UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000020897
Receipt number R000022951
Scientific Title Biosignal monitoring in cardiovascular patients for development of new driver safety system
Date of disclosure of the study information 2016/02/05
Last modified on 2017/02/07 14:12:22

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Basic information

Public title

Biosignal monitoring in cardiovascular patients for development of new driver safety system

Acronym

Biosignal monitoring for cardiovascular stress during driving.

Scientific Title

Biosignal monitoring in cardiovascular patients for development of new driver safety system

Scientific Title:Acronym

Biosignal monitoring for cardiovascular stress during driving.

Region

Japan


Condition

Condition

arrhythmia

Classification by specialty

Cardiology Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Biosignal monitoring in cardiovascular patients for development of new driver safety system

Basic objectives2

Others

Basic objectives -Others

Biosignal monitoring

Trial characteristics_1

Exploratory

Trial characteristics_2

Others

Developmental phase

Not applicable


Assessment

Primary outcomes

Changes in electrocardiography during driving

Key secondary outcomes

Driving-induced changes in pulse wave, blood pressure, body temperature, behavior patterns (walking pattern, pedaometer, sleep period, blood glucose fluctuation)


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Prevention

Type of intervention

Device,equipment

Interventions/Control_1

exercise challenge by Treadmill test or cardiopulmonary exercise test.

Interventions/Control_2

driving challenge by simulator

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

Cardiovascular patients who have been diagnosed arrhythmia and healthy counterparts who have driver license with informed consent.

Key exclusion criteria

Unstable angina, lethal arrhythmia, patients who is contraindicated for exercise challenge.
limiting condition for exercise.

Target sample size

100


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Toyoaki Murohara

Organization

Nagoya University

Division name

Department of Cardiology

Zip code


Address

65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, Japan

TEL

052-744-2147

Email

murohara@med.nagoya-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Yasuko K Bando

Organization

Nagoya University

Division name

Department of Cardiology

Zip code


Address

65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, Japan

TEL

052-744-2147

Homepage URL


Email

ybando@med.nagoya-u.ac.jp


Sponsor or person

Institute

Nagoya University

Institute

Department

Personal name



Funding Source

Organization

Nagoya University

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor

Toyota Motor Corporation

Name of secondary funder(s)

Denso Corporation


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

名古屋大学医学部附属病院、名古屋大学National Innovation Complex(健常者のみ)


Other administrative information

Date of disclosure of the study information

2016 Year 02 Month 05 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

Preinitiation

Date of protocol fixation

2015 Year 02 Month 05 Day

Date of IRB


Anticipated trial start date

2016 Year 02 Month 15 Day

Last follow-up date

2018 Year 03 Month 31 Day

Date of closure to data entry

2018 Year 03 Month 31 Day

Date trial data considered complete

2018 Year 03 Month 31 Day

Date analysis concluded

2019 Year 03 Month 31 Day


Other

Other related information



Management information

Registered date

2016 Year 02 Month 05 Day

Last modified on

2017 Year 02 Month 07 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000022951


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name