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effect of beta glucan on pediatric obesity

The effects of beta-glucan supplementation on anthropometric indices and cardiometabolic risk factors in children and adolescents with overweight and obesity: a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180805040703N3
Enrollment
70
Registered
2025-01-26
Start date
2024-12-21
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

obesity. Obesity due to excess calories

Interventions

Intervention 1: Intervention group: 8 week beta glucan supplementation. Intervention 2: Control group: 8-week 7grams of maltodextrin daily.

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 17 Years

Inclusion criteria

Inclusion criteria: Children and adolescents aged 6 to 17 overweight, body mass index score in the range of positive one to positive two standard deviations compared to the standard median determined for age and sex by the World Health Organization for children or adolescents between 5-19 A person with obesity with a body mass index higher than positive 2 standard deviations compared to the standard median determined for age and gender by the World Health Organization for children or adolescents between 5-19 years old Willingness to participate in the study

Exclusion criteria

Exclusion criteria: taking any drugs or supplements that affect the metabolism and mechanisms of blood sugar and insulin, lipid profile and liver enzymes, such as metformin for more than 3 days in the last 1 month Participation in other weight loss programs in the previous 3 months and weight fluctuations of more than 5 kg in the last 2 months. Not suffering from any type of renal, cardiovascular, thyroid, liver and digestive metabolic diseases. Not suffering from secondary obesity such as Cushing's syndrome, obesity, hypogonadal hypothyroidism or hypophysis. Current use of more corticosteroid drugsFrom 5 days in a month. history of surgery in the last 3 months, history of bariatric surgery) Use of drugs to treat psychosis or Manic depression such as lithium, carbamazepine, or Valproic acid

Design outcomes

Primary

MeasureTime frame
Weight. Timepoint: At the beginning and end of the study (2 months after starting the intervention). Method of measurement: Digital scales.;Body mass index. Timepoint: At the beginning and end of the study (2 months after starting the intervention). Method of measurement: calculation.;Waist circumference. Timepoint: At the beginning and end of the study (2 months after starting the intervention). Method of measurement: tape measure.;Body mass index Z-score. Timepoint: At the beginning and end of the study (2 months after starting the intervention). Method of measurement: Measurement.

Secondary

MeasureTime frame
Fasting serum glucose concentration. Timepoint: At the beginning and end of the study (2 months after starting the intervention). Method of measurement: Colorimeter/ laboratory kit.;Fasting serum insulin concentration. Timepoint: At the beginning and end of the study (2 months after starting the intervention). Method of measurement: enzyme-linked immunosorbent assay/laboratory kit.;Total serum cholesterol level. Timepoint: At the beginning and end of the study (2 months after starting the intervention). Method of measurement: Colorimeter/ laboratory kit.;Serum triglyceride level. Timepoint: At the beginning and end of the study (2 months after starting the intervention). Method of measurement: Colorimeter/ laboratory kit.;Serum Low density lipoprotein level. Timepoint: At the beginning and end of the study (2 months after starting the intervention). Method of measurement: Blood biochemical test / colorimetry.;Serum high density lipoprotein level. Timepoint: At the beginning and end of the study (2 months after starting the intervention). Method of measurement: Blood biochemical test / colorimetry.;Alanine amino transferase enzyme. Timepoint: At the beginning and end of the study (2 months after starting the intervention). Method of measurement: photometry.;Aspartate amino transferase. Timepoint: At the beginning and end of the study (2 months after starting the intervention). Method of measurement: photometry.;Gamma glutamyl transferase enzyme. Timepoint: At the beginning and end of the study (2 months after starting the intervention). Method of measurement: Enzymatic colorimetry.;HOMA-IR index. Timepoint: At the beginning and end of the study (2 months after starting the intervention). Method of measurement: formula.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahdi Amani Farani

Shahid Beheshti University of Medical Sciences

navidamani14@gmail.com+98 939 296 4546

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026