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

Sponsor: East and North Hertfordshire NHS Trust

NCT ID: NCT06400927

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Access to the study treatment being tested
Type of study
Interventional (receives a drug or procedure)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
HF-guided VA (other), Standard-of-care (other)
How long the study runs
Study runs about 40 months (dates as stated)
About the drug or intervention
HF-guided VA — other: VA guided recommendation · Standard-of-care — other: Standard-of-care
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
18 Years and over
Who
All
Number of participants
60
Started
2024-05-07
Last checked
2024-07

Plain English Summary

What is this study?

  • • Testing a new treatment for heart failure
  • • NA - 60 participants
  • • 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

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with heart failure

Where?

  • • Stevenage - East and North Hertfordshire NHS Trust

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

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.

Heart Failure

How this trial compares with your answers

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What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

What the study is looking for

  • ✓Age ≥ 18 years
  • ✓Newly diagnosed HF with New York Heart Association class II-III symptoms at discharge
  • ✓Exclusion Criteria
  • ✓Known prior history of HF
  • ✓Severe other health conditions that could affect protocol adherence, in the opinion of the investigator
See the full criteria
Inclusion Criteria: * Age ≥ 18 years * Newly diagnosed HF with New York Heart Association class II-III symptoms at discharge Exclusion Criteria * Known prior history of HF * 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

Where Is This Study? (1 UK site)

East and North Hertfordshire NHS Trust

Stevenage SG1 4AB, United Kingdom

Recruiting
Site contact (verified)

How to Get in Touch

Joshua H Leader, MBChB, BSc

Sponsor contact

CONTACT

07376188768 joshua.leader@nhs.net

Diana A Gorog, MD, PhD

Sponsor contact

CONTACT

01707247512 d.gorog@imperial.ac.uk
Data sourced from ClinicalTrials.gov · Last verified: 2024-07