UMIN-CTR Clinical Trial

Basic information
Public title	The transferability of systematic review educational workshop between facilities in Japanese hospitals
Acronym	The transferability of systematic review educational workshop between facilities
Scientific Title	The transferability of systematic review educational workshop between facilities in Japanese hospitals
Scientific Title:Acronym	The transferability of systematic review educational workshop between facilities
Region	Japan

Condition
Condition	workers in hospitals
Classification by specialty	Adult
Classification by malignancy	Others
Genomic information	NO

Objectives
Narrative objectives1	The objective is to verificate the effectiveness of the educational workshop to conduct systematic review
Basic objectives2	Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase

Assessment
Primary outcomes	the proportion of those who designed the protocol
Key secondary outcomes	The proportion of those who registrate to the PROSPERO, and who success to Cochrane title registration, present the result in scientific meeting, publish the result in scientific journal.

Base
Study type	Interventional

Study design
Basic design	Single arm
Randomization	Non-randomized
Randomization unit
Blinding	Open -no one is blinded
Control	Uncontrolled
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	We will conduct a total of 9 workshops(WS) approximately every 2-3 weeks. Each WS is planning about one hour. We will directly give lectures and feedback at this time. Draw research questions from participants, create groups of about 2 with similar research questions, and make it a review team. Each review team receives a lecture using YouTube(r) after each WS and tackles the homework according to the lecture. Participants submit the homework form using Google Drive(r) once for each WS and receive feedback from operators and facilitators from time to time. It is possible to re-submit based on the result of feedback. In addition, we will respond to the question that appeared during the homework. On the day of the workshop, we will provide feedback on mistakes that were frequent in submission tasks, questions from participants and comments on the next issue.
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	Not applicable
Age-upper limit	Not applicable
Gender	Male and Female
Key inclusion criteria	health care worker who can participate the workshops in each facilities
Key exclusion criteria	those who has already conducted a systematic review
Target sample size	150

Research contact person
Name of lead principal investigator	1st name Middle name Last name Yuki Kataoka
Organization	Hyogo Prefectural Amagasaki General Medical Center
Division name	Department of Respiratory Medicine, Hospital Care Research Unit
Zip code
Address	Higashi-Naniwa-Cho 2-17-77, Amagasaki, Hyogo
TEL	06-6480-7000
Email	youkitikk@gmail.com

Public contact
Name of contact person	1st name Middle name Last name Yuki Kataoka
Organization	Hyogo Prefectural Amagasaki General Medical Center
Division name	Department of Respiratory Medicine, Hospital Care Research Unit
Zip code
Address	Higashi-Naniwa-Cho 2-17-77, Amagasaki, Hyogo
TEL	06-6480-7000
Homepage URL	https://www.facebook.com/SRworkshop
Email	youkitikk@gmail.com

Sponsor
Institute	Hyogo Prefectural Amagasaki General Medical Center
Institute
Department

Funding Source
Organization	self funding
Organization
Division
Category of Funding Organization	Other
Nationality of Funding Organization

Other related organizations
Co-sponsor	Japan Primary Care Association
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	堺市立総合医療センター、倉敷中央病院、近畿中央胸部疾患センター、聖隷三方原病院、尼崎医療生協病院

Other administrative information
Date of disclosure of the study information	2017 Year 01 Month 10 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	Main results already published
Date of protocol fixation	2017 Year 01 Month 09 Day
Date of IRB	2017 Year 02 Month 01 Day
Anticipated trial start date	2017 Year 02 Month 08 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	2017 Year 01 Month 09 Day
Last modified on	2022 Year 01 Month 13 Day

Link to view the page
URL(English)	https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000029438