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Artifical IntelligenceNCT07909083

The Effect of Two Different Generative AI Tools on Nursing Students' Patient Counseling Skills and Motivation Regarding Instructional Materials

A study testing Interactive AI Avatar Simulation and Written AI Chatbot Simulation in people with Artifical Intelligence and Generative Artificial Intelligence, run by Manisa Celal Bayar University.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Official record
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Trial summary

The goal of this parallel-group randomized controlled trial is to compare the effects of two different generative artificial intelligence (AI) tools (a video/audio interactive AI avatar versus a written AI learning assistant (chatbot)) on patient counseling skills self-assessment levels and instructional materials… Read more about this study

Who is it for?
Any ageHealthy volunteers can take part
What is being tested?
Interactive AI Avatar Simulation and Written AI Chatbot Simulation
Could I receive a placebo?
No, everyone receives an active treatment
How many people
70 participants
Where
No sites listed yet
Study dates
15 Oct 2026to 31 Jan 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

  • Being enrolled as a 2nd-year undergraduate nursing student
  • Possessing appropriate technological equipment (e.g., smartphone, tablet, or personal computer) capable of accessing and running the study's generative artificial intelligence tools
  • Voluntarily agreeing to participate in the study

Who cannot join

  • Prior experience with the specific AI tools developed or utilized in this study
  • Concurrent participation in another research study involving AI-supported teaching or learning strategies
  • Requesting to withdraw from the study at any point during the intervention period

About this study

Official title: The Effect of Two Different Generative AI Tools on Nursing Students' Patient Counseling Skills and Motivation Regarding Instructional Materials: A Randomized Controlled Study

The goal of this parallel-group randomized controlled trial is to compare the effects of two different generative artificial intelligence (AI) tools (a video/audio interactive AI avatar versus a written AI learning assistant (chatbot)) on patient counseling skills self-assessment levels and instructional materials motivation in undergraduate nursing students.

The main questions it aims to answer are:

Read more
  • Is there a difference in health services counseling skills self-assessment scores between nursing students using an interactive AI avatar and those using a written AI chatbot?
  • Is there a difference in instructional materials motivation scores between nursing students using an interactive AI avatar and those using a written AI chatbot? Researchers will compare Intervention Group 1 (students interacting asynchronously with a video and audio interactive AI avatar) to Intervention Group 2 (students interacting asynchronously with a written AI chatbot) to see if the AI interaction channel (video/audio avatar vs. text chatbot) significantly impacts student counseling self-efficacy and learning motivation.

Participants will:

  • Complete baseline pre-test questionnaires, including a Demographic Information Form, the Generative Artificial Intelligence Usage and Competence Scale, and the Counseling Skills Self-Assessment Scale.
  • Conduct patient education and counseling practice over at least 2 to 3 asynchronous sessions using their assigned AI tool on a standardized clinical case scenario.
  • Complete post-intervention questionnaires, including the Counseling Skills Self-Assessment Scale, the Instructional Materials Motivation Scale, and an Application Feedback Form.
Being tested
Interactive AI Avatar Simulation, Written AI Chatbot Simulation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Interactive AI Avatar SimulationOther

    Students engage in virtual patient education and counseling simulation using a video/audio interactive AI avatar trained on a standardized nursing clinical case scenario. The simulation is completed asynchronously across at least 2 to 3 practice sessions. The intervention aims to develop students' health counseling self-efficacy and learning motivation.

  • Written AI Chatbot SimulationOther

    Students engage in virtual patient education and counseling simulation using a text-based AI chatbot trained on the same standardized nursing clinical case scenario and learning objectives. The simulation is completed asynchronously across at least 2 to 3 practice sessions. The intervention aims to develop students' health counseling self-efficacy and learning motivation.

Study groups in NCT07909083
Study groupRoleWhat they receive
Interactive AI Video Avatar GroupExperimentalNot described
Receives: Other: Interactive AI Avatar Simulation
Written AI Chatbot GroupExperimentalNot described
Receives: Other: Written AI Chatbot Simulation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in Counseling Skills Self-Assessment Score

    Evaluated using the Self-Assessment Scale for Counselling Skills in Health Services. The scale consists of 44 items rated on a 5-point Likert scale ranging from 1 ("Strongly Disagree") to 5 ("Strongly Agree"). It encompasses three subscales: Communication Skills (items 1-10), Professionalism (items 11-25), and Counseling Application Skills (items 26-44). Total scores range from 44 to 220, with higher scores reflecting higher self-assessed levels of counseling competence in healthcare services.

    Measured: Baseline (Pre-intervention) and Post-Intervention (upon completion of 2 to 3 asynchronous practice sessions, within a 15-week academic period)

  2. Instructional Materials Motivation Score

    Evaluated using the Instructional Materials Motivation Survey. The scale is a single-dimensional 14-item instrument scored on a 5-point Likert scale. Higher overall or mean scores indicate higher positive motivation toward the specific generative AI instructional tool utilized during the intervention.

    Measured: Post-Intervention (upon completion of 2 to 3 asynchronous practice sessions, within a 15-week academic period)

Secondary outcomes (1)
  1. User Application Feedback Score

    It is aimed to assess students' subjective evaluations, user experience, and overall satisfaction with the assigned AI instructional tool.

    Measured: Post-Intervention (upon completion of 2 to 3 asynchronous practice sessions, within a 15-week academic period)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Nov 2026
  2. Study start15 Oct 2026 (estimated)
  3. Primary completion31 Jan 2027 (estimated)
  4. Study completion31 Jan 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
70 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07909083
Sponsor's protocol ID
MCBU05.10.2026/20.478.486/4569
Status last verified
Oct 2026
First submitted
14 Oct 2026
Last updated
2 Nov 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Interactive AI Avatar Simulation and Written AI Chatbot Simulation in people with Artifical Intelligence and Generative Artificial Intelligence, run by Manisa Celal Bayar University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 2 Nov 2026. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Counseling Skills Self-Assessment Score (time frame: Baseline (Pre-intervention) and Post-Intervention (upon completion of 2 to 3 asynchronous practice sessions, within a 15-week academic period)). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Nov 2026.

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