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临床试验/NCT07124728
NCT07124728终止不适用

Impact of Syntrillo's Telehealth Service on Stroke Risk Factor Reduction in At-risk Patients

Syntrillo, Inc1 个研究点 分布在 1 个国家目标入组 11 人开始时间: 2025年7月30日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
终止
发起方
入组人数
11
试验地点
1
主要终点
Change in Systolic Blood Pressure

研究概览

简要总结

A prospective, single-arm, open-label study evaluating the impact of Syntrillo's telehealth program on stroke risk factors, particularly blood pressure, among 68 high-risk patients. The 6-month intervention includes personalized remote care with blood pressure monitoring, wearable tracking, and multidisciplinary telehealth visits.

详细描述

Participants ≥30 years old with hypertension and at least one of the following conditions: atrial fibrillation, diabetes, chronic kidney disease (stage 2 or higher), obesity (class 2 or higher), obstructive sleep apnea, coronary artery disease, hyperlipidemia, carotid stenosis (of 50% or greater), and/or congestive heart failure will be enrolled in a 6-month telehealth intervention focused on stroke risk reduction. The program includes use of home blood pressure monitors, smart pillboxes, wearable activity trackers, and a multidisciplinary team for personalized care. Primary endpoint is change in systolic blood pressure. Additional endpoints include diastolic BP, inflammatory markers (hs-CRP), and cardiovascular biomarkers (resting heart rate, HRV). The study is single-arm, non-randomized, and exploratory in design.

研究设计

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

入排标准

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

入选标准

  • Age greater than or equal to 30
  • Diagnosis of hypertension
  • One or more of the following:
  • Dtrial fibrillation
  • Chronic kidney disease (stage 2+)
  • Obesity (class 2+)
  • Obstructive sleep apnea
  • Coronary artery disease
  • Hyperlipidemia
  • Carotid stenosis (greater than or equal to 50%)
  • Congestive heart failure

排除标准

  • History of stroke or TIA
  • Inability to consent or understand study
  • Residence in long-term acute care facility
  • Inability to ambulate independently
  • Non-English speaking
  • No internet access
  • Not residing in Virginia
  • Pregnancy or suspected pregnancy

研究组 & 干预措施

Telemedicine Stroke Prevention Program

Experimental

Participants will receive a 6-month personalized telehealth intervention including remote patient monitoring, blood pressure management, lifestyle counseling, wearable monitoring, and multidisciplinary telemedicine visits via the Healthie platform.

干预措施: Laboratory Blood Test Collection (Procedure)

Telemedicine Stroke Prevention Program

Experimental

Participants will receive a 6-month personalized telehealth intervention including remote patient monitoring, blood pressure management, lifestyle counseling, wearable monitoring, and multidisciplinary telemedicine visits via the Healthie platform.

干预措施: Wearable Activity Trackers (Fitbit or Apple Watch) (Device)

Telemedicine Stroke Prevention Program

Experimental

Participants will receive a 6-month personalized telehealth intervention including remote patient monitoring, blood pressure management, lifestyle counseling, wearable monitoring, and multidisciplinary telemedicine visits via the Healthie platform.

干预措施: Healthie EHR (Other)

Telemedicine Stroke Prevention Program

Experimental

Participants will receive a 6-month personalized telehealth intervention including remote patient monitoring, blood pressure management, lifestyle counseling, wearable monitoring, and multidisciplinary telemedicine visits via the Healthie platform.

干预措施: Secure Messaging Platforms (TigerConnect, Weave, AirCall) (Other)

Telemedicine Stroke Prevention Program

Experimental

Participants will receive a 6-month personalized telehealth intervention including remote patient monitoring, blood pressure management, lifestyle counseling, wearable monitoring, and multidisciplinary telemedicine visits via the Healthie platform.

干预措施: Antihypertensive Medication Management (Drug)

Telemedicine Stroke Prevention Program

Experimental

Participants will receive a 6-month personalized telehealth intervention including remote patient monitoring, blood pressure management, lifestyle counseling, wearable monitoring, and multidisciplinary telemedicine visits via the Healthie platform.

干预措施: Statin Medication Management (Drug)

Telemedicine Stroke Prevention Program

Experimental

Participants will receive a 6-month personalized telehealth intervention including remote patient monitoring, blood pressure management, lifestyle counseling, wearable monitoring, and multidisciplinary telemedicine visits via the Healthie platform.

干预措施: Antiplatelet or Anticoagulant Therapy (Drug)

Telemedicine Stroke Prevention Program

Experimental

Participants will receive a 6-month personalized telehealth intervention including remote patient monitoring, blood pressure management, lifestyle counseling, wearable monitoring, and multidisciplinary telemedicine visits via the Healthie platform.

干预措施: Tenovi Smart Pillbox (Device)

Telemedicine Stroke Prevention Program

Experimental

Participants will receive a 6-month personalized telehealth intervention including remote patient monitoring, blood pressure management, lifestyle counseling, wearable monitoring, and multidisciplinary telemedicine visits via the Healthie platform.

干预措施: Technology-enabled Telehealth Care Plan (Behavioral)

Telemedicine Stroke Prevention Program

Experimental

Participants will receive a 6-month personalized telehealth intervention including remote patient monitoring, blood pressure management, lifestyle counseling, wearable monitoring, and multidisciplinary telemedicine visits via the Healthie platform.

干预措施: Blood Pressure Monitoring Device (Device)

结局指标

主要结局

Change in Systolic Blood Pressure

时间窗: Baseline to 6 months

This measure evaluates the average change in systolic blood pressure (SBP), which is the pressure in the arteries when the heart beats. Blood pressure is measured by participants at home using a Tenovi FDA-cleared digital blood pressure monitor. Baseline SBP is calculated using the first 10 valid readings taken during the initial week of monitoring. The 6-month value is calculated from the last 10 valid readings taken in the final week of the intervention. The study aims to observe a reduction of at least 10 mmHg in average SBP over the intervention period.

次要结局

  • Change in Diastolic Blood Pressure(Baseline to 6 months)
  • Change in Pulse Pressure(Baseline to 6 months)
  • Change in High-Sensitivity C-Reactive Protein (hs-CRP)(Baseline to 6 months)
  • Change in Resting Heart Rate(Baseline to 6 months)
  • Change in Systolic Blood Pressure Variability(Baseline to 6 months)
  • Change in Heart Rate Variability(Baseline to 6 months)

研究者

发起方
Syntrillo, Inc
申办方类型
Other
责任方
Sponsor

研究点 (1)

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