UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000058334
Receipt number R000066688
Scientific Title Confirmatory study of the effects of food component intake on QOL (Quality of Life)
Date of disclosure of the study information 2025/07/28
Last modified on 2025/07/01 16:04:04

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Basic information

Public title

Confirmatory study of the effects of food component intake on QOL (Quality of Life)(SWE-2025-01)

Acronym

Confirmatory study of the effects of food component intake on QOL (Quality of Life)

Scientific Title

Confirmatory study of the effects of food component intake on QOL (Quality of Life)

Scientific Title:Acronym

Confirmatory study of the effects of food component intake on QOL (Quality of Life)

Region

Japan


Condition

Condition

Not applicable

Classification by specialty

Not applicable Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Evaluate the impact of food intake on QOL (Quality of Life)

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Health related Quality of Life(SF-36)

Key secondary outcomes



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

Consumption of test foods (4 weeks)

Interventions/Control_2

Consumption of control foods(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

40 years-old <=

Age-upper limit

64 years-old >=

Gender

Male and Female

Key inclusion criteria

1) Healthy men and women aged 40 to 64 years old
2) Subjects who can understand the purpose and content of this study and agree in writing to participate in this study.

Key exclusion criteria

1) With previous and present serious disease such as cardiac affection, liver disorder, kidney disorder, cardiovascular disorder, lung disorder, diabetes mellitus.
2) Subjects who keep irregular hours such as shift work.
3) Heavy drinker of alcohol.
4) Use of products affecting the data of this study, such as food for specified health use, food with function claims, and medicine.
5) Investigator's judgment for other reason.

Target sample size

400


Research contact person

Name of lead principal investigator

1st name Daisuke
Middle name
Last name Takemoto

Organization

Suntory Wellness Limited

Division name

Institute for Science of Life

Zip code

619-0284

Address

8-1-1 Seikadai, Seika-cho, Soraku-gun, Kyoto, Japan

TEL

050-1804-0274

Email

Daisuke_Takemoto@suntory.co.jp


Public contact

Name of contact person

1st name Yuhei
Middle name
Last name Kamei

Organization

Suntory Wellness Limited

Division name

Institute for Science of Life

Zip code

619-0284

Address

8-1-1 Seikadai, Seika-cho, Soraku-gun, Kyoto, Japan

TEL

050-1734-9397

Homepage URL


Email

Yuhei_Kamei@suntory.co.jp


Sponsor or person

Institute

Suntory Wellness Limited

Institute

Department

Personal name



Funding Source

Organization

Suntory Wellness Limited

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

Institutional Review Board of Chiyoda Paramedical Care Clinic

Address

2F Daiwa Bldg. 3-3-10, Nihonbashi Hongokucho, Chuo-ku, Tokyo, Japan

Tel

03-6225-9005

Email

IRB@cpcc.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

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 07 Month 01 Day

Date of IRB

2025 Year 06 Month 27 Day

Anticipated trial start date

2025 Year 10 Month 11 Day

Last follow-up date

2025 Year 11 Month 29 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 07 Month 01 Day

Last modified on

2025 Year 07 Month 01 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000066688