UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000058618 |
|---|---|
| Receipt number | R000066567 |
| Scientific Title | The effects of lactic acid bacteria ingestion combined with resistance training on intestinal barrier related indices. |
| Date of disclosure of the study information | 2025/07/28 |
| Last modified on | 2025/07/28 16:35:00 |
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Basic information
Public title
The effects of lactic acid bacteria ingestion combined with resistance training on intestinal barrier related indices.
Acronym
The effects of lactic acid bacteria ingestion combined with resistance training on intestinal barrier related indices.
Scientific Title
The effects of lactic acid bacteria ingestion combined with resistance training on intestinal barrier related indices.
Scientific Title:Acronym
The effects of lactic acid bacteria ingestion combined with resistance training on intestinal barrier related indices.
Region
| Japan |
Condition
Condition
Healthy adults
Classification by specialty
| Not applicable | Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To assess the effects of lactic acid bacteria ingestion during 12 weeks of resistance training on intestinal barrier related indices.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Exploratory
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Intestinal barrier related indices
Key secondary outcomes
Base
Study type
Others,meta-analysis etc
Study design
Basic design
Randomization
Randomization unit
Blinding
Control
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
Purpose of intervention
Type of intervention
Interventions/Control_1
Interventions/Control_2
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
| 30 | years-old | <= |
Age-upper limit
| 60 | years-old | > |
Gender
Male
Key inclusion criteria
1.Subjects who participated in the previous study (UMIN000054363)
2.Subjects must read and sign the informed consent form
Key exclusion criteria
1.Subjects who were determined to be discontinued in the previous study (UMIN000054363)
Target sample size
36
Research contact person
Name of lead principal investigator
| 1st name | Chiaki |
| Middle name | |
| Last name | Sanbongi |
Organization
Meiji Co., Ltd.
Division name
R&D Division
Zip code
192-0919
Address
1-29-1 Nanakuni, Hachioji, Tokyo
TEL
+81-42-632-5847
chiaki.sanbongi@meiji.com
Public contact
Name of contact person
| 1st name | Aya |
| Middle name | |
| Last name | Yoshimura |
Organization
Meiji Co., Ltd.
Division name
R&D Division
Zip code
92-0919
Address
1-29-1 Nanakuni, Hachioji, Tokyo
TEL
+81-42-632-5847
Homepage URL
aya.yoshimura.aa@meiji.com
Sponsor or person
Institute
Meiji Co., Ltd.
Institute
Department
Personal name
Funding Source
Organization
Meiji Co., Ltd.
Organization
Division
Category of Funding Organization
Profit organization
Nationality of Funding Organization
Other related organizations
Co-sponsor
Ritsumeikan University
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Meiji Institutional Review BoardMeiji Institutional Review Board
Address
1-29-1 Nanakuni, Hachiouji, Tokyo, Japan
Tel
81-42-632-5900
MEIJI.IRB@meiji.com
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
株式会社 明治 研究本部
Other administrative information
Date of disclosure of the study information
| 2025 | Year | 07 | Month | 28 | 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
Preinitiation
Date of protocol fixation
| 2025 | Year | 05 | Month | 18 | Day |
Date of IRB
| 2025 | Year | 05 | Month | 22 | Day |
Anticipated trial start date
| 2025 | Year | 06 | Month | 20 | Day |
Last follow-up date
| 2025 | Year | 08 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
In this study, the blood samples obtained in the previous study(UMIN000054363) are analyzed. There is no intervention and invasion in this study.
Management information
Registered date
| 2025 | Year | 07 | Month | 28 | Day |
Last modified on
| 2025 | Year | 07 | Month | 28 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000066567
