跳至主要内容
临床试验/NCT07539597
NCT07539597招募中不适用

Innovative Approaches to Hypertension Management in High-Risk Emergency Department Populations: A Feasibility Study

Icahn School of Medicine at Mount Sinai1 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2026年2月12日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
15
试验地点
1
主要终点
Number of participants on study at 3 months

研究概览

简要总结

This single-center, single-arm quasi-experimental study will assess the feasibility and acceptability of a community health worker (CHW)-led intervention to address social determinants of health (SDOH) among emergency department patients with hypertension. At enrollment, participants (N=15) will complete standardized SDOH surveys in REDCap, and CHWs will facilitate referrals to local community-based organizations that address identified social needs. With participant consent, the study will also include medical record review through EPIC and Healthix to evaluate healthcare utilization-including emergency department visits, hospitalizations, and outpatient encounters-during the one-year period before and after the index ED visit.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Health Services Research
盲法
None

入排标准

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

入选标准

  • 18 years and older who reside in the 5 boroughs of NYC,
  • whom speak English or Spanish,
  • have a known diagnosis of hypertension, and
  • have uncontrolled hypertension, defined as two measures of systolic blood pressure (SBP) ≥140 mmHg or diastolic blood pressure (DBP) ≥ 90 mmHg obtained during their ED visit.

排除标准

  • Patients who are unable to consent,
  • pregnant patients,
  • patients with a history of end stage renal disease, a history of heart failure or a BMI of greater than 50.

研究组 & 干预措施

Participants with Hypertension

Experimental

Participants with hypertension in high-risk Emergency Department populations

干预措施: Community Health Worker engagement (Behavioral)

结局指标

主要结局

Number of participants on study at 3 months

时间窗: 3 months

Number of participants on study at 3 months to assess retention

Number of intervention engagement

时间窗: 6 months

Number of interventions engagement based on number of types of CHW encounters

次要结局

  • Acceptability of Intervention Measure (AIM)(baseline, 3 months, 6 months)
  • Intervention Appropriateness Measure (IAM)(baseline, 3 months, 6 months)

研究者

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

Marcee Wilder

Assistant Professor

Icahn School of Medicine at Mount Sinai

研究点 (1)

Loading locations...

相似试验