UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000019187 |
|---|---|
| Receipt number | 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 10:07:35 |
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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 | Obstetrics 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
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
hanshin.crt@gmail.com
Sponsor or person
Institute
Hyogo Prefectural Amagasaki General Medical Center
Institute
Department
Personal name
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
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
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000022178
