UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000036630
Receipt number R000041726
Scientific Title Can humanoid robot EMIEW be effective support system for medical staffs? : a prospective controlled study
Date of disclosure of the study information 2019/05/01
Last modified on 2021/03/17 10:51:19

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Basic information

Public title

Can humanoid robot EMIEW be effective support system for medical staffs? : a prospective controlled study

Acronym

Can humanoid robot EMIEW be effective support system for medical staffs? : a prospective controlled study

Scientific Title

Can humanoid robot EMIEW be effective support system for medical staffs? : a prospective controlled study

Scientific Title:Acronym

Can humanoid robot EMIEW be effective support system for medical staffs? : a prospective controlled study

Region

Japan


Condition

Condition

non

Classification by specialty

Not applicable

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate duty reduction effect for medical workers by using humanoid robot "EMIEW3"

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Changes in Patient Response Time for Admission/Discharge Explanation with or without Support by EMIEW 3

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

Self control

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Educational,Counseling,Training

Type of intervention

Other

Interventions/Control_1

Humanoid robot EMIES3 does the routine explanation instead of medical worker.

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

80 years-old >

Gender

Male and Female

Key inclusion criteria

Persons who obtain written consent to participate in the study.

Key exclusion criteria

Persons for whom it is difficult to confirm their intention.
More than one person to explain.
Persons whose research director has determined that inclusion in research is inappropriate.

Target sample size

100


Research contact person

Name of lead principal investigator

1st name Tokuhara
Middle name
Last name Makoto

Organization

National Center for Global Health and Medicine

Division name

Admission support center

Zip code

162-8655

Address

1-21-1 Toyama Shinjuku-ku Tokyo

TEL

03-3202-7181

Email

mtokuha@hosp.ncgm.go.jp


Public contact

Name of contact person

1st name Tokuhara
Middle name
Last name Makoto

Organization

National Center for Global Health and Medicine

Division name

Admission support center

Zip code

162-8655

Address

1-21-1 Toyama Shinjuku-ku Tokyo

TEL

03-3202-7181

Homepage URL


Email

mtokuha@hosp.ncgm.go.jp


Sponsor or person

Institute

National Center for Global Health and Medicine

Institute

Department

Personal name



Funding Source

Organization

HITACHI Corporation

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

National Center for Global Health and Medicine

Address

1-21-1 Toyama Shinjuku-ku Tokyo

Tel

03-3202-7181

Email

rinrijm@hosp.ncgm.go.jp/ rinrijm@hosp.ncgm.go.jp


Secondary IDs

Secondary IDs

YES

Study ID_1

NCGM-G-003095-01

Org. issuing International ID_1

National Center for Global Health and Medicine

Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions

国立国際医療研究センター


Other administrative information

Date of disclosure of the study information

2019 Year 05 Month 01 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

2019 Year 03 Month 19 Day

Date of IRB

2019 Year 04 Month 05 Day

Anticipated trial start date

2019 Year 05 Month 13 Day

Last follow-up date

2020 Year 03 Month 31 Day

Date of closure to data entry

2020 Year 03 Month 31 Day

Date trial data considered complete

2020 Year 03 Month 31 Day

Date analysis concluded

2021 Year 03 Month 07 Day


Other

Other related information



Management information

Registered date

2019 Year 04 Month 30 Day

Last modified on

2021 Year 03 Month 17 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000041726


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name