Acute Coronary Syndrome, Smoking
Conditions
Keywords
Smoking, nicotine replacement, psychological behaviour, Smoking > 5 cigarettes per day, Hospitalisation for acute coronary syndrome
Brief summary
The aim of the present study is to assess if a personal care program of smokers hospitalised for acute coronary syndrome can change the smoking habits as compared with similar patients in conventional care program at 6 months. The program includes a cognitive-behavioural approach associated with a nicotine replacement treatment presented as an obligatory non optional treatment. Patients are men and women of less than 70 years old hospitalised for acute coronary syndrome. Major exclusion criteria is the presence of another dependence. The program includes a cognitive-behavioural approach based on the specific technique of exposure and the prescription of nicotine patch considered as other usual cardiologic treatments for at least 6 months. The end point is the smoking habits at 6 months classified as: no smoking confirmed by CO measurement, smoking or doubtful (declaration of no smoking by the patient but a CO level \> 10 ppm). 72 patients in each group will be included in 2 majors sites.
Detailed description
The cognitive behavioural approach group : This group will receive an inclusion visit at first, then two cigaret exposures cessions during hospitalisation. Thereafter-one week after he's out- the patient will come for 5 follow up visits consisting in the specific technique of cigaret exposure and nicotinic treatment adjustment. Then the last visit, at six months, will tell us if the patient is an effective non smoker or not; We'll be also collecting psychological and medical informations (such as the treatment, IMC, cardiovascular check up and psychological tests). The control group : This group is managed as usual : the nurse gives very rapid recommendations to the patients concerning smoking cessation. Nicotinic substitutes are proposed to the patients but the patient must find them by itself.
Interventions
BEHAVIORALTechnique of in-vivo exposure (cigarette) and mental image exposure (craving)
Nicotine replacement
BEHAVIORALconventional follow-up
nicotinic substitutes
Sponsors
Ministry of Health, France
National Cancer Institute, France
Assistance Publique - Hôpitaux de Paris
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
* Patients are men and women of less than 70 years old * Hospitalised for acute coronary syndrome in cardiology Intensive Care Unit * Active smoking \>5 cigarettes/day * Has given consent to participate in the study and haven't expressed its opposition the exploitation of data as part of the study
Exclusion criteria
* Presence of another dependence : alcohol abuse avowed or strongly suspected, addiction to drugs, high dose benzodiazepine dependence. clinical assessment * Major psychiatric disorders or history. clinical assessment * Treatment with lithium and neuroleptic. clinical assessment * Patient whose cardiac problem could lead to hemodynamic instability during 48 h after admission. * Patient scheduled for programmed hospitalisation within 6 months after release from hospital (\>3 days long, including coronary bypass) * Patients presenting another severe pathology requiring 6 months specific treatments. clinical assessment * Patient which cannot understand or read French * Patient with possible side-effect to nicotine substitute * Patient unaffiliated to any social security regime
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The smoking habits at 6 months classified as : no smoking confirmed by CO measurement, smoking or doubtful (declaration of no smoking by the patient but a CO level > 10 ppm). | 6 month |
Secondary
| Measure | Time frame |
|---|---|
| Assessment depending of age classes, sex, anxiety scale and other psychological characteristics | 6 month |
Countries
France
Outcome results
None listed