UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000036370
Receipt number R000041436
Scientific Title An MEG study regarding the effect of subjective air hunger using a mask on affection and cognitive function
Date of disclosure of the study information 2020/03/31
Last modified on 2020/01/16 17:34:15

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Basic information

Public title

An MEG study regarding the effect of subjective air hunger using a mask on affection and cognitive function

Acronym

An MEG study regarding the effect of subjective air hunger using a mask on affection and cognitive function

Scientific Title

An MEG study regarding the effect of subjective air hunger using a mask on affection and cognitive function

Scientific Title:Acronym

An MEG study regarding the effect of subjective air hunger using a mask on affection and cognitive function

Region

Japan


Condition

Condition

Healthy

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To clarify the effect of the air hunger on affection and coginitve function

Basic objectives2

Others

Basic objectives -Others

To investigate the neural mechanisms of air hunger

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The MEG data

Key secondary outcomes

Questionnaires


Base

Study type

Interventional


Study design

Basic design

Cross-over

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

Placebo

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

6

Purpose of intervention

Prevention

Type of intervention

Behavior,custom

Interventions/Control_1

Condition 1, condition 2, condition 3

Interventions/Control_2

Condition 1, condition 3, condition 2

Interventions/Control_3

Condition 2, condition 1, condition 3

Interventions/Control_4

Condition 2, condition 3, condition 1

Interventions/Control_5

Condition 3, condition 1, condition 2

Interventions/Control_6

Condition 3, condition 2, condition 1

Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

20 years-old <=

Age-upper limit

60 years-old >

Gender

Male and Female

Key inclusion criteria

Healthy adult

Key exclusion criteria

Participants with past or current history of serious medical illness and/or brain organic disease, who take central nerve system acting drugs, who have allergic rhinitis or bronchial asthma, who are contradicted for the use of MRI, and who are judged as not suitable for participation in this study.

Target sample size

20


Research contact person

Name of lead principal investigator

1st name Masato
Middle name
Last name Uji

Organization

Osaka City University Graduate School of Medicine

Division name

Sports medicine

Zip code

545-8585

Address

1-4-3, Asahi-machi, Abeno-ku, Osaka, 545-8585

TEL

06-6645-3790

Email

m2036283@med.osaka-cu.ac.jp


Public contact

Name of contact person

1st name Masato
Middle name
Last name Uji

Organization

Osaka City University Graduate School of Medicine

Division name

Sports medicine

Zip code

545-8585

Address

1-4-3, Asahi-machi, Abeno-ku, Osaka, 545-8585

TEL

06-6645-3790

Homepage URL


Email

m2036283@med.osaka-cu.ac.jp


Sponsor or person

Institute

Department of Sports Medicine, Osaka City University Graduate School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Japan Science and Technology Agency

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

Osaka City University Hospital Certified Review Board

Address

1-2-7, Asahi-machi, Abeno-ku, Osaka, 545-8533

Tel

06-6645-3435

Email

ethics@med.osaka-cu.ac.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

大阪市立大学医学部附属病院(大阪府), Osaka City University Hospital (Osaka Prefecture)


Other administrative information

Date of disclosure of the study information

2020 Year 03 Month 31 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

16

Results

While those who wear mask(group M) feel significantly subjective air hunger compared with those who do not wear mask (group C), no difference of cognitive function using reverse Stroop test is detected between group M and C.

Results date posted

2020 Year 01 Month 16 Day

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 02 Month 25 Day

Date of IRB

2018 Year 12 Month 27 Day

Anticipated trial start date

2020 Year 03 Month 31 Day

Last follow-up date

2020 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2019 Year 04 Month 01 Day

Last modified on

2020 Year 01 Month 16 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000041436


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name