UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000056965
Receipt number R000065104
Scientific Title Development of a Simplified Questionnaire Specializing in Eating Behavior Based on Personality Types
Date of disclosure of the study information 2025/03/17
Last modified on 2025/10/29 09:33:43

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Basic information

Public title

Development of a Simplified Questionnaire Specializing in Eating Behavior Based on Personality Types

Acronym

Development of a Simplified Questionnaire Specializing in Eating Behavior Based on Personality Types

Scientific Title

Development of a Simplified Questionnaire Specializing in Eating Behavior Based on Personality Types

Scientific Title:Acronym

MBP STUDY

Region

Japan


Condition

Condition

Healthy subjects

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The aim is to develop a simplified questionnaire specializing in personality types related to eating behavior, the Mealtime Behavior Questionnaire based on Personality (MBP).

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

"The aim is to develop a simplified questionnaire specializing in personality types related to eating behavior, the Mealtime Behavior Questionnaire based on Personality (MBP)."

Key secondary outcomes



Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


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

20 years-old <=

Age-upper limit

69 years-old >

Gender

Male and Female

Key inclusion criteria

Ages 20 and above but under 69

Key exclusion criteria

Individuals who are unable to use web-based surveys.
Cases where the principal investigator or co-investigators determine that participation in this study is not appropriate

Target sample size

300


Research contact person

Name of lead principal investigator

1st name Sakane
Middle name
Last name Naoki

Organization

National Hospital Organization Kyoto Medical Center

Division name

Division of Preventive Medicine, Clinical Research Institute

Zip code

612-8555

Address

1-1 Mukaihata-cho, Fukakusa, Fushimi-ku, Kyoto

TEL

075-641-9161

Email

404-j-doit1@mail.hosp.go.jp


Public contact

Name of contact person

1st name Sakane
Middle name
Last name Naoki

Organization

National Hospital Organization Kyoto Medical Center

Division name

Division of Preventive Medicine, Clinical Research Institute

Zip code

612-8555

Address

1-1 Mukaihata-cho, Fukakusa, Fushimi-ku, Kyoto

TEL

075-641-9161

Homepage URL


Email

404-j-doit1@mail.hosp.go.jp


Sponsor or person

Institute

Division of Preventive Medicine, Clinical Research Institute, National Hospital Organization Kyoto Medical Center, Kyoto

Institute

Department

Personal name



Funding Source

Organization

JSPA KAKENNHI

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

National Hospital Organization Kyoto Medical Center

Address

1-1 Mukaihata-cho, Fukakusa, Fushimi-ku, Kyoto, Japan.

Tel

075-641-9161

Email

404-j-doit1@mail.hosp.go.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 03 Month 17 Day


Related information

URL releasing protocol


Publication of results

Published


Result

URL related to results and publications


Number of participants that the trial has enrolled

300

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

Main results already published

Date of protocol fixation

2025 Year 03 Month 17 Day

Date of IRB

2025 Year 03 Month 17 Day

Anticipated trial start date

2025 Year 03 Month 18 Day

Last follow-up date

2028 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Survey Research


Management information

Registered date

2025 Year 02 Month 07 Day

Last modified on

2025 Year 10 Month 29 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000065104