Smoking Cessation Clinical Trial
— ESCIMOfficial title:
Effectiveness of a Smoking Cessation Intervention in a Mental Health Day Hospital
Background: Nicotine contained in tobacco is highly addictive and tobacco use is a major risk factor for cardiovascular and respiratory diseases. Every year, more than 8 million people die from tobacco use. Smoking-related mortality is significantly higher in people with serious mental illness. Is estimated that half of all deaths among individuals with mental illnesses are attributable to tobacco use. People with serious mental illness have greater daily tobacco consumption, nicotine dependence, and smoking relapse. While significant progress has been made in reducing tobacco use within the general population, rates of tobacco use remain high among individuals with mental illness. Smoking cessation often requires numerous attempts by these people. Thus, smokers with mental health illnesses may find it more difficult to quit, although highly motivated to quit. Smoking cessation during hospitalization (total or partial) is cost-effective, as it reduces hospital readmissions, and mortality, and improves smokers' quality of life. Available quitting aids are both safe and effective in supporting cessation in tobacco users with mental illness and stopping smoking is associated with an improvement in mental health. The investigators aimed to evaluate the feasibility and efficacy of adding an intensive smoking intervention to the usual treatment for patients with psychiatric disorders attending a day hospital of a tertiary hospital.
Status | Recruiting |
Enrollment | 150 |
Est. completion date | July 30, 2024 |
Est. primary completion date | July 27, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Mental health day hospital inpatient. - Smoker of at least 1 cigarette per day, electronic cigarette, or heated tobacco product daily for at least 1 month. - Individuals who accept to participate in the study and give informed consent. Exclusion Criteria: - Cognitive impairment, dementia, or brain damage. - Medically unstable. - Explicitly demanding tobacco treatment. - Trying to quit smoking using another intervention. - Insufficient comprehension skills in Spanish or Catalan. |
Country | Name | City | State |
---|---|---|---|
Spain | Hospital Clínic de Barcelona | Barcelona |
Lead Sponsor | Collaborator |
---|---|
Hospital Clinic of Barcelona |
Spain,
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* Note: There are 20 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Tobacco use changes from baseline to post-intervention | Number of cigarettes smoked in past 24 hours. | An average of 2 months | |
Primary | Motivation to quit smoking changes from baseline to post-intervention | Individuals will be assessed with the Richmond test. | An average of 2 months | |
Primary | Cotinine levels in urine changes from baseline to post-intervention | Urine cotinine levels | An average of 2 months | |
Secondary | Nicotine dependence changes from baseline to post-intervention | Change of self reported tobacco dependence using Fagerström Test for Nicotine Dependence. | An average of 2 months | |
Secondary | Self-efficacy to quit smoking changes from baseline to post-intervention | Change of self reported self-efficacy (using a Likert scale from 0 to 10). Minimum value: 0. Maximum value: 10. Higher scores indicate more self-efficacy to quit smoking. | An average of 2 months | |
Secondary | Smoking knowledge changes from baseline to post-intervention | Changes in smoking knowledge obtained through a knowledge questionnaire developed by the researchers. | An average of 2 months | |
Secondary | Trait and state anxiety changes from baseline to post-intervention | Changes in anxiety obtained through the State-Trait Anxiety Inventory. Minimum value: 20. Maximum value: 80. Higher scores indicate greater anxiety. | An average of 2 months | |
Secondary | Depressive symptoms changes from baseline to post-intervention | Changes in depressive symptoms obtained through the Montgomery and Asberg Depression. Minimum value: 0 Maximum value: 60. A score of less than 10 points indicate the absence of depressive disorder. | An average of 2 months | |
Secondary | Self-reported clinically relevant psychological symptoms changes from baseline to post-intervention | Changes in self-reported clinically relevant psychological symptoms through the Brief Symptom Inventory. Minimum value: 0. Maximum value: 72. Higher scores indicate higher levels of psychological distress. | An average of 2 months |
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