Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06400927

Safety of AI-Powered Virtual Assistant in Outpatient Management of Heart Failure

Led by East and North Hertfordshire NHS Trust · Updated on 2024-07-29

60

Participants Needed

1

Research Sites

174 weeks

Total Duration

On this page

Sponsors

E

East and North Hertfordshire NHS Trust

Lead Sponsor

C

Clinical and Interventional Cardiology, Sassari University Hospital, Sassari, Italy

Collaborating Sponsor

AI-Summary

What this Trial Is About

The aim of this pilot randomized study is to examine whether integrating the SIRIO-HF virtual assistant (VA) into the outpatient management of participants recently discharged from hospital with a new diagnosis of heart failure (HF), may reduce the need for regular medical assessment and the healthcare burden, reduce variability in healthcare, and meet with participant satisfaction, without compromising participant safety and overall care quality.

CONDITIONS

Official Title

Safety of AI-Powered Virtual Assistant in Outpatient Management of Heart Failure

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 63; 18 years
  • Newly diagnosed heart failure with New York Heart Association class II-III symptoms at discharge
Not Eligible

You will not qualify if you...

  • Known prior history of heart failure
  • Severe comorbidities that could affect protocol adherence, in the opinion of the investigator
  • Alternative diagnosis for symptoms such as chronic obstructive pulmonary disease
  • Dementia or other cognitive impairment
  • Currently involved in another interventional clinical trial

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

East and North Hertfordshire NHS Trust

Stevenage, Hertfordshire, United Kingdom, SG1 4AB

Actively Recruiting

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Research Team

J

Joshua H Leader, MBChB, BSc

CONTACT

D

Diana A Gorog, MD, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

2

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