EducationAI-CriticalNCT07762261
Impact of Generative AI on University Students' Learning Processes and Critical Thinking
A study testing Behavioral in people with Education and Academic Performance, run by Ataturk University.
Trial summary
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. Read more about this study
- Who is it for?
- Ages 18 to 25 months
- Conditions the study is for
- Education, Academic Performance, Learning Efficiency
- What is being tested?
- Behavioral
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 100 participants
- Where
- No sites listed yet
- Study dates
- 1 Nov 2026to 1 Mar 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 18 to 25 months
- All sexes
- No healthy volunteers
- Child
Who may be able to join
- 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
Who cannot join
- 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)
Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
About this study
Official title: 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).
Read the detailed description
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.
- Being tested
- Behavioral
- Keywords
- Generative Artificial Intelligence, Artificial Intelligence in Education, Academic Success, Learning Efficiency, Critical Thinking
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
BehavioralBehavioural
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.
| Study group | Role | What they receive |
|---|---|---|
| Generative AI-Supported Education | Experimental | 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. Receives: Behavioral: Behavioral |
| Standard Education | No intervention | 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. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Academic Achievement
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.
Measured: Baseline (Week 0) and immediately after the intervention (Week 4)
Secondary outcomes (1)
Critical Thinking Disposition
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.
Measured: Baseline (Week 0) and immediately after the intervention (Week 4)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted13 Aug 2026
- Study start1 Nov 2026 (estimated)
- Primary completion1 Dec 2026 (estimated)
- Study completion1 Mar 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for EducationStudies of the same condition, open and under way.
- More trials run by Ataturk UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Health services research
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- This study employs a two-arm, parallel-group, pretest-posttest experimental (or quasi-experimental) design. Participants are assigned to either the Intervention Group (Generative AI-assisted learning approach) or the Control Group (traditional/standard learning methods). Outcomes, including academic achievement, learning efficiency, and critical thinking skills, are measured before and immediately after the educational intervention
- Masking
- None (open label)
- Enrolment
- 100 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Ataturk University
- Sponsor type
- University, hospital or other
- Collaborators
- Bingol University
- Responsible party
- Principal investigator, Mahmut Coban, Bingol University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07762261
- Sponsor's protocol ID
- 2026/06-12
- Acronym
- AI-Critical
- Status last verified
- Oct 2026
- First submitted
- 4 Aug 2026
- Last updated
- 28 Oct 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: 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
Study at a glance
From the registry record, last updated by the sponsor on 28 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- An Experimental Investigation of the Effects of Generative Artificial Intelligence-Supported Learning on University Students' Academic Success, Learning Efficiency, and Critical Thinking Skills
- ClinicalTrials.gov ID
- NCT07762261
- Acronym / sponsor ID
- AI-Critical / 2026/06-12
- Keywords
- Generative Artificial Intelligence, Artificial Intelligence in Education, Academic Success, Learning Efficiency, Critical Thinking
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 100 participants (estimated)
- Lead sponsor
- Ataturk UniversityUniversity, hospital or other
- Collaborators
- Bingol University
- Study start
- 1 Nov 2026 (estimated)
- Primary completion
- 1 Dec 2026 (estimated)
- Study completion
- 1 Mar 2027 (estimated)
- First posted
- 13 Aug 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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).
Detailed description
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.
Study design
- Primary purpose
- Health services research
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- This study employs a two-arm, parallel-group, pretest-posttest experimental (or quasi-experimental) design. Participants are assigned to either the Intervention Group (Generative AI-assisted learning approach) or the Control Group (traditional/standard learning methods). Outcomes, including academic achievement, learning efficiency, and critical thinking skills, are measured before and immediately after the educational intervention
| Arm | Type | Receives |
|---|---|---|
| Generative AI-Supported Education | Experimental | Behavioral: BehavioralParticipants 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. |
| Standard Education | No intervention | –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. |
Who may qualify
- Ages
- 18 to 25 months
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (5 listed)
- 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
Key exclusion criteria (5 listed)
- 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)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| BehavioralParticipants 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. | Behavioural | Generative AI-Supported Education |
Primary outcome
Academic Achievement
Time frame: 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.
1 secondary outcome
Critical Thinking Disposition
Time frame: Baseline (Week 0) and immediately after the intervention (Week 4)
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 28 Oct 2026.
- Individual participant dataSharing planned: No. 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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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Questions about this trial
What is this clinical trial studying?
A study testing Behavioral in people with Education and Academic Performance, run by Ataturk 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 5 inclusion and 5 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 28 Oct 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?
Contact Mahmut Çoban, phd (+905387022343, mahmutcoban@bingol.edu.tr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Academic Achievement (time frame: Baseline (Week 0) and immediately after the intervention (Week 4)). 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 28 Oct 2026.