- Microvascular Coronary Rehabilitation For Improving Treatment – Feasibility Study — Recruiting • Non-phase study • Cardiology / Cardiovascular • NCT06681896.
- What is being tested: A personalised cardiac rehabilitation programme called MICROFIT combining high-intensity interval exercise (HIIT) and dietary advice, designed to improve outcomes in patients with microvascular coronary disease.
- Patient eligibility overview: This feasibility study targets patients with microvascular coronary dysfunction (microvascular angina), a condition characterised by chest pain and ischaemia despite normal coronary arteries on angiography.
- Quick orientation before opening the registry record.
- Checking recruitment status, phase and sponsor at a glance.
- Connecting this trial to nearby guidelines, Drug Science and education.
The goal of this clinical trial is to assess the feasibility of undertaking a randomized controlled trial assessing the impact of a personalised, intense cardiac rehabilitation programme involving high intensity interval exercise (HIIT) and dietary advice (termed MICROFIT) on symptom burden in patients with microvascular coronary dysfunction. The main questions it aims to answer are: 1. Feasibility of undertaking randomised controlled trial of MICROFIT in patients with coronary microvascular dysfunction (recruitment rates, retention and adherence, acceptability of MICROFIT and participants' and practitioners' experiences of trial participation) 2. Preliminary data on…
- : * Age ≥18 * Angina or angina equivalent symptoms * Unobstructed coronary arteries at the time of coronary angiogram. This will be defined as plaque causing
Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.