UMIN-ICDS Clinical Trial
| Unique ID issued by UMIN | UMIN000061083 |
|---|---|
| Receipt number | R000069861 |
| Scientific Title | The effects of a test food on attenuating fatigue sensation |
| Date of disclosure of the study information | 2026/03/27 |
| Last modified on | 2026/03/25 17:13:23 |
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Basic information
Public title
The effects of a test food on attenuating fatigue sensation
Acronym
The effects of a test food on attenuating fatigue sensation
Scientific Title
The effects of a test food on attenuating fatigue sensation
Scientific Title:Acronym
The effects of a test food on attenuating fatigue sensation
Region
| Japan |
Condition
Condition
Healthy volunteers
Classification by specialty
| Not applicable | Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To examine the effects of the test food on attenuating fatigue sensation
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
VAS (fatigue sensation) daily upon waking
Key secondary outcomes
VAS (fatigue sensation) at the time of visit, Chalder fatigue scale
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
Intake of test food for 4 weeks
Interventions/Control_2
Intake of a placebo for 4 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
| 20 | years-old | <= |
Age-upper limit
| 65 | years-old | > |
Gender
Male and Female
Key inclusion criteria
1)Males and females aged 20 years or more and less than 65 years
2)Persons having fatigue sensation in daily life
3)Persons with a BMI of 18.5 kg/m2 or more, and less than 25.0 kg/m2
4)Persons receiving sufficient briefing of the objective and content of the present study, fully understanding and agreeing to voluntarily participate in the study, and being able to personally sign a written informed consent
Key exclusion criteria
1)Persons receiving medical treatment for serious cardio-vascular, hepatic, renal, respiratory, endocrine, or metabolic disorders or having a medical history of these disorders
2)Persons having been diagnosed with chronic fatigue syndrome or idiopathic chronic fatigue
3)Persons whose pure alcohol intake per day is 60 g or more
4)Persons who may develop allergic symptoms from consuming the test food
5)Persons whose lifestyles are irregular such as those who work a night shift
6)Persons planning an oversea trip during the study period
7)Persons regularly taking medicines or quasi-drug products that affect fatigue
8)Persons regularly taking "Food with Functional Claims" that affect fatigue sensation
9)Persons who are pregnant or lactating, or intending to become pregnant during the study period
10)Persons who took part in another clinical study within 3 months prior to the start of the present study or who are currently taking part in another clinical study
11)Persons deemed unsuitable by the investigator
Target sample size
200
Research contact person
Name of lead principal investigator
| 1st name | Mikako |
| Middle name | |
| Last name | Sato |
Organization
NH Foods Ltd.
Division name
Research & Development Center
Zip code
300-2646
Address
3-3 Midorigahara, Tsukuba, Ibaraki
TEL
029-847-7811
m.satou@nipponham.co.jp
Public contact
Name of contact person
| 1st name | Tomohiro |
| Middle name | |
| Last name | Sugino |
Organization
Soiken Inc.
Division name
R&D Division
Zip code
560-0082
Address
Senri Life Science Center 13F, 1-4-2, Shinsenri-higashimachi, Toyonaka, Osaka
TEL
06-6871-8888
Homepage URL
sugino@soiken.com
Sponsor or person
Institute
NH Foods Ltd.
Institute
Department
Personal name
Funding Source
Organization
None
Organization
Division
Category of Funding Organization
Self funding
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
IRB of Fukuda Clinic
Address
Shin-Osaka brick building 2F, 1-6- 1 Miyahara, Yodogawa, Osaka, Osaka
Tel
06-6398-0203
fukudaclinicIRB@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 | 03 | Month | 27 | 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
| 2026 | Year | 01 | Month | 17 | Day |
Date of IRB
| 2026 | Year | 01 | Month | 17 | Day |
Anticipated trial start date
| 2026 | Year | 05 | Month | 22 | Day |
Last follow-up date
| 2026 | Year | 06 | Month | 30 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2026 | Year | 03 | Month | 27 | Day |
Last modified on
| 2026 | Year | 03 | Month | 25 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000069861
