Further development and evaluation of a training for general practitioners in delivering brief stop-smoking advice as an implementation strategy of the S3-guideline screening, diagnosis and treatment of harmful and addictive tobacco use in general practice

Not Applicable

• Conditions: Tobacco Smoking, tobacco addiction; F17.2

• Registration Number: DRKS00012786
• Lead Sponsor: Medical Faculty, Heinrich Heine University Duesseldorf

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2017-08-22
• Study Completion: 2020-02-26
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 1937

Inclusion Criteria

Smoking tobacco daily or at least occasionally, consultation of a GP who participates in the trial (arm 1 or2 )

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

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
1) Patient-reported rates of delivery of behavioural treatment (single or group intervention) to assist their quit attempt by their GP during routine consultation.<br><br>2) Patient-reported rates of delivery of nicotine replacement therapy to assist their quit attempt by their GP during routine consultation.<br><br>3) Patient-reported rates of delivery of Varenicline or Bupropion to assist their quit attempt by their GP during routine consultation.<br><br>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.<br><br>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.