UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000049047
Receipt number R000055879
Scientific Title Verification of the relationship between the dissemination of information on the promotion of social participation using social network services and well-being and bustle of the city
Date of disclosure of the study information 2022/10/14
Last modified on 2023/03/31 16:55:54

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

Verification of the relationship between the dissemination of information on the promotion of social participation using social network services and well-being and bustle of the city

Acronym

Verification of the relationship between the dissemination of information on the promotion of social participation using social network services and well-being and bustle of the city

Scientific Title

Verification of the relationship between the dissemination of information on the promotion of social participation using social network services and well-being and bustle of the city

Scientific Title:Acronym

Verification of the relationship between the dissemination of information on the promotion of social participation using social network services and well-being and bustle of the city

Region

Japan


Condition

Condition

Community-dwelling adults

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To verify the relationship between the dissemination of information about local events and social participation using SNS and well-being and bustle of the city

Basic objectives2

Safety

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Well-being(2 months after the start of the intervention)

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Behavior,custom

Interventions/Control_1

Providing information on local events, recommended spots, and columns on social participation

Interventions/Control_2

Providing information on health

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

18 years-old <=

Age-upper limit

100 years-old >=

Gender

Male and Female

Key inclusion criteria

Men and women over 18 years old
mobile application LINE user
given consent for this study

Key exclusion criteria

Minors
Those who live outside the study area
unable to give consent for this study

Target sample size

250


Research contact person

Name of lead principal investigator

1st name Katsunori
Middle name
Last name Kondo

Organization

Chiba university

Division name

Center for preventive medicine

Zip code

263-8522

Address

1-33, Yayoi-cho, Inage ku, Chiba city, Chiba

TEL

043-290-3177

Email

kkondo@kkondo.net


Public contact

Name of contact person

1st name Noriyuki
Middle name
Last name Abe

Organization

Chiba university

Division name

Center for preventive medicine

Zip code

263-8522

Address

1-33, Yayoi-cho, Inage ku, Chiba city, Chiba

TEL

043-290-3177

Homepage URL


Email

abe.n@chiba-u.jp


Sponsor or person

Institute

Chiba university

Institute

Department

Personal name



Funding Source

Organization

Japan Science and Technology Agency

Organization

Division

Category of Funding Organization

Government offices of other countries

Nationality of Funding Organization



Other related organizations

Co-sponsor

NTT DOCOMO, INC.

Name of secondary funder(s)



IRB Contact (For public release)

Organization

Chiba university

Address

1-33, Yayoi-cho, Inage ku, Chiba city, Chiba

Tel

043-290-3177

Email

abe.n@chiba-u.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 10 Month 14 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

384

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

2022 Year 10 Month 01 Day

Date of IRB

2022 Year 09 Month 15 Day

Anticipated trial start date

2022 Year 10 Month 14 Day

Last follow-up date

2023 Year 01 Month 31 Day

Date of closure to data entry

2023 Year 02 Month 05 Day

Date trial data considered complete

2023 Year 02 Month 05 Day

Date analysis concluded

2023 Year 03 Month 01 Day


Other

Other related information



Management information

Registered date

2022 Year 09 Month 28 Day

Last modified on

2023 Year 03 Month 31 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000055879


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name