UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000047307
Receipt number R000053952
Scientific Title Investigation of oral frail prevention program for community dwelling older adults
Date of disclosure of the study information 2022/04/01
Last modified on 2023/09/29 11:06:45

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Basic information

Public title

Investigation of oral frail prevention program for community dwelling older adults

Acronym

Investigation of Oral frail prevention program

Scientific Title

Investigation of oral frail prevention program for community dwelling older adults

Scientific Title:Acronym

Investigation of Oral frail prevention program

Region

Japan


Condition

Condition

healthy adults

Classification by specialty

Dental medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study is to investigate the effects of oral health program on oral health literacy, nutritional status, and physical function in community dwelling older adults

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Oral function (tongue pressure, lip tongue motor function, masticatory function)
Self reported oral health status before and after intervention

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

NO

Dynamic allocation

NO

Institution consideration

Institution is not considered as adjustment factor.

Blocking

NO

Concealment

No need to know


Intervention

No. of arms

1

Purpose of intervention

Educational,Counseling,Training

Type of intervention

Food Behavior,custom

Interventions/Control_1

3 month Comprehensive program
1. Physical exercise
2. Oral exercise
3. Eating munchy texture lunch twice a month
4. Receiving lectures about oral health and nutrition once a month for each

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

65 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Individuals who can participate for t months

Key exclusion criteria

1. individuals who have food allergy
2. individuals who have severe renal failure
3. individuals who have severe dysphagia

Target sample size

200


Research contact person

Name of lead principal investigator

1st name Koichiro
Middle name
Last name Matsuo

Organization

Tokyo Medical and Dental University

Division name

Oral Health Sciences for Community Welfare

Zip code

113-8549

Address

1-5-45 Yushima, Bunkyo, Tokyo,

TEL

03-5803-4545

Email

matsuo.ohcw@tmd.ac.jp


Public contact

Name of contact person

1st name Koichiro
Middle name
Last name Matsuo

Organization

Tokyo Medical and Dental University

Division name

Oral Health Sciences for Community Welfare

Zip code

113-8549

Address

1-5-45 Yushima, Bunkyo, Tokyo,

TEL

03-5803-4545

Homepage URL

https://www.ohcw-tmd.com/research/

Email

matsuo.ohcw@tmd.ac.jp


Sponsor or person

Institute

Japan Science and Technology Agency

Institute

Department

Personal name



Funding Source

Organization

Japan Science and Technology Agency

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Tokyo Medical and Dental University

Address

1-5-45 Yushima, Bunkyo, Tokyo

Tel

03-3813-6111

Email

d-hyoka.adm@tmd.ac.jp


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

2022 Year 04 Month 01 Day


Related information

URL releasing protocol


Publication of results

Published


Result

URL related to results and publications

https://link.springer.com/article/10.1007/s12603-023-1913-1

Number of participants that the trial has enrolled

271

Results


Kihon checklist (KCL) and CAMCAM checklist scores were significantly lower in the Oral frailty (OF) group at the initial assessment. Oral Frailty Index-8 (OFI-8) and KCL findings were significantly improved in the OF group after completing the program (all P <0.05). Regarding the CAMCAM checklist, awareness of chewing improved significantly in the Robust group (P=0.009), with a similar tendency in the OF group (P=0.080).

Results date posted

2023 Year 09 Month 29 Day

Results Delayed


Results Delay Reason


Date of the first journal publication of results

2023 Year 04 Month 28 Day

Baseline Characteristics


Participant flow


Adverse events

none

Outcome measures

Oral Frailty Index-8 (OFI-8), Kihon checklist (KCL), and CAMCAM checklist

Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Main results already published

Date of protocol fixation

2022 Year 03 Month 29 Day

Date of IRB

2022 Year 05 Month 23 Day

Anticipated trial start date

2022 Year 07 Month 01 Day

Last follow-up date

2024 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2022 Year 03 Month 29 Day

Last modified on

2023 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=R000053952


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name