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临床试验/NCT04640519
NCT04640519已完成不适用

Telehealth After Stroke Care (TASC): Integrated Multidisciplinary Access to Post-stroke Care

Columbia University1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2020年10月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
50
试验地点
1
主要终点
Percentage of Participants With Systolic BP Control

研究概览

简要总结

The Telehealth After Stroke Care (TASC) trial is a pilot randomized controlled trial. It aims to evaluate the feasibility of a telehealth based model providing multidisciplinary access including nursing, pharmacy and physician care, and obtain preliminary evidence of efficacy of an integrated telehealth approach to blood pressure management after stroke.

详细描述

Hypertension is the most modifiable risk factor for recurrent stroke. Blood pressure (BP) reduction is associated with decreased risk of stroke recurrence but remains poorly controlled in most survivors. Minority groups have a higher prevalence of uncontrolled BP and higher rates of stroke. Limited access contributes to challenges in post-stroke care. Telehealth After Stroke Care (TASC) will be a telehealth intervention that integrates remote BP monitoring and telehealth visits to enhance BP control and promote self-efficacy, with a multidisciplinary approach to improve clinical processes and health outcomes. The investigators will assess for feasibility and obtain preliminary evidence of efficacy. Fifty (50) eligible patients will be screened for inclusion prior to hospital discharge and randomized to TASC or usual care. TASC patients will receive a BP monitoring kit and electronic tablet. They will be scheduled with 5 telehealth visits over 3 months, including primary care nurse practitioner, pharmacy at 4 and 8 weeks and stroke neurologist. Usual care patients will be seen by a primary care nurse practitioner at 1-2 weeks and a stroke neurologist at 1 and 3 months. Data will be collected at 0 and 3 months. The primary outcome will be BP control (BP <140/90 mmHg) at 3 months. The secondary outcome will be self-efficacy in medication adherence and treatment. Interdisciplinary team competency, fidelity, and telehealth satisfaction surveys will be administered. Patient reported outcomes including depression, cognitive function, and socioeconomic determinants will also be collected. Integrated team-based interventions are needed to improve BP control and reduce racial disparities in post-stroke care. It may be feasible and effective in enhancing post-stroke BP control and promoting self-efficacy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Presence of hypertension (by clinical history or hospital BP ≥140/90 on two occasions)
  • •Plan for discharge home after stroke
  • •Ability to provide consent (patient or caregiver)

排除标准

  • •Modified Rankin scale ≥ 4 at time of enrollment (severely disabled)
  • •Pregnancy
  • •Severe psychiatric illness
  • •Dialysis or diagnosis of end stage renal disease
  • •Life expectancy < 1 year or terminal illness
  • •Symptomatic flow limiting cerebrovascular stenosis without plan for intervention, or long-term BP goal ≥ 140/90

研究组 & 干预措施

TASC Intervention

Experimental

TASC patients will receive a BP monitoring kit and electronic tablet and tailored infographics, and attend 5 telehealth visits over 3 months, including primary care nurse practitioner, pharmacy and stroke neurologist.

干预措施: TASC intervention (Other)

TASC Control

Active Comparator

Usual care patients will be seen by a primary care nurse practitioner and a stroke neurologist.

干预措施: Usual care (Other)

结局指标

主要结局

Percentage of Participants With Systolic BP Control

时间窗: Up to 3 months

The outcome of BP control will be defined by change in mean awake systolic blood pressure from baseline at the time of discharge through remote monitoring at 3 months to be \< 130 mmHg. BP control will be determined by the mean 24-hr blood pressure through remote monitoring at 3 months and survey patient reported outcomes for all participants.

Percentage of Participants Who Completed at Least 1 Video Visit

时间窗: 3 months

This measures the feasibility of the TASC model, the interdisciplinary team competency, fidelity of implementation.

次要结局

  • Medication Adherence Percentage(3 months)

研究者

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

Imama A. Naqvi

Assistant Professor of Neurology

Columbia University

研究点 (1)

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