UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000048740
Receipt number R000055530
Scientific Title Trial of the efficacy of food ingredients on sleep quality
Date of disclosure of the study information 2022/09/08
Last modified on 2022/12/01 10:18:45

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Basic information

Public title

Trial of the efficacy of food ingredients on sleep quality (SWE-2022-03- HCRINK)

Acronym

Trial of the efficacy of food ingredients on sleep quality

Scientific Title

Trial of the efficacy of food ingredients on sleep quality

Scientific Title:Acronym

Trial of the efficacy of food ingredients on sleep quality

Region

Japan


Condition

Condition

Not applicable

Classification by specialty

Not applicable Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the effects of food ingredients on sleep quality

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Sleep quality

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

Intake of the test foods for 2 weeks.

Interventions/Control_2

Intake of the control foods for 2 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

64 years-old >=

Gender

Male and Female

Key inclusion criteria

1) Healthy men and women aged 20 to 64 years.
2) Subjects who feel tired on daily basis.
3) Subjects who can understand the purpose and content of this study and agree in writing to participate in this study.

Key exclusion criteria

1) Subjects who keep irregular hours such as shift work.
2) Heavy drinker of alcohol.
3) Use of products affecting the data of this study, such as food for specified health use, food with function claims, and medicine.
4) Presence of previous and present diseases such as chronic fatigue syndrome, sleep apnea syndrome, menopausal disorder, lung disorder, cardiovascular disorder, diabetes mellitus, food allergy.
5) Investigator's judgment for other reason.

Target sample size

180


Research contact person

Name of lead principal investigator

1st name Hidenori
Middle name
Last name Obata

Organization

Suntory Wellness Limited

Division name

Institute For Health Care Science

Zip code

619-0284

Address

8-1-1 Seikadai, Seika-cho, Soraku-gun, Kyoto. 619-0284, Japan.

TEL

050-3182-0568

Email

Hidenori_Obata@suntory.co.jp


Public contact

Name of contact person

1st name Izumi
Middle name
Last name Yamasaki

Organization

Suntory Wellness Limited

Division name

Institute For Health Care Science

Zip code

619-0284

Address

8-1-1 Seikadai, Seika-cho, Soraku-gun, Kyoto. 619-0284, Japan.

TEL

050-3182-0648

Homepage URL


Email

Izumi_Yamasaki@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

Profit organization

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

2022 Year 09 Month 08 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

Completed

Date of protocol fixation

2022 Year 08 Month 22 Day

Date of IRB

2022 Year 08 Month 19 Day

Anticipated trial start date

2022 Year 09 Month 09 Day

Last follow-up date

2022 Year 11 Month 14 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2022 Year 08 Month 24 Day

Last modified on

2022 Year 12 Month 01 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000055530


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name