Atrial Fibrillation Circulatory System Atrial Fibrillation
Conditions
Interventions
Each participant will attend their GP surgery for one visit. Each participant will be tested using 4 devices in random sequence, followed by a standard 12 lead ECG. Each test is performed immediately
Sponsors
University of Southampton
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: AF Participants: 1. Aged 65 years an over 2. Coded as AF on their GP records Control participants: 1. Aged 65 years an over 2. No known AF
Exclusion criteria
Exclusion criteria: All participants: 1. Aged under 65 2. Permanent pacemaker in situ 3. Dementia / lacking in capacity 4. Previous moderate or severe skin reaction to electrode gel
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Diagnostic accuracy of WatchBP, AliveCor, Polar heart rate monitor belt (with diagnostic algorithm), Firstbeat Bodyguard2 (with diagnostic algorithm) are determined through comparison with the 12-lead ECG reference test at the study visit. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Comfort is measured using a visual analogue scale immediately after all tests are completed 2. Ease of use for each device is measured using a visual analogue scale immediately after all tests are completed | — |
Countries
United Kingdom
Contacts
Public ContactMark Lown
Outcome results
None listed