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A Systematic Review of the effect of intake of functional ingredients of barley-derived beta glucan in reducing postprandial Blood Glucose rise

A Systematic Review of the effect of intake of functional ingredients of barley-derived beta glucan in reducing postprandial Blood Glucose rise - SR of the effect of Barley-derived beta-glucan in reducing postprandial Blood Glucose rise

Status
Active, not recruiting
Phases
Unknown
Study type
Unknown
Source
JPRN
Registry ID
JPRN-UMIN000056843
Enrollment
Unknown
Registered
2025-01-31
Start date
2025-01-31
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Male and female adults whose fasting or postprandial blood glucose in borderline or high levels, and healthy male and female adults. Those who are planning to become pregnant, expectant or nursing mothers, and breastfeeding women are excluded.

Interventions

None listed

Sponsors

Kyushu University
Lead Sponsor
Evaluation Center of Health and Nutrition Inc. Kenichi Kakino
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (PICOS) P (Participant): Male and female adults whose fasting or postprandial blood glucose level: 110-125 mg/dl, 75gOGTT 2 hour after value: 110-125 mg/dl, casual blood glucose level: 140-199 mg/dl, and healthy male and female adults. Minors, pregnant women (including those planning pregnant), lactating mothers, patients with diabetes mellitus, BMI less than 18.5, 30 or above are excluded. I (Intervention): Foods containing barley-derived beta-glucan (regardless of food form) should be taken orally. The duration of intake is one time. Studies with unknown barley-derived beta-glucan content are excluded. C (Comparison): Comparison target, Intake of barley-derived beta-glucan-free placebo O (Outcome measurement): The primary outcome is the evaluated value of the effect of intake of barley-derived beta-glucan on Area under the blood concentration curve (AUC) and the postprandial blood glucose levels. S (Study design): Randomised controlled trials are conducted. A significant difference test is performed on the test results by statistical analysis. The test arm must contain a food or beverage containing barley-derived beta-glucan. Intervention trials without a placebo group and studies using foods with multiple ingredients other than barley-derived beta-glucan as functional components are not included. Only peer-reviewed original papers are eligible.

Exclusion criteria

Exclusion criteria: Trials that include women who are pregnant or breastfeeding, women who are planning to become pregnant, or people who are being treated for hypertension Studies with unknown barley-derived beta-glucan content Papers citing the test results of the original paper, explanatory papers, abstracts of conference presentations, conference proceedings

Design outcomes

Primary

MeasureTime frame
The effect of intake of barley-derived beta-glucan on Area under the blood concentration curve (AUC) and the postprandial blood glucose levels

Countries

Japan

Contacts

Public ContactSeiichi Hattori

Kurume Research Park Co., Ltd. Bio Project Division

fbv@kurume-rp.co.jp0942-37-6124

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026