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NCT05596175Active, not recruiting

Super-Rehab: a Novel Approach to Treat Atrial Fibrillation

Effectiveness of a Novel Intervention (Super Rehab) in Overweight Patients With Atrial Fibrillation (SuRe AF), a Randomised Controlled Trial.

Source: ClinicalTrials.gov · Last updated 12 Aug 2025

Brief summary (registry, in English)

This study proposes to evaluate the effectiveness of a novel lifestyle intervention (Super Rehab), in addition to standard care, for patients with symptomatic atrial fibrillation (AF) requiring rhythm control strategy who are overweight. As the main driver behind the selection of a rhythm-control strategy for patients with AF, the primary outcome will be an improvement in AF-related symptoms with Super Rehab versus Usual Care only. Secondary outcomes will include the burden of AF, biochemical and cardiac functional and structural changes, and markers of quality-of-life and health resource use.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
36 (estimated)
First submitted
27 Sept 2022
Start date
3 Apr 2023
Primary completion date
30 Nov 2025
Lead sponsor
Royal United Hospitals Bath NHS Foundation Trust
NCT number
NCT05596175

What you commit to

  • Study type: Interventional
  • Planned participants: 36
  • From 3 Apr 2023 to the primary completion date, 30 Nov 2025
  • 1 site in 1 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

  • Prior AF ablation

Other illness

  • Prognostic coronary artery disease, defined as left main stem \>50% stenosis and/or ≥ moderate disease in ≥3 major epicardial vessels requiring revascularisation.
  • Unstable angina
  • New York Heart Association class III/IV heart failure or severe left ventricular impairment
  • Severe heart valve disease
  • Severe hypertension (BP \>180/120mmHg) despite optimising anti-hypertensive therapy
  • Uncontrolled arrhythmia or higher degree heart block
  • History of aortic dissection
  • Recent acute pulmonary embolus, deep vein thrombosis, stroke or transient ischaemic attack (\<6 months)
  • Significant acute or chronic renal failure that would preclude contrast use at CT
  • Significant pulmonary fibrosis or interstitial lung disease (as assessed by a pulmonary physician)
  • A clinically significant ECG abnormality at the screening visit, which in the opinion of the investigators exposes the subject to risk by enrolling in the trial, including but not limited to: sustained ventricular tachycardia, high-grade atrioventricular block (second-degree Mobitz type II or third-degree heart block), evidence of acute ischemia (ST-segment elevation or depression \>1 mm), or other arrhythmias deemed clinically significant by the study cardiologist.

Other

  • Significant cardiomyopathy (as assessed by Cardiologist, e.g. hypertrophic cardiomyopathy or arrhythmogenic right ventricular cardiomyopathy)
  • Severe autonomic or peripheral neuropathy
  • Physically unable to participate in high-intensity exercise
  • Pregnancy
  • Participation in another intervention-based research study
  • Inability to fully understand the instructions provided during the study

Who the study is looking for

  • Aged \>18
  • Symptomatic AF (paroxysmal or persistent \<12-months) with a rhythm control management strategy selected including consideration of referral for a cardioversion or ablation forming part of their planned pathway
  • BMI ≥27m/kg2

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

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Royal United Hospitals Bath NHS Foundation Trust
Coordinator of this site? Confirm its status
BathUnited KingdomUnknown status

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