Atrial Fibrillation Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You are 50 years of age or older
- You are mostly independent in daily life with little to no disability (confirm with trial site)
- You have recently (within the last 2 weeks) had a mini-stroke (TIA) AND either have a high risk score, an irregular heart rhythm called atrial fibrillation, or significant narrowing/hardening of major arteries
- You have recently (within the last 2 weeks) had an ischemic stroke (caused by a blockage) AND either have atrial fibrillation or significant narrowing/hardening of major arteries
- You have an irregular heart rhythm (atrial fibrillation or flutter) AND are either not taking blood thinners or taking a reduced dose, AND have a high risk score for stroke (confirm with trial site)
- You have recently (within the last 2 weeks) had a bleeding stroke in the brain AND have atrial fibrillation
- You have agreed in writing to take part after being fully informed about the study
- You have been a smartphone user for at least one year
Who may not be able to join:
- You have already taken part in this study before
- You have weakness or reduced movement in your arm due to any previous medical condition
- You are not able to give your own consent to join the study
- You do not speak or read any of the languages available in the study's smartphone app
- You do not have access to a smartphone that works with the study's app
- You have other health conditions or circumstances that would make it too difficult to use the app or attend follow-up appointments
- You do not wish to participate
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Ulrika Anderson, Ms., Lund University
Phone: 800-555-5555
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Alarm from device within 3 hours of onset of stroke with unilateral arm motor deficit.
Can't join this trial?
Data last synced from ClinicalTrials.gov: 5 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.