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Imaging on Core Muscles Function in Patients With Visceral Adiposity

D

Deraya University

Status

Completed

Conditions

Obesity, Abdominal

Treatments

Other: device and exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT05690659
P.T.REC/012/003449

Details and patient eligibility

About

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.

Full description

  • 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

Enrollment

45 patients

Sex

All

Ages

25 to 45 years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

45 participants in 3 patient groups

cavitation ultrasonic lipolysis
Experimental group
Description:
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
Treatment:
Other: device and exercise
RUSI guided core muscle exercise
Experimental group
Description:
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
Treatment:
Other: device and exercise
combination of cavitation and RUSI
Experimental group
Description:
combination of cavitation and RUSI 2 sesions / week for 10 sessions
Treatment:
Other: device and exercise

Trial contacts and locations

1

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Central trial contact

Soad Ali Mohamed; omar mohamed mabrouk

Data sourced from clinicaltrials.gov

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