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OpenTrials
Active, Not Recruiting

NCT Number: NCT07684651

Artificial Intelligence Chatbots as an Educational Tool for Statistical Analysis Among Dental Students

The goal of this randomized crossover trial is to learn if ChatGPT-5.2 is usable and effective as a supplementary educational tool for teaching statistical data analysis to fifth-year undergraduate dental students. The study will also compare ChatGPT-5.2 with conventional statistical tools, such as Microsoft Excel and online statistical calculators.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Age range

21 year–25 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Faculty of Dentistry, Alexandria University

Alexandria, Egypt

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Fifth-year undergraduate dental students enrolled at the Faculty of Dentistry, Alexandria University, Egypt.
  • Students officially registered in the Research Project course (211082502) during the Spring 2026 semester.
  • Provided written informed consent and agreed to participate voluntarily in the study.

Exclusion criteria

  • Postgraduate students and undergraduate students not enrolled in the fifth year of the dental program, Faculty of Dentistry, Alexandria University, Egypt.
  • Students not registered in the Research Project course during the Spring 2026 semester.
  • Students who decline to provide written informed consent to participate in the study

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Treatment and study plan

ChatGPT 5.2

Other

ChatGPT 5.2 will be used for solving the statistical analysis assignment

Conventional methods

Other

Microsoft excel and online calculators will be used to solve the statistical analysis assignment

Primary outcomes

  1. The efficacy of technological tools for completing the statistical analysis assignments.

    Time frame: 21 days

    Efficacy will be evaluated by comparing participants' performance scores across the two tools (AI-ChatGPT-5.2 and conventional tools). Scores will be calculated as the percentage of correct answers in the two assignments.

    Score = (Number of correct answers)/(total number of questions)×100

  2. The usability of the technological tools for completing the statistical analysis assignments

    Time frame: 21 days

    Usability is defined as "the extent to which a product can be used by specified users to achieve specific goals with effectiveness, efficiency, and satisfaction in a specified context of use. it will be assessed using system usability questionnaire(SUS), SUS yields a single number representing a composite measure of the overall usability of the system being studied. Note that scores for individual items are not meaningful on their own.

    To calculate the SUS score, first sum the score contributions from each item. Each item's score contribution will range from 0 to 4. For items 1,3,5,7,and 9 the score contribution is the scale position minus 1. For items 2,4,6,8 and 10, the contribution is 5 minus the scale position. Multiply the sum of the scores by 2.5 to obtain the overall value of SU.

    SUS scores have a range of 0 to 100.

Sponsors and collaborators

Lead sponsor

Rowan Elshabrawy

Other

Registry information

Official study title

Usability and Efficacy of Artificial Intelligence Chatbots as an Educational Aid for Statistical Data Analysis Among Dental Students: A Randomized Crossover Trial

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jul 6, 2026
Registry last updated
Jul 6, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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