants in 2 patient groups

low volume High-intensity interval training (HIIT)

Experimental group

Description:

group A (n =24) will receive low volume High-intensity interval training (HIIT) three times /week for 3 months,

Treatment:

Device: High intensity interval training

Dietary Supplement: Caloric restricted diet

caloric restricted diet.

Experimental group

Description:

group B (24) will receive caloric restricted diet.

Treatment:

Device: High intensity interval training

Dietary Supplement: Caloric restricted diet