ACTRN12622000134729尚未招募未知
Investigating feasibility and efficacy of a virtual UNSW Lifestyle Clinic exercise physiologist intervention for people with hypertension: a pilot randomised controlled trial
A/Prof Xiaoqi Feng0 个研究点目标入组 60 人开始时间: 2022年1月27日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 o limit(—)
- 性别
- All
入选标准
- •be 18 years of age or older;
- •diagnosed with hypertension and recent clinic systolic blood pressure greater than or equal to 130 mmHg and/or diastolic blood pressure greater than or equal to 80 mmHg;
- •willing to wear wrist-based blood pressure device for seven consecutive days at baseline and after 3 months;
- •willing to undergo initial exercise tests by an Exercise Physiologist to determine eligibility;
- •have access to a smartphone and the internet and feel comfortable to use it to download an App for use with a blood-pressure device, complete online assessments, and join online video consultations with an Accredited Exercise Physiologist;
- •no plan to change medications;
- •have a personal weighing bathroom scale; and
- •independently ambulant for 200m (be confident to walk 200m or around the block unassisted).
排除标准
- •significant alcohol or drug use;
- •pregnancy (or planned pregnancy);
- •unstable cardiovascular, respiratory and neurological disorders; established chronic kidney disease (eGFR <60ml/kg/1.73m2); known arrhythmias (irregular heart rhythms); known vascular aneurysm; implanted electrical devices (e.g. cardiac pacemakers or defibrillators); severe or untreated mental health illnesses (including eating disorders); active cancer or requiring treatment for cancer; other health conditions, (e.g. orthopaedic or neuromuscular limitations) or hospital admissions within the last 6 months that would make it difficult or unsafe to participate in the exercise sessions at home safely. prior mastectomy (breast removal);
- •wrist circumference >22cm and upper arm circumference >64 cm because of the BP device size;
- •participation in any other behaviour change program or clinical trial that may interfere with the outcomes of this study, e.g. weight loss, physical activity or drug;
- •unable to speak English (a translator is not available) or give written informed consent;
- •allergy to the silicone material from the BP device.
研究者
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