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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05372328
Other study ID # IRB00319633
Secondary ID 139475
Status Completed
Phase N/A
First received
Last updated
Start date August 9, 2022
Est. completion date June 1, 2023

Study information

Verified date September 2023
Source Johns Hopkins University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Primary Objectives 1. Determine the effect of an unsupported and poorly positioned arm on initial and average triplicate blood pressure done according to clinical practice guidelines with an automated device. a. Hypothesis: Compared to blood pressure measurements obtained with the arm supported with mid-cuff positioned at heart level, blood pressures measured with an unsupported arm and/or with mid-cuff below heart level will be significantly higher. Secondary Objective 1. To determine if the effects differ based on the following patient characteristics: - Hypertensive blood pressure (SBP≥130 mmHg vs. <130 mmHg). - Age (≥ 60 years vs. < 60 years) Greater vascular stiffness > lesser vascular stiffness - Regular health care (Last BP measured >1 year ago vs. ≤1 year ago) - Arm length:cuff width


Description:

The investigators propose a cross-sectional study of adult participants recruited from the community. Enrolled participants will have four sets of three automated blood pressure measurements, with each set taken with the arm positioned and supported as follows: - Arm supported on a desk, with mid-cuff at mid-heart level (4th intercostal space) - Desk1 - Reference measurement - Arm supported on the participant's lap - Lap - Arm hanging at the participant's side, unsupported - Side - The last period of triplicate BP measurements will always have the arm supported and mid-cuff positioned at mid-heart level - Desk2 In the prior 3 periods, the arm position and support conditions are randomly ordered. Each participant will undergo a total of 12 systolic and 12 diastolic BP measurements


Recruitment information / eligibility

Status Completed
Enrollment 134
Est. completion date June 1, 2023
Est. primary completion date June 1, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Age = 18 years Exclusion Criteria: - Presence of the following on both arms: rashes, gauze dressings, casts, edema, paralysis, tubes, open sores or wounds, A-V shunts. - Being mentally impaired - Being pregnant - Arm circumference exceeding 55 cm. - >80 years of age

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Position of arm while taking blood pressure measurement
Each participant will have 4 sets of 3 blood pressure measurements taken. The participants will be randomized to the order in which their arm position changes prior to each set of measurements.

Locations

Country Name City State
United States Johns Hopkins University Baltimore Maryland

Sponsors (2)

Lead Sponsor Collaborator
Johns Hopkins University Vital Strategies

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Difference in systolic blood pressure in lap1 vs desk arm position Absolute difference between (1) 1st systolic BP and (2) average of 3 systolic BP from measurements (mmHg) obtained in: Lap vs Desk1 Time of measurement up to 90 minutes
Primary Difference in diastolic blood pressure in side vs desk 1 arm position Absolute difference between (1) 1st diastolic BP and (2) average of 3 diastolic BP from measurements (mmHg) obtained with: Side vs Desk1 Time of measurement up to 90 minutes
Primary Difference of systolic and diastolic differences Systolic and Diastolic BP difference of differences between: (Desk1-Desk2) and (Lap-Desk1) from measurements (mmHg) Time of measurement up to 90 minutes
Primary Difference of diastolic differences Systolic and Diastolic Difference of differences in BP measurements (mmHg) between: (Desk1-Desk2) and (Side-Desk1) Time of measurement up to 90 minutes
Secondary Difference in blood pressure based on hypertension status To determine the blood pressure difference based on hypertensive (=140/90) vs. non-hypertensive participants Time of measurement up to 90 minutes
Secondary Difference in blood pressure based on age To determine the blood pressure difference based on age (= 60 years vs. <60 years). Time of measurement up to 90 minutes
Secondary Difference in blood pressure based on regular healthcare visits To determine the blood pressure difference between participants receiving regular health care visits (>1 year vs. = 1 year). Time of measurement up to 90 minutes
Secondary Difference in blood pressure based on arm length to cuff width ratio To determine the blood pressure difference of arm length to cuff width ratio Time of measurement up to 90 minutes
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