UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000029356
Receipt number R000033551
Scientific Title Effect of chewing and histidine intake for prevention and improvement of metabolic syndrome
Date of disclosure of the study information 2017/09/30
Last modified on 2017/09/29 19:27:41

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Basic information

Public title

Effect of chewing and histidine intake for prevention and improvement of metabolic syndrome

Acronym

Chewing and histidine intake

Scientific Title

Effect of chewing and histidine intake for prevention and improvement of metabolic syndrome

Scientific Title:Acronym

Chewing and histidine intake

Region

Japan


Condition

Condition

Healthy volunteers

Classification by specialty

Not applicable

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To assess the effects of chewing and histidine intake for improvement of obesity.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Anthropometry (Height, Weight, Body fat percentage)

Key secondary outcomes

Blood pressure, Food intake, Blood (Glucose, Hemoglobin A1c, Triacylglycerol, Free fatty acid, T-Chol, HDL-Chol, LDL-Chol, Insulin, cortisol, AST, ALT, gamma-GTP)


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Placebo

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

3

Purpose of intervention

Educational,Counseling,Training

Type of intervention

Food Behavior,custom

Interventions/Control_1

Control

Interventions/Control_2

Thirty -times chewing per bite ( for 12 weeks)

Interventions/Control_3

Intake of histidine 1g/day ( for 12 weeks)

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

50 years-old >=

Gender

Male

Key inclusion criteria

Obtained written informed consent from the men before the participation

Key exclusion criteria

Those who felt this study was inconvenient to everyday life

Target sample size

30


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Toshiko Kuwano

Organization

The university of shizuoka

Division name

School of Food and Nutritional Sciences

Zip code


Address

52-1 Yada, Suruga-Ward, Shizuoka-City 422-8526, Japan

TEL

054-264-5513

Email

kuwano@u-shizuoka-ken.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Toshiko Kuwano

Organization

The university of shizuoka

Division name

School of Food and Nutritional Sciences

Zip code


Address

52-1 Yada, Suruga-Ward, Shizuoka-City 422-8526, Japan

TEL

054-264-5513

Homepage URL


Email

kuwano@u-shizuoka-ken.ac.jp


Sponsor or person

Institute

The university of shizuoka

Institute

Department

Personal name



Funding Source

Organization

Ministry of Education, Culture, Sports, Science and Technology

Organization

Division

Category of Funding Organization

Local Government

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



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

2017 Year 09 Month 30 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

2013 Year 05 Month 27 Day

Date of IRB


Anticipated trial start date

2013 Year 08 Month 28 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2017 Year 09 Month 29 Day

Last modified on

2017 Year 09 Month 29 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000033551


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name