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| Tracking Information | |||||||||
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| First Received Date ICMJE | January 4, 2007 | ||||||||
| Last Updated Date | January 4, 2007 | ||||||||
| Start Date ICMJE | January 2007 | ||||||||
| Primary Completion Date | |||||||||
| Current Primary Outcome Measures ICMJE |
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| Original Primary Outcome Measures ICMJE | Same as current | ||||||||
| Change History | No Changes Posted | ||||||||
| Current Secondary Outcome Measures ICMJE |
Number of days admitted to hospital | ||||||||
| Original Secondary Outcome Measures ICMJE | Same as current | ||||||||
| Descriptive Information | |||||||||
| Brief Title ICMJE | Optimizing the Effect of COPD Rehabilitation | ||||||||
| Official Title ICMJE | Rehabilitation of COPD Patients: Can the Effect be Prolonged by Follow-up and Continued Rehabilitation | ||||||||
| Brief Summary | Patients with Chronic Obstructive Pulmonary Disease (COPD) may benefit from an 8-week pulmonary rehabilitation programme. However, the effect of the programme tends to attenuate with time. Patients who complete the programme are randomized to continued rehabilitation follow-up and control follow-up. |
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| Detailed Description | Patients with Chronic Obstructive Pulmonary Disease (COPD) may benefit from an 8-week pulmonary rehabilitation programme according to guidelines of the Danish Society of Pulmonary Medicine. However, the effect of programme tends to attenuate with time. Patients who complete the programme are randomized to continued rehabilitation follow-up and control follow-up. |
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| Study Phase | |||||||||
| Study Type ICMJE | Interventional | ||||||||
| Study Design ICMJE | Prevention, Randomized, Open Label, Placebo Control, Parallel Assignment, Efficacy Study | ||||||||
| Condition ICMJE | Chronic Obstructive Pulmonary Disease | ||||||||
| Intervention ICMJE | Behavioral: follow-up rehabilitation of participants with COPD | ||||||||
| Study Arms / Comparison Groups | |||||||||
| Publications * | |||||||||
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* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline. |
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| Recruitment Information | |||||||||
| Recruitment Status ICMJE | Not yet recruiting | ||||||||
| Enrollment ICMJE | 120 | ||||||||
| Completion Date | June 2008 | ||||||||
| Primary Completion Date | |||||||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both | ||||||||
| Ages | |||||||||
| Accepts Healthy Volunteers | No | ||||||||
| Contacts ICMJE |
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| Location Countries ICMJE | Denmark | ||||||||
| Administrative Information | |||||||||
| NCT ID ICMJE | NCT00419289 | ||||||||
| Responsible Party | |||||||||
| Study ID Numbers ICMJE | KA20060179 | ||||||||
| Study Sponsor ICMJE | Glostrup University Hospital,Copenhagen | ||||||||
| Collaborators ICMJE | Ministry of the Interior and Health, Denmark | ||||||||
| Investigators ICMJE |
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| Information Provided By | Glostrup University Hospital,Copenhagen | ||||||||
| Verification Date | January 2007 | ||||||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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