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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).

研究概览

详细说明

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.

研究类型

介入性

注册 (估计的)

100

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 孩子

接受健康志愿者

不

描述

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)

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:卫生服务研究
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的: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.
无干预: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.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Academic Achievement
大体时间: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)

次要结果测量

结果测量
措施说明
大体时间
Critical Thinking Disposition
大体时间: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)

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年9月1日

初级完成 (估计的)

2026年10月1日

研究完成 (估计的)

2027年1月1日

研究注册日期

首次提交

2026年8月4日

首先提交符合 QC 标准的

2026年8月8日

首次发布 (实际的)

2026年8月13日

研究记录更新

最后更新发布 (实际的)

2026年8月13日

上次提交的符合 QC 标准的更新

2026年8月8日

最后验证

2026年8月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

IPD 计划说明

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

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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