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The effect of probiotic supplementation on obesity

Phase 3
Recruiting
Conditions
Obesity.
Obesity due to excess calories
E66.0
Registration Number
IRCT20131228015968N5
Lead Sponsor
Vice chancellor for research, Shahid Beheshti University of Medical sciences- School of Nutrition
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
60
Inclusion Criteria

Body Mass Index 30-39.99
The desire to participate in the study
Confirmation of food addiction after obtaining the necessary points from the relevant questionnaire
Being in the age range of 20-50 years

Exclusion Criteria

Having a Weight loss diet in the last two months
Pregnancy or lactation
Menopause
Continuous use (more than once a week) of vitamin and mineral supplements in the past month
Use of any type of antibiotic in the last three weeks
Use of weight loss and appetite suppressants
Sports activity that lasted more than three weeks from the start
Cancer, cardiovascular disease, diabetes
Acute gastrointestinal disease
Chronic kidney or liver disease, with the exception of non-alcoholic fatty liver
Infectious diseases up to 1 month before the start of the study

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Weight. Timepoint: Before intervention, after 6 Weeks of intervention and after 12 Weeks of intervention. Method of measurement: Seca scale.;Body Mass Index. Timepoint: Before intervention, after 6 Weeks of intervention and after 12 Weeks of intervention. Method of measurement: Calculation (kg/m2).;Waist circumference. Timepoint: Before intervention, after 6 Weeks of intervention and after 12 Weeks of intervention. Method of measurement: Meter strip.;Fat Mass. Timepoint: Before intervention, after 6 Weeks of intervention and after 12 Weeks of intervention. Method of measurement: Bio Impedance Analyzer.;Fat Free Mass. Timepoint: Before intervention, after 6 Weeks of intervention and after 12 Weeks of intervention. Method of measurement: Bio Impedance Analyzer.
Secondary Outcome Measures
NameTimeMethod
Serum level of Leptin. Timepoint: Before intervention and after 12 weeks of intervention. Method of measurement: Elisa.;Serum Neuropeptide Y. Timepoint: Before intervention and after 12 weeks of intervention. Method of measurement: Elisa.;Appetite. Timepoint: Before intervention and after 12 weeks of intervention. Method of measurement: Simple appetite questionnaire.;Serum level of Oxytocin. Timepoint: Before intervention and after 12 weeks of intervention. Method of measurement: Elisa.;Eating behavior. Timepoint: Before intervention and after 12 weeks of intervention. Method of measurement: The Three-Factor Eating Questionnaire.
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