UMIN-CTR Clinical Trial

BACK TOP
UMIN-CTR English Home Glossary (Simple) FAQ Search clinical trials

Name:
UMIN ID:

Recruitment status Enrolling by invitation
Unique ID issued by UMIN UMIN000019187
Receipt No. R000022178
Scientific Title PROTOCOL(PRotocol cOnsTruction wOrkshop for the healthCare professiOnaLs): action research
Date of disclosure of the study information 2015/10/01
Last modified on 2016/10/01

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information
Public title PROTOCOL(PRotocol cOnsTruction wOrkshop for the healthCare professiOnaLs): action research
Acronym PROTOCOL
Scientific Title PROTOCOL(PRotocol cOnsTruction wOrkshop for the healthCare professiOnaLs): action research
Scientific Title:Acronym PROTOCOL
Region
Japan

Condition
Condition healthcare professionals in hospitals
Classification by specialty
Medicine in general Surgery in general Obsterics and gynecology
Pediatrics Ophthalmology Dermatology
Psychiatry Oto-rhino-laryngology Orthopedics
Urology Radiology Anesthesiology
Oral surgery Neurosurgery Cardiovascular surgery
Plastic surgery Aesthetic surgery Laboratory medicine
Operative medicine Emergency medicine Blood transfusion
Intensive care medicine Rehabilitation medicine Dental medicine
Nursing Adult
Classification by malignancy Others
Genomic information NO

Objectives
Narrative objectives1 The purpose of our project is to develop a model workshop for hospital healthcare professionals to acquire skills of writing clinical research proposals based on their clinical questions.
Basic objectives2 Others
Basic objectives -Others medical education
Trial characteristics_1
Trial characteristics_2
Developmental phase

Assessment
Primary outcomes the number of accomplished proposals of clinical research by participants
Key secondary outcomes the number of protocol applications to local ethical comittee, conference presentations, and papers by participants every 6 months.

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 plan to held around 8 times workshops per period.
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 professionals or students who are accessible to the workshop in Hyogo Prefectural Amagasaki General Medical Center.
If someone want to conduct the workshop in other facilities, we will modify the protocol and demand re-examination by IRB.
Key exclusion criteria dissidence
Target sample size 20

Research contact person
Name of lead principal investigator
1st name
Middle name
Last name KATAOKA Yuki
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 660-8550, Japan.
TEL 06-6480-7000
Email hanshin.crt@gmail.com

Public contact
Name of contact person
1st name
Middle name
Last name KATAOKA Yuki
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 660-8550, Japan.
TEL 06-6480-7000
Homepage URL
Email hanshin.crt@gmail.com

Sponsor
Institute Hyogo Prefectural Amagasaki General Medical Center
Institute
Department

Funding Source
Organization Hyogo Prefectural Amagasaki General Medical Center
Organization
Division
Category of Funding Organization Self funding
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

Other administrative information
Date of disclosure of the study information
2015 Year 10 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 Enrolling by invitation
Date of protocol fixation
2015 Year 10 Month 01 Day
Date of IRB
Anticipated trial start date
2015 Year 10 Month 01 Day
Last follow-up date
Date of closure to data entry
Date trial data considered complete
Date analysis concluded

Other
Other related information

Management information
Registered date
2015 Year 10 Month 01 Day
Last modified on
2016 Year 10 Month 01 Day


Link to view the page
URL(English) https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000022178

Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name


Contact us.