- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07693699
Optimizing Sustainable Cuff Access and Training Pathways for Self-Measured Blood Pressure Monitoring in Primary Care
Optimizing Sustainable Cuff Access and Training Pathways for Self-Measured Blood Pressure Monitoring in Primary Care: A Pragmatic Randomized Controlled Trial
연구 개요
상태
정황
상세 설명
The study team developed a clinical integration package as a multicomponent primary care-based approach to increase SMBP adoption through structured workflows, patient training, blood pressure logs, reminders/support, and clinical follow-up. Pilot work demonstrated that SMBP uptake can be significantly improved in underserved primary care settings. However, the pilot relied on research funds to purchase cuffs, which is not sustainable for health-system scale. A scalable model must identify practical pathways for patients to obtain standard validated blood pressure cuffs through routine care mechanisms, including vendor-supported, insurance-billed, consignment, or mail-order pathways, without depending on research-purchased devices.
In addition to cuff access, effective SMBP implementation also requires feasible approaches to patient training. Many patients do not receive standardized instruction on how to correctly measure and record home blood pressure readings, and intensive in-person training models may be difficult to sustain in routine primary care workflows. Health systems therefore need practical training strategies that balance effectiveness with scalability, ranging from brief hands-on education delivered during clinic visits to lower-touch written or self-guided educational materials.
Patients will be randomized to one of four arms:
- Mail-order cuff delivery with enhanced return conversation
- Mail-order cuff delivery with written instructions
- In-clinic cuff distribution with enhanced return conversation
- In-clinic cuff distribution with written instructions
All other intervention components will be standardized across study arms, including receipt of a blood pressure log, written instructions on when and how to obtain home blood pressure readings, and routine clinic processes for documenting or reviewing SMBP readings returned by patients. The design is intended to evaluate implementation pathways for SMBP delivery in routine care rather than to test the clinical efficacy of SMBP itself. This design is intended to evaluate operational implementation pathways for SMBP delivery in routine care rather than to test the clinical efficacy of SMBP itself.
연구 유형
등록 (추정된)
단계
- 해당 없음
연락처 및 위치
연구 연락처
- 이름: Rasha Khatib, PhD
- 전화번호: 7086843691
- 이메일: Rasha.Alkhatib@aah.org
연구 장소
-
-
Illinois
-
Chicago, Illinois, 미국, 60617
- 모병
- Advocate Medical Group Chicago (Southeast)
-
연락하다:
- Nicole Glowacki, MPH
- 전화번호: 708-684-3691
- 이메일: nicole.glowacki@aah.org
-
Chicago, Illinois, 미국, 60619
- 모병
- Advocate Medical Group Chicago (Imani Village)
-
연락하다:
- Nicole Glowacki, MPH
- 전화번호: 708-684-3691
- 이메일: nicole.glowacki@aah.org
-
Chicago, Illinois, 미국, 60643
- 모병
- Advocate Medical Group Beverly
-
연락하다:
- Nicole Glowacki, MPH
- 전화번호: 708-684-3691
- 이메일: nicole.glowacki@aah.org
-
Merrionette Park, Illinois, 미국, 60803
- 모병
- Advocate Medical Group Merrionette Park
-
연락하다:
- Nicole Glowacki, MPH
- 전화번호: 708-684-3691
- 이메일: nicole.glowacki@aah.org
-
Oak Lawn, Illinois, 미국, 60453
- 모병
- Advocate Medical Group Oak Lawn (IM)
-
연락하다:
- Nicole Glowacki, MPH
- 전화번호: 708-684-3691
- 이메일: nicole.glowacki@aah.org
-
Oak Lawn, Illinois, 미국, 60453
- 모병
- Advocate Medical Group Oak Lawn (FP)
-
연락하다:
- Nicole Glowacki, MPH
- 전화번호: 708-684-3691
- 이메일: nicole.gowacki@aah.org
-
-
참여기준
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
설명
Inclusion Criteria:
- Age 18 years or older.
- Diagnosed hypertension documented prior to the index clinic visit.
- Scheduled for and attends an in-person visit with a participating clinician at a study clinic.
- Elevated BP (blood pressure) documented in Epic during rooming or the clinic visit before study enrollment, defined as systolic BP >=140 mmHg or diastolic BP >=90 mmHg.
Exclusion Criteria:
- Visit is canceled, rescheduled, or the patient does not attend the visit.
- Patient already has a usable home BP cuff provide through insurance within the past 5 years.
- Patient declines assistance obtaining a BP cuff.
- Patient declines submitting cuff order to insurance.
- Patient unable to participate for operational reasons.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 지지 요법
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
활성 비교기: Mail-order cuff delivery - Enhanced Return Conversation
Patients will receive a blood pressure cuff in the mail and have a conversation with the medical assistant on when and how to return their blood pressure log with the care team.
|
Complete vendor form; provide blood pressure log/instructions; discuss with patient how and when to return bp log; submit vendor form for mail delivery; complete envelope checklist.
|
|
활성 비교기: Mail-order cuff delivery - Written instructions
Patients will receive a blood pressure cuff in the mail and receive written training on who and when to return their blood pressure log with the care team.
|
Complete vendor form; provide blood pressure log/instructions; submit vendor form for mail delivery; complete envelope checklist.
|
|
활성 비교기: In-clinic cuff distribution - Enhanced Return Conversation
Patients will receive a blood pressure cuff in the clinic and have a conversation with the medical assistant on when and how to return their blood pressure log with the care team.
|
Complete vendor form; provide blood pressure log/instructions; discuss with patient how and when to return bp log; provide blood pressure cuff in clinic; submit vendor form as required; complete envelope checklist.
|
|
활성 비교기: In-clinic cuff distribution - Written instructions
Patients will receive a blood pressure cuff in the mail and receive written training on who and when to return their blood pressure log with the care team.
|
Complete vendor form; provide blood pressure log/instructions; provide blood pressure cuff in clinic; submit vendor form as required; complete envelope checklist.
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Rate of Blood Pressure Receipt
기간: up to day 14
|
Number of participants that have received their blood pressure cuff documented through the envelope checklist, vendor records, or vendor delivery confirmation when available
|
up to day 14
|
|
Rate of Cuff Order Completion
기간: up to day 14
|
Number of participants that have ordered their blood pressure cuff documented through the envelope checklist, vendor records, or vendor delivery confirmation when available.
|
up to day 14
|
|
Rate of Return Modality Completion
기간: up to day 14
|
Number of participants that completed the assigned return modality as documented on the envelope checklist.
|
up to day 14
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Time to Complete Intervention
기간: up to day 14
|
Number of days from index clinic visit to documentation of both cuff receipt and completion of assigned training modality.
|
up to day 14
|
|
Number of Participants Documenting at Least One Blood Pressure Reading
기간: up to day 21
|
Number of participants with at least one self-monitored blood pressure reading documented in the EHR within 21 days of cuff receipt.
|
up to day 21
|
|
Time Between Cuff Receipt and First Documented Reading
기간: up to day 21
|
Number of days between cuff receipt and first documented self-monitored blood pressure reading.
|
up to day 21
|
|
Rate of Workflow Barriers
기간: up to day 14
|
Number of participants with documented workflow barriers contributing to incomplete or non-concordant intervention delivery, including shipment issues, incomplete vendor forms, patient decline after workflow initiation, return modality not completed, missing documentation, clinic cuff inventory depletion, supply limitations, or other workflow disruptions identified through routine workflow documentation or operational follow-up activities.
|
up to day 14
|
|
Rate of Fidelity
기간: up to day 14
|
Number of participants that received the assigned cuff delivery modality and assigned return modality without crossover, reassignment, or missing assigned workflow components.
|
up to day 14
|
|
Rate of Differential Implementation Success
기간: up to day 14
|
Number of participants with successful delivery of both blood pressure cuff and return modality.
|
up to day 14
|
기타 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Change in Systolic Blood Pressure
기간: up to day 90
|
Change in systolic blood pressure using routinely documented clinic blood pressure values in Epic.
|
up to day 90
|
|
Rate of Medication Intensification
기간: up to day 90
|
Number of participants with addition of a new antihypertensive medication class, dose increase, or regimen intensification consistent with clinician-directed care using Epic medication order data.
|
up to day 90
|
공동 작업자 및 조사자
수사관
- 수석 연구원: Rasha Khatib, PhD, Advocate Health
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
기타 연구 ID 번호
- IRB00151173
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
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