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临床试验/NCT07325617
NCT07325617尚未招募不适用

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

Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital2 个研究点 分布在 1 个国家目标入组 400 人开始时间: 2026年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
400
试验地点
2
主要终点
Pre-visit Anxiety (VAS 0-10)

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Cross Sectional

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 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)

研究组 & 干预措施

AI/LLM users

Participants who report prior use of AI chat tools based on large language models (e.g., ChatGPT or similar) for health information before the outpatient urology visit, as assessed by the study questionnaire.

non AI/LLM users

Participants who report no prior use of AI/LLM chat tools (e.g., ChatGPT or similar) for health information before the outpatient urology visit, as assessed by the study questionnaire.

结局指标

主要结局

Pre-visit Anxiety (VAS 0-10)

时间窗: 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.

次要结局

  • Post-visit Anxiety (VAS 0-10)(Day 0 (immediately after the outpatient visit))
  • Visit Satisfaction (VAS 0-10)(Day 0 (immediately after the outpatient visit))
  • Disease Awareness/Understanding (VAS 0-10)(Day 0 (during the outpatient clinic visit))

研究者

发起方
Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Tuncel Uzel

Principal Investigator

Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital

研究点 (2)

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