Skip to content

QuitPick: Best practice smoking cessation care for individuals receiving mental health services

QuitPick: A pilot intervention of direct-to-consumer best practice smoking cessation care for individuals accessing mental health services

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12624000159550
Enrollment
10
Registered
2024-02-20
Start date
2024-03-22
Completion date
2024-08-31
Last updated
2024-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Smoking is the leading cause of preventable death in people with severe mental illness (SMI). Although smokers with SMI want to quit, tailored interventions are rarely delivered in practice. This pilot feasibility study will assess the acceptability of the QuitPick intervention for smoking cessation among individuals living with severe mental illness. 30 participants who are accessing any treatment, support or care service for a mental health condition from Mind Australia Limited in Victoria will be recruited. All participants will receive the QuitPick intervention. Participants will be contacted by Quitline and offered a targeted smoking cessation counselling intervention with a choice of pharmacotherapy (NRT or NVP) and peer support over a 12-week period. Assessments will be conducted at baseline, 3 months (end of treatment), and 6 months (3 months post-treatment). After completing the QuitPick intervention, one-on-one semi-structured interviews will be conducted with 20 participants to investigate the experience of participants and understand acceptability of the intervention, with a focus on further enhancing engagement with the intervention.

Interventions

QuitPick intervention: - Quit pack of written resources from Quitline Victoria will be mailed to participants. Extended and tailored Quitline counselling with a dedicated counsellor: Proactive referral (opt-out; where Quitline contacts the participant) made by the research team (with consent via REDCap) to tailored counselling for people with SMI. Following the Quitpick treatment protocol (i.e., different from standard Quitline practice) including offer of weekly calls within the 12-week period;

QuitPick intervention: - Quit pack of written resources from Quitline Victoria will be mailed to participants. Extended and tailored Quitline counselling with a dedicated counsellor: Proactive referral (opt-out; where Quitline contacts the participant) made by the research team (with consent via REDCap) to tailored counselling for people with SMI. Following the Quitpick treatment protocol (i.e., different from standard Quitline practice) including offer of weekly calls within the 12-week period; structured monitoring of mental health symptoms, nicotine withdrawal symptoms and medication side effects (the latter may increase due to medication interactions with smoking cessation); and the use of mood management strategies that dually act to aid mood and cessation (e.g., exercise, scheduling pleasant activities). A dedicated counsellor will manage counselling for each participant. Counsellors will monitor and encourage correct use of nicotine replacement therapy and nicotine vaping products and will address barriers to use. Quitline has established protocols to support people using nicotine vaping products for smoking cessation and also offers support to people wanting to reduce or cease vaping, with a focus on preventing smoking relapse or increases in smoking. - Peer support forum: Access to study website with peer worker videos sharing lived experienced of mental health conditions / smoking and recovery (including recommendation and encouragement with engage with Quitline) and online forum where participants can ask questions, share experiences and support each other. This messaging style forum will be monitored by peer workers (supervised by the chief investigator) and enhance engagement with the intervention by providing lived experienced expertise, encouragement, and resources to tackle smoking and other areas of physical health. The online forum will be hosted on Facebook. Participants will be offered the opportunity to join the study’s Facebook support group page. The group will be set up using the ‘secret’ group setting from Facebook; a secret group that involves only those an administrator allows to participate. Participants are not required to post to the Facebook group page. Upon enrolment, we will advise participants that if we become concerned about any one individual’s need for additional counselling, we will refer him or her to appropriate services. We have successfully used this method in previous studies (ACTRN12621001315808). Approximately bi-weekly (depending on participant recruitment rate) material on tackling smoking, stories of lived experience and encouragement for quitting will be posted on the Facebook group. Peer workers will monitor postings weekly and respond when appropriate (clarifying, answering questions, offering encouragement, or asking additional facilitating questions). Use and acceptability of the forum will be assessed using self-report items within the follow up assessments. - Pharmacotherapy (12 weeks choice of state-of-the-art nicotine vaping products or combined nicotine replacement therapy and GP support: o Week 1 trial pack: The study GP will review participants’ baseline assessments for relevant information (e.g., nicotine dependence, current medications likely to be affected by smoking cessation and take action/make appropriate referrals). An initial assessment via telehealth will be conducted with the trial GP to address health and safety issues and any concerns and to help the participant for when they make an informed choice to proceed with either nicotine vaping products or combination nicotine replacement therapy for the remainder of the intervention period. An e-script will be sent to our partnering Australian pharmacy and a 1-week supply of nicotine vaping products and combination nicotine replacement therapy (patches plus lozenges as per best practice) with written resource guides for use will be sent to the participant to trial, matched to nicotine dependence. Allo vapes are a quality, nicotine delivery system that has been selected for their simplicity and ease of use. Participants’ nominated GP will be advised what treatments have been prescribed. o Week 2: Participants will be sent their choice of either a remaining 11 week supply of nicotine replacement therapy or nicotine vaping products. Use of nicotine replacement therapy and nicotine vaping products will be assessed within follow up assessments using participant self-report items. The study links together three existing supports already available to participants in the community/through their mental health service – Quitline counselling, peer workers and nicotine replacement therapy. Following the 12-week intervention period, participants can continue to access these resources. - Engagement with GP and mental health providers: Participants will be asked to provide the details of their current GP and/or psychiatrist. A letter will be sent by the research team to these health professionals with information about their client’s trial participation and a link to Australia’s smoking cessation guidelines for health professionals (includes a list of medications affected by smoking) and peer-reviewed articles that provide practical advice to assist doctors in helping people with SMI to quit smoking. Participants will receive a Quitting Mood and Experiences diary which they will be encouraged to use and discuss with the study GP, Quitline counsellor and other health professionals as relevant. Quitline will provide written feedback to treatment providers at the end of the telephone counselling program. They will be encouraged to monitor and support cessation efforts whenever appropriate. In addition, Quitline will contact the mental health treatment provider, if concerns arise about mental health issues. - Quitline engagement of support network: A Quitline brochure for carers which offers Quitline as a resource for supporters of people with SMI to address any queries/concerns about quitting.

Sponsors

The University of Newcastle
Lead SponsorUniversity

Study design

Allocation
Non-randomised trial
Primary purpose
Treatment

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

To be eligible, participants must: (i) be aged at least 18 years; (ii) have a self-reported diagnosis or receipt of SMI (including major depressive disorder, psychosis, schizophrenia, schizophrenia spectrum or bipolar disorder) and/or receiving treatment or support from Mind services; (iii) be residing in Victoria; and (iv) be a current tobacco smoker (smoke at least 10 cigarettes per day and currently smokes cigarettes).

Exclusion criteria

Participants will be excluded if they: (i) are currently smoking less than 10 cigarettes per day; (ii) are currently engaged in Quitline’s callback service; (iii) have no ready access to a phone; (iv) are unable to complete informed consent and/or the screening survey; (v) show signs of acute suicidality; and (vi) are pregnant, breastfeeding or planning pregnancy in the next 12 months.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026