Skip to main content
Clinical Trials/NCT07408492
NCT07408492
Not yet recruiting
Not Applicable

The Impact of Artificial Intelligence-Powered Research Training Course on Nursing Students' Research Literacy, Attitude, and Readiness to Use Artificial Intelligence

Shahid Beheshti University of Medical Sciences0 sites104 target enrollmentStarted: March 1, 2026Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
104
Primary Endpoint
Readiness to use artificial intelligence: Medical Artificial Intelligence Readiness Scale for Medical Students (MAIRS-MS)

Overview

Brief Summary

The goal of this clinical trial is to find out whether an artificial intelligence (AI)-powered research training course can improve nursing students' research skills, attitudes toward artificial intelligence, and readiness to use AI in research and education.

The main questions this study aims to answer are:

Does AI-powered research training improve nursing students' understanding of research methods?

Does this training improve nursing students' attitudes toward artificial intelligence?

Does the course increase nursing students' readiness and confidence to use artificial intelligence in research-related activities?

Researchers will compare nursing students who take an AI-powered research training course with students who receive usual education without AI-based training.

Participants will:

Be randomly assigned to either the AI-powered research training group or the usual education group

Complete online questionnaires about research skills, attitudes toward artificial intelligence, and readiness to use AI

Attend assessments at three time points: before the course, immediately after the course, and three months later

The AI-powered research training course includes structured sessions on research methods and the responsible use of artificial intelligence tools for literature review, research design, data analysis support, and academic writing. The results of this study may help improve research education and support the safe and effective use of artificial intelligence in nursing education and research.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Enrolled in a nursing program (bachelor's, master's, or doctoral level) at one of the participating universities during the study term.
  • Completion of at least one course in research methodology in their program curriculum.
  • Willingness to participate and to provide written informed consent.

Exclusion Criteria

  • Prior completion of advanced courses specifically on research-oriented AI or formal AI certification programs.
  • Inability to attend the scheduled intervention sessions or to access the online learning platform.
  • Not complete the study questionnaires at all required time points
  • Withdrawal of consent or failure to complete baseline assessments.

Arms & Interventions

AI-Powered Research Training Course

Experimental

Participants in the intervention group will take part in an artificial intelligence (AI)-powered research training course. The course includes eight structured sessions delivered over approximately four weeks and combines core research methods with practical use of AI tools to support research activities.

The training covers key stages of the research process, including selecting a research topic, reviewing scientific literature, developing research questions, choosing study designs, understanding research ethics, managing references, and preparing research reports. Participants will learn how AI tools can support tasks such as literature searching, organizing information, drafting research text, and critically reviewing research outputs, while emphasizing responsible and ethical use of AI.

Sessions include short lectures, hands-on exercises, and practical workshops using commonly available AI-based research tools. Course materials are delivered through an online learning platform,

Intervention: AI-Powered Research Training Course (Other)

Standard education

No Intervention

Participants in the control group will continue with their usual academic education and will not receive any artificial intelligence (AI)-based research training during the study period. They will complete the same outcome assessments as the intervention group at baseline, immediately after the intervention period, and three months later.

After completion of the final follow-up assessment, participants in the control group will be given full access to the AI-powered research training course materials and recorded sessions to ensure ethical fairness and equal access to educational resources.

Outcomes

Primary Outcomes

Readiness to use artificial intelligence: Medical Artificial Intelligence Readiness Scale for Medical Students (MAIRS-MS)

Time Frame: baseline (T0, pre-intervention), immediately after course completion (T1), and three months after course completion (T2).

Readiness to use AI will be conceptualized as technical expertise, positive attitudes, and self-confidence in adopting AI tools for research and clinical tasks (29). It will be assessed using the Persian version of the Medical Artificial Intelligence Readiness Scale for Medical Students (MAIRS-MS), a validated 20-item, 4-domain tool (Cognition, Ability, Vision, Ethics) with 5-point Likert items (total score 20-100). Higher scores will indicate greater readiness. The instrument will have demonstrated acceptable reliability (Cronbach's α ≥ 0.80) and structural validity in prior Iranian studies (24,25). Domain and total scores will be calculated for all participants.

Secondary Outcomes

  • Research literacy: a researcher-developed Research Literacy Questionnaire(baseline (T0, pre-intervention), immediately after course completion (T1), and three months after course completion (T2).)
  • Attitude toward artificial intelligence: AI Attitude Scale (AIAS-4)(baseline (T0, pre-intervention), immediately after course completion (T1), and three months after course completion (T2).)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Sogand Sarmadi

Principal Investigator

Shahid Beheshti University of Medical Sciences

Similar Trials