UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000027278 |
|---|---|
| Receipt number | R000031255 |
| Scientific Title | Trial of the educational program enforcement to bring transformation in the manner of the critical care center nurse corresponding to the attempted suicide patient |
| Date of disclosure of the study information | 2017/05/09 |
| Last modified on | 2019/11/12 11:50:55 |
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Basic information
Public title
Trial of the educational program enforcement to bring transformation in the manner of the critical care center nurse corresponding to the attempted suicide patient
Acronym
Trial of the educational program enforcement to bring transformation in the manner of the critical care center nurse corresponding to the attempted suicide patient
Scientific Title
Trial of the educational program enforcement to bring transformation in the manner of the critical care center nurse corresponding to the attempted suicide patient
Scientific Title:Acronym
Trial of the educational program enforcement to bring transformation in the manner of the critical care center nurse corresponding to the attempted suicide patient
Region
| Japan |
Condition
Condition
Psychiatric disorder
Classification by specialty
| Nursing |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
Clarify whether the manner to an attempted suicide patient brings an affirmative change by a critical care center nurse with the correspondence experience to an attempted suicide patient attending relation attempted suicide patient educational program
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
At the time of an attitude toward attempted suicide patient standard educational program start of the nurse
I perform it after the educational program end four weeks after three weeks
Key secondary outcomes
At the time of Japanese edition The Understanding Suicidal PatientsScale educational program start
I perform it after the educational program end four weeks after three weeks
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
| Behavior,custom |
Interventions/Control_1
I carry out two times of educational program.
I perform it in 90 minutes at program time of the first and the second.
I set aside program enforcement of the first and the second for two weeks.
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
| 22 | years-old | <= |
Age-upper limit
| 60 | years-old | >= |
Gender
Male and Female
Key inclusion criteria
Critical care center nurse
Key exclusion criteria
Critical care center nurse for an attempted suicide patient without the correspondence experience
Target sample size
60
Research contact person
Name of lead principal investigator
| 1st name | Takako |
| Middle name | |
| Last name | Okawa |
Organization
Fukushima Medical College School of Nursing
Division name
Family nursing section
Zip code
960-1295
Address
Hikarigaoka, Fukushima-shi, Fukushima
TEL
024-547-1825
ohkawa@fmu.ac.jp
Public contact
Name of contact person
| 1st name | Chie |
| Middle name | |
| Last name | Saito |
Organization
Fukushima Medical College graduate school
Division name
Nursing science graduate course
Zip code
960-1295
Address
Hikarigaoka, Fukushima-shi, Fukushima
TEL
024-547-1111
Homepage URL
mn165003@fmu.ac.jp
Sponsor or person
Institute
Fukushima Medical College graduate school
Institute
Department
Personal name
Funding Source
Organization
Fukushima Medical College graduate school
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
Fukushima Medical University Research Promotion Section
Address
1 Hikarigaoka, Fukushima City, Fukushima Prefecture
Tel
0245471825
rs@fmu.ac.jp
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
| 2017 | Year | 05 | 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
| 2017 | Year | 06 | Month | 15 | Day |
Date of IRB
| 2017 | Year | 05 | Month | 20 | Day |
Anticipated trial start date
| 2017 | Year | 06 | Month | 15 | Day |
Last follow-up date
| 2018 | 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 | 05 | Month | 09 | Day |
Last modified on
| 2019 | Year | 11 | Month | 12 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000031255
