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Effect of oral Probiotic supplementation in children with Obesity: evaluation of the impact on body weight and variables associated with Obesity

Effect of oral Probiotic supplementation in children with Obesity: avaluation of the impact on nutritional status and variables associated with Obesity

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-9qg9qhh
Enrollment
Unknown
Registered
2023-03-01
Start date
2023-04-11
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Obesity

Interventions

This is a double-blind, parallel, placebo-controlled clinical trial lasting 12 weeks, with participants being randomly selected. Experimental group: 35 children with obesity and severe obesity will re
G07.203.300.456.500

Sponsors

Fundação Universidade Federal de São João Del Rei
Lead Sponsor
Secretaria municipal de saúde de Divinópolis
Collaborator

Eligibility

Age
7 Years to 10 Years

Inclusion criteria

Inclusion criteria: Kids; both genders; age between 7 and 10 years; with a nutritional diagnosis of obesity or severe obesity

Exclusion criteria

Exclusion criteria: Children with liver diseases; nephropathy; heart disease; cancer; inflammatory bowel disease using probiotic supplements; prebiotics; symbiotics

Design outcomes

Primary

MeasureTime frame
It is expected to find a 15% decrease in body weight, assessed by anthropometric methods (weight, height and waist circumference measurements) and body composition (body fat percentage). The nutritional status will be verified by the body mass index (BMI) by age, according to the parameters of the WHO growth curves. Data collected at 0, 30, 60 and 90 days of intervention.—

Secondary

MeasureTime frame
No outcomes are expected secondary—

Countries

Brazil

Contacts

Public ContactKelly Santos

Fundação Universidade Federal de São João Del Rei

kellyfreitass83@hotmail.com+55 (37)98847-0178

Outcome results

None listed

Source: REBEC (via WHO ICTRP)