Imaging on Core Muscles Function in Patients With Visceral Adiposity

NCT ID: NCT05690659

Last Updated: 2023-09-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

45 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-08-01

Study Completion Date

2023-01-20

Brief Summary

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The purpose of this study is to determine the effect of cavitation ultrasonic lipolysis, RUSI guided core muscle exercise and their combination (cavitation ultrasonic lipolysis and RUSI guided core muscles exercise) on diaphragmatic excursion, transverse abdominis activation ratio, visceral fat thickness and waist circumference in patients with visceral adiposity patients with visceral adiposity will be recognized by nutrition specialist. 45 patients were distributed randomly into three groups. The first group will be treated with Cavitation lipolysis twice weekly. The second group was treated with rehabilitative ultrasound imaging (RUSI) guided core muscle exercise. The third group was treated with combination of cavitation and RUSI. patients will be examined with medical ultrasound imaging and tape measurement.

Detailed Description

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\- Inclusion criteria: Forty five subjects participated in this study. Age of participants ranged from 25 to 45 years. 3. Waist circumference was more than 102 cm for men and 88 cm for women 4. Body mass index (BMI) ranged from 25 to 29.9 (Kg / m2). 5. Subjects hadn't received drugs

Exclusion criteria:

1. history of spinal surgery or spinal fracture.
2. Serious diseases, such as heart disease, kidney, liver diseases, gastric ulcer or duodenal ulcer.
3. A history of bronchial asthma or any chest disease.
4. Uncontrolled diabetes or hypertension.
5. Patients with peacemaker or any metal implant on the treated area.
6. Cancer or patient with past history of tumor excision

Conditions

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Obesity, Abdominal

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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cavitation ultrasonic lipolysis

on abdomen 2 sesions / week for 10 sessions , Treatment head was griped perpendicular to abdomen, and make slow circular motion with marked pressure.2 sesions / week for 10 sessions

Group Type EXPERIMENTAL

device and exercise

Intervention Type OTHER

cavitation ultrasonic device therapeutic exercise guided ultrasonography imaging

RUSI guided core muscle exercise

2 sesions / week for 10 sessions For diaphragm muscle the transducer was placed on the sub costal region to visualize diaphragm muscle on the screen aiming to use US as a visual feedback procedure. instructed to have 5 seconds to contract the diaphragm muscle by deep breathing and hold the contraction. At the end of the 5-second period, the image was saved on the screen, and the measurement of the resultant increase in thickness was performed. Each subject performed a total of 10 contractions (intervention session) For transverse abdominis exercise,. draw in your umbilicus toward the spine without moving back or pelvis, while comfortably breathing in and out," for 10 seconds hold and then 15 seconds rest in between, it was repeated 3 sets of ten while keeping the transducer perpendicular to the surface of the skin in a transverse plane halfway between the ASIS and the lower ribcage along the anterior axillary line

Group Type EXPERIMENTAL

device and exercise

Intervention Type OTHER

cavitation ultrasonic device therapeutic exercise guided ultrasonography imaging

combination of cavitation and RUSI

combination of cavitation and RUSI 2 sesions / week for 10 sessions

Group Type EXPERIMENTAL

device and exercise

Intervention Type OTHER

cavitation ultrasonic device therapeutic exercise guided ultrasonography imaging

Interventions

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device and exercise

cavitation ultrasonic device therapeutic exercise guided ultrasonography imaging

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Forty five subjects participated in this study.
* Age of participants ranged from 25 to 45 years.
* Waist circumference was more than 102 cm for men and 88 cm for women
* Body mass index (BMI) ranged from 25 to 29.9 (Kg / m2).
* Subjects hadn't received drugs

Exclusion Criteria

.history of spinal surgery or spinal fracture.

* Serious diseases, such as heart disease, kidney, liver diseases, gastric ulcer or duodenal ulcer.
* A history of bronchial asthma or any chest disease.
* Uncontrolled diabetes or hypertension.
* Patients with peacemaker or any metal implant on the treated area.
* Cancer or patient with past history of tumor excision.
Minimum Eligible Age

25 Years

Maximum Eligible Age

45 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Deraya University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Deraya university

Minya, , Egypt

Site Status

Countries

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Egypt

Other Identifiers

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P.T.REC/012/003449

Identifier Type: -

Identifier Source: org_study_id

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