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NCT07069998Not yet recruiting

AI-guided AF Treatment

Artificial Intelligent Guided Treatment of Atrial Fibrillation: A Randomized Controlled Pilot Study

Source: ClinicalTrials.gov · Last updated 17 Jul 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Two-centre, prospective, randomized, open-label, controlled pilot study to examine whether integrating an artificial intelligence virtual assistant (VA), instructed with the latest international guidelines on optimal patient management into the outpatient management of patients diagnosed with atrial fibrillation (AF) in the last 6 months, is feasible, acceptable and effective in reducing the need for regular medical assessment and the healthcare burden, reduce variability, and meets with participant satisfaction, without compromising participant safety and overall care quality.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
60 (estimated)
First submitted
21 May 2025
Start date
15 Jul 2025
Primary completion date
26 May 2028
Lead sponsor
East and North Hertfordshire NHS Trust
NCT number
NCT07069998

What you commit to

  • Study type: Interventional
  • Planned participants: 60
  • From 15 Jul 2025 to the primary completion date, 26 May 2028
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Alternative potentially reversible causes of AF (such as surgery, sepsis, or thyroid dysfunction)

Other illness

  • Severe comorbidities (such as physical impairment, cognitive impairment, and hearing loss) that could affect protocol adherence, in the opinion of the investigator
  • Chronic Kidney Disease (CKD) stage 4-5 or on dialysis
  • Medical illness with a life expectancy of less than 1 year
  • Dementia or other cognitive impairment

Other

  • Currently involved in another AF interventional clinical trial
  • Being pregnant

Who the study is looking for

  • Age ≥ 18 years
  • Documented diagnosis of AF within the last 6 months
  • Patient is at least mildly symptomatic. Presence of at least one of the symptoms like palpitation, dizziness, breathlessness, pre-syncope, and syncope with at least mild intensity
  • Ability to understand and comprehend the study rationale, design, and process.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.