We hypothesize that the accuracy of four selected types of smartphone compatible blood pressure monitors does not differ significantly from the handheld sphygmanometer
ID
Bron
Verkorte titel
Aandoening
Not applicable
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
All measured blood pressures by all devices
Achtergrond van het onderzoek
Rationale: Smartphone-connected blood pressure monitors are being released on the market. An independent study comparing the accuracy of these devices has not been done yet.
Objective: To validate and compare smartphone-connected blood pressure monitors produced by Withings, Qardio and iHealth with the gold standard and a validated automatic blood pressure monitor.
Study design: Crossover trial
Study population: Two study populations will be investigated. The first population (population one) will consists of young, healthy individuals aged 18-30. The second population (population two) will consist of patients who visit the outpatient clinic within one year after having suffered from a ST elevation myocardial infarction for which they received primary percutaneous coronary intervention in the LUMC.
Intervention: All study subjects will receive three blood pressure measurements with a handheld manometer, three measurements with an automatic device and 12 measurements with 4 automatic devices (1 device will be used 3 times in 1 patient). The order in which the devices are used will be randomized
Main study parameters/endpoints: The study parameter will be per study subject 18 systolic blood pressure measurements (SBP), 18 diastolic blood pressure measurements (DBP) and 18 heart rates (HR).
Doel van het onderzoek
We hypothesize that the accuracy of four selected types of smartphone compatible blood pressure monitors does not differ significantly from the handheld sphygmanometer
Onderzoeksopzet
not applicable
Onderzoeksproduct en/of interventie
Four smartphone compatible blood pressure monitors:
- iHealth BP 5
- iHealth BP 7
- QardioArm
- Withings Blood Pressure Monitor
Publiek
Wetenschappelijk
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
Patients with a ST-elevation myocardial infarction and subsequently primary percutaneous coronary intervention (PCI) one year or less ago at the time of their outpatient clinic visit.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
Patients with diagnosed irregular cardiac arrhythmias
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL5109 |
NTR-old | NTR5241 |
CCMO | NL52863.058.15 |
OMON | NL-OMON42703 |