UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000053192
Receipt number R000060706
Scientific Title Research to verify the effectiveness of long-term care cost containment
Date of disclosure of the study information 2023/12/22
Last modified on 2023/12/22 10:32:28

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Basic information

Public title

Study to verify the effectiveness of Kumagai's Frailty Preventive System (face-to-face and remote frailty prevention exercise) in reducing the cost of nursing care.

Acronym

Study to verify the effectiveness of reducing nursing care costs by introducing exercise to prevent frailty

Scientific Title

Research to verify the effectiveness of long-term care cost containment

Scientific Title:Acronym

validation study

Region

Japan


Condition

Condition

Frail, sarcopenia, lifestyle-related diseases, depression in the elderly, sleep disorders, cognitive decline

Classification by specialty

Medicine in general Neurology Psychosomatic Internal Medicine
Geriatrics Laboratory medicine Rehabilitation medicine
Nursing Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To examine the effectiveness evaluation associated with long-term remote and face-to-face exercise intervention to improve sarcopenia and frailty.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Effects of Exercise Therapy on the Risk of Needing Assistance or Nursing Care
Effects of Exercise Therapy on Reducing the Cost of Nursing Care
Effects of Exercise Therapy on Frailty

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

Behavior,custom Other

Interventions/Control_1

exercise guidance

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

senior residents of Sakai City and Katsuyama City, Fukui Prefecture

Key exclusion criteria

(1) Residents who did not give consent for this study
(2) Residents who are hospitalized or admitted to a medical institution
(3) Other residents deemed inappropriate by the researcher.

Target sample size

300


Research contact person

Name of lead principal investigator

1st name Yamaura
Middle name
Last name Osamu

Organization

Faculty of Medical Science, University of Fukui

Division name

Deparement of Community Medicine

Zip code

910-1193

Address

23-3, Shimoaizuki, Matsuoka, Eiheiji, Yoshida, Fukui

TEL

0776-61-3111

Email

kapi@u-fukui.ac.jp


Public contact

Name of contact person

1st name Onishi
Middle name
Last name Hidenori

Organization

Faculty of Medical Science, University of Fukui

Division name

Deparement of Community Medicine

Zip code

910-1193

Address

23-3, Shimoaizuki, Matsuoka, Eiheiji, Yoshida, Fukui

TEL

0776-61-3111

Homepage URL


Email

o-hide68@u-fukui.ac.jp


Sponsor or person

Institute

Faculty of Medical Science, University of Fukui

Institute

Department

Personal name



Funding Source

Organization

Fukui prefecture

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

The Research Ethics Committee of University of Fukui

Address

23-3 Shimoaizuki Matsuoka Eiheiji Yoshida Fukui

Tel

0776-61-8529

Email

chiken@ml.u-fukui.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

2023 Year 12 Month 22 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

Open public recruiting

Date of protocol fixation

2022 Year 06 Month 01 Day

Date of IRB

2022 Year 06 Month 24 Day

Anticipated trial start date

2022 Year 06 Month 24 Day

Last follow-up date

2027 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

2023 Year 12 Month 22 Day

Last modified on

2023 Year 12 Month 22 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000060706


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name