- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06785155
AI Chatbot-Based Learning on Dry Eye and Eye Strain Knowledge
March 4, 2025 updated by: İbrahim Edhem Yılmaz, Gaziantep Islam Science and Technology University
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.
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
63
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Center
-
Kilis, Center, Turkey, 79100
- Deparment of Nursing, Kilis 7 Aralık University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- to be actively enrolled in the nursing program
- to demonstrate baseline digital literacy.
Exclusion Criteria:
- diagnosed visual impairments,
- those with prior specialized ophthalmological training,
- individuals with limited digital technology proficiency
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: website group
Participants explored these topics using the website.
|
Participants explored the topics using the website platform
|
|
Experimental: Chatbot group
Participants explored the topics using the AI chatbot platform
|
Participants explored the topics using the AI chatbot platform.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Dry Eye and eye strain knowledge questionnaire
Time Frame: From enrollment to the end of training at 4 weeks
|
From enrollment to the end of training at 4 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 4, 2025
Primary Completion (Actual)
March 4, 2025
Study Completion (Actual)
March 4, 2025
Study Registration Dates
First Submitted
January 9, 2025
First Submitted That Met QC Criteria
January 17, 2025
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
March 4, 2025
Last Verified
March 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- GaziantepIslamSTU-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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