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Comparative Effects of 16:8 Intermittent Fasting and Continuous Caloric Restriction on Metabolic Syndrome Components in obese Women: A Non-randomized Controlled Clinical Trial

Comparative Effects of 16:8 Intermittent Fasting and Continuous Caloric Restriction on Metabolic Syndrome Components in obese Women: A Non-randomized Controlled Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202409898073796
Enrollment
100
Registered
2024-09-02
Start date
2022-10-01
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Nutritional, Metabolic, Endocrine

Interventions

intermittent fasting
CCR continuous calorie restriction

Sponsors

none
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: women aged between 18 and 50 years, with a BMI = 30 kg/m², who consented to adhere to the study protocol.

Exclusion criteria

Exclusion criteria: pregnant, breastfeeding or menopausal; diabetic or hypertensive; consuming medications (such as corticosteroids) or specific supplements (like probiotics) that might affect weight evolution; diagnosed with dysthyroidism (hyperthyroidism or hypothyroidism); or affected by any other conditions potentially impacting weight evolution. bariatric surgery, modified their diets within the 12 weeks preceding the study commencement severe eating disorders or psychiatric illnesses

Design outcomes

Primary

MeasureTime frame
At baseline anthropometric parameters, weight, waist circumference and body composition will be assessed and it will be re-evaluated at 3 months after the intervention.

Secondary

MeasureTime frame
laboratorys tests were performed, fasting blood glucose, glycated hemoglobin, HOMA-IR (Homeostasis Model Assessment) index, calculated as fasting insulin (µU/dL) multiplied by fasting blood glucose (mmol/L) divided by 22.5 and lipid profile. they were assessed at baseline and 3 months after the intervention

Countries

Tunisia

Contacts

Public Contacthenda jamoussi

institut national de nutrition et de technologie alimentaire de tunis

hendajamoussi@gmail.com+21698648225

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026