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Impact of Generative AI on University Students' Learning Processes and Critical Thinking (AI-Critical)

2026年8月8日 更新者:Mahmut Coban、Ataturk University

An Experimental Investigation of the Effects of Generative Artificial Intelligence-Supported Learning on University Students' Academic Success, Learning Efficiency, and Critical Thinking Skills

This study is a randomized, controlled trial with a pre-test/post-test design, conducted to determine the effects of Generative AI (GenAI)-supported learning on academic achievement, learning efficiency, and critical thinking within a university setting. The study population consists of students from the Dialysis Program at Bingöl University's Vocational School of Health Services; the sample comprises 100 volunteer students who met the inclusion criteria and were randomly assigned to either an experimental group (n=50) or a control group (n=50). The experimental group will participate in a "Generative AI-Supported Learning Program" over the course of one month-meeting two days a week for a total of eight 60-minute sessions-covering topics ranging from effective prompting techniques to case analysis and academic ethics; meanwhile, the control group will continue with their routine educational activities. Data will be collected using a Demographic Information Form, the Academic Achievement Inventory, the Critical Thinking Disposition Scale, and the Artificial Intelligence Dependency Scale, and will be analyzed using biostatistical methods (t-tests, ANCOVA, and effect size calculations).

調査の概要

状態

まだ募集していません

介入・治療

詳細な説明

Study Design and Methodology Type of Study: This study will be conducted as a randomized experimental design with a pretest-posttest control group to determine the impact of generative artificial intelligence-assisted learning on university students' academic achievement, learning efficiency, and critical thinking skills.

Setting and Time of Study: The study will be carried out with students enrolled in the Dialysis Program at Bingöl University Vocational School of Health Services. It is planned to be completed within approximately one month following the receipt of institutional permissions and approval from the Ethics Committee.

Population and Sample: The population of the study will consist of students studying in the Dialysis Program at Bingöl University Vocational School of Health Services. The sample will comprise a total of 100 students who voluntarily agree to participate in the study. Participants will be divided into two equal groups-50 in the experimental group and 50 in the control group-using a computer-assisted simple random randomization method.

Data Collection Tools: Demographic Information Form: Developed by the researchers in line with the literature, this form will be used to determine the sociodemographic and educational characteristics of the students. It will consist of approximately 10-15 items covering age, gender, grade level, cumulative grade point average (CGPA), daily internet usage time, generative AI usage status, frequency of use, purpose of use, and prior AI training.

Academic Success Inventory for College Students (ASICS): Originally developed by Prevatt, Roberson, and Peterson (2011) as the Academic Success Inventory for College Students (ASICS) to evaluate university students' behaviors, efforts, and performance perceptions related to academic success. The Turkish adaptation, validity, and reliability study was conducted by Orçanlı, Bekmezci, and Boztoprak (2021). In the adaptation study, confirmatory factor analysis for the first-order multi-factor model demonstrated good fit indices . The overall Cronbach's alpha internal consistency coefficient was reported as 0.937, indicating high internal reliability. Higher scores on this Likert-type scale indicate higher levels of academic achievement.

Disposition Towards Critical Thinking Scale: Based on the "Disposition Towards Critical Thinking" model developed by Facione and Facione, this widely recognized international tool was adapted into Turkish by Hülya Ertaş Kılıç and Ahmet İlhan Şen. In the Turkish validity and reliability study, the five-factor structure (Analysis, Open-Mindedness, Inquisitiveness, Systematization, Cognitive Maturity/Self-Confidence) showed good fit indices, and the overall Cronbach's alpha coefficient ranged between 0.85 and 0.95. Responses are recorded on a 5-point Likert scale (1 = "Strongly Disagree" to 5 = "Strongly Agree"), where higher overall scores indicate a greater disposition toward critical thinking.

Dependence on Artificial Intelligence Scale: Developed globally by Morales-García et al. (2024) as the Dependence on Artificial Intelligence Scale to measure AI addiction behaviors among college students, its Turkish adaptation was performed by Buğra Çağatay Savaş (2024). Confirmatory factor analysis for the single-factor structure revealed excellent fit indices and an overall Cronbach's alpha internal consistency coefficient of 0.937. The Likert-type scale will be administered as a pretest and posttest in both groups to evaluate changes in students' AI dependence levels resulting from generative AI-assisted learning applications.

Study Implementation After obtaining written informed consent from participating students, randomization into experimental and control groups will be performed. At baseline, both groups will complete:Demographic Information FormAcademic Achievement Assessment ToolsMotivated Strategies for Learning Questionnaire (MSLQ)California Critical Thinking Disposition Inventory (CCTDI) / Disposition Towards Critical Thinking Scale.

The experimental group will undergo a Generative AI-Assisted Learning Program developed by the researchers.

Duration: 1 month Frequency: 2 days per week (Total of 8 sessions) Session Length: Approximately 60 minutes each Intervention Materials: Educational booklets, instructor presentations, implementation guides, prompt engineering handbooks, worksheets, and infographics.

Session Outline:

Session 1: Introduction to Generative AI Technologies Session 2: Effective Prompt Engineering Techniques Session 3: AI-Assisted Study Methods Session 4: Content Summarization and Knowledge Organization Session 5: Question Generation and Exam Preparation with AI Session 6: Case Analysis and Clinical Problem-Solving Applications Session 7: Critical Evaluation of AI Outputs and Academic Integrity Session 8: Practical Synthesis, Overall Evaluation, and Feedback Students in the control group will continue their standard curriculum without receiving any educational intervention. Upon completing the one-month period, all posttests will be re-administered to both groups.

Data Analysis:Data will be analyzed using IBM SPSS Statistics software with support from a biostatistics consultant. Initial procedures will include data cleaning, missing value checks, outlier analysis, data coding, and assessing suitability for parametric testing.Statistical Methods to be Applied:Descriptive Statistics: Mean, standard deviation, median, minimum-maximum, frequencies, and percentages.Normality & Homogeneity Tests: Shapiro-Wilk test and Levene's test for equality of variances.Comparative Inferential Tests: Chi-square test, Independent Samples t-test, Paired Samples t-test, Mann-Whitney U test, and Wilcoxon Signed-Rank test.Advanced & Covariate Analysis: Analysis of Covariance (ANCOVA) for repeated measures and multiple linear regression models if indicated.Effect Size & Reliability: Cohen's d, Partial Eta Squared , and Cronbach's alpha internal consistency analysis.All statistical tables, figures, and reporting will strictly follow scientific publication standards. The threshold for statistical significance will be set at p < 0.05.

研究の種類

介入

入学 (推定)

100

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 子

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  • Being an active undergraduate student enrolled in the university program/course during the study period
  • Willingness to voluntarily participate in the study and providing written informed consent
  • Having regular access to a digital device (e.g., smartphone, laptop, tablet) and an internet connection
  • Basic digital literacy to use educational software and AI tools
  • Agreeing to complete all course activities, pre-tests, and post-test

Exclusion Criteria:

  • Prior formal or advanced training in generative AI tools (e.g., prompt engineering certification)
  • Transfer students or students repeating the course who have prior experience with the course material
  • Having cognitive, visual, or physical impairments that prevent participation in online learning or completing evaluation surveys
  • Unwillingness to participate in the study or withdrawing consent at any stage
  • Missing more than 20% of the course sessions or failing to complete the outcome assessment tools (pre-test/post-test)

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:ヘルスサービス研究
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Generative AI-Supported Education
Participants in the intervention group will receive a 4-week generative artificial intelligence (GenAI)-supported educational program integrated into the course curriculum. Students will use generative AI tools, such as ChatGPT, to support learning course content, develop study materials, solve subject-specific problems, access information, and enhance critical thinking skills under structured guidance and educational instructions provided by the researchers. The intervention will be delivered in 8 sessions over 4 weeks, with two sessions per week.
Participants in the intervention group will receive a 4-week generative artificial intelligence (GenAI)-supported educational program integrated into the course curriculum. Students will use generative AI tools, such as ChatGPT, to support learning course content, develop study materials, solve subject-specific problems, access information, and enhance critical thinking skills under structured guidance and educational instructions provided by the researchers. The intervention will be delivered in 8 sessions over 4 weeks, with two sessions per week.
介入なし:Standard Education
Participants in the control group will continue to receive the standard/traditional educational program for 4 weeks. No study-specific training, guidance, or structured intervention regarding the use of generative artificial intelligence tools will be provided. The course content, curriculum, educational duration, and assessment methods will be the same as those of the intervention group; however, generative AI-supported learning activities will not be implemented.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Academic Achievement
時間枠:Baseline (Week 0) and immediately after the intervention (Week 4)
Academic success will be assessed using the Academic Success Inventory for College Students (ASICS), developed by Prevatt et al. (2011) and adapted into Turkish by Orçanlı, Bekmezci, and Boztoprak (2021). The Turkish version consists of 46 items across 9 dimensions. Items are rated on a 7-point Likert scale ranging from 1 (Strongly Disagree) to 7 (Strongly Agree). Seventeen negatively worded items are reverse scored. The total score ranges from 46 to 322, and the unit of measurement is points. Higher scores indicate a higher level of academic success orientation and academic functioning.
Baseline (Week 0) and immediately after the intervention (Week 4)

二次結果の測定

結果測定
メジャーの説明
時間枠
Critical Thinking Disposition
時間枠:Baseline (Week 0) and immediately after the intervention (Week 4)
Critical thinking disposition will be assessed using the University of Florida Engagement, Maturity, and Innovativeness Critical Thinking Disposition Instrument (UF/EMI), developed by Irani et al. (2007) and adapted into Turkish by Ertaş Kılıç and Şen (2014). The Turkish version consists of 25 items across 3 dimensions: Engagement (11 items), Cognitive Maturity (7 items), and Innovativeness (7 items). Items are rated on a 5-point Likert scale ranging from 1 (Strongly Disagree) to 5 (Strongly Agree). There are no reverse-scored items. The total score ranges from 25 to 125, and the unit of measurement is points. Higher scores indicate a stronger critical thinking disposition.
Baseline (Week 0) and immediately after the intervention (Week 4)

協力者と研究者

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協力者

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年9月1日

一次修了 (推定)

2026年10月1日

研究の完了 (推定)

2027年1月1日

試験登録日

最初に提出

2026年8月4日

QC基準を満たした最初の提出物

2026年8月8日

最初の投稿 (実際)

2026年8月13日

学習記録の更新

投稿された最後の更新 (実際)

2026年8月13日

QC基準を満たした最後の更新が送信されました

2026年8月8日

最終確認日

2026年8月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

IPD プランの説明

Individual participant data will not be shared in order to protect participant confidentiality and privacy, as explicit consent for open data sharing was not obtained from the participants in accordance with institutional ethics board approval and data protection regulations

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米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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