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Effect of kettogenic diet on weight management and apptite

Not Applicable
Recruiting
Conditions
E66.0
Obesity.
Obesity due to excess calories
Registration Number
IRCT20220418054574N1
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
All
Target Recruitment
50
Inclusion Criteria

Overweight or obese people between 18-60 years old
Body mass index 40-26 kg / m2
Food addiction based on YFAS4 questionnaire
Weight regain One-third to two-thirds of the weight lost in 1 year, or almost all of them in 5 years
Do not be pregnant or breastfeeding

Exclusion Criteria

gout and chronic diseases such as diabetes, cardiovascular, liver, etc.
mental illness (depression, bipolar disorder and obsessive-compulsive disorder)
Failure to follow a specific diet
take drugs that affect appetite and weight
use any probiotic products in a recent month
use antibiotics during the last month

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Weight. Timepoint: before intervention and 8 weeks after intervention. Method of measurement: seca scale.;Body Mass Index. Timepoint: before intervention, 4 weeks and 8 weeks after intervention. Method of measurement: Calculation (kg/m2).;Waist circumference. Timepoint: before intervention, 4 weeks and 8 weeks after intervention. Method of measurement: Meter strip.;Fat Mass. Timepoint: before intervention and 8 weeks after intervention. Method of measurement: Bio Impedance Analyzer.;Fat Free Mass. Timepoint: before intervention and 8 weeks after intervention. Method of measurement: Bio Impedance Analyzer.
Secondary Outcome Measures
NameTimeMethod
Serum serotonin level. Timepoint: before intervention, 8 weeks after intervention. Method of measurement: Elisa.;Serum BDNF. Timepoint: before intervention, 8 weeks after intervention. Method of measurement: Elisa.;Gut microbiota. Timepoint: before intervention, 8 weeks after intervention. Method of measurement: PCR.
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