UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000027718
Receipt number R000031654
Scientific Title Effectiveness of educational intervention (EASE program) introductory training on the patient education of nurses.
Date of disclosure of the study information 2017/06/11
Last modified on 2023/08/28 13:53:38

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Basic information

Public title

Effectiveness of educational intervention (EASE program) introductory training on the patient education of nurses.

Acronym

Effectiveness of educational intervention (EASE program) introductory training on the patient education of nurses.

Scientific Title

Effectiveness of educational intervention (EASE program) introductory training on the patient education of nurses.

Scientific Title:Acronym

Effectiveness of educational intervention (EASE program) introductory training on the patient education of nurses.

Region

Japan


Condition

Condition

Nurse

Classification by specialty

Nursing

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To be able to obtain a future direction of effective nurse in continuing education, the introductory training in educational intervention program is carried out and determined its effect to the clinical nurses.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

1.By taking the educational intervention (EASE program) introductory training, this will help determine if patient education in the program is improved through scientific basis.

Key secondary outcomes

2.By taking the educational intervention (EASE program) introductory training, this will determine the effectiveness and improvement of knowledge through research.
3.By taking the educational intervention (EASE program) introductory training, this will help determine an improvement in terms of motivation for individuals to work as nurse.


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 Maneuver

Interventions/Control_1

The interventional education (EASE program) introductory training program will help to collect and compare data.
Before and after training, the participants will be 1. Collect, interpret, compare data, measure characteristic and changes through questionnaire. 2.knowledgeable in measurement of attitude to nursing research.3. Measure motivation through scientific motivation measureme.

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

This includes hospital nurses who understand the contents of the description of this study and gave written informed consent, agreeing to cooperate during the investigations.

Key exclusion criteria

This includes hospital nurses who did not give written informed consent.

Target sample size

50


Research contact person

Name of lead principal investigator

1st name Mitsuhiro
Middle name
Last name Matsumoto

Organization

Gunma University, Graduate School of Health Sciences

Division name

Nursing

Zip code

3718514

Address

3-39-22 Showa-machi, Maebashi, Gunma

TEL

027-220-7111

Email

matsumoto_32@yahoo.co.jp


Public contact

Name of contact person

1st name Mitsuhiro
Middle name
Last name Matsumoto

Organization

Gunma University, Graduate School of Health Sciences

Division name

Nursing

Zip code

3718514

Address

3-39-22 Showa-machi, Maebashi, Gunma

TEL

027-220-7111

Homepage URL


Email

matsumoto_32@yahoo.co.jp


Sponsor or person

Institute

Gunma University, Graduate School of Health Sciences

Institute

Department

Personal name



Funding Source

Organization

Gunma University, Graduate School of Health Sciences

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

Gunma University, Graduate School of Health Sciences

Address

3-39-22 Showa-machi, Maebashi, Gunma

Tel

027-220-7111

Email

matsumoto_32@yahoo.co.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 06 Month 11 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

44

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

Open public recruiting

Date of protocol fixation

2017 Year 07 Month 01 Day

Date of IRB

2017 Year 08 Month 25 Day

Anticipated trial start date

2017 Year 07 Month 01 Day

Last follow-up date

2028 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 06 Month 11 Day

Last modified on

2023 Year 08 Month 28 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000031654