UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000019706
Receipt number R000022590
Scientific Title Investigation research of stress relieving effect on optimization environmental of a high-resolution sound source in university hospital.
Date of disclosure of the study information 2015/11/09
Last modified on 2017/10/30 10:38:37

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Basic information

Public title

Investigation research of stress relieving effect on optimization environmental of a high-resolution sound source in university hospital.

Acronym

Investigation of stress relieving effect of a high-resolution sound source.

Scientific Title

Investigation research of stress relieving effect on optimization environmental of a high-resolution sound source in university hospital.

Scientific Title:Acronym

Investigation of stress relieving effect of a high-resolution sound source.

Region

Japan


Condition

Condition

Not specified

Classification by specialty

Not applicable

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Evaluate the change of satisfaction with placing the system of hyper resolution sound at the outpatient waiting.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

Questionnaire of satisfaction

Key secondary outcomes



Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


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) more than 20 years old
2) no difficulty of reading and writing
3) subjects who accept the answer

Key exclusion criteria

Refer to inclusion criteria

Target sample size

200


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Toshinori Ito

Organization

Osaka University School of Medicine

Division name

Department of Integrative Medicine

Zip code


Address

2-2 Yamadaoka, Suita, Osaka, Japan

TEL

06-6879-3498

Email

a-yasueda@cam.med.osaka-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Asuka Yasueda

Organization

Osaka University School of Medicine

Division name

Department of Integrative Medicine

Zip code


Address

2-2 Yamadaoka, Suita, Osaka, Japan

TEL

06-6879-3498

Homepage URL


Email

a-yasueda@cam.med.osaka-u.ac.jp


Sponsor or person

Institute

Osaka University School of Medicine Department of Integrative Medicine

Institute

Department

Personal name



Funding Source

Organization

None

Organization

Division

Category of Funding Organization

Other

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

大阪大学医学部附属病院


Other administrative information

Date of disclosure of the study information

2015 Year 11 Month 09 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

2015 Year 09 Month 09 Day

Date of IRB


Anticipated trial start date

2015 Year 11 Month 09 Day

Last follow-up date

2015 Year 12 Month 15 Day

Date of closure to data entry

2015 Year 12 Month 31 Day

Date trial data considered complete

2015 Year 12 Month 31 Day

Date analysis concluded

2016 Year 02 Month 15 Day


Other

Other related information

Evaluate the change of patient's satisfaction whether with or without system of high resolution sound source

Study design: cross sectional method
Recruit method: Patients who come to ophthalmology of our hospital in 16-20th November or 14-18th December.

Subjects: Patients who accept to answer the survey and meet our inclusion criteria.

Evaluation Item: survey of satisfaction rate of our hospital.


Management information

Registered date

2015 Year 11 Month 09 Day

Last modified on

2017 Year 10 Month 30 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000022590


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name