UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000045427
Receipt number R000051861
Scientific Title The effects of mouse exercise program on oral function in the elderly
Date of disclosure of the study information 2021/09/10
Last modified on 2022/09/12 14:56:38

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Basic information

Public title

The effects of mouse exercise program on oral function in the elderly

Acronym

The effects of mouse exercise program on oral function in the elderly

Scientific Title

The effects of mouse exercise program on oral function in the elderly

Scientific Title:Acronym

The effects of mouse exercise program on oral function in the elderly

Region

Japan


Condition

Condition

Healthy adult

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

"Oral Exercise Program" for the elderly and its effect on oral fuction

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

Occlusal force and occlusal contact area test
Gum for check of chewing
Oral moisture
Swallowing screening questionnaire
Tongue pressure test
Tongue and lip movement function
Hirai-style intake available food questionnaire
Height, weight, and BMI
Intraoral examination

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Educational,Counseling,Training

Type of intervention

Food Behavior,custom

Interventions/Control_1

Mouse exercise program

Interventions/Control_2

No intervention

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) Individuals who are able to exercise their mouths
(2) Subjects giving written informed consent

Key exclusion criteria

(1)Individuals with symptoms that
may affect mouth exercise or gum chewing
(2)Individuals may develop allergies in relation to the test
(3) Individuals who are judged by the principal investigator to be inappropriate for participation in this study

Target sample size

60


Research contact person

Name of lead principal investigator

1st name Kenji
Middle name
Last name Osawa

Organization

Lotte Co., Ltd.

Division name

Central Laboratory, Kamukoto Research Department

Zip code

336-8601

Address

1-1, Numakage-3chome, Minami-ku, Saitama

TEL

048-837-0744

Email

oosawa_kenji@lotte.co.jp


Public contact

Name of contact person

1st name Kenji
Middle name
Last name Osawa

Organization

Lotte Co., Ltd.

Division name

Central Laboratory, Kamukoto Research Department

Zip code

336-8601

Address

1-1, Numakage-3chome, Minami-ku, Saitama

TEL

048-837-0744

Homepage URL


Email

oosawa_kenji@lotte.co.jp


Sponsor or person

Institute

Lotte Co., Ltd.

Institute

Department

Personal name



Funding Source

Organization

Lotte Co., Ltd.

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Shiba Palace Clinic

Address

6F DaiwaA Hamamatucho Bld., 1-9-10 Hamamatsucho, Minato-ku, Tokyo, 105-0013, Japan

Tel

03-5408-1590

Email

jimukyoku@mail.souken-r.com


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

2021 Year 09 Month 10 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

64

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

2021 Year 08 Month 23 Day

Date of IRB

2021 Year 08 Month 23 Day

Anticipated trial start date

2021 Year 10 Month 01 Day

Last follow-up date

2022 Year 05 Month 12 Day

Date of closure to data entry

2022 Year 05 Month 12 Day

Date trial data considered complete

2022 Year 05 Month 31 Day

Date analysis concluded

2022 Year 06 Month 23 Day


Other

Other related information



Management information

Registered date

2021 Year 09 Month 09 Day

Last modified on

2022 Year 09 Month 12 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000051861


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name