Study Results
Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.
View full resultsBasic Information
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COMPLETED
NA
65 participants
INTERVENTIONAL
2010-02-28
2014-02-28
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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Control group
Participants in the control group receive usual care.
No interventions assigned to this group
Self monitoring for patients with COPD
self-monitoring for patients with severe COPD
Intervention Group entering vital parameters via Web Portal or automatic call center.
Nurse monitoring for patients with COPD
nurse-monitoring for patients with severe COPD
Nurses are entering vital parameters of the patient with mobile devices.
Interventions
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self-monitoring for patients with severe COPD
Intervention Group entering vital parameters via Web Portal or automatic call center.
nurse-monitoring for patients with severe COPD
Nurses are entering vital parameters of the patient with mobile devices.
Eligibility Criteria
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Inclusion Criteria
* Be able to use the system provided
* Life expectancy \> 12 months
ALL
No
Sponsors
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European Commission
OTHER
Landeskrankenanstalten-Betriebsgesellschaft
INDUSTRY
Responsible Party
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Locations
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LKH Laas
Kötschach, Carintha, Austria
Klinikum Klagenfurt
Klagenfurt, Carinthia, Austria
LKH Villach
Villach, Carinthia, Austria
Countries
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Other Identifiers
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C250487
Identifier Type: -
Identifier Source: org_study_id
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