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Tracking AI/LLM Literacy and Knowledge in Urology Outpatients (TALK-U)

The TALK-U Study: Tracking AI/LLM Knowledge and Use in Urology Outpatients and Its Association With Anxiety, Satisfaction, and Health Awareness-A Cross-Sectional Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07325617
Acronym
TALK-U
Enrollment
400
Registered
2026-01-08
Start date
2026-01-01
Completion date
2026-03-01
Last updated
2026-01-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Health Information Seeking Behavior

Keywords

Artificial intelligence, Anxiety, ChatGPT, Gemini, Health information seeking, Large language model (LLM), Patient satisfaction

Brief summary

This study is a one-time, questionnaire-based survey of adults attending a urology outpatient clinic. The investigators will examine whether patients who use AI chat tools based on large language models (LLMs), such as ChatGPT, before seeking care differ from non-users in (1) anxiety, (2) satisfaction with the clinic visit, and (3) awareness/understanding of their health condition. Participants who provide written informed consent will complete a brief survey during their clinic visit (about 5-7 minutes). The survey includes a standardized anxiety scale (GAD-7), visual analog scales (0-10) for anxiety before and after the visit, satisfaction, and disease awareness, as well as questions about AI/LLM knowledge and use. Treating clinicians will not have access to participants' survey responses, and participation will not affect clinical care.

Detailed description

The TALK-U study is a cross-sectional, observational survey conducted in the urology outpatient clinic of Dr. Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital. The primary exposure is self-reported AI/LLM knowledge and use for health information (e.g., whether participants have used ChatGPT or similar tools, frequency, awareness of AI, and purpose of use). The primary outcome is anxiety measured by GAD-7 at the time of the clinic encounter. Secondary outcomes include (i) anxiety assessed on a 0-10 visual analog scale before and after the visit, (ii) outpatient visit satisfaction (0-10 VAS), and (iii) perceived disease awareness/understanding (0-10 VAS). Eligible adult first-time urology outpatients who can complete the survey independently and provide informed consent will be invited during a 2-month recruitment period. Analyses will compare outcomes between AI/LLM users and non-users and explore associations with age group (\<40, 40-60, \>60), education level, and urology subspecialty category. Data will be analyzed using appropriate parametric/nonparametric tests depending on distribution, with p \< 0.05 considered statistically significant.

Interventions

None listed

Sponsors

Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age 18 years or older * First-time visit to the Urology Outpatient Clinic * Able to read and write and complete the questionnaire independently * Able to provide written informed consent

Exclusion criteria

* Age under 18 years * Insufficient literacy to understand and complete the questionnaire * Severe hearing or visual impairment, or a neurological/psychiatric condition that prevents understanding and completing the survey * Refusal or inability to provide informed consent * Currently under follow-up for a known urologic condition (i.e., not a first-time urology outpatient visit)

Design outcomes

Primary

MeasureTime frameDescription
Pre-visit Anxiety (VAS 0-10)Day 0 (immediately before the outpatient visit)Self-rated anxiety on a 0-10 visual analog scale (VAS), where 0 indicates no anxiety and 10 indicates the highest possible anxiety. This measure reflects visit-related state anxiety prior to clinician encounter.

Secondary

MeasureTime frameDescription
Post-visit Anxiety (VAS 0-10)Day 0 (immediately after the outpatient visit)Self-rated anxiety on a 0-10 VAS (0 = none, 10 = highest).
Visit Satisfaction (VAS 0-10)Day 0 (immediately after the outpatient visit)Self-rated satisfaction with the outpatient visit on a 0-10 VAS (0 = not satisfied at all, 10 = maximum satisfaction).
Disease Awareness/Understanding (VAS 0-10)Day 0 (during the outpatient clinic visit)Self-rated awareness/understanding of one's condition on a 0-10 VAS (0 = none, 10 = complete).

Other

MeasureTime frameDescription
Baseline General Anxiety Symptoms (GAD-7 Total Score)Day 0 (at enrollment; prior to or during the clinic visit)Total score on the 7-item GAD-7 questionnaire (range 0-21; higher scores indicate greater generalized anxiety symptoms). This measure will be used to account for baseline anxiety (trait-like symptoms) and to adjust analyses of VAS-based state anxiety out

Countries

Turkey (Türkiye)

Contacts

Primary ContactTuncel Uzel, MD
tunceluzelmd@gmail.com+90 312 336 09 09
Backup ContactMehmet Duvarcı, MD
mehmet_duvarci@hotmail.com+90 312 336 09 09

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026