UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000054932
Receipt number R000062738
Scientific Title Effects of Ingestion of Lactic Acid Bacteria on Subjective Physical Symptoms in Healthy Adults: A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Comparison Study.
Date of disclosure of the study information 2024/07/11
Last modified on 2025/01/09 09:08:23

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

Effects of Ingestion of Lactic Acid Bacteria on Subjective Physical Symptoms in Healthy Adults: A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Comparison Study.

Acronym

Effects of Ingestion of Lactic Acid Bacteria on Subjective Physical Symptoms in Healthy Adults.

Scientific Title

Effects of Ingestion of Lactic Acid Bacteria on Subjective Physical Symptoms in Healthy Adults: A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Comparison Study.

Scientific Title:Acronym

Effects of Ingestion of Lactic Acid Bacteria on Subjective Physical Symptoms in Healthy Adults.

Region

Japan


Condition

Condition

Healthy adult

Classification by specialty

Not applicable Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To prove the clinical benefits of lactic acid bacteria intake on subjective physical symptoms in healthy adults.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Subjective symptoms of physical conditions

Key secondary outcomes

Immunological functions


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Double blind -all involved are blinded

Control

Placebo

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Prevention

Type of intervention

Food

Interventions/Control_1

Daily ingestion of powdered lactic acid bacteria for 16 weeks.

Interventions/Control_2

Daily ingestion of placebo powder for 16 weeks.

Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

18 years-old <=

Age-upper limit

65 years-old >

Gender

Male and Female

Key inclusion criteria

Subjects who are between the ages of 18 and 64 years old.

Key exclusion criteria

1. Subjects with serious cancer, respiratory, hepatic, renal, cardiac, lung, gastrointestinal, blood, endocrine or metabolic diseases, and/or with serious medical history of those disease.
2. Subjects who have any autoimmune disease.
3. Subjects at risk of allergic reactions to drugs or foods.
4. Pregnant or breastfeeding women or women who expect to become pregnant during this study.
5. Subjects whose BMI is >=30 kg/m2.
6. Heavy smokers, alcoholics or subjects with a disordered lifestyle.
7. Subjects who regularly take medications that affect immune function for more than 1 day per week.
8. Subjects who are at risk of having allergic reactions during this study.
9. Subjects who regularly consume foods that affect immune function.
10. Subjects who have donated either 400 ml whole blood within 16 weeks (women), 12 weeks (men), 200 ml whole blood within 4 weeks (men and women), or blood components within 2 weeks (men and women), prior to this study.
11. Subjects who were vaccinated within 4 weeks prior to this study.
12. Subjects who are ineligible based on the judgement of the principal investigator.

Target sample size

200


Research contact person

Name of lead principal investigator

1st name Naoyuki
Middle name
Last name HONMA

Organization

Hokkaido Information University

Division name

Department of Medical Management and Informatics

Zip code

069-8585

Address

59-2, Nishi-nopporo, Ebetsu, Hokkaido, 069-8585, Japan

TEL

011-385-4430

Email

hisc-acad.res@s.do-johodai.ac.jp


Public contact

Name of contact person

1st name Naoyuki
Middle name
Last name HONMA

Organization

Hokkaido Information University

Division name

Health Information Science Center

Zip code

069-8585

Address

59-2, Nishi-nopporo, Ebetsu, Hokkaido, 069-8585, Japan

TEL

011-385-4430

Homepage URL


Email

hisc-acad.res@s.do-johodai.ac.jp


Sponsor or person

Institute

Hokkaido Information University

Institute

Department

Personal name



Funding Source

Organization

Morinaga Milk Industry Co., Ltd.

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor

Department of Nutritional Sciences for Well-being, Faculty of Health Sciences for Welfare, Kansai University of Welfare Sciences

Name of secondary funder(s)



IRB Contact (For public release)

Organization

The ethics committee of Hokkaido Information University

Address

59-2, Nishi-nopporo, Ebetsu, Hokkaido, 069-8585, Japan

Tel

011-385-4411

Email

soumu@do-johodai.ac.jp


Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions

北海道情報大学 保健センター(北海道)


Other administrative information

Date of disclosure of the study information

2024 Year 07 Month 11 Day


Related information

URL releasing protocol


Publication of results

Unpublished


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

No longer recruiting

Date of protocol fixation

2024 Year 06 Month 19 Day

Date of IRB

2024 Year 06 Month 19 Day

Anticipated trial start date

2024 Year 07 Month 25 Day

Last follow-up date

2025 Year 04 Month 05 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2024 Year 07 Month 11 Day

Last modified on

2025 Year 01 Month 09 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000062738