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

NCT07320339 | Recruiting

• 1 other identifier: 0111-25
• Study Type: interventional
• Target: 500
• Locations: 1 country
• Sites: 1

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

Conditions

Blood Pressure Measurement in Pregnancy

Outcome Measures

Primary Outcomes (1)

• Mean difference in systolic blood pressure (mmHg) between guideline-based and routine clinical measurement

  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.

  1 year

Secondary Outcomes (2)

• Mean difference in diastolic blood pressure (mmHg) between guideline-based and routine clinical measurement

  1 year

• Mean difference in mean arterial pressure (mmHg) between guideline-based and routine clinical measurement

  1 yaer

Study Arms (1)

variation in blood pressure between an optimal measurement and a 'common' measurement

EXPERIMENTAL

Procedure: blood pressure measurement

Interventions

blood pressure measurement PROCEDURE

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

variation in blood pressure between an optimal measurement and a 'common' measurement

Eligibility Criteria

• Age: 18 Years - 40 Years
• Gender Eligibility Details: • Women aged 18-40
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Women aged 18-40
• Informed consent to participate.

You may not qualify if:

• Inability to cooperate with BP measurement under optimal conditions
• Women with complex underlying disease that may bias the data (e.g. significant vasculopathy)

Sponsors & Collaborators

• Hillel Yaffe Medical Center: lead

Study Sites (1)

Hille Yaffe Medical Center

Hadera, Israel, 3881000, Israel

RECRUITING

Central Study Contacts

Ikhlas IM Ammash, M.D

CONTACT

+972-4-7744602; AnnaTu@hymc.gov.il

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: SCREENING
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER GOV
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: November 16, 2025
• First Posted: January 6, 2026
• Study Start: August 24, 2025
• Primary Completion (Estimated): August 24, 2026
• Study Completion (Estimated): August 24, 2026
• Last Updated: January 6, 2026

Record last verified: 2025-12

Locations

IL (1)