UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000054927
Receipt number R000062753
Scientific Title A comparative study of pre and post intervention in a facilitator educational program to support nursing reflection
Date of disclosure of the study information 2024/08/10
Last modified on 2025/01/09 09:11:15

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Basic information

Public title

Evaluation of a facilitator educational program to support nursing reflection

Acronym

Evaluation of a facilitator educational program to support nursing reflection

Scientific Title

A comparative study of pre and post intervention in a facilitator educational program to support nursing reflection

Scientific Title:Acronym

Nursing reflection facilitator educational study

Region

Japan


Condition

Condition

None

Classification by specialty

Nursing

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Evaluation of the appropriateness of the developed "Facilitator Educational Program to Support Nursing Reflection"

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2


Developmental phase

Not applicable


Assessment

Primary outcomes

Questionnaire to evaluate the appropriateness of the program (presence of new awareness, implementation environment, support of action plan, reconstructing the meaning of the experience, trust, problem identification, program structure, time required, and potential for utilization)

Key secondary outcomes

Check the presence or absence of new awareness from the video recording data and the presence or absence of awareness not included in the self-reflective process.
As supportive techniques, the type of questions, the order in which they are utilized, and the behavior of the learners in response to the questions will be observed.


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 Other

Interventions/Control_1

Practice of facilitation

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

Facilitator role: Nurses who have attended the reflection training course and have 5 to 10 years of experience in facilitating reflections in their departments.
The learner role: Nurses who have attended the reflection training, who belong to a different team in the same department as the facilitator, and who have 1 to 3 years of experience.
Written consent for participation in the study has been obtained from the subjects themselves.

Key exclusion criteria

Inability to participate in the program to the end.
Unable to obtain consent to participate in the research.

Target sample size

15


Research contact person

Name of lead principal investigator

1st name Etsuko
Middle name
Last name Ikenishi

Organization

Osaka Medical and Pharmaceutical University

Division name

Faculty of Nursing

Zip code

659-0095

Address

7-6 Hatchonishimachi Takatsuki Osaka

TEL

072-683-1221

Email

e.ikenishi@ompu.ac.jp


Public contact

Name of contact person

1st name Etsuko
Middle name
Last name Ikenishi

Organization

Osaka Medical and Pharmaceutical University

Division name

Faculty of Nursing

Zip code

569-0095

Address

7-6 Hatchonishimachi Takatsuki Osaka

TEL

072-683-1221

Homepage URL


Email

e.ikenishi@ompu.ac.jp


Sponsor or person

Institute

Osaka Medical and Pharmaceutical University

Institute

Department

Personal name

Etsuko Ikenishi


Funding Source

Organization

MEXT

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor

Kyoto Notre Dome University
Kansai University of Nursing and Health Sciences

Name of secondary funder(s)



IRB Contact (For public release)

Organization

Research Promotion Section, Osaka Medical and Pharmaceutical University

Address

2-7 Daigakumachi Takatsuki Osaka

Tel

072-683-1221

Email

rinri@ompu.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

大阪医科薬科大学(大阪府)


Other administrative information

Date of disclosure of the study information

2024 Year 08 Month 10 Day


Related information

URL releasing protocol

None

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

2024 Year 07 Month 07 Day

Date of IRB

2024 Year 07 Month 24 Day

Anticipated trial start date

2024 Year 07 Month 17 Day

Last follow-up date

2026 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

2024 Year 07 Month 10 Day

Last modified on

2025 Year 01 Month 09 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000062753