Smoking Cessation Interventions in Stroke Patients

Not Applicable

• Conditions: Ischemic Stroke

• Registration Number: NCT01574001
• Lead Sponsor: Institute of Psychiatry and Neurology, Warsaw

Brief Summary

The primary objective of the present randomized controlled trial is to compare the effectiveness of three anti-smoking interventions of different intensities. It has been hypothesised that early follow-up visits facilitate post-stroke smoking cessation in patients hospitalized because of first-ever ischemic stroke.

Detailed Description

BACKGROUND: It is well known, that continued smoking after stroke increases the risk of death and stroke recurrence within a few years after the first stroke. Searching for more efficient methods of antismoking interventions is therefore justified.

OBJECTIVES: The primary objective of the present study is to compare the effectiveness of three anti-smoking interventions of different intensities.

DESIGN: Randomized, controlled trial.

METHODS: Study participants will be recruited among patients of neurological clinics of Institute of Psychiatry and Neurology, hospitalized because of their first in a lifetime ischemic stroke. All stroke patients will be screened regarding their smoking status. The subjects will be patients smoking cigarettes immediately before their first-ever stroke, able to understand the research protocol procedures and able to cooperate during the investigation.

Antismoking interventions will be based on the "5A's" method. Study participants will be randomized to one of three interventions differing in follow-up intensity.

Study Timeline

• Status Verified: 2012-04
• Study Start: 2012-04
• Study First Submitted: 2012-04-01
• Study First Submitted QC: 2012-04-06
• Study First Posted: 2012-04-10
• Last Update Submitted: 2013-05-14
• Last Update Posted: 2013-05-15
• Primary Completion: 2013-12
• Study Completion: 2014-12

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 240

Inclusion Criteria

• Patients smoking immediately prior to stroke
• The first in the lifetime ischemic stroke
• Ability to understand the research protocol procedures and cooperation during the investigation
• Reported availability of and declaration to participate in follow-up
• Informed consent to participate in the study

Exclusion Criteria

• Severe stroke
• Stroke onset more than 3 weeks before admission
• History of previous stroke with clinical symptoms
• Hemorrhagic stroke
• Diagnosis of dementia or presence of other neurological disease (Parkinson's disease, amyotrophic lateral sclerosis, multiple sclerosis, Huntington's chorea, a previous subarachnoid haemorrhage, meningitis, cerebral trauma in an interview)

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Smoking cessation rate	12 months

Trial Locations

Locations (1)

Institute of Psychiatry and Neurology; 🇵🇱 Warsaw, Poland