View all studies | Atrial Fibrillation (A-Fib)

Atrial Fibrillation (A-Fib) Research Study

Atrial fibrillation (A-fib) is an irregular and often very rapid heart rhythm which is associated with an increased risk of stroke and/or heart failure and the earlier it is detected, the higher the chances of preventing A-Fib-related strokes. Common A-Fib symptoms include dizziness, shortness of breath, chest pain, and fatigue.

We are currently enrolling volunteers to take part in our research studies for people who have or have not been diagnosed with Atrial Fibrillation but experience symptoms.

By taking part in a study, you will:

  • Receive regular monitoring during study visits, which may include heart rhythm assessments, ECGs, blood pressure measurements, pulse checks, blood and urine tests, and other study-related evaluations.
  • Have the results of any additional study-related assessments shared with your doctor, where appropriate.
  • Receive study-related care at no cost.
  • Be reimbursed for travel and other qualifying study-related expenses.
  • Contribute to medical research that may help advance future treatment options for people living with heart rhythm disorders such as atrial fibrillation and other arrhythmias.

For further information and to discuss your eligibility with our team, please complete our online form.

Register your interest


When you register your interest with Accellacare, our clinical research specialists will review your information at no cost and connect you with studies you may be eligible for. When we find a match, Accellacare may contact you for further pre-screening or we may share your information with a local site office for them to contact you directly. Your data will be processed as outlined in the Accellacare Privacy Notice.


Data Protection

As the data controller for accellacare.us, Accellacare is committed to protecting the information that you provide. Where you give us your consent, we may use your information to: (a) identify appropriate clinical trials for you and to let you know about them; and/or (b) send you invitations to participate in future study opportunities. You can withdraw your consent at any time, but we may continue some limited processing where we have other legal grounds for doing so.

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Please note: You may or may not benefit medically from taking part and you are able to opt out at anytime and do not have to give us a reason for doing so. Your primary care physician will be informed about your participation and all medical assessments that will be carried out as part of the study. If during screening any abnormal results are found your primary care physician will also be informed.