Long Term Effect of an Education and Training Program for Patients With Chronic Obstructive Pulmonary Disease
This study has been completed.
Sponsor:
Norwegian University of Science and Technology
Collaborator:
The Royal Norwegian Ministry of Health
Information provided by:
Norwegian University of Science and Technology
ClinicalTrials.gov Identifier:
NCT00159549
First received: September 8, 2005
Last updated: November 18, 2005
Last verified: November 2005
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
A parallell group study comparing the effect of an education program with an education and training program for patients with COPD. 30 participants in each group. Participants self-select which group they wanted to be in. Main outcome is SGRQ (a HQoL for patients with COPD).
| Condition | Intervention | Phase |
|---|---|---|
|
Chronic Obstructive Pulmonary Disease |
Behavioral: education and training program |
Phase 2 Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Long Term Effect of an Education and Training Program for Patients With Chronic Obstructive Pulmonary Disease |
Resource links provided by NLM:
Further study details as provided by Norwegian University of Science and Technology:
Primary Outcome Measures:
- St Geoprg Respiratory Questionnaire (SGRQ)
Secondary Outcome Measures:
- COPD-Efficacy scale (Norwegian short version), Breathing Problems Questionnaire (BPQ), journal examinations, FVC, FEV1, six minutes walking test with registration of shortness of breath and pulseoxymetrical data.
| Estimated Enrollment: | 60 |
| Study Start Date: | January 2000 |
| Estimated Study Completion Date: | December 2005 |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Patients diagnosed with COPD (FEV1<75% of expected) who have the ability to conversation and active participation will be included.
Exclusion Criteria:
-
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00159549
Locations
| Norway | |
| Department of Community Medicine and General Practice | |
| Trondheim, Norway, N-7489 | |
Sponsors and Collaborators
Norwegian University of Science and Technology
The Royal Norwegian Ministry of Health
Investigators
| Principal Investigator: | Aslak Steinsbekk, PhD | Norwegian University of Science and Technology |
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00159549 History of Changes |
| Other Study ID Numbers: | DMF 05/414 |
| Study First Received: | September 8, 2005 |
| Last Updated: | November 18, 2005 |
| Health Authority: | Norway: Norwegian Social Science Data Services |
Keywords provided by Norwegian University of Science and Technology:
|
Patient education |
Additional relevant MeSH terms:
|
Lung Diseases Respiration Disorders Pulmonary Disease, Chronic Obstructive Lung Diseases, Obstructive Respiratory Tract Diseases |
ClinicalTrials.gov processed this record on May 23, 2013