- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06711458
Using Generative Artificial Intelligence (AI) to Create Patient-Friendly Discharge Summaries
Using Generative Artificial Intelligence to Transform Discharge Summaries Into Patient-Friendly Language and Format
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
New York
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New York, New York, United States, 10016
- NYU Langone Health
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Admitted to Inpatient Medicine unit at NYULH
- Able to read and understand English
- Willing and able to consent to this research
Exclusion Criteria:
- Inpatient Hospice
- Discharged on home hospice
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Generative AI Discharge Instructions
At the time of discharge, patients will receive patient-friendly discharge instructions generated by GPT-4, an advanced natural language processing model, with the aim of enhancing patient readability and understandability in the discharge information.
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Patient-friendly hospital discharge instructions generated by GPT-4, an advanced natural language processing model.
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Active Comparator: Standard of Care Discharge Instructions
At the time of discharge, patients will receive standard discharge instructions (i.e., not generated by GPT-4).
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Standard hospital discharge instructions.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of Summaries with Positive Outcome on Composite Measure of Readability and Understandability
Time Frame: Day 1 (At Discharge)
|
This is a composite outcome measure. Readability of discharge summaries will be measured using the Flesch-Kincaid Grade Level assessment, which measures how challenging a text may be for readers. Scores on the Flesch-Kincaid assessment are rated as follows: 0-3: Basic reading level, (kindergarten or elementary school) 3-6: Basic reading level, (elementary school ) 6-9: Average reading level, (middle school) 9-12: Average reading level, (high school) 11-18: Skilled readers. Understandability will be evaluated by the presence of simplified description of primary diagnosis and hospital intervention. Summaries with both 1) presence of simplified description of primary diagnosis and hospital intervention, and 2) a Flesch-Kincaid grade level greater than or equal to 6 and less than 8, will be considered to have a "positive outcome." |
Day 1 (At Discharge)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes made to AI-Generated Content
Time Frame: Day 1 (At Discharge)
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Changes made to content will be assessed using edit distance.
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Day 1 (At Discharge)
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AI-Generated Content Perception Survey: Safety
Time Frame: Day 1 (At Discharge)
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Patients will be given a survey in which they are asked whether they feel safe with the discharge instructions they were provided.
The total score is the number of participants who respond "Yes, definitely" or "Yes, somewhat" to the question.
|
Day 1 (At Discharge)
|
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AI-Generated Content Perception Survey: Understandability
Time Frame: Day 1 (At Discharge)
|
Patients will be given a survey in which they are asked whether the instructions were easy to understand.
The total score is the number of participants who respond "Yes, definitely" or "Yes, somewhat" to the question.
|
Day 1 (At Discharge)
|
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AI-Generated Content Perception Survey: Empathy
Time Frame: Day 1 (At Discharge)
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Patients will be given a survey in which they are asked whether the instructions were written in an empathetic manner.
The total score is the number of participants who respond "Yes, definitely" or "Yes, somewhat" to the question.
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Day 1 (At Discharge)
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Jonah Zaretsky, NYU Langone Health
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 23-01544
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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