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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

Standard vs. Routine Blood Pressure Measurement in Pregnancy: Effects of Position and Diurnal Variation

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07320339
Enrollment
500
Registered
2026-01-06
Start date
2025-08-24
Completion date
2026-08-24
Last updated
2026-01-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Blood Pressure Measurement in Pregnancy

Brief 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

Detailed description

Accurate blood pressure measurement is a cornerstone of the diagnosis and management of hypertension. The latest Clinical Practice Guidelines (AHA2020- International Society of Hypertension Global) emphasize several important steps for accurate blood pressure measurement, including choosing the correct cuff size, resting for five minutes, sitting with support for the back, feet flat on the floor, and legs uncrossed, and proper arm positioning (i.e., positioning the midpoint of the cuff at heart level with the arm supported on a table or work surface). Sitting measurements are preferred because of the large amount of data linking blood pressure measurements in this position to health outcomes.

Interventions

PROCEDUREblood 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

Sponsors

Hillel Yaffe Medical Center
Lead SponsorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
Yes

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)

Design outcomes

Primary

MeasureTime frameDescription
Mean difference in systolic blood pressure (mmHg) between guideline-based and routine clinical measurement1 yearMean 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.

Secondary

MeasureTime frameDescription
Mean difference in mean arterial pressure (mmHg) between guideline-based and routine clinical measurement1 yaerMean arterial pressure (MAP) will be calculated as MAP = (SBP + 2×DBP) / 3 for each measurement method. The outcome will be the within-participant difference between methods
Mean difference in diastolic blood pressure (mmHg) between guideline-based and routine clinical measurement1 yearAs above, for diastolic blood pressure (DBP).

Countries

Israel

Contacts

Primary ContactIkhlas IM Ammash, M.D
AnnaTu@hymc.gov.il+972-4-7744602

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026