Prebiotic and functional effects of Ora-pro-nobis (Pereskia aculleata) in overweight wome

Not Applicable

• Conditions: Overweight; Obesity

• Registration Number: RBR-57c9wnd
• Lead Sponsor: niversidade Vila Velha

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2023-01-17
• Last Update Posted: 29 May 2023
• Study Completion: 2023-12-01

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

Volunteer women; age between 18-59 years; diagnosed with overweight or obesity by BMI>24.5;

Exclusion Criteria

Disease diagnosis; consumption of food supplements in the last 6 months; consumption of laxatives in the last 6 months; consumption of antibiotics in the last 6 months; surgical procedures in the last 6 months; vegetarianism; consumption of herbal remedies; consumption of herbal preparations; known allergic reactions to product components; intake of probiotics in the previous year; use of hypoglycemic drugs; use of lipid-lowering drugs; use of hypotensive; presence of other comorbidities; smokers

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
It is expected to find an improvement in biochemical parameters and weight loss, evaluated by biochemical tests and anthropometric assessment. It is expected that there will be weight reduction corresponding to a decrease in BMI greater than 24.5 for a BMI less than this value, during the intervention time of 12 weeks. Furthermore, it is expected that biochemical values ??will be adjusted to based on the reference values ??for each analyzed variable, within the 12 weeks of intervention.

Secondary Outcome Measures

Name	Time	Method
Secondary outcomes are not expected.