DRKS00000239
Completed
Phase 4
Acceptance of a Telemedical Intervention in Patients with COPD - ATICO
Robert Bosch Healthcare GmbH0 sites43 target enrollmentStarted: November 3, 2009Last updated:
Overview
- Phase
- Phase 4
- Status
- Completed
- Sponsor
- Robert Bosch Healthcare GmbH
- Enrollment
- 43
Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
- Allocation
- N/a: Single Arm Study
- Masking
- Open (masking not used)
Eligibility Criteria
- Ages
- one to one (—)
- Sex
- All
Inclusion Criteria
- •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
Exclusion Criteria
- •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
Investigators
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