UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000026087
Receipt number R000029978
Scientific Title Examination of the relationship between cognitive indicator and taste sensitivity as well as dietary survey
Date of disclosure of the study information 2017/02/11
Last modified on 2019/03/20 11:38:32

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Basic information

Public title

Examination of the relationship between cognitive indicator and taste sensitivity as well as dietary survey

Acronym

Examination of the relationship between cognitive indicator and taste sensitivity as well as dietary survey

Scientific Title

Examination of the relationship between cognitive indicator and taste sensitivity as well as dietary survey

Scientific Title:Acronym

Examination of the relationship between cognitive indicator and taste sensitivity as well as dietary survey

Region

Japan


Condition

Condition

Alzheimer's disease, mild cognitive impairment, elderly persons without cognitive impairment

Classification by specialty

Neurology Geriatrics Psychiatry

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The aim of this study is to investigate the usefulness of taste-related tests for early diagnosis of Alzheimer's disease.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Gustatory test (the whole mouth test method)

Key secondary outcomes

Touch Panel-type Dementia Assessment Scale (TDAS), amount of saliva secretion, blood tests, blood pressure measurement, height and weight measurement


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Prevention

Type of intervention

Other

Interventions/Control_1

Gustatory test, examination of cognitive function, measurement of saliva secretion, blood tests, blood pressure measurement, height and weight measurement

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

40 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

1) Subjects who are more than 40 years old at the time of registration
2) Alzheimer's disease patients who fulfill of the DSM-5 and NINCDS-ADRDA criteria, or mild cognitive impairment patients who fulfill of the Petersen criteria, or subjects who don't have cognitive impairment.
3) The consent from proxies is necessary.

Key exclusion criteria

1) Patients who are diagnosed taste disturbance.
2) Patients who are assessed by the principal investigator due to other reasons.

Target sample size

150


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Katsuya Urakami

Organization

School of Health Science, Faculty of Medicine, Tottori University

Division name

Department of Biological Regulation

Zip code


Address

86 Nishicho, Yonago, Tottori, Japan

TEL

0859-38-6354

Email

kurakami@med.tottori-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Minoru Kouzuki

Organization

School of Health Science, Faculty of Medicine, Tottori University

Division name

Department of Biological Regulation

Zip code


Address

86 Nishicho, Yonago, Tottori, Japan

TEL

0859-38-6358

Homepage URL


Email

kouzuki@med.tottori-u.ac.jp


Sponsor or person

Institute

Department of Biological Regulation, School of Health Science, Faculty of Medicine, Tottori University

Institute

Department

Personal name



Funding Source

Organization

Ajinomoto Co., Inc.

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


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 02 Month 11 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

2017 Year 01 Month 27 Day

Date of IRB

2017 Year 01 Month 27 Day

Anticipated trial start date

2017 Year 03 Month 01 Day

Last follow-up date

2019 Year 01 Month 23 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2017 Year 02 Month 10 Day

Last modified on

2019 Year 03 Month 20 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000029978


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name