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Anti-fatigue Effects of Yogurt Fermented with Lactobacillus delbrueckii subsp. bulgaricus OLL1073R-1.

Anti-fatigue Effects of Yogurt Fermented with Lactobacillus delbrueckii subsp. bulgaricus OLL1073R-1. - Anti-fatigue Effects of Yogurt

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000025974
Enrollment
60
Registered
2017-02-02
Start date
2017-02-03
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

N/A (healthy adults)

Interventions

Oral intake of the test food (112 mL) twice a day for 4 weeks. Washout period for 3 weeks. Oral intake of the placebo (112mL) twice a day for 4 weeks. Oral intake of the placebo (112 mL) twice a d

Sponsors

Center for Health Science Innovation, Osaka City University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: [1]Individuals whose written informed consent has been obtained. [2]Healthy adults aged 30-59 years.

Exclusion criteria

Exclusion criteria: [1]Individuals under medication or using medial products. [2]Individuals who have medical history of circulatory system diseases. [3]Individuals who have autonomic nervous system disorders. [4]Individuals who have medical history of neurological diseases such as unconsciousness, coma, convulsion, etc. [5]Individuals who have sleep disorders. [6]Individuals who have serious diseases such as diabetes, liver diseases, renal diseases, heart diseases. [7]Individuals who have serious pollinosis. [8]Individuals who are sensitive to foods or intolerant to lactose. [9]Individuals who excessively take alcohol(expressed in amount of alcohol: over 60 g/day) [10]Smokers. [11]Individuals who have a habit to take fermented milk or lactic acid bacteria beverage two days a week or more in the past 3 months. [12]Individuals who work the night shift. [13]Individuals whose BMI is not 17.0-30.9. [14]Individuals who have meal restrictions. [15]Women who are pregnant, breastfeeding, or wish to be pregnant in this study period. [16]Individuals who participated in other clinical trials in the past 1 month or are going to participate in other trials in this study period. [17]Individuals who are judged not suitable to participate in this trial by investigators.

Design outcomes

Primary

MeasureTime frame
[1]Autonomic nerve function [2]Cognitive function [3]Subjective Fatigue

Secondary

MeasureTime frame
[1]Condition of sleep [2]Physical active mass [3]Fatigue biomarker in blood

Countries

Japan

Contacts

Public ContactMika Furusawa

Osaka City University Center for Health Science Innovation

chsi-b@ado.osaka-cu.ac.jp+81-6-6485-0288

Outcome results

None listed

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