DRKS00000239已完成4 期
Acceptance of a Telemedical Intervention in Patients with COPD - ATICO
Robert Bosch Healthcare GmbH0 个研究点目标入组 43 人开始时间: 2009年11月3日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 43
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
- N/a: Single Arm Study
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- one 至 one（—）
- 性别
- All
入选标准
- •1. written consent
- •2. male or female ambulatory treated patients
- •3. patients with COPD - GOLD classification III and IV
- •4. patients with COPD - GOLD classification I and II -, with an inpatient treatment of COPD lasting not longer than 3 months
- •5. patient has blood pressure when resting not higher than 180/100 mmHg
- •6. patient has the cognitive ability and intention to use the Health Buddy® with its peripherals
- •7. patient has adequate knowledge of the German language
- •8. patient has an active telephone connection, preferably analogue
- •9. patient is motivated to take part in the trial
排除标准
- •1. patient is currently participating in another trial or finished participation within the previous 4 weeks
- •2. patient is pregnant or breastfeeding
- •3. patient currently has known malignant or virulent illnesses
- •4. patient has a severe restriction of movements (e.g. paresis after stroke)
- •5. patient is invasively ventilated
研究者
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