UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000018033
Receipt number R000020891
Scientific Title A feasibility study of smoking cessation artificial intellgence application for patients with nicotine addiction
Date of disclosure of the study information 2015/06/22
Last modified on 2017/07/13 11:17:02

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Basic information

Public title

A feasibility study of smoking cessation artificial intellgence application for patients with nicotine addiction

Acronym

A study of smoking cessation application for patients with nicotine addiction

Scientific Title

A feasibility study of smoking cessation artificial intellgence application for patients with nicotine addiction

Scientific Title:Acronym

A study of smoking cessation application for patients with nicotine addiction

Region

Japan


Condition

Condition

nicotine addiction

Classification by specialty

Pneumology Psychiatry

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Investigate the safety and efficacy of smoking cessation aid application for patients with nicotine addiction.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2


Developmental phase

Not applicable


Assessment

Primary outcomes

The normal operation of the application
The safety of the application

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

Device,equipment

Interventions/Control_1

smoking cessation aid application

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

nicotine addiction patients who entitled to get health care services provided by health insurance and who agree to participate in the study after enough explanation about the study.

Key exclusion criteria

exclusion criteria
1. a patient does not agree
2. a patient who the attending physician think is does not seem able to use a smartphone.
3. a patient with severe mental disorder who the attending physician think is not followable in the study.

Target sample size

30


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Fukunaga Koichi

Organization

Keio University school of medicine

Division name

pulmonary devision

Zip code


Address

shinanomachi35,shinjyukuku,tokyo

TEL

03-3353-1211

Email

k-fuku@jf7.so-net.ne.jp


Public contact

Name of contact person

1st name
Middle name
Last name Fukunaga koichi

Organization

Keio University school of medicine

Division name

pulmonary devision

Zip code


Address

shinanomachi35,shinjyukuku,tokyo

TEL

03-3353-1211

Homepage URL


Email

k-fuku@jf7.so-net.ne.jp


Sponsor or person

Institute

Keio University school of medicine pulmonary devision

Institute

Department

Personal name



Funding Source

Organization

CureApp, Inc.

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



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

2015 Year 06 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

Completed

Date of protocol fixation

2014 Year 12 Month 08 Day

Date of IRB


Anticipated trial start date

2015 Year 01 Month 21 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2015 Year 06 Month 22 Day

Last modified on

2017 Year 07 Month 13 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000020891