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Enrolling by invitation NCT07217366

Speech-to-text Tool for Heart Failure Patient-Reported Data

No phase Interventional Heart Failure

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Artificial intelligence speech-to-text tool.
Who it may be relevant to
Registry conditions: Heart Failure. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Testing a Speech-to-text Tool for Heart Failure Patient-Reported Data

Overview

The goal of this study is to see whether this type of Artificial Intelligence (AI) Voice Assistant can reliably capture patient-reported health information to support communication between patients and their healthcare team.

Interventions

  • Other Artificial intelligence speech-to-text tool
    Pilot testing of speech-to-text tool using artificial intelligence

Primary outcome measures

  • Accuracy of AI Voice Assistant Compared With Expert Extraction [Time frame: ~3 months]
Secondary outcome measures (4)
  • Usability of AI Voice Assistant [Time frame: ~3 months]
  • Agreement between AI Voice Assistant Compared With Patient Self-Reported Written Responses [Time frame: ~3 months]
  • Kansas City Cardiomyopathy Questionnaire Scores [Time frame: ~3 months]
  • Qualitative Feedback [Time frame: ~3 months]

Eligibility criteria

Inclusion criteria

  • Adults with heart failure receiving cardiology care at Stanford University

Exclusion criteria

  • Diminished decision-making capacity
  • Inability to understand and communicate in English sufficiently to complete study procedures
  • Inability to complete study procedures to the best of the participant's and investigator's knowledge
  • Any disorder or condition that, in the opinion of the investigator would pose a risk to participant safety or interfere with the study evaluation, procedures or completion

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Diagnostic

Study locations

United States · 1 center
  • Stanford University — Palo Alto

Identifiers

NCT: NCT07217366 · 79867

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗