UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000012497
Receipt number R000014628
Scientific Title Evaluation of the health effects by daily intake of "Calpis"; a pilot study
Date of disclosure of the study information 2013/12/05
Last modified on 2013/12/06 10:23:25

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Basic information

Public title

Evaluation of the health effects by daily intake of "Calpis"; a pilot study

Acronym

"Calpis" Communication Project

Scientific Title

Evaluation of the health effects by daily intake of "Calpis"; a pilot study

Scientific Title:Acronym

"Calpis" Communication Project

Region

Japan


Condition

Condition

Nothing

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this pilot study is to evaluate the health effects for elders by daily intake of "Calpis" mainly to QOL(Quality Of Life) and brain function.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

QOL Score (SF-8)

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

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Food

Interventions/Control_1

A participant prepares 150ml "Calpis" per day by himself and drinks it for 8 weeks.

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

60 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

(1) Those who live in Kamijima-town, Ehime prefecture
(2) That whose age at the time of informed consent is aged 60 and over.
(3) Those who can understand the purpose and the contents of this study, and can agree with participation to this study by letter.

Key exclusion criteria

(1) Those who show an allergic reaction to dairy products and a soybean.
(2) The person under diabetes medical treatment, or those who need to treat diabetes.
(3) Those who have taken medical supplies or supplements which investigator judged that this trial would be affected.
(4) Those who are during the medical treatment of critical diseases, such as cancer
(5) In addition, those who were judged inadequate by investigator.

Target sample size

40


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Takeshi Tanigawa

Organization

Graduate School of Medicine, Ehime University

Division name

Department of Public Health

Zip code


Address

Shizukawa, Toon-city, Ehime

TEL

089-960-5283

Email

tt9178tt9178@gmail.com


Public contact

Name of contact person

1st name
Middle name
Last name Tetsu Kinoshita

Organization

Community SHIN Science Co., Ltd.

Division name

Social Epidemiology Institute

Zip code


Address

160-4 Kishimachi, Matsuyama-city, Ehime

TEL

089-904-7811

Homepage URL


Email

tetsu.prospective@gmail.com


Sponsor or person

Institute

Department of Public Health, Graduate School of Medicine, Ehime University

Institute

Department

Personal name



Funding Source

Organization

Calpis 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


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

2013 Year 12 Month 05 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


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

2012 Year 09 Month 26 Day

Date of IRB


Anticipated trial start date

2012 Year 10 Month 02 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

2013 Year 12 Month 05 Day

Last modified on

2013 Year 12 Month 06 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000014628


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name