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Where Should Automated Blood Pressures be Done in Primary Care Offices?

2014년 4월 2일 업데이트: Michelle Greiver, North Toronto Primary Care Research Network

Where Should Automated Blood Pressures be Done? RCT of BpTRU Measurement in Private or Non-private Areas of Primary Care Offices

The use of automated blood pressure measurement (ABPM) devices in the office setting is increasingly recognized as superior to manual BP measurement. Current guidelines recommend that patients be alone in a quiet room, with no interactions with health care professionals during the readings; in practice, this means using an exam room. However, we found no evidence supporting the location of ABPM. Furthermore, exam rooms are constantly being used in primary care offices, so this may not be practical in routine care.

For this study, fifty consecutive consenting patients age 18 or more in each of seven community based primary care offices will randomly be allocated to either ABPM in an exam room, or in a non-private area of the clinic. After being tested in the first location they will then be tested in the second location with the same device. The main outcome will be the mean value of the last five systolic blood pressures for each location within offices. Secondary measures will include blood pressures for patients with or without hypertension, a comparison of the initial and second set of blood pressures and of the effect of office noise in decibels on BP readings.

New technology is more readily adopted if barriers to use are minimized. If we find no differences in BP readings between office locations, clinicians will then have the option to use an additional office area to implement the automated BP measurement device.

연구 개요

상태

빼는

정황

상세 설명

Following the design of our pilot study, patients consenting to two sets of blood pressure readings will be randomly allocated using a random number table to either automated blood pressure measurement using a BpTRU device in an exam room (private area without any traffic or staff) with the door closed, or BpTRU in an open (non-private area) of the clinic with routine office traffic and noise levels. Patients randomized to the private area first will be subsequently tested in the non-private area and those randomized to the non-private area first will then be tested in the private area. A single portable BpTRU machine will be used for all recordings. A research assistant will be trained on the use of the equipment with at least five supervised training readings. The BpTRU device will be placed on the patient's arm and readings will be recorded by the research assistant. The first reading will be done with the research assistant present to ensure proper placement and recording. The patient will then be left alone for the subsequent five measurements separated by one minute intervals. This will be immediately followed by a second set of readings in the alternate location. During both sets of readings the patient will be seated comfortably in a chair with arms and will be instructed not to talk or cross their legs. The same arm will be used for both sets of measurements with the blood pressure cuff at heart level. The research assistant will record the average of the last five out of six blood pressure readings for each office location, in accordance with the manufacturer's recommendations and previous studies.

The research assistant will record decibel levels in each location during BP readings using a Reed Sound Level Meter C-322 (Reed Instruments, Ste-Anne-de-Bellevue, Quebec, Canada). The sound level meter includes a data logger, and the mean decibel level per location for each set of readings will be recorded. The assistant will be trained in the use of the sound meter and logger and will use it during the five supervised BP training readings. The research assistant will also measure and record the patient's weight in kg, height in cm, and will collect information on patient's gender and self reported history of hypertension.

Planned sample size and analysis Our sample size is based on equivalence of BpTRU measurement done in non private office areas as compared to measurement done in private office areas, using the results of our pilot study. We consider differences of less than 5 mm Hg in systolic blood pressure to be clinically equivalent. In order to demonstrate equivalence for our primary outcome, and accounting for clustering effect in primary care offices, using a power of 80% and a two sided alpha level of 0.05 to conclude equivalency for a difference of 5 mm Hg or less, we will need to recruit 350 patients. Our planned recruitment is therefore fifty patients per office and seven office locations. 175 patients (25 per office location) will be randomly allocated to BpTRU measurement in a private exam room first and 175 will be allocated to an open area first.

Following the analytic methods used in our pilot study, we will use a random effect regression model to account for repeated measures within each participant for analyzing the data. Regression analysis will be undertaken to compare the measures and results will be adjusted for clustering effect. All tests will be two-sided using an alpha level of 0.05.

연구 유형

관찰

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • Ontario
      • Toronto, Ontario, 캐나다, M3B 3S6
        • North Toronto Primary Care Research Network

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 이상 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

샘플링 방법

비확률 샘플

연구 인구

Consecutive consenting patients age eighteen or over will be recruited from the waiting rooms of participating practices in Toronto, Ontario

설명

Inclusion Criteria:

  • Age eighteen and over
  • Able to consent

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 관찰 모델: 케이스 크로스오버
  • 시간 관점: 유망한

코호트 및 개입

그룹/코호트
BpTRU readings in private office area
Consenting patients will be randomly allocated using a random number table to BpTRU in an exam room. The first reading will be done with the research assistant present to ensure proper placement and recording and will then be left alone for the subsequent five measurements at one minute intervals. This will be immediately followed by a second set of readings in the alternate location. During both sets of readings the patient will be seated comfortably in a chair with arms and will be instructed not to talk or cross their legs. The same arm will be used for both sets of measurements with the blood pressure cuff at heart level. The average of the last five out of six blood pressure readings for each office location will be recorded. The decibel levels in each location will be recorded during BP readings using a Reed Sound Level Meter C-322. The patient's weight in kg, height in cm, gender and self reported history of hypertension will also be recorded.
BpTRU readings in open office area
Consenting patients will be randomly allocated using a random number table to BpTRU in an open office area The first reading will be done with the research assistant present to ensure proper placement and recording and will then be left alone for the subsequent five measurements at one minute intervals. This will be immediately followed by a second set of readings in the alternate location. During both sets of readings the patient will be seated comfortably in a chair with arms and will be instructed not to talk or cross their legs. The same arm will be used for both sets of measurements with the blood pressure cuff at heart level. The average of the last five out of six blood pressure readings for each office location will be recorded. The decibel levels in each location will be recorded during BP readings using a Reed Sound Level Meter C-322. The patient's weight in kg, height in cm, gender and self reported history of hypertension will also be recorded.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
mean value of the last five systolic blood pressures for each location within the offices
기간: 1 hour
comparison between the mean systolic values of the automated blood pressure measurements using a BpTRU device in private (quiet, no interactions with health care personnel) and non private areas of the offices.
1 hour

2차 결과 측정

결과 측정
측정값 설명
기간
comparison of first and second sets of blood pressure readings
기간: 1 hour
Determination of rank effect on automated blood pressure measurements
1 hour
comparisons of automated BP readings for patients with and without previously documented hypertension
기간: 1 hour
1 hour
effect of office decibel levels on automated office BP readings
기간: 1 hour
1 hour

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: Michelle Greiver, MD MSc, North Toronto Primary Care Research Network

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작

2014년 3월 1일

기본 완료 (예상)

2014년 9월 1일

연구 완료 (예상)

2014년 11월 1일

연구 등록 날짜

최초 제출

2012년 2월 17일

QC 기준을 충족하는 최초 제출

2012년 2월 22일

처음 게시됨 (추정)

2012년 2월 23일

연구 기록 업데이트

마지막 업데이트 게시됨 (추정)

2014년 4월 4일

QC 기준을 충족하는 마지막 업데이트 제출

2014년 4월 2일

마지막으로 확인됨

2014년 4월 1일

추가 정보

이 연구와 관련된 용어

추가 관련 MeSH 약관

기타 연구 ID 번호

  • 12-0217

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

3
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