NCT07698509尚未招募不适用
A Scalable, Lifestyle Medicine Intervention for Hypertension Using Virtual Group Shared Medical Appointments
The University of Texas Health Science Center, Houston1 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2026年8月3日最近更新:
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 18
- 试验地点
- 1
- 主要终点
- Change in diastolic blood pressure readings
研究概览
简要总结
The purpose of this study is to learn whether virtual Lifestyle medicine shared medical appointments (LMSMAs) can help people better manage their blood pressure and improve their overall health.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 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
- 否
入选标准
- •Current diagnosis of hypertension (ICD codes I10.0-I14.0 billed within the last 5 years Essential HTN, Essential HTN, Primary HTN)
- •Currently receives care at a UTPhysicians; Last seen by a PCP at Victory location within the last 1 year.
- •Able to participate in a virtual format
- •Willingness to participate and engage in home blood pressure monitoring
排除标准
- •Unstable cardiovascular disease (recent Myocardial Infarction (MI), unstable angina, decompensated HF)
- •Advanced Chronic kidney disease (CKD) (eGFR < 30) without nephrology co-management
- •Active cancer treatment
- •Severe cognitive impairment (unable to engage)
- •Uncontrolled psychiatric illness (e.g., active psychosis)
- •Resistant hypertension (requiring> 3 medications at maximum doses)
- •Unable to participate in English class format
- •Unstable internet or lack of smartphone
研究组 & 干预措施
Lifestyle Medicine Virtual Group Visit Program plus usual medical care
Experimental
干预措施: Lifestyle Medicine Virtual group (Behavioral)
Lifestyle Medicine Virtual Group Visit Program plus usual medical care
Experimental
干预措施: Usual Care Group (Behavioral)
Usual medical care only
Active Comparator
干预措施: Usual Care Group (Behavioral)
结局指标
主要结局
Change in diastolic blood pressure readings
时间窗: 2-4 weeks after randomization,6 months after randomization
Change in systolic blood pressure readings
时间窗: 2-4 weeks after randomization,6 months after randomization
次要结局
- Percentage of eligible participants who agree to participate(end of study (6 months after randomization))
- Number of primary care physicians (PCPs) whose patients are included in the program(end of study (6 months after randomization))
- Median number of sessions attended by each participant(end of study (6 months after randomization))
- Adherence as assessed by the number of of blood pressure (BP) readings submitted between each session(end of study (6 months after randomization))
- Adherence to home BP monitoring as assessed by the number of of home BP sessions submitted between each session(end of study (6 months after randomization))
研究者
Puja Bharat Gandhi
Assistant Professor
The University of Texas Health Science Center, Houston
研究点 (1)
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