Smoking cessation treatment for patients with common mental illness Other
Conditions
Interventions
A two-armed, pragmatic, online, randomised, and controlled feasibility and pilot trial will be used to test the acceptability and feasibility of an online smoking cessation intervention, and the trial
Sponsors
University of Bath
Eligibility
Sex/Gender
All
Age
18 Years to 100 Years
Inclusion criteria
Inclusion criteria: 1. Adult (aged 18+ years), 2. Self-reported regular (daily or non-daily) smokers 3. Eligible for SilverCloud treatment, according to therapists/psychological wellbeing practitioners 4. Comorbidities are allowed
Exclusion criteria
Exclusion criteria: 1. Aged under 18 2. Non-smoker 3. Not eligible for SilverCloud treatment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Self-reported quit attempt (at least 24 hours quit) measured using an online questionnaire at 2, 4, 6, 8 and 10 weeks, and 3-month follow up | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Engagement with, and completion of, the online smoking cessation and mental health programmes measured using SilverCloud data over 12 weeks. 2. Self-reported smoking cessation medicine and e-cigarette use measured using an online questionnaire at baseline, 2, 4, 6, 8 and 10 weeks, and 3 and 6 months follow up. 3. Depression and anhedonia (Patient Health Questionnaire; PHQ-9) measured using SilverCloud data at baseline and at 2, 4, 6, 8 and 10 weeks, and 3 and 6 months follow up by online questionnaire 4. Anxiety (General Anxiety Disorder Questionnaire; GAD-7) measured using SilverCloud data at baseline and at 2, 4, 6, 8 and 10 weeks, and 3 and 6 months follow up by online questionnaire 5. Quality of health measured using an online questionnaire at 3 and 6 months follow up 6. Self-reported smoking cessation measured using an online questionnaire at the 3-month follow-up (4-weeks abstinent) and 6-month follow-up (prolonged 12-week abstinence) 7. Saliva cotinine (i.e., 15 nanograms per millilitre), or salivary anabasine (<1ng/ml) if using nicotine, measured to confirm smoking abstinence, using saliva sample testing kits that will be posted to participants with a pre-paid envelope to send to ACM Bioanalytical Services (https://www.acmgloballab.com/bioanalytical-services) laboratory for testing at the 3 and 6-month follow-ups (for those reporting cessations) 8. Patient acceptability and satisfaction with the intervention measured using an online questionnaire and qualitative interview conducted remotely online or by telephone (intervention arm only) at the 6-month follow-up 9. Patient acceptability with the trial procedures measured using an online questionnaire at the 6-month follow-up 9. Clinician acceptability of the intervention measured using an online questionnaire and qualitative interview conducted remotely online or by telephone at the end of the trial 10. Engagement with the mental health treatment service (e.g., number of attended/missed appointments, di | — |
Countries
England, United Kingdom
Contacts
Public ContactDeborah Roy
Outcome results
None listed