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Name:
UMIN ID:

Recruitment status Completed
Unique ID issued by UMIN UMIN000027278
Receipt No. 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

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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
Email 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
Email mn165003@fmu.ac.jp

Sponsor
Institute Fukushima Medical College graduate school
Institute
Department

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
Email 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
URL(English) https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000031255

Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name


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