UMIN-ICDS Clinical Trial
| Unique ID issued by UMIN | UMIN000060178 |
|---|---|
| Receipt number | R000068826 |
| Scientific Title | Effects of 6-week intake of krill oil on physical and mental health in healthy adults: a randomized, double-blind, placebo-controlled, parallel-group comparison |
| Date of disclosure of the study information | 2026/11/10 |
| Last modified on | 2025/12/23 14:19:18 |
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Basic information
Public title
Effects of 6-week intake of krill oil on physical and mental health in healthy adults
Acronym
The effects of krill oil intake on physical and mental health
Scientific Title
Effects of 6-week intake of krill oil on physical and mental health in healthy adults: a randomized, double-blind, placebo-controlled, parallel-group comparison
Scientific Title:Acronym
The effects of krill oil intake on physical and mental health
Region
| Japan |
Condition
Condition
Healthy adult
Classification by specialty
| Not applicable | Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To examine the effects of krill oil on the physical and mental health of healthy adults
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Cognitive function evaluation
Key secondary outcomes
Knee pain assessment
Muscle strength evaluation
Base
Study type
Interventional
Study design
Basic design
Parallel
Randomization
Randomized
Randomization unit
Individual
Blinding
Open -but assessor(s) 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
Take 1000mg of krill oil for 6 weeks (42 days)
Interventions/Control_2
Placebo intake for 6weeks (42 days)
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
| 60 | years-old | <= |
Age-upper limit
| 80 | years-old | >= |
Gender
Male and Female
Key inclusion criteria
(1) persons who is generally judged as healthy
(2) Persons who can give voluntary written consent to participate in the present trial
(3) Persons who are aware of their physical and mental fatigue and stress
Key exclusion criteria
(1) persons who have any dietary supplements, quasi drugs or medicines which cause same or similar efficacy with the effect evaluated in this study
(2) persons who have changed their habitats to take supplements within past 4 weeks.
(3) Persons who work in night shift or in day and night shift
(4) persons who have been treated their illness or prevention in a clinic at their informed consent
(5) persons with their medical histories as follows: serious diseases of sugar metabolism, lipid metabolism, hepatic function, renal function, heart, circulatory, respiratory, endocrine system, immune system, or mental illness of the nervous system
(6) persons with the medical histories of alcoholism or drug dependence
(7) persons who might be developed allergic reaction to foods
(8) Persons who are pregnant, breast-feeding, or hope to be pregnant during the study period
(9) persons who had always participated in or will participate in any other clinical trial (to use foods/medicine/quasi medicine/medical device)
(10) persons who will not be judged suitable to the participants by the investigator
Target sample size
30
Research contact person
Name of lead principal investigator
| 1st name | Kouichirou |
| Middle name | |
| Last name | Ohnuki |
Organization
User Life Science Co.,Ltd.
Division name
The research and development part
Zip code
820-0115
Address
372-3,Niho,Iiduka-shi,Fukuoka,Japan
TEL
0948-82-3123
ohnuki.rinp@gmail.com
Public contact
Name of contact person
| 1st name | Keiko |
| Middle name | |
| Last name | Ohnuki |
Organization
User Life Science Co.,Ltd.
Division name
The research and development part
Zip code
820-0115
Address
372-3,Niho,Iiduka-shi,Fukuoka,Japan
TEL
0948-82-3123
Homepage URL
userlifescience@gmail.com
Sponsor or person
Institute
Others
Institute
Department
Personal name
Funding Source
Organization
Others
Organization
Division
Category of Funding Organization
Profit organization
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
User Life Science Co., Ltd. Ethics Committee
Address
372-3 Niho, Iizuka City, Fukuoka
Tel
0948-82-3123
userlifesciense@gmail.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
Other administrative information
Date of disclosure of the study information
| 2026 | Year | 11 | Month | 10 | 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
37
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
| 2025 | Year | 10 | Month | 14 | Day |
Date of IRB
| 2025 | Year | 02 | Month | 27 | Day |
Anticipated trial start date
| 2025 | Year | 11 | Month | 15 | Day |
Last follow-up date
| 2025 | Year | 12 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2025 | Year | 12 | Month | 23 | Day |
Last modified on
| 2025 | Year | 12 | Month | 23 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000068826
