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Ultrasound-induced Adipose Tissue Cavitation and Training in Obesity

Ultrasound-induced Adipose Tissue Cavitation: Effects on Cardiometabolic Risk and Body Composition in Persons With Obesity

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04417816
Acronym
UATC
Enrollment
28
Registered
2020-06-05
Start date
2018-04-15
Completion date
2020-02-28
Last updated
2021-08-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Brief summary

The addition of ultrasound-induced adipose tissue cavitation (UATC) at the level of the abdominal subcutaneous adipose tissue may seem relevant as an additive treatment option to exercise intervention in individuals with obesity. However, whether individuals with obesity who participate in an exercise intervention and additionally undergo UATC, are more likely to develop a metabolically healthy phenotype, as opposed to subjects with obesity undergoing exercise training or UATC only, remains to be studied. Therefore, the first aim of this study is to examine the impact of combined UATC during exercise intervention on abdominal subcutaneous and whole-body adipose tissue mass, quality of life and cardiometabolic risk in individuals with abdominal obesity.

Interventions

OTHERExercise training intervention with ultrasound induced adipose tissue cavitation

Exercise training intervention with ultrasound induced adipose tissue cavitation

OTHERExercise training intervention without ultrasound induced adipose tissue cavitation

Exercise training intervention with ultrasound induced adipose tissue cavitation

Sponsors

Hasselt University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* male/female (1:1), * age 18-65 y, * abdominal obesity (waist circumference \>102cm or \>88cm) -

Exclusion criteria

* involvement in dietary or exercise intervention in the last year, * intake of any medication, * clinically diagnosed diseases (cardiovascular disease, hypertension, venous thromboses blood diseases, presence of a pacemaker/defibrillator, brain or nervous system diseases, kidney, thyroid or liver disease, chronic inflammatory diseases, cancer, osteoporosis and epilepsy). * Persons with a pregnancy, * a recent bone injury or the presence of a metal prothese

Design outcomes

Primary

MeasureTime frameDescription
oral glucose tolerance testBaselineglucose and insulin levels at 0, 15, 30, 45, 60, 90 and 120 min post glucose load
kidney functionBaselineurea, creatinine
inflammationBaselineCRP
BloodpressureBaselinesystolic and diastolic blood pressure
DEXA scanbaselineBody composition (fat mass, fat free mass, android and gynoid fat mass), clinical measures (waist circumference, hip circumference, weight, height)
Fasting blood sampleBaseline(glycated haemoglobin)
lipid profileBaselinetotal LDL, HDL, triglycerides

Secondary

MeasureTime frameDescription
SF-36 questionaireBaselineQuality of Life questionaire, a 36-item, patient-reported survey of patient health. The SF-36 is a measure of health status
Food intakeBaseline3-day food diary
Overall physical fitnessBaselineMaximal oxygen uptake (during cardiopulmonary exercise testing)

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026