UMIN-CTR Clinical Trial

BACK TOP
UMIN-CTR English Home Glossary (Simple) FAQ Search clinical trials

Name:
UMIN ID:

Recruitment status Completed
Unique ID issued by UMIN UMIN000029356
Receipt No. 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

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


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
Institute The university of shizuoka
Institute
Department

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
URL(English) https://upload.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


Contact us.