Nocturnal hypertension Circulatory System Hypertensive diseases
Conditions
Interventions
This is an observational study that involves the participant wearing a wrist-worn blood pressure monitoring device (Aktiia) for 1 week while otherwise behaving as normal. Each participant visits the l
Sponsors
University of Oxford
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Adults aged between 21 and 69 years of age
Exclusion criteria
Exclusion criteria: 1. Individuals outside of the specified age range 2. Individuals suffering from tachycardia or atrial fibrillation 3. Individuals suffering from diabetes or renal dysfunction 4. Individuals who are pregnant
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Systolic blood pressure estimated continuously using the Aktiia device and averaged 2 hourly. 7 days' data will be collected per participant and the 24-hour pattern will be averaged. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Diastolic blood pressure estimated using the Aktiia device and averaged 2 hourly for 7 days 2. Heart rate estimated using the Aktiia device averaged 2 hourly for 7 days | — |
Countries
England, United Kingdom
Outcome results
None listed