Clinical trial

Effect of High Intensity Interval Training and Ultrasound Cavitation on Lipid Profile in Type 2 Diabetes Patients

Opening soon · Not applicable · 1 countries · Registry ID NCT06926725

Opening soonNot applicableInterventional

What this study is about

The study aim to find out the combined effect of high intensity interval training and ultrasound cavitation on lipid profile in type two diabetic patient with abdominal obesity.

A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.

Basic eligibility

Age30 Years to Not listed

SexAll

Healthy volunteersNot accepted

ConditionDiabetes Mellitus Type 2

Full registry criteria

Inclusion Criteria: * patient with type 2 diabetes. * waist circumference \>102 cm in male ,\>88 cm in female * lipid profile range will be (between border line and high risk ). Exclusion criteria: Kidney disease Heart disease Lung disease ,Liver disease ,Neurological disorders ,Pregnant women , breast feeding, immune deficiency , cancer Heavy smoker Exclusion Criteria: \-

Treatments and study arms

Cavitation : Study group A only will receive one session per week for three months (total 12 sessions ). Ultrasound treatments are performed using an applicator head with diameter 7 cm . Intensity :

Device

Cavitation : Study group A only will receive one session per week for three months (total 12 sessions ). Ultrasound treatments are performed using an applicator head with diameter 7 cm . Intensity : 0.1-0.5 w/cm2 (low) Frequency : 30-40 KHZ (low) Duration : 30 minutes

high intenisty exercise

Other

type: alternate high intensity exercise (aerobic or strength training) with recovery stages Intensity: high intensity (75%-95% HRmax) or RPE(14-16 hard to very hard ) ( according to patient tolerance), followed by active or passive recovery stage (30%-60% HRmax) or RPE(7-11 extremely light to light) . frequency : 3 days per week for three months (with no more than 2 consecutive days between sessions) Duration: 10 seconds to 4 minutes high intensity ,12 seconds to 5 minutes active or passive recovery .(according to patient tolerance) 5 minutes warm up pre exercise . 5 minutes cool down post exercise . Progress gradually. total duration :20-40 minutes (according to patient tolerance and progression)

Diet

Dietary Supplement

In all groups (both study groups A\&B and control group).

Primary outcomes

Anthropometric Measurements3 months

It will be performed before and after the treatment . Weight in (kg) is measured by in body scale During the measurement of height in( cm) patient is barefoot . Body mass index (BMI): weight (kg)/ \[ height (m)\] 2

Lipid profile3 months

contains (cholesterol, triglycerides, Low-density lipoprotein cholesterol (LDL), and high-density lipoprotein cholesterol (HDL)).

Study locations

1 locations were listed when this page was built. The first 40 are shown.

Beni-Suif University Hospital🇪🇬 GIZA, Cairo Governorate, Egypt

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Sara El-dinContact