Actively Recruiting

Age: 18Years +
All Genders
NCT06566911

Voice Analysis for Monitoring Patients With Heart Failure

Led by Noah Labs · Updated on 2024-08-22

70

Participants Needed

2

Research Sites

31 weeks

Total Duration

On this page

Sponsors

N

Noah Labs

Lead Sponsor

C

Charite University, Berlin, Germany

Collaborating Sponsor

AI-Summary

What this Trial Is About

This observational study involves ADHF patients at two sites in the United States and Germany. After informed consent and screening assessments, participants will perform daily voice recordings during their hospital stay, from admission until discharge. Alongside voice data, additional clinical information such as left ventricular ejection fraction, NTpro-BNP levels, and ECG-data will be collected for comprehensive analysis. The study's goal is to identify voice-based indicators of heart failure progression, with the potential to enhance remote monitoring and self-management strategies for heart failure patients.

CONDITIONS

Official Title

Voice Analysis for Monitoring Patients With Heart Failure

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Clinically diagnosed with Acutely Decompensated Heart Failure.
  • At least 18 years of age.
Not Eligible

You will not qualify if you...

  • Disabling mental diseases (e.g., Alzheimer's disease)
  • Clinically diagnosed chronic obstructive pulmonary disease (COPD)
  • Treatment in ICU or IMU
  • Dialysis treatment
  • Previous operations on organs involved in generation of voice (vocal tract, vocal folds, etc.)
  • Neurodegenerative diseases
  • Pregnancy
  • Inability to provide consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Mayo Clinic

Rochester, Minnesota, United States, 55902

Actively Recruiting

2

Deutsches Herzzentrum der Charité

Berlin, Germany, 13353

Completed

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Research Team

L

Leonhard Riehle, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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