UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000054088
Receipt number R000061760
Scientific Title The Effect of Learning Support Tools Utilizing Auditory Perception on the Consolidation of Medical Knowledge in Nursing Students
Date of disclosure of the study information 2024/05/31
Last modified on 2024/10/09 08:02:52

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Basic information

Public title

The Effect of Learning Support Tools Utilizing Auditory Perception on the Consolidation of Medical Knowledge in Nursing Students

Acronym

The Effect of Learning Support Tools Utilizing Auditory Perception on the Consolidation of Medical Knowledge in Nursing Students

Scientific Title

The Effect of Learning Support Tools Utilizing Auditory Perception on the Consolidation of Medical Knowledge in Nursing Students

Scientific Title:Acronym

The Effect of Learning Support Tools Utilizing Auditory Perception on the Consolidation of Medical Knowledge in Nursing Students

Region

Japan


Condition

Condition

Nursing faculty students

Classification by specialty

Nursing Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study is to clarify whether educational support utilizing auditory methods can contribute to the retention of medical knowledge among nursing students. To achieve this, the following will be elucidated:

1. Whether nursing students can actually utilize post-study support tools employing auditory elements.
2. Whether the level of medical knowledge among nursing students who utilized post-study support tools incorporating auditory methods increased compared to nursing students who did not use such support tools.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Compare the difference in the change of scores between Mini-tests 1 and 2 based on whether participants listened to the audio files or not.

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking

YES

Concealment



Intervention

No. of arms

2

Purpose of intervention

Educational,Counseling,Training

Type of intervention

Other

Interventions/Control_1

Listening to the audio files at least once a week during the intervention period (2 months). 15 to 20 minutes per audio file.
The intervention group undergoes two rounds of mini-tests, one before and one after the intervention.

Interventions/Control_2

The control group undergoes two rounds of mini-tests at the same time intervals as the intervention group.

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

1) Students enrolled in the second year of the Nursing faculty of Kansai Medical University
2) Faculty students who have received sufficient explanation and consent of the research subject's free will to participate in this research with full understanding.

Key exclusion criteria

1) Students who feel resistance to wearing earphone.
2) Students deemed inappropriate as research participants by the principal investigator.

Target sample size

60


Research contact person

Name of lead principal investigator

1st name Ohashi
Middle name
Last name Atsushi

Organization

Kansai Medical University

Division name

Faculty of Nursing

Zip code

5731004

Address

2-2-2 Shinmachi, Hirakata, Osaka

TEL

0728040101

Email

ohashia@hirakata.kmu.ac.jp


Public contact

Name of contact person

1st name Atsushi
Middle name
Last name Ohashi

Organization

Kansai Medical University

Division name

Faculty of nrsing

Zip code

5731004

Address

2-2-2 Shinmachi, Hirakata, Osaka

TEL

0728040101

Homepage URL


Email

ohashia@hirakata.kmu.ac.jp


Sponsor or person

Institute

Kansai Medical University, Faculty of Nursing

Institute

Department

Personal name



Funding Source

Organization

Japan Society for the Promotion of Science

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

Kansai Medical University

Address

2-2-2, Shinmachi, Hirakata, Osaka

Tel

0728040101

Email

ohashia@hirakata.kmu.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

2024 Year 05 Month 31 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

2024 Year 04 Month 10 Day

Date of IRB

2024 Year 07 Month 06 Day

Anticipated trial start date

2024 Year 07 Month 06 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 04 Month 08 Day

Last modified on

2024 Year 10 Month 09 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000061760