The Aim of the Study is to Examine the Variation in Blood Pressure Between an Optimal Measurement (According to Established Guidelines in the Literature - Per Guidelines) and a 'Common' Measurement (Used by Nursing Teams - Per Common Practice) Among Women of Reproductive Age With and Without Hyperte
blood pressure measurement: examine the variation in blood pressure between an optimal measurement (according to established guidelines in the literature - per guidelines) and a 'common' measurement (used by nursing teams - per common practice) among women of reproductive age with and without hypertention
Study summary
The aim of the study is to examine the variation in blood pressure between an optimal measurement (according to established guidelines in the literature - per guidelines) and a 'common' measurement (used by nursing teams - per common practice) among women of reproductive age with and without hyperte
Eligibility
Sex
FEMALE
Min age
18 Years
Max age
40 Years
Healthy volunteers
Accepted
Inclusion Criteria:
* Women aged 18-40
* Informed consent to participate.
Exclusion Criteria:
* Inability to cooperate with BP measurement under optimal conditions
* Women with complex underlying disease that may bias the data (e.g. significant vasculopathy)
Primary outcome measure(s)
Mean difference in systolic blood pressure (mmHg) between guideline-based and routine clinical measurement — 1 year Mean difference in systolic blood pressure (mmHg) between guideline-based and routine clinical measurement
Description:
Systolic blood pressure (SBP) will be measured in each participant using two methods:
1. guideline-based blood pressure measurement performed according to international hypertension guidelines (seated position, appropriate cuff size, arm supported at heart level after ≥5 minutes of rest), and
2. routine clinical blood pressure measurement as performed by nursing staff under usual clinical conditions.
The primary outcome will be the within-participant mean difference in SBP (mmHg) between the two measurement methods.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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