COPD Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have been diagnosed with COPD (a long-term lung condition that makes breathing difficult)
- People who have had a flare-up (worsening of symptoms) of their COPD at least once in the past year
- People who live in Høje Taastrup or Copenhagen
- People who are cognitively able to participate (able to think and understand clearly enough to take part)
- People who score at certain levels on a quality-of-life questionnaire called the ICECAP-SCM, with specific score thresholds across seven areas (confirm with trial site for exact scoring details)
Who may not be able to join:
- People who have dementia
- People who have a psychotic condition
- People who have a substance abuse problem
- People who have a hearing or speech impairment that would affect their ability to participate
- People who have cancer
- People who are already receiving specialised palliative care or a similar type of support program
- People who are in the final stage of life and considered to be imminently dying
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Kirstine Benthien, Ph.d., Copenhagen University Hospital, Hvidovre
Phone: +45 24 34 21 35
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
ICECAP-SCM
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.