The University of Texas Health Science Center at Houston
Houston, Texas, 77030, United States
Location contact
Krislynn M Mueck, MD, MS, MPH
CONTACT
William D Rieger
CONTACT
NCT Number: NCT07222644
The purpose of this study is to refine and test existing enterprise-grade large language model (LLM) based on generative artificial intelligence (AI), to assess the feasibility and acceptability of LLM-based feedback, to assess the ability of LLM-based feedback to improve residents' communications,to explore the ability of standardized patients to assess residents' communication and to explore the ability of residents to self-assess their communication complexity
Trial opening soon.
Get Notified18 year–50 year
All sexes
Interventional
Not applicable
Houston, Texas, 77030, United States
Krislynn M Mueck, MD, MS, MPH
CONTACT
William D Rieger
CONTACT
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Participants will have their verbal communications with standardized patients (SP) regarding 3 different scenarios recorded, transcribed, and analyzed in real-time by the large language model (LLM) and will receive feedback as suggestions and alternative scripts. These will be reviewed by residents between SP scenarios
Time frame: end of intervention ( 1 hour after baseline)
This will be scored by the by Cohen's Kappa values from 1-5. Higher Cohen's kappa scores mean better outcome
Time frame: end of intervention ( 1 hour after baseline)
This will be scored by the by Cohen's Kappa values from 1-5. Higher Cohen's kappa scores mean better outcome
Time frame: end of intervention ( 1 hour after baseline)
This will be reported on a 5 point Likert scale form 1 very incorrect to 5 very correct
Time frame: end of intervention ( 1 hour after baseline)
This will be reported on a 5 point Likert scale form 1 very inapplicable to 5 very applicable
Time frame: end of intervention ( 1 hour after baseline)
This will be categorically reported in the following categories:
Elementary middle high college graduate
Time frame: end of intervention ( 1 hour after baseline)
This is scored from 1( very unconfident) to 5 (very confident)
Time frame: end of intervention ( 1 hour after baseline)
This is scored from 1( very useless) to 5 (very useful)
Time frame: end of intervention ( 1 hour after baseline)
This is scored from 1( very unlikely) to 5 (very likely)
Time frame: end of intervention ( 1 hour after baseline)
This is scored from 1( very unrealistic) to 5 (very realistic)
Time frame: end of intervention ( 1 hour after baseline)
Readability of resident-SP encounter transcripts will be assessed using the Flesch-Kincaid Grade Level formula, which estimates the U.S. school grade level required to understand the text. Higher scores indicate a higher reading grade level (i.e., lower readability).
Formula used:
Grade level= 0.39(total words/total sentences) + 11.8 (total syllables/total words)-15.59
Time frame: end of intervention ( 1 hour after baseline)
Percentage score based on a validated questionnaire This has 20 questions and each is scored from 1(yes), 0.5(partly), 0 (no) and question is removed if it does not apply.Scores are reported as a percentage and higher percentage score indicates better quality
Time frame: end of intervention ( 1 hour after baseline)
This will be categorically reported in the following categories:
Elementary middle high college graduate
Time frame: end of intervention ( 1 hour after baseline)
This is scored from 1( very unconfident) to 5 (very confident)
Contact information is provided by the study sponsor or research team.
Krislynn M Mueck, MD, MS, MPH
CONTACT
William D Rieger
CONTACT
The University of Texas Health Science Center, Houston
Other
Clinical Language Evaluation With AI for Residents (CLEAR2) - A Pilot Randomized Controlled Trial
Acronym: CLEAR2
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.