UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000049633
Receipt number R000056497
Scientific Title AI Hospital program study based upon a research about retention rate of the diabetes diagnostic support service system and effectiveness and acceptability of the applications
Date of disclosure of the study information 2022/11/28
Last modified on 2023/04/03 14:10:07

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Basic information

Public title

AI Hospital program study based upon a research about retention rate of the diabetes diagnostic support service system and effectiveness and acceptability of the applications

Acronym

AI Hospital program study based upon a research about retention rate of the diabetes diagnostic support service system and effectiveness and acceptability of the applications

Scientific Title

AI Hospital program study based upon a research about retention rate of the diabetes diagnostic support service system and effectiveness and acceptability of the applications

Scientific Title:Acronym

AI Hospital program study based upon a research about retention rate of the diabetes diagnostic support service system and effectiveness and acceptability of the applications

Region

Japan


Condition

Condition

type 2 diabetes

Classification by specialty

Endocrinology and Metabolism

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Try out the applications of diabetes diagnostic support service system through research participants in order to confirm effectiveness and acceptability of the system and check presence and absence of problems.

Basic objectives2

Others

Basic objectives -Others

[1] Can data be collected and recorded continuously?
[2] Has the diabetes therapy knowledge been increased through the use of the applications?
[3] Has people's interest in the diabetes therapy grown through the use of the applications?
[4] Has the user-friendly design of the applications been confirmed through actual operations?

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

-Weight, blood pressure value, blood glucose level, steps, sleep duration, meal, height, and age of research participants (data collected via the applications)
-Applications' problems and any harmful events therefrom caused to suffer research participants
-Questionnaires answered by research participants
-Opinions expressed by research participants at web meetings

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

Educational,Counseling,Training

Type of intervention

Behavior,custom

Interventions/Control_1

Help improve lifestyle by using the applications to receive input data and return feedbacks

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

20 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

1.Outpatients that consented at an age at 20 years old or more
(regardless of gender)
2. Patients of Type 2 Diabetes as diagnosed (HbA1c6.5% or more)
3. Patients capable of taking photos and emailing via their iPhone (of 15 or more iOS) or Android smartphone (of AndroidOS9 or more)
Patients without iPhone or Android smartphone can use iPhone (of 15 or more iOS) or Android smartphone (AndroidOS9 or more) of their families.
4. Patients that express intention to participate in the study for 6 weeks (42 days) or more in the period from the study initiation date to January 31, 2023 (Reiwa 5)

Key exclusion criteria

Patients that indicated rejection to participating in this study

Target sample size

25


Research contact person

Name of lead principal investigator

1st name Yutaka
Middle name
Last name Hatori

Organization

Hatori Clinic Medical Corporation

Division name

Internal medicine

Zip code

212-0058

Address

1-8-33 Kashimada, Saiwai-ku, Kwasaki, Kanagawa

TEL

044-522-0033

Email

yutaka@hatori.or.jp


Public contact

Name of contact person

1st name Shungo
Middle name
Last name Oki

Organization

BIPROGY Inc.

Division name

Social & Public Business Services 1

Zip code

135-8560

Address

1-1-1 Toyosu, Koto-ku, Tokyo

TEL

050-3132-9113

Homepage URL


Email

shungo.oki@biprogy.com


Sponsor or person

Institute

Hatori Clinic Medical Corporation

Institute

Department

Personal name



Funding Source

Organization

National Institutes of Biomedical Innovation, Health and Nutrition.

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

Japan Medical Association

Address

2-28-16 Hon-komagome, Bunkyou-ku, Tokyo

Tel

03-3946-2121

Email

rinri@po.med.or.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 11 Month 28 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

28

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 11 Month 15 Day

Date of IRB

2022 Year 11 Month 15 Day

Anticipated trial start date

2022 Year 11 Month 15 Day

Last follow-up date

2023 Year 02 Month 28 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 11 Month 28 Day

Last modified on

2023 Year 04 Month 03 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000056497