UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000045417
Receipt number R000051855
Scientific Title Assessment of the efficacy of the dietary instruction using two biomarkers in workplace health promotion
Date of disclosure of the study information 2021/09/10
Last modified on 2023/03/10 13:10:51

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Basic information

Public title

Assessment of the efficacy of the dietary instruction using two biomarkers in workplace health promotion

Acronym

Assessment of the efficacy of the dietary instruction using two biomarkers in workplace health promotion

Scientific Title

Assessment of the efficacy of the dietary instruction using two biomarkers in workplace health promotion

Scientific Title:Acronym

Assessment of the efficacy of the dietary instruction using two biomarkers in workplace health promotion

Region

Japan


Condition

Condition

healthy subjects

Classification by specialty

Not applicable Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To assess the efficacy of a new dietary instruction method using two biomarkers in the workplace health promotion

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Blood pressure, BMI, Measured levels of biomarker A and B, Scores of concious and behaviour for eating habits

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Self control

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Educational,Counseling,Training

Type of intervention

Behavior,custom Other

Interventions/Control_1

Dietary instructoin using two biomarkers, and monitoring of the biomarkers

Interventions/Control_2


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

18 years-old <=

Age-upper limit

65 years-old >

Gender

Male and Female

Key inclusion criteria

Subjects who agree to participate in this study with a written informed consent

Key exclusion criteria

NA

Target sample size

100


Research contact person

Name of lead principal investigator

1st name Yusuke
Middle name
Last name Ushida

Organization

KAGOME CO., LTD.

Division name

Innovation Division

Zip code

329-2762

Address

17 Nishitomiyama, Nasushiobara-shi, Tochigi

TEL

0287362935

Email

Yusuke_Ushida@kagome.co.jp


Public contact

Name of contact person

1st name Yusuke
Middle name
Last name Ushida

Organization

KAGOME CO., LTD.

Division name

Innovation Division

Zip code

329-2762

Address

17 Nishitomiyama, Nasushiobara-shi, Tochigi

TEL

0287362935

Homepage URL


Email

Yusuke_Ushida@kagome.co.jp


Sponsor or person

Institute

KAGOME CO., LTD.

Institute

Department

Personal name



Funding Source

Organization

KAGOME 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

Kagome Ethics Committee

Address

3-21-1 Nihonbashi-hamacho, Chuo-ku, Tokyo

Tel

03-5623-8501

Email

Takuji_Hayakawa@kagome.co.jp


Secondary IDs

Secondary IDs

YES

Study ID_1

2021-R10

Org. issuing International ID_1

Kagome Ethics Committee

Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2021 Year 09 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

110

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

2021 Year 09 Month 02 Day

Date of IRB

2021 Year 09 Month 02 Day

Anticipated trial start date

2021 Year 10 Month 08 Day

Last follow-up date

2022 Year 10 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

2021 Year 09 Month 08 Day

Last modified on

2023 Year 03 Month 10 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000051855