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Using the Blood Pressure TRU in Clinical Settings: a Knowledge Translation Study

Using the Bp TRU in Clinical Settings: a Knowledge Translation Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01357226
Enrollment
50
Registered
2011-05-20
Start date
2011-05-31
Completion date
2012-01-31
Last updated
2012-04-26

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

Conditions

Blood Pressure

Keywords

measurement in two environments

Brief summary

Context: Use of automated blood pressure (BP) measurement devices in the office setting is increasingly recognized as superior to manual BP measurement. Current recommendations are to have the patient alone in a quiet room, with no interactions with health care professionals during the readings. However, this may not be practical in primary care offices where the exam rooms are constantly being used. Objective: To compare measurements with an automated BP device in private examination rooms with measurements in non-private areas of a primary care office. Design: Randomized controlled trial with cross-over. Setting: Community based primary care office participating in the NorTReN Practice Based Research Network in Toronto, Ontario. Participants: Fifty consecutive consenting patients over the age of 18 having their BP checked as part of their routine care. Intervention: Patients will be randomly allocated to either automated BP measurement in an exam room, or in a non-private area of the clinic. After being tested in the first location they will subsequently be tested in the second location with the same device. Main outcome measure: The primary outcome measure is a comparison between the mean systolic values of the automated BP measurements in the two office areas. The investigators will use the t-test for paired samples. The secondary outcome is a comparison of systolic values for patients with previously documented hypertension. The investigators define a clinically meaningful result as a difference of 5 mmHg or more in systolic BP. Conclusion: New technology is more readily adopted if barriers to use are minimized. If the investigators find no differences in BP readings between office locations, physicians will then have the convenience of an additional office area to implement the automated BP measurement device.

Interventions

None listed

Sponsors

North Toronto Primary Care Research Network
Lead SponsorNETWORK

Study design

Observational model
CASE_CROSSOVER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Able to consent * Over the age of 18

Design outcomes

Primary

MeasureTime frameDescription
Automated Blood Pressure measurements in two different environmentsDay of consentComparison of the mean systolic values of the automated blood pressure measurement in the private exam room and the common area (laboratory area).

Secondary

MeasureTime frameDescription
Automated Blood Pressure values of hypertensive patients in two different environmentsDay of consentComparison of the mean systolic blood pressure measurements for patients with previously documented hypertension in the private exam room and the common area (laboratory area).

Countries

Canada

Outcome results

None listed

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