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A randomised controlled trial examining the efficacy of a smoking cessation intervention initiated during psychiatric hospitalisation on post-discharge smoking reduction, nicotine dependence and abstinence.

The effect of an integrated smoking care program on the reduction and abstinence of smoking in mental health inpatients following discharge from hospital.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12609000465257
Enrollment
200
Registered
2009-06-16
Start date
2009-10-30
Completion date
2011-05-30
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

The purpose of this study is to explore inpatient psychiatric settings as a platform for initiating smoking cessation treatment to patients smokers. We hypothesise that patients who commence smoking cessation treatment in hospital and receive ongoing support post-hospitalisation will be more likely to quit than smokers who receive standard hospital care only.

Interventions

*Provision of 3 quit smoking pamphlets upon recruitment to the intervention condition *Active referral to the telephone support Quitline (occurring once at discharge from hospital) *Up to 16 weeks provision of Nicotine Replacement Therapy (NRT), including patches, Gum, lozenges and Inhalers. * A weekly, one hour smoking support group (occurring for 4 weeks in total) * A one page referral to a general practitioner (GP) and other health professionals (for example psychologists, occupational ther

*Provision of 3 quit smoking pamphlets upon recruitment to the intervention condition *Active referral to the telephone support Quitline (occurring once at discharge from hospital) *Up to 16 weeks provision of Nicotine Replacement Therapy (NRT), including patches, Gum, lozenges and Inhalers. * A weekly, one hour smoking support group (occurring for 4 weeks in total) * A one page referral to a general practitioner (GP) and other health professionals (for example psychologists, occupational therapists) to inform them of their clients participation in a smoking study. *Telephone support calls, made once every two weeks for up to 4 months.

Sponsors

University of Newcastle
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Primary purpose
Treatment

Eligibility

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

Inclusion criteria

Inpatient at mental health hospital, smoker.

Exclusion criteria

non-smoker

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026