Health BehaviorsNCT06785155
AI Chatbot-Based Learning on Dry Eye and Eye Strain Knowledge
A study testing Chatbot group and website assisted in people with Health Behaviors and Artificial Intelligence (AI), run by Gaziantep Islam Science and Technology University at 1 site in Turkey (Türkiye).
Trial summary
The aim of this project is to evaluate the effectiveness of using chatbots for patient education about dry eye disease. The study will examine how the chatbot affects patients' levels of information, managing symptoms, and overall satisfaction. Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Health Behaviors, Artificial Intelligence (AI), Chatbot
- What is being tested?
- Chatbot group and website assisted
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 63 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 4 Feb 2025to 4 Mar 2025
- Phase
- Interventional
- Are there results?
- None posted in the registry
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 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- to be actively enrolled in the nursing program
- to demonstrate baseline digital literacy.
Who cannot join
- diagnosed visual impairments,
- those with prior specialized ophthalmological training,
- individuals with limited digital technology proficiency
Trial locations and contacts
1 site in 1 country.
Turkey (Türkiye)1 site
Deparment of Nursing, Kilis 7 Aralık University
Kilis, Center, 79100
About this study
Official title: AI Chatbot-Based Learning on Dry Eye and Eye Strain Knowledge Among Nursing Students
The aim of this project is to evaluate the effectiveness of using chatbots for patient education about dry eye disease. The study will examine how the chatbot affects patients' levels of information, managing symptoms, and overall satisfaction.
- Conditions
- Health Behaviors, Artificial Intelligence (AI), Chatbot, Dry Eye, Eye Strain
- Being tested
- Chatbot group, website assisted
- Medical subject headings
- Health Behavior, Dry Eye Syndromes, Asthenopia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Chatbot groupOther
Participants explored the topics using the AI chatbot platform.
website assistedOther
Participants explored the topics using the website platform
| Study group | Role | What they receive |
|---|---|---|
| website group | Active comparator | Participants explored these topics using the website. Receives: Other: website assisted |
| Chatbot group | Experimental | Participants explored the topics using the AI chatbot platform Receives: Other: Chatbot group |
What is being measured
The primary outcome is the main question the study is designed to answer.
Dry Eye and eye strain knowledge questionnaire
Measured: From enrollment to the end of training at 4 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 Jan 2025
- Study start4 Feb 2025
- Primary completion4 Mar 2025
- Study completion4 Mar 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Health BehaviorsStudies of the same condition, open and under way.
- 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
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 63 participants (actual)
Sponsor and investigators
- Lead sponsor
- Gaziantep Islam Science and Technology University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, İbrahim Edhem Yılmaz, Gaziantep Islam Science and Technology University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06785155
- Sponsor's protocol ID
- GaziantepIslamSTU-01
- Status last verified
- Mar 2025
- First submitted
- 9 Jan 2025
- Last updated
- 5 Mar 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 5 Mar 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- AI Chatbot-Based Learning on Dry Eye and Eye Strain Knowledge Among Nursing Students
- ClinicalTrials.gov ID
- NCT06785155
- Acronym / sponsor ID
- GaziantepIslamSTU-01
- Conditions
- Health Behaviors, Artificial Intelligence (AI), Chatbot, Dry Eye, Eye Strain
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 63 participants (actual)
- Lead sponsor
- Gaziantep Islam Science and Technology UniversityUniversity, hospital or other
- Study start
- 4 Feb 2025 (actual)
- Primary completion
- 4 Mar 2025 (actual)
- Study completion
- 4 Mar 2025 (actual)
- First posted
- 21 Jan 2025 (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.
The aim of this project is to evaluate the effectiveness of using chatbots for patient education about dry eye disease. The study will examine how the chatbot affects patients' levels of information, managing symptoms, and overall satisfaction.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| website group | Active comparator | Other: website assistedParticipants explored these topics using the website. |
| Chatbot group | Experimental | Other: Chatbot groupParticipants explored the topics using the AI chatbot platform |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (2 listed)
- to be actively enrolled in the nursing program
- to demonstrate baseline digital literacy.
Key exclusion criteria (3 listed)
- diagnosed visual impairments,
- those with prior specialized ophthalmological training,
- individuals with limited digital technology proficiency
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 |
|---|---|---|
| Chatbot groupParticipants explored the topics using the AI chatbot platform. | Other | Chatbot group |
| website assistedParticipants explored the topics using the website platform | Other | website group |
Primary outcome
Dry Eye and eye strain knowledge questionnaire
Time frame: From enrollment to the end of training at 4 weeks
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 5 Mar 2025.
- Individual participant dataSharing planned: No
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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. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Chatbot group and website assisted in people with Health Behaviors and Artificial Intelligence (AI), run by Gaziantep Islam Science and Technology University at 1 site in Turkey (Türkiye).
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 2 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: finished, as of the sponsor's last update on 5 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
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?
Dry Eye and eye strain knowledge questionnaire (time frame: From enrollment to the end of training at 4 weeks). 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 5 Mar 2025.