COPD
Conditions
Interventions
All patients in the *result oriented* group will be asked, when motivated to
initiate a quit attempt, to compose treatment goals in a contract and attend an
intense smoking-cessation program.
After
Sponsors
Universitair Medisch Centrum Utrecht
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: COPD patients (FEV1/FVC
Exclusion criteria
Exclusion criteria: not familiar with the Dutch language patients in the end stage of a disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary study endpoint: point prevalence after 24 months, measured by self-reported smoking and biochemical verification (urinary cotinine measurement). | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary study endpoint: abstinence after 12 en 24 months, functional status, quality of life, attitude, social stimulation, self-efficacy, patiënt perception, motivation, smoking habits and pulmonary function. | — |
Countries
Netherlands
Outcome results
None listed