Background: Many people who smoke use vaping products to help them quit. Levels of toxicants in urine samples are substantially lower in those who exclusively vape compared to those who smoke, suggesting that vaping poses only a fraction of the harms as smoking. However, vaping is still not risk free, with some studies finding higher levels of some toxicants among vapers compared to those who do not smoke or vape. People with mental health conditions have different smoking patterns compared with the wider general population. It is not known if people with mental health conditions have different vaping pattens, therefore researchers do not know if they are exposed to different levels of vaping related toxicants. Also, smoking exposes people to high levels of polycyclic aromatic hydrocarbons (PAHs), which can reduce the effectiveness of some psychotropic medication and management of symptoms. Vaping exposes people to lower levels of PAHs than smoking, however it is unknown if the levels of PAHs from vaping affect the metabolization of psychotropic medicines. The goal of this observational study is to learn about levels of tobacco toxicants among people with mental health conditions who vape, smoke, dual use or do neither. The main question\[s\] it aims to answer are: What are the levels of biomarkers of toxicant exposure among those who use community mental health services who exclusively vape, exclusively smoke, dual use or do neither, and how do they change over time? What is the difference in clozapine excretion levels and metabolism among those who use community mental health services who exclusively vape, exclusively smoke or dual use or do neither? Participants will self report smoking and vaping characteristics and provide blood and urine samples at baseline and six months later. Urine will be analysed for tobacco toxicants. Blood will be analysed for levels of clozapine and other prescribed anti psychotic medication. Researchers will compare levels of toxicants between people who vape, smoke, dual use, or do neither to see if these is a difference.
This is a longitudinal observational study. It aims to investigate four groups each with 40 participants (160 in total) and follow them up at 6 months (smokers, vapers and non-users) or 3 months and 6 months (dual users). Participants will complete questionnaires and provide urine and blood samples at each data collection session. Urine samples will be tested for a range of tobacco toxicants and markers of inflammation and oxidative stress. Blood samples will be tested for levels of clozapine an other anti-psychotic medication.
Study Type
OBSERVATIONAL
Enrollment
160
No intervention, participants own tobacco products
No intervention, participants own e-cigarette products
No intervention, participants own tobacco and e-cigarette products
No intervention
South London and Maudsley NHS Foundation Trust
London, United Kingdom
Nicotine
Levels of nicotine and its metabolites (nicotine, 3-hydroxycotinine) in urine
Time frame: Baseline
Nicotine
Levels of nicotine and its metabolites (nicotine, 3-hydroxycotinine) in urine
Time frame: 6 months after baseline
Tobacco-specific nitrosamines
Levels of NNN, NNK(NNAL), NAB, NAT in urine
Time frame: Baseline
Tobacco-specific nitrosamines
Levels of NNN, NNK(NNAL), NAB, NAT in urine
Time frame: 6 months after baseline
Volatile organic compounds
Levels of Acrolein, Acrylamide, Acrylonitrile, Benzene and Crotonaldehyde in urine
Time frame: Baseline
Volatile organic compounds
Levels of Acrolein, Acrylamide, Acrylonitrile, Benzene and Crotonaldehyde in urine
Time frame: 6 months after baseline
Polycyclic aromatic hydrocarbons
Levels of 2-napthol in urine
Time frame: Baseline
Polycyclic aromatic hydrocarbons
Levels of 2-napthol in urine
Time frame: 6 months after baseline
Metals
Levels of Cadmium, Lead, Mercury, Nickle, Selenium in urine
Time frame: Baseline
Metals
Levels of Cadmium, Lead, Mercury, Nickle, Selenium in urine
Time frame: 6 months after baseline
Clozapine
Levels of clozapine in blood
Time frame: Baseline
Clozapine
Levels of clozapine in blood
Time frame: 6 months after baseline
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