UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000039420
Receipt number R000044941
Scientific Title Nurse's knowledge before and after heart failure patient guidance tool use and investigation of a conscious change
Date of disclosure of the study information 2020/02/20
Last modified on 2021/02/07 15:05:53

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Basic information

Public title

Nurse's knowledge before and after heart failure patient guidance tool use and investigation of a conscious change

Acronym

Nurse's knowledge before and after heart failure patient guidance tool use and investigation of a conscious change

Scientific Title

Nurse's knowledge before and after heart failure patient guidance tool use and investigation of a conscious change

Scientific Title:Acronym

Nurse's knowledge before and after heart failure patient guidance tool use and investigation of a conscious change

Region

Japan


Condition

Condition

Heart failure

Classification by specialty

Nursing

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

A heart failure patient guidance tool is utilized, a change in knowledge and consciousness of a ward nurse is investigated before and after utilization and it's used for future's heart failure patient guidance.

Basic objectives2

Others

Basic objectives -Others

The validity of the heart failure patient guidance tool

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Before and after a heart failure guidance tool is used, a survey by questionnaire is performed. Something by which the question contents can grasp the guidance contents to a heart failure patient. I deal with an answer of a questionnaire in statistical way.

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

Historical

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

Before and after a ward nurse used a heart failure patient guidance tool, a change in knowledge by a questionnaire and consciousness is investigated.
A heart failure patient guidance tool is used for about 1 month and patient guidance is performed. A questionnaire is distributed before and behind it, and you answer.

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

50 years-old >=

Gender

Male and Female

Key inclusion criteria

An investigation of a change in knowledge after use and consciousness was taken charge of daily and 22 nurses doing business were selected because a patient guidance tool was made to the nurse who is taking charge of a patient and is guiding in the business daily at a ward.
There is a possibility of the heart failure or the heart failure, and the patient guided using a patient guidance tool guides with the patient who can understand. At most 22 nurses make it number of people about 10 people possible to concern about 5 times by guidance.

Key exclusion criteria

The nurse who doesn't take charge of and do business.
The patient hospitalized besides the heart failure.

Target sample size

22


Research contact person

Name of lead principal investigator

1st name Tomoko
Middle name
Last name Tutiya

Organization

Gunma University hospital

Division name

The 4th floor of the south ward

Zip code

3718511

Address

3-39-15, Showamachi, Maebashi-shi, Gunma

TEL

0272208153

Email

tomococo@gunma-u.ac.jp


Public contact

Name of contact person

1st name Takehiro
Middle name
Last name Saito

Organization

Gunma University Hospital

Division name

The 4th floor of the south ward

Zip code

3718511

Address

3-39-15, Showamachi, Maebashi-shi, Gunma

TEL

0272208153

Homepage URL


Email

saitotak@gunma-u.ac.jp


Sponsor or person

Institute

Gunma University Hospital
The 4th floor of the south ward

Institute

Department

Personal name



Funding Source

Organization

None

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

Gunma University hospital The medical science course study ERB which makes a person the subject

Address

3-39-15, Showamachi, Maebashi-shi, Gunma

Tel

027-220-8740

Email

hitotaisho-ciru@ml.gunma-u.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 02 Month 20 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

2020 Year 02 Month 20 Day

Date of IRB

2020 Year 02 Month 05 Day

Anticipated trial start date

2020 Year 02 Month 20 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 02 Month 07 Day

Last modified on

2021 Year 02 Month 07 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000044941


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name