UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000062140
Receipt number R000071100
Scientific Title Development of an AI-Based Practicum Support Agent for Nursing Students: Feasibility Evaluation of Classroom Implementation
Date of disclosure of the study information 2026/07/06
Last modified on 2026/07/05 09:10:32

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Basic information

Public title

Development of an AI-Based Practicum Support Agent for Nursing Students: Feasibility Evaluation of Classroom Implementation

Acronym

Classroom Feasibility NAIS Trial (Nursing-AI Support)

Scientific Title

Development of an AI-Based Practicum Support Agent for Nursing Students: Feasibility Evaluation of Classroom Implementation

Scientific Title:Acronym

Classroom Feasibility NAIS Trial (Nursing-AI Support)

Region

Japan


Condition

Condition

None

Classification by specialty

Not applicable

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the feasibility of implementing, in classroom settings, an AI agent based on generative artificial intelligence (AI) that provides autonomous guidance to support nursing students in resolving challenges and questions encountered during clinical practicums.

Basic objectives2

Safety

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Change in self-efficacy for clinical practicum documentation

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Single blind -participants are blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Educational,Counseling,Training

Type of intervention

Other

Interventions/Control_1

A web-based application utilizing generative AI was provided to deliver autonomous guidance to nursing students regarding questions and challenges encountered during clinical practice.

Interventions/Control_2

No-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

* Undergraduate nursing students enrolled at a nursing university.
* Students scheduled to take a course in the subject area for which the AI model was developed.
* Students who understood the purpose and procedures of the study and provided written informed consent.

Key exclusion criteria

* Individuals unable to use the required device (e.g., a personal computer or tablet).
* Individuals judged to be unable to provide continuous study data because of poor health or other reasons.
* Individuals who withdrew their consent to participate in the study.

Target sample size

60


Research contact person

Name of lead principal investigator

1st name Asahiko
Middle name
Last name Higashitusji

Organization

Chiba prefectural university of health sciences

Division name

Faculty of Healthcare Sciences

Zip code

2610014

Address

2-10-1 Wakaba, Mihama-ku, Chiba City

TEL

0432722000

Email

cpuhs1@mz.pref.chiba.lg.jp


Public contact

Name of contact person

1st name Asahiko
Middle name
Last name Higashitsuji

Organization

Chiba prefectural university of health sciences

Division name

Faculty of Healthcare Sciences

Zip code

2610014

Address

2-10-1 Wakaba, Mihama-ku, Chiba City

TEL

0432722000

Homepage URL


Email

cpuhs1@mz.pref.chiba.lg.jp


Sponsor or person

Institute

Chiba prefectural university of health sciences

Institute

Department

Personal name



Funding Source

Organization

Chiba prefectural university of health sciences

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

Research Ethics Committee of Chiba Prefectural University of Health Sciences

Address

2-10-1 Wakaba, Mihama-ku, Chiba City

Tel

0432722000

Email

cpuhs1@mz.pref.chiba.lg.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

2026 Year 07 Month 06 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

Open public recruiting

Date of protocol fixation

2026 Year 05 Month 01 Day

Date of IRB

2026 Year 05 Month 01 Day

Anticipated trial start date

2026 Year 05 Month 01 Day

Last follow-up date

2026 Year 09 Month 01 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2026 Year 07 Month 05 Day

Last modified on

2026 Year 07 Month 05 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000071100