EFFECT OF BLOOD PRESSURE MEASUREMENT IN DIFFERENT POSITIONS ON BLOOD PRESSURE VALUES AND ANXIETY LEVELS IN PREGNANT WOMEN WITH PREECLAMPSIA (PREECLAMPSIA)

March 26, 2025 updated by: Şerife Kelle Dikbaş, Istanbul University - Cerrahpasa

Aim: This study examined the effects of blood pressure measurement in different positions on diastolic and systolic blood pressure values and anxiety levels in pregnant women diagnosed with preeclampsia.

Method: The study was conducted between March and June 2024 as a pre-test post-test quasi-experimental study with 96 pregnant women diagnosed with preeclampsia in the perinatology department of a training and research hospital. Participants were divided into three groups and their blood pressures were measured in the left lateral, right lateral and semi-Fowler positions. Data were collected using an introductory information form and the State Anxiety Scale.

Study Overview

Detailed Description

Aim: This study examined the effects of blood pressure measurement in different positions on diastolic and systolic blood pressure values and anxiety levels in pregnant women diagnosed with preeclampsia.

Method: The study was conducted between March and June 2024 as a pre-test post-test quasi-experimental study with 96 pregnant women diagnosed with preeclampsia in the perinatology department of a training and research hospital. Participants were divided into three groups and their blood pressures were measured in the left lateral, right lateral and semi-Fowler positions. Data were collected using an introductory information form and the State Anxiety Scale.

Study Type

Interventional

Enrollment (Actual)

96

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Üsküdar
      • Istanbul, Üsküdar, Turkey, 34668
        • Zeynep Kamil Women's and Children's Diseases Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Being primigravida (first pregnancy),

    • Being in the third trimester of pregnancy,
    • Being between the ages of 18-45,
    • Being diagnosed with preeclampsia,
    • Having an arm circumference of less than 36 cm,
    • Having a history of hospitalization of at least 24 hours (in order to minimize anxiety, uncertainty, lack of information and disorientation related to hospitalization).

Exclusion Criteria:

  • • Presence of a physical disability that would make it difficult to perform the positions included in the study (e.g. loss of extremity),

    • Presence of decompensated disease (e.g. eclampsia, pulmonary edema),
    • Presence of a history of cardiological disease,
    • Diagnosis of obstructive sleep apnea,
    • Presence of additional risk factors other than preeclampsia (e.g. threat of premature birth, placental anomalies).

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Factorial Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Right Lateral Position
The pregnant woman was placed in the right lateral position on the patient bed. Her head was supported by a medium-height pillow. The right arm to be measured was held at heart level and extended at a 45° angle to the body. Considering that taking measurements from the left arm above heart level could lower blood pressure values, both measurements were made only from the right arm.
Participants rested for 10 minutes in a fully seated position, leaning their backs on a chair, without crossing their legs and placing their feet parallel to the floor. During this time, the arm to be measured was kept at heart level.
Experimental: Left Lateral Position
The pregnant patient was lying in the left lateral position on her bed, her head supported by a pillow of medium height. The left arm to be measured was positioned at heart level and supported by a pillow underneath. Blood pressure was measured using the arm extended at a 45° angle to the body in the left lateral position. Considering that taking measurements from the right arm above heart level may lower blood pressure values, both measurements were taken from the left arm only.
Left Lateral Position
Experimental: Semi Fowler Position (45° Fowler)
The pregnant woman was laid on her back at a 45° angle on the patient bed. Her head was supported with a medium-height pillow. The arm to be measured was held at heart level and supported with a pillow underneath to provide the appropriate position.
Semi Fowler Position (45° Fowler)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
blood pressure measurement
Time Frame: 4 month
The effect of blood pressure measurement in different positions on diastolic and systolic blood pressure values in pregnant women diagnosed with preeclampsia will be examined. Measurement will be made with a blood pressure device. Systolic pressure and diastolic pressure will be measured in mmhg.
4 month
anxiety levels
Time Frame: 4 month
The effects of blood pressure measurement in different positions on anxiety levels in pregnant women diagnosed with preeclampsia will be measured. The anxiety level will be measured with the state anxiety scale. The score obtained from the scale varies between 20 and 80. A high score indicates a high level of anxiety, a low score indicates a low level of anxiety. The same applies when interpreting scores according to percentile rank. In other words, a low percentile rank (1, 5, 10) indicates low anxiety. The average score level determined in applications varies between 36 and 41.
4 month

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 1, 2024

Primary Completion (Actual)

June 1, 2024

Study Completion (Actual)

June 1, 2024

Study Registration Dates

First Submitted

March 8, 2025

First Submitted That Met QC Criteria

March 26, 2025

First Posted (Actual)

March 27, 2025

Study Record Updates

Last Update Posted (Actual)

March 27, 2025

Last Update Submitted That Met QC Criteria

March 26, 2025

Last Verified

March 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • Preeclampsia (Other Identifier: Al-Ahliyya Amman University)
  • 29.01.2024 2024/06 (Registry Identifier: Üsküdar University Non-Interventional Research Ethics Committee approval)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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