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Effect of non-invasive devises on fat reductio

Phase 4
Conditions
Overweight and obesity.
Overweight and obesity
Registration Number
IRCT20110726007117N8
Lead Sponsor
ational Institute for Medical Research Development(NIMAD)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
52
Inclusion Criteria

BMI more than 25
Age between 18 and 65 years

Exclusion Criteria

Pregnancy
Lactation
Active implant device such as pacemaker, defibrillator or drug delivery
Tooth infection
History of previous surgery in the desired area
History of stroke or facial paralysis (Bell's palsy)
Botulinum toxin or injection of aesthetic drugs in the area (abdomen) during the last 6 months.
Treatment with dermal fillers, radioactive methods or laser

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
?Anthropometric indices. Timepoint: before and after of the intervention. Method of measurement: bio impedance analyser(BIA).
Secondary Outcome Measures
NameTimeMethod
Examine the satisfaction of the body composition. Timepoint: before and after of the intervention. Method of measurement: body satisfaction questionnaire(BSQ).;psychological distress scale evaluation. Timepoint: before and after of the intervention. Method of measurement: kessler psychological distress scale k10 score interpretation.;Lipid profile measurement. Timepoint: before and after of the intervention. Method of measurement: blood sampling.;Liver enzyme measurement. Timepoint: before and after of the intervention. Method of measurement: blood sampling.
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