UMIN-CTR Clinical Trial

Basic information
Public title	Dementia nursing intervention developing nursing practical capability program for nurses in hospitals
Acronym	Dementia nursing intervention developing nursing practical capability program for nurses in hospitals
Scientific Title	Dementia nursing intervention developing nursing practical capability program for nurses in hospitals
Scientific Title:Acronym	Dementia nursing intervention developing nursing practical capability program for nurses in hospitals
Region	Japan

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

Objectives
Narrative objectives1	A purpose of the study is to determine the effectiveness of the dementia nursing intervention ability upbringing program by e-learning which we developed.
Basic objectives2	Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase

Assessment
Primary outcomes	Consciousness about the reduction of the physical restriction 3. An ethical sensitivity standard of the clinical nurse 4A nursing intervention self-assessment standard aiming at the person-centred care for elderly people with cognitive impairment of the acute phase hospital
Key secondary outcomes

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	Maneuver
Interventions/Control_1	Dementia nursing intervention ability upbringing program by e-learning which we developed
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	21 years-old <
Age-upper limit	60 years-old >=
Gender	Male and Female
Key inclusion criteria	Regular nurse The person who belongs to the surgical system, internal medicine system ward which we work in a hospital for acute phase, and elderly people with dementia of the somatotherapy are admitted to One (the person whom the mobile terminals such as a smartphone and a tablet, the PC, and the like are available to) in the environment that can reply e-learning attendance and WEB questionnaire
Key exclusion criteria	It is all clinical nurse specialists, all authorized nurses regardless of the field 2. Person of part-time service and the part-time job 3. Person of a maternity leave plan and the retirement plan 4. Nurse of the ward where hospitalization is not at all of elderly people with dementia including children, the maternity ward
Target sample size	162

Research contact person
Name of lead principal investigator	1st name Mizue Middle name Last name Suzuki
Organization	Hamamatsu University School of Medicine
Division name	Faculty of Nursing
Zip code	431-3192
Address	1-20-1 Handayama, Higashi-ku, Hamamatsu
TEL	053-435-2826
Email	mizuesuzuki@gmail.com

Public contact
Name of contact person	1st name Mizue Middle name Last name suzuki
Organization	Hamamatsu University School of Medicine
Division name	Faculty of Nursing
Zip code	431-3192
Address	1-20-1 Handayama, Higashi-ku, Hamamatsu
TEL	053-435-2826
Homepage URL
Email	mizuesuzuki@gmail.com

Sponsor
Institute	Hamamatsu University School of Medicine Faculty of Nursing 1-20-1 Handayama, Higashi-ku, Hamamatsu 431-3192, Japan
Institute
Department

Funding Source
Organization	Hamamatsu University School of Medicine Faculty of Nursing 1-20-1 Handayama, Higashi-ku, Hamamatsu 431-3192, Japan
Organization
Division
Category of Funding Organization	Japanese Governmental office
Nationality of Funding Organization

Other related organizations
Co-sponsor
Name of secondary funder(s)

IRB Contact (For public release)
Organization	Hamamatsu University School of Medicine
Address	1-20-1 Handayama, Higashi-ku, Hamamatsu
Tel	053-435-2826
Email	m~suzuki@hama-med.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	2020 Year 07 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	Preinitiation
Date of protocol fixation	2020 Year 03 Month 31 Day
Date of IRB	2020 Year 03 Month 05 Day
Anticipated trial start date	2020 Year 05 Month 01 Day
Last follow-up date	2020 Year 12 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	2020 Year 04 Month 19 Day
Last modified on	2020 Year 04 Month 19 Day

Link to view the page
URL(English)	https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000045839