跳至主要内容
临床试验/NCT04797403
NCT04797403进行中(未招募)不适用

Effectiveness of Implementing an Intensive Blood Pressure Reduction Intervention on Cognitive Decline in Low-Income and Minority Hypertensive Patients

Tulane University1 个研究点 分布在 1 个国家目标入组 1,306 人开始时间: 2019年10月22日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
1,306
试验地点
1
主要终点
Net difference in mean change in cognitive decline

研究概览

简要总结

The study will test a multifaceted strategy for implementing an intensive blood pressure intervention protocol targeting systolic BP <120 mmHg on cognitive decline in racial minority and low-income hypertensive patients in primary care. The proposed study will generate urgently needed data on effective, adoptable, and equitable intervention strategies to reduce blood pressure-related cognitive decline in low- income and minority populations. If proven effective, the implementation strategy for intensive blood pressure reduction could be adapted and scaled up in diverse primary care settings to prevent cognitive decline and clinical dementia.

详细描述

African American and low-income populations bear a disproportionate burden of dementia and have been underrepresented in trials of cognitive impairment. The Systolic Blood Pressure Intervention Trial (SPRINT) showed that an intensive blood pressure (BP) intervention (target systolic BP <120 mmHg) lowered the risk of cognitive impairment compared to a standard BP intervention (systolic BP target <140 mmHg). The next important step is to determine how the successful SPRINT intensive blood pressure intervention can be implemented in a real-world clinic setting to prevent cognitive decline. The overall objective of the proposed study is to test a multifaceted strategy for implementing an intensive BP intervention protocol adapted from SPRINT targeting systolic BP <120 mmHg on cognitive decline in racial minority and low-income hypertensive patients in resource-constrained primary care practices in Louisiana and Mississippi. The RE-AIM (Reach Effectiveness Adoption Implementation Maintenance) framework has been used to guide the development and evaluation of the multifaceted implementation strategy, including protocol-based treatment that employs the SPRINT stepped-care intensive BP management algorithm, dissemination of SPRINT findings, shared- decision making, team-based collaborative care, BP audit and feedback, home BP monitoring, and patient health coaching. Building on the ongoing Implementation of Multifaceted Patient-Centered Treatment Strategies for Intensive Blood Pressure Control (IMPACTS-BP) trial, the investigators will cost-effectively conduct a cluster- randomized trial in 40 primary care clinics that serve low-income populations in Louisiana and Mississippi. The primary outcome in the proposed trial is the net difference in mean change of global cognitive composite z-score from baseline to an average of 36 months between the intervention and enhanced usual care groups. Secondary outcomes include net difference in mean change of executive function and memory composite z-scores, systolic and diastolic BP, adverse effects, and quality of life. Implementation outcomes, including acceptability, adaptation, adoption, feasibility, fidelity, penetrance, and cost-effectiveness, will also be collected and used to improve intervention delivery during the trial. The proposed trial, with a sample size of 40 clinics (31.5 patients/clinic), has 93% statistical power to detect a 0.30 or higher difference in the global cognitive composite z-score at a 2-sided significance level of 0.05 assuming 20% loss to follow-up and an intra-cluster correlation of 0.05. In a meta-analysis of 5 clinical trials, the pooled effect size was 0.35 (95% CI 0.32, 0.38) for the global cognitive composite z-score. This study will generate urgently needed data on effective, adoptable, and equitable intervention strategies to reduce blood pressure-related cognitive decline in low-income and minority populations. If proven effective, the implementation strategy for intensive blood pressure reduction could be adapted and scaled up in diverse primary care settings to prevent cognitive decline and clinical dementia.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
40 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •for Primary Care Clinics
  • •Predominantly managing underserved populations with health disparities (ethnic minorities, low-income groups, and residents of rural areas and inner cities).
  • •Having electronic medical record systems.
  • •Serving >200 hypertension patients (ICD-10-CM I10-I15) during the previous year.
  • •Not participating in other hypertension control programs
  • •Not sharing providers or nurses/pharmacists with other participating clinics.
  • •Inclusion Criteria for Study Participants
  • •Men or women aged ≥40 years (2/3 of participants ≥60 years) who receive primary care from participating clinics.
  • •Systolic BP ≥ 140 mmHg at two screening visits for those not taking antihypertensive medication or systolic BP ≥ 130 mmHg at two screening visits for those taking antihypertensive medications
  • •Pregnant women, women planning to become pregnant in the near future, women of childbearing potential and not practicing birth control, and persons who cannot give informed consent will be excluded.
  • •No diagnosis of dementia at baseline
  • •Baseline MoCA score ≥
  • •No diagnosis of end-stage renal disease, defined as dialysis or transplantation
  • •Speak English as first language
  • •No plans to change to a primary healthcare provider outside of their clinic in the near future
  • •No individuals unlikely to complete the study, such as those who plan to move out of the study area in the near future and temporary migrant and homeless people
  • •No immediate family members are staff at their clinic

排除标准

  • 未提供

研究组 & 干预措施

Enhanced Usual Care

No Intervention

Enhanced usual care will include an education session on the ACC/AHA hypertension guideline to providers and proper BP measurement to providers and staff at enhanced usual care clinics.Otherwise, no active intervention will take place, and all usual care clinics will follow their routine clinic practice.

Intervention

Experimental

The core component of the intervention is protocol-based treatment using the SPRINT intensive BP management algorithm. Implementation strategies include dissemination of SPRINT study findings, team-based collaborative care and shared-decision making, blood pressure audit and feedback, home blood pressure monitoring, and health coaching.

干预措施: Stepped-care protocol adapted from the SPRINT intensive-treatment algorithm (Behavioral)

结局指标

主要结局

Net difference in mean change in cognitive decline

时间窗: Baseline to an average of 36 months

The net difference in mean change of global cognitive composite z-score over an average 36 months between intervention and enhanced usual care groups

次要结局

  • Net difference in mean change in MoCA score(Baseline to an average of 36 months)
  • Net difference in mean change in memory function(Baseline to an average of 36 months)
  • Net difference in mean change in diastolic blood pressure(Baseline to an average of 36 months)
  • Net difference in mean change in executive function(Baseline to an average of 36 months)
  • Net difference in mean change in systolic blood pressure(Baseline to an average of 36 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Katherine T Mills

Assistant Professor

Tulane University

研究点 (1)

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