- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06108037
DHL Survey on Generative AI for MyChart Messaging
Duke Health Listens Survey on Generative Artificial Intelligence (AI) for MyChart Messaging
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
- The investigators will create short surveys online to ask patients how they feel about using computer programs that create messages in their medical records.
- The surveys will show fictional situations where patients ask questions and get answers from either real people or computer programs, with or without a disclosure about how the response was written.
- The investigators will ask the people taking the survey to share what they think about these situations using tools like rating scales, comparison scales, or written responses.
- If patients want to, they can provide their contact information to be part of future discussion groups. Participants do not have to give any personal information to complete the survey.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
North Carolina
-
Durham, North Carolina, United States, 27710
- Duke University Health System
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Member of the Duke Health Listens patient advocacy community
Exclusion Criteria:
- Age < 18
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Arm A
Each arm will receive 3 clinical scenarios spaced over time across 3 Sends. The 6 groups (Arms A-F) will be arranged with naming conventions as such:
Arm A receives AHN in Send 1, BAIC in Send 2, and CHH in Send 3 |
We will use a large language model such as GPT 3.5 to automatically generate responses to fictional messages to a physician.
We will disclose whether the message was generated using this technology or not.
There are 3 clinical scenarios and 6 pairs of human/AI response and human disclosure/AI disclosure/not disclosed that will test patient attitudes toward this technology.
|
|
Other: Arm B
Each arm will receive 3 clinical scenarios spaced over time across 3 Sends. The 6 groups (Arms A-F) will be arranged with naming conventions as such:
Arm B receives BHC in Send 1, CAIH in Send 2, and AAIN in Send 3 |
We will use a large language model such as GPT 3.5 to automatically generate responses to fictional messages to a physician.
We will disclose whether the message was generated using this technology or not.
There are 3 clinical scenarios and 6 pairs of human/AI response and human disclosure/AI disclosure/not disclosed that will test patient attitudes toward this technology.
|
|
Other: Arm C
Each arm will receive 3 clinical scenarios spaced over time across 3 Sends. The 6 groups (Arms A-F) will be arranged with naming conventions as such:
Arm C receives CHC in Send 1, AHH in Send 2, and BAIN in Send 3 |
We will use a large language model such as GPT 3.5 to automatically generate responses to fictional messages to a physician.
We will disclose whether the message was generated using this technology or not.
There are 3 clinical scenarios and 6 pairs of human/AI response and human disclosure/AI disclosure/not disclosed that will test patient attitudes toward this technology.
|
|
Other: Arm D
Each arm will receive 3 clinical scenarios spaced over time across 3 Sends. The 6 groups (Arms A-F) will be arranged with naming conventions as such:
Arm D receives AAIH in Send 1, BHN in Send 2, and CAIC in Send 3 |
We will use a large language model such as GPT 3.5 to automatically generate responses to fictional messages to a physician.
We will disclose whether the message was generated using this technology or not.
There are 3 clinical scenarios and 6 pairs of human/AI response and human disclosure/AI disclosure/not disclosed that will test patient attitudes toward this technology.
|
|
Other: Arm E
Each arm will receive 3 clinical scenarios spaced over time across 3 Sends. The 6 groups (Arms A-F) will be arranged with naming conventions as such:
Arm E receives BAIH in Send 1, CHN in Send 2, and AHC in Send 3 |
We will use a large language model such as GPT 3.5 to automatically generate responses to fictional messages to a physician.
We will disclose whether the message was generated using this technology or not.
There are 3 clinical scenarios and 6 pairs of human/AI response and human disclosure/AI disclosure/not disclosed that will test patient attitudes toward this technology.
|
|
Other: Arm F
Each arm will receive 3 clinical scenarios spaced over time across 3 Sends. The 6 groups (Arms A-F) will be arranged with naming conventions as such:
Arm F receives CAIN in Send 1, AAIC in Send 2, and BHH in Send 3 |
We will use a large language model such as GPT 3.5 to automatically generate responses to fictional messages to a physician.
We will disclose whether the message was generated using this technology or not.
There are 3 clinical scenarios and 6 pairs of human/AI response and human disclosure/AI disclosure/not disclosed that will test patient attitudes toward this technology.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Patient satisfaction, as measured by survey
Time Frame: Up to 2 weeks
|
Likert-scale responses to satisfaction question: "I am satisfied with this interaction", on a scale from 1-5 with answer options of Strongly Disagree (1), Disagree (2), Neither agree nor disagree (3), Agree (4), and Strongly agree (5).
|
Up to 2 weeks
|
|
Patient attitudes towards utility, as measured by survey
Time Frame: Up to 2 weeks
|
Likert-scale responses to utility question: "The information is useful", on a scale from 1-5 with answer options of Strongly Disagree (1), Disagree (2), Neither agree nor disagree (3), Agree (4), and Strongly agree (5).
|
Up to 2 weeks
|
|
Patient empathy, as measured by survey
Time Frame: Up to 2 weeks
|
Likert-scale responses to empathy question: "I feel cared for during this interaction", on a scale from 1-5 with answer options of Strongly Disagree (1), Disagree (2), Neither agree nor disagree (3), Agree (4), and Strongly agree (5).
|
Up to 2 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Anand Chowdhury, MD, MMCi, Duke University
Publications and helpful links
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 (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- Pro00113587
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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