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RECRUITING Not applicable ClinicalTrials.gov

Human Voice vs AI-Cloned Voice Audio Added to Written Consent Before Ureteroscopy or Retrograde Intrarenal Surgery (AUDIO-CONSENT)

Sponsor: Aydin Adnan Menderes University • ClinicalTrials.gov ID: NCT07859436

Registry updated: 2026-10-07
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Description

Before kidney stone surgery with a flexible or semirigid ureteroscope, patients must read and sign a written consent form, but many patients find these forms long and hard to understand. This study tests whether listening to an audio recording of the same consent form, in addition to the usual written form and the surgeon's explanation, helps patients understand the operation better. It also asks whether it matters if the recording is read by a real urologist or produced by artificial intelligence (AI) from a clone of that same urologist's voice. Adults scheduled for their first ureteroscopy or retrograde intrarenal surgery at three hospitals in Turkey will be randomly assigned to one of three groups: (A) standard written consent only, (B) standard consent plus an audio recording read by a urologist, or (C) standard consent plus the same text produced by an AI-cloned version of the same urologist's voice. All three groups receive exactly the same information, word for word; only the way it is delivered differs. Patients in group C are told that the voice was produced by AI. The main outcome is a 10-question knowledge test on the content of the consent form, taken immediately after the consent process. Anxiety (State-Trait Anxiety Inventory) and satisfaction are also measured on the same day. No forms are completed on the day of surgery.

Interventions

  • Standard written informed consent (Other)
    The institution's unified written informed consent form for ureteroscopy and retrograde intrarenal surgery, read and signed by the patient, together with the physician's usual verbal explanation. Delivered identically in all three arms.
  • Human-voice audio consent recording (Behavioral)
    An approximately 12-minute audio recording of the complete consent text, read word for word by one urologist (the same recording at all centers; not the patient's own surgeon). Presented after the standard written consent and physician explanation, on a tablet with headphones in the patient's room without companions; the patient may replay it and the number of replays is recorded. Loudness-normalized to -24 LUFS. Introduced to the patient as "a recording of the entire consent form read by a urologist".
  • AI-cloned-voice audio consent recording (Behavioral)
    The same consent text, generated once with Resemble.ai from a voice clone of the same urologist (reference sample: a separate recording of at least 5 minutes of a different text), frozen before enrollment with no live AI calls. Duration approximately 12 minutes; loudness-matched (-24 LUFS), codec and delivery identical to the human-voice recording, presented after the standard written consent and physician explanation, on a tablet with headphones; replay allowed and counted. Patients are informed that the voice was generated with AI from a urologist's voice.

Eligibility criteria

Inclusion Criteria: * Age 18 years or older * Scheduled for elective ureteroscopy (URS) or retrograde intrarenal surgery (RIRS) * Able to read, understand and communicate verbally in Turkish * Provides written informed consent to participate in the study Exclusion Criteria: * Hearing or visual impairment preventing use of the study materials * Confusion, dementia, psychosis or any other condition affecting capacity to consent * Emergency surgery * Previous URS or RIRS * Current psychiatric treatment or use of anxiolytics * Health-care professional

Conditions

Urolithiasis Kidney Calculi Ureteral Calculi Informed Consent

Locations

  • Aydin Adnan Menderes University, Department of Urology — Aydin, Aydın, Turkey (Türkiye)
  • Aydin City Hospital, Department of Urology — Aydin, Aydın, Turkey (Türkiye)
  • Kutahya Health Sciences University, Department of Urology — Kütahya, Kütahya, Turkey (Türkiye)
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Official Source

Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

View Official Record