UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000037986
Receipt number R000043292
Scientific Title Effect on concentration (and cognitive function) by single ingestion of a test food
Date of disclosure of the study information 2019/09/17
Last modified on 2019/12/27 09:45:49

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Basic information

Public title

Effect on concentration (and cognitive function) by single ingestion of a test food

Acronym

Effect on concentration (and cognitive function) by single ingestion of a test food

Scientific Title

Effect on concentration (and cognitive function) by single ingestion of a test food

Scientific Title:Acronym

Effect on concentration (and cognitive function) by single ingestion of a test food

Region

Japan


Condition

Condition

Healthy subjects

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study is to examine the influence on concentration by single intake of test food for healthy Japanese men aged 30 years or older and younger than 60 years.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Cognitrax

Key secondary outcomes

VAS questionnaire,POMS2 shorter version,Uchida Kraepelin test


Base

Study type

Interventional


Study design

Basic design

Cross-over

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

On the day intake of the test food
Wash out
On the day intake of the placebo

Interventions/Control_2

On the day intake of the placebo
Wash out
On the day intake of the test food

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. Japanese male aged 30 years or older and younger than 60 years at the time of the informed consent.
2. Non smoker
3. Subject who has understood the purpose of the study, and agreed to participate it by signing the written informed consent.

Key exclusion criteria

1. Subject who is taking medication or under medical treatment because of some serious illness.
2.Subject who is under exercise therapy or dietetic therapy.
3. Subject who has an allergy for test food.
4. Subject who has or had a history of either medicine or alcohol dependence syndrome.
5. Subject who has or had a history of mental illness (depression) or sleep disturbance.
6. Subject who is on a night-shift or is a shift worker.
7. Subject whose lifestyle is extremely irregular.
8. Subject who has an unbalanced diet.
9. Subject who is disease or history such severe diseases such as brain disease, malignant tumor, immune disease, diabetes, liver disease (hepatitis), kidney disease, heart disease, thyroid disease, adrenal disease, other metabolic diseases person.
10. Subject who uses health foods ,supplements and medicines that affect concentration (theanine, caffeine, polyphenols, soy lecithin, DHA / EPA, taurine, Ginkgo biloba etc.)
11. Subject who has participated in other clinical studies within the past 3 months from the day of the consent acquisition or who is planning to participate in other clinical studies during the current study.
12. Subject who has blood drawn 200mL within the past 1 months or 400mL within the past 3 months from the day of the consent acquisition.
13. Subject who can't keep the daily records.
14.Subject who is considered as an inappropriate candidate by the doctor in charge.

Target sample size

90


Research contact person

Name of lead principal investigator

1st name Daisuke
Middle name
Last name Ochitani

Organization

HUMA R&D CORP

Division name

Clinical Development Division

Zip code

108-0014

Address

Round Cross Tamachi 10F 5-31-19 Shiba Minato-ku Tokyo 108-0014 Japan

TEL

03-3431-1260

Email

ochitani@huma-rd.co.jp


Public contact

Name of contact person

1st name Daisuke
Middle name
Last name Ochitani

Organization

HUMA R&D CORP

Division name

Clinical Development Division

Zip code

108-0014

Address

Round Cross Tamachi 10F 5-31-19 Shiba Minato-ku Tokyo 108-0014 Japan

TEL

03-3431-1260

Homepage URL


Email

ochitani@huma-rd.co.jp


Sponsor or person

Institute

HUMA R&D CORP

Institute

Department

Personal name



Funding Source

Organization

Asahi Quality and Innovations Co., Ltd.

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

Ethics Committees of Nihonbashi Egawa Clinic

Address

2F Kotobuki Build. 1-1-3 Yaesu Chuo-ku, Tokyo 103-0028 Japan

Tel

03-5204-0311

Email

jim@medipharma.co.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



Other administrative information

Date of disclosure of the study information

2019 Year 09 Month 17 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

89

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

Completed

Date of protocol fixation

2019 Year 07 Month 03 Day

Date of IRB

2019 Year 07 Month 16 Day

Anticipated trial start date

2019 Year 08 Month 07 Day

Last follow-up date

2019 Year 10 Month 18 Day

Date of closure to data entry

2019 Year 10 Month 24 Day

Date trial data considered complete

2019 Year 10 Month 28 Day

Date analysis concluded

2019 Year 12 Month 26 Day


Other

Other related information



Management information

Registered date

2019 Year 09 Month 11 Day

Last modified on

2019 Year 12 Month 27 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000043292


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name