UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000016263
Receipt number R000018873
Scientific Title A cross-sectional study to assess the effects of interprofessional working and inter-unit cooperation on the employee satisfaction in Japanese tertiary hospitals.
Date of disclosure of the study information 2015/01/19
Last modified on 2015/01/19 14:44:51

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Basic information

Public title

A cross-sectional study to assess the effects of interprofessional working and inter-unit cooperation on the employee satisfaction in Japanese tertiary hospitals.

Acronym

Effects of interprofessional working and inter-unit cooperation on the employee satisfaction in Japanese tertiary hospitals.

Scientific Title

A cross-sectional study to assess the effects of interprofessional working and inter-unit cooperation on the employee satisfaction in Japanese tertiary hospitals.

Scientific Title:Acronym

Effects of interprofessional working and inter-unit cooperation on the employee satisfaction in Japanese tertiary hospitals.

Region

Japan


Condition

Condition

none

Classification by specialty

Not applicable Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

a) To assess the extent to which the interprofessional working and inter-unit cooperation are taken in tertiary hospitals in Japan.
b) To investigate the facilitator or inhibitor of the interprofessional working and inter-unit cooperation.
c) To investigate whether the interprofessional working effect satisfaction and well-being of employees.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

+ Units with which frequently cooperate
+ the extent to which the interprofessional working and inter-unit cooperation are taken

Key secondary outcomes

+ Employee satisfaction
+ Life satisfaction
+ Subjective well-being


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

+ Employees at a tertiary hospitals in which the present research is conducted, AND
+ Persons who voluntarily agree to both (a) participate the research and (b) use their data to the research

Key exclusion criteria

+ not applicable

Target sample size

5000


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name ICHIKAWA Shuhei

Organization

Mie University Graduate School of Medicine

Division name

Department of education and research in family and community medicine

Zip code


Address

2-174 Edobashi, Tsu-city, Mie, 514-8507 Japan.

TEL

059-231-5290

Email

Jwellyfish@outlook.com


Public contact

Name of contact person

1st name
Middle name
Last name ICHIKAWA Shuhei

Organization

Mie University Graduate School of Medicine

Division name

Department of education and research in family and community medicine

Zip code


Address

2-174 Edobashi, Tsu-city, Mie, 514-8507 Japan.

TEL

059-231-5290

Homepage URL


Email

Jwellyfish@outlook.com


Sponsor or person

Institute

Department of education and research in family and community medicine, Mie University Graduate School of Medicine.

Institute

Department

Personal name



Funding Source

Organization

MEXT (JAPAN)

Organization

Division

Category of Funding Organization

Nationality of Funding Organization

JAPAN


Other related organizations

Co-sponsor

Primary Care and Medical Education, Tsukuba University
Notocord corporation.

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

三重大学医学部付属病院 (三重県) / Mie University Hospital (Mie)
さいたま赤十字病院 (埼玉県) / Saitama Red Cross Hospital (Saitama)
日本赤十字社医療センター (東京都) / Japanese Red Cross Medical Center (Tokyo)


Other administrative information

Date of disclosure of the study information

2015 Year 01 Month 19 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

No longer recruiting

Date of protocol fixation

2014 Year 11 Month 30 Day

Date of IRB


Anticipated trial start date

2014 Year 12 Month 22 Day

Last follow-up date

2015 Year 01 Month 16 Day

Date of closure to data entry

2015 Year 02 Month 10 Day

Date trial data considered complete

2015 Year 02 Month 28 Day

Date analysis concluded

2015 Year 05 Month 30 Day


Other

Other related information

The cross-sectional study using some questionnaires


Management information

Registered date

2015 Year 01 Month 19 Day

Last modified on

2015 Year 01 Month 19 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000018873


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name