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Fasting mimicking diet compared with low calorie diet among premenopausal obese women

The effects of fasting mimicking diet versus low calorie diet on anthropometric measurements, body composition, insulin sensitivity and regulatory hormones of food intake on premenopausal obese women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190717044244N1
Enrollment
60
Registered
2019-08-19
Start date
2019-08-21
Completion date
Unknown
Last updated
2020-05-18

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

Conditions

obesity. Overweight and obesity

Interventions

Intervention 1: Intervention group: fasting mimicking diet will be administered during the first 5 days of a month (In total, 2 five-days cycles for 2 months). Fasting mimicking diet is a plant-based

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: healthy women aged 18-50 years BMI ranged from 30 to 35 not to use any tobacco regular menstrual cycle not to have symptoms of hyperandrogenism or PCOS not to use contraceptive drugs negative pregnancy test not having metabolic disorder affecting gluconeogenesis not having medical history of heart diseases not having considerable food allergies weight change less than 3 kg in the last 3 months not having psychotic disorder affecting the patients' adherence

Exclusion criteria

Exclusion criteria: not to have adherence to the diet unwilling to continue the trial

Design outcomes

Primary

MeasureTime frame
Body weight. Timepoint: Body weight will be measured just before the inclusion in the trial and at the end of the intervention (after 2 months). Method of measurement: digital scale.

Secondary

MeasureTime frame
Body fat mass. Timepoint: Body fat mass will be measured just before the inclusion in the trial and at the end of the intervention (after 2 months). Method of measurement: Body composition analyzer.;Fat free mass. Timepoint: Fat free mass will be measured just before the inclusion in the trial and at the end of the intervention (after 2 months). Method of measurement: Body composition analyzer.;Serum glucose. Timepoint: Serum glucose will be measured just before the inclusion in the trial and at the end of the intervention (after 2 months). Method of measurement: enzymatic methods.;Serum insulin. Timepoint: Serum glucose will be measured just before the inclusion in the trial and at the end of the intervention (after 2 months). Method of measurement: ELISA.;Ghrelin. Timepoint: Serum ghrelin will be measured just before the inclusion in the trial and at the end of the intervention (after 2 months). Method of measurement: ELISA.;Leptin. Timepoint: Serum leptin will be measured just before the inclusion in the trial and at the end of the intervention (after 2 months). Method of measurement: ELISA.;Neuropeptide Y. Timepoint: Serum neuropeptide Y will be measured just before the inclusion in the trial and at the end of the intervention (after 2 months). Method of measurement: ELISA.;Waist circumference. Timepoint: Waist circumference will be measured just before the inclusion in the trial and at the end of the intervention (after 2 months). Method of measurement: Meter.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehdi Sadeghian

Ahvaz University of Medical Sciences

mehdisad69@gmail.com+98 61 3373 8253

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 24, 2026