ClinicalTrials.gg
CompletedNCT06785155Updated Mar 5, 2025

AI Chatbot-Based Learning on Dry Eye and Eye Strain Knowledge

An interventional study of Chatbot group and website assisted in Health Behaviors, Artificial Intelligence (AI) and Chatbot, sponsored by Gaziantep Islam Science and Technology University. Completed at 1 site in Turkey. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-03-05.

Sponsored by Gaziantep Islam Science and Technology University · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
63
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study 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.

02

Conditions studied

  • Health Behaviors
  • Artificial Intelligence (AI)
  • Chatbot
  • Dry Eye
  • Eye Strain
03

In context

Health Behavior

967 studies on the registry are indexed under Health Behavior; 165 are open to participants now.

This study's enrollment of 63 is below the median of 150 across 824 interventional studies indexed under Health Behavior.

Browse Health Behavior studies →

Lead sponsor

Gaziantep Islam Science and Technology University is the lead sponsor of 43 studies on the registry; 10 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • to be actively enrolled in the nursing program
  • to demonstrate baseline digital literacy.

Exclusion criteria

Exclusion Criteria:

  • diagnosed visual impairments,
  • those with prior specialized ophthalmological training,
  • individuals with limited digital technology proficiency
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
63 participants (actual)

Study arms

  • Active comparator
    website group

    Participants explored these topics using the website.

    Other: website assisted

  • Experimental
    Chatbot group

    Participants explored the topics using the AI chatbot platform

    Other: Chatbot group

Interventions

  • OtherChatbot group

    Participants explored the topics using the AI chatbot platform.

  • Otherwebsite assisted

    Participants explored the topics using the website platform

06

What researchers measure

Primary outcomes

  1. Dry Eye and eye strain knowledge questionnaire

    Time frame: From enrollment to the end of training at 4 weeks

07

Study locations

1 site
  • Deparment of Nursing, Kilis 7 Aralık University
    Kilis, Center 79100, Turkey
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 5, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06785155
Lead sponsor
Gaziantep Islam Science and Technology University
Responsible party
İbrahim Edhem Yılmaz (Assistant Professor, Gaziantep Islam Science and Technology University) — Principal investigator
First posted
Jan 21, 2025
Start date
Feb 4, 2025
Primary completion
Mar 4, 2025
Completion
Mar 4, 2025
Last update
Mar 5, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2025. You cannot join it, but the record below documents what was studied.

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