- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06520852
The Effect of the Use of Artificial Intelligence in the Preparation of Patient Education Material
July 21, 2024 updated by: Sevda Korkut, TC Erciyes University
The Effect of the Use of Artificial Intelligence in the Preparation of Patient Education Material on the Comprehensibility, Actionability and Quality of the Material
This research was conducted to examine the effect of students' use of AI tools while preparing patient education material on the quality, understandability and actionability of the material in terms of content.
Students in the control group used auxiliary tools such as books, journals and websites while preparing patient education materials.
Students in the intervention group used AI tools in addition to tools such as books, journals, and websites.
Study Overview
Status
Completed
Conditions
Detailed Description
This research was conducted to examine the effect of students' use of AI tools while preparing patient education material on the quality, understandability and actionability of the material in terms of content.
Students in the control group used auxiliary tools such as books, journals and websites while preparing patient education materials.
Students in the intervention group used AI tools in addition to tools such as books, journals, and websites.
Patient Education Materials Assessment Tool and Global Quality Scale were used to evaluate the educational materials.
Study Type
Interventional
Enrollment (Actual)
180
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
-
-
Kayseri
-
Talas, Kayseri, Turkey, 0(553) 310 49 51
- Sevda Korkut
-
-
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
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- agreeing to participate in the study,
- taking the Fundamentals of Nursing II course for the first time,
- not working as a nurse in a hospital or any health institution.
Exclusion Criteria:
- not agreeing to participate in the study
- having prepared patient education materials before
- repeating the Fundamentals of Nursing II course
- not having internet access
- not having a computer or smartphone.
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: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention group
Group using artificial intelligence tools in addition to traditional tools in preparing educational materials
|
Students in the intervention group used AI tools in addition to tools such as books, journals, and websites.
Other Names:
|
|
No Intervention: Control group
Group using traditional tools in preparing educational materials
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Understandability of the material
Time Frame: After the students have completed the materials (5 days later)
|
Patient Education Materials Assessment Tool for Printable Materials: The tool consists of a total of 26 items, 19 items evaluating the understandability of the materials and 7 items evaluating their actionability.
PEMAT scores materials from 0 to 100 points for understandability and actionability.
|
After the students have completed the materials (5 days later)
|
|
Actionability of the material
Time Frame: After the students have completed the materials (5 days later)
|
Patient Education Materials Assessment Tool for Printable Materials: The tool consists of a total of 26 items, 19 items evaluating the understandability of the materials and 7 items evaluating their actionability.
PEMAT scores materials from 0 to 100 points for understandability and actionability.
|
After the students have completed the materials (5 days later)
|
|
Quality of the material
Time Frame: After the students have completed the materials (5 days later)
|
Global Quality Scale : According to this scale, the quality of the training materials was evaluated on a 5-point scale (1: poor quality, 2: low quality - limited use, 3: somewhat useful, 4: useful, 5: useful-excellent quality).
|
After the students have completed the materials (5 days later)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: SEVDA KORKUT, TC Erciyes University
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 5, 2024
Primary Completion (Actual)
May 31, 2024
Study Completion (Actual)
June 7, 2024
Study Registration Dates
First Submitted
July 21, 2024
First Submitted That Met QC Criteria
July 21, 2024
First Posted (Actual)
July 25, 2024
Study Record Updates
Last Update Posted (Actual)
July 25, 2024
Last Update Submitted That Met QC Criteria
July 21, 2024
Last Verified
July 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 2024-04/14
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
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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