Tobacco Smoking, tobacco addiction F17.2
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Smoking tobacco daily or at least occasionally, consultation of a GP who participates in the trial (arm 1 or2 )
Exclusion criteria
Exclusion criteria: Limited literacy, incapability to provide informed consent (e.g. dementia), patients who can not be interviewed due to other reasons (e.g. limited visual or auditory abilities), patients who will not see their GP in person
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Patient-reported rates of delivery of brief advice to quit smoking by their GP during routine consultation. This parameter will be collected by personal-oral-questioning immediately after the consultation. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1) Patient-reported rates of delivery of behavioural treatment (single or group intervention) to assist their quit attempt by their GP during routine consultation. 2) Patient-reported rates of delivery of nicotine replacement therapy to assist their quit attempt by their GP during routine consultation. 3) Patient-reported rates of delivery of Varenicline or Bupropion to assist their quit attempt by their GP during routine consultation. 4-9) Patient-reported rates of quit attempts 4, 12 and 26 weeks following GP consultation and patient-reported smoke status 4,12 and 26 weeks after consultation. Parameter 1-3) will be collected by personal-oral-questioning immediately after the consultation. Parameter 4-9) will be collected by paper-and-pencil follow-up survey. | — |
Countries
Germany
Contacts
Institut of General Practice; Addiction research and clinical epidemiology; Medical Faculty of the Heinrich Heine University