ACTRN12621000552886Not yet recruiting未知
Feasibility assessment of an ambulatory monitoring and management of chronic obstructive pulmonary disease
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Not yet recruiting
- Enrollment
- 20
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
- Allocation
- Non-randomised trial
- Primary Purpose
- Prevention
- Masking
- Open (masking not used)
Eligibility Criteria
- Ages
- 18 Years to o limit (—)
- Sex
- All
Inclusion Criteria
- •1. Evidence of spirometrically confirmed airflow obstruction, defined as a post-bronchodilator FEV1/FVC ratio <0.7 and post-bronchodilator FEV1 between 30% and 70% predicted, recorded within 1 year of screening
- •2. Report one or more of the following symptoms within the preceding two weeks: shortness of breath, chronic cough and sputum
- •3. Hospitalisation for worsening COPD (exacerbation) on one or more occasions in the two years prior to commencement of study procedures
- •4. Be ambulatory and self-caring at the time of recruitment
Exclusion Criteria
- •1. Have experienced an exacerbation in the 30 days prior to screening
- •2. In the opinion of the investigator will not complete the study or adhere to the intervention
- •3. In the opinion of the investigator, have an inadequate mastery of English to communicate with study staff
- •4. Is unable to independently provide consent
Investigators
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