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Trial registered on ANZCTR
Registration number
ACTRN12612000368831
Ethics application status
Approved
Date submitted
26/03/2012
Date registered
30/03/2012
Date last updated
15/06/2021
Date data sharing statement initially provided
15/06/2021
Date results provided
15/06/2021
Type of registration
Prospectively registered
Titles & IDs
Public title
GIVE UP FOR GOOD- A study to evaluate the effectiveness of a pharmacist-led multidisciplinary smoking cessation intervention for smokers admitted to public hospitals.
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Scientific title
A multi-centre, randomized, controlled study to evaluate the effectiveness of pharmacist-led multidisciplinary system-change smoking cessation intervention in comparison with usual care for smokers admitted to public hospitals.
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Secondary ID [1]
280244
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Nil
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Universal Trial Number (UTN)
U1111-1128-6290
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Trial acronym
GIVE UP FOR GOOD
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Tobacco use and dependence
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Smoking Cessation
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Condition category
Condition code
Public Health
286151
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0
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Health service research
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Mental Health
286243
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0
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Addiction
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Participants randomized to intervention arm will receive a series of smoking cessation counselling sessions by a specially trained pharmacist over the course of at least three sessions: the first during hospital stay, second on discharge or immediately after discharge and third within one month post-discharge. Each participant will be counselled individually and each counselling session will take approximately 15 minutes. All smoking cessation medications during hospital stay and for at least one week after discharge will be provided free of charge. When participants are discharged from hospital, the pharmacist will communicate with participant's General Practitioner and community pharmacist about further smoking cessation support.
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Intervention code [1]
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Lifestyle
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Intervention code [2]
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Treatment: Other
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Intervention code [3]
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Behaviour
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Comparator / control treatment
Control group will receive the current standard care provided by the hospital. Current policy at each participating hospital includes brief (up to 5 mins) advice and /or pharmacotherapy provided by hospital staff as part of usual care to all inpatients who are smokers.
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Control group
Active
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Outcomes
Primary outcome [1]
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Carbon Monoxide (CO) validated 7-day point prevalence abstinence
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Assessment method [1]
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Timepoint [1]
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6 months and 12 months
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Secondary outcome [1]
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Continuous abstinence will be assessed using patient self report during interviews.
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Assessment method [1]
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Timepoint [1]
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1 month, 6 months and 12 months
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Secondary outcome [2]
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24hr/7-day/30-day point prevalence abstinence will be assessed using patient self report during interviews.
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Assessment method [2]
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Timepoint [2]
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1 month, 6 months and 12 months
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Eligibility
Key inclusion criteria
Age 18 years and above, who are smokers at the time of hospital admission and available for follow-up on discharge, and at 1, 6, and 12 months post-discharge
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Physical or mental inability to participate in the study, unable to provide written informed consent, unable to communicate in English, terminal illness, pregnancy and on another smoking cessation therapy or program at the time of hospital admission
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Sealed opaque envelope method.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Stratified block randomisation - Participants will be stratified based on Heaviness of Smoking Index -Light Smokers and Heavy smokers
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
2/04/2012
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Actual
2/04/2012
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Date of last participant enrolment
Anticipated
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Actual
6/06/2013
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Date of last data collection
Anticipated
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Actual
30/06/2014
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Sample size
Target
600
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Accrual to date
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Final
600
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Recruitment in Australia
Recruitment state(s)
VIC
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Funding & Sponsors
Funding source category [1]
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Government body
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Name [1]
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Australian Research Council
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Address [1]
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Level 2, 11 Lancaster Place
Majura Park ACT 2609
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Country [1]
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Australia
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Funding source category [2]
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Commercial sector/Industry
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Name [2]
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Pfizer Australia Pty Ltd
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Address [2]
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38-42 Wharf Road
West Ryde NSW 2114
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Country [2]
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Australia
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Primary sponsor type
University
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Name
Monash University
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Address
381 Royal Parade
Parkville
Victoria 3052
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
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Country [1]
283787
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Other collaborator category [1]
260597
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University
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Name [1]
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The University of Newcastle
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Address [1]
260597
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Cnr King and Auckland Streets
Newcastle NSW 2300
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Country [1]
260597
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Australia
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Other collaborator category [2]
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Hospital
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Name [2]
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The Alfred
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Address [2]
260598
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Commercial Road,
Melbourne. VIC 3004
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Country [2]
260598
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Australia
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Other collaborator category [3]
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Hospital
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Name [3]
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Austin Hospital
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Address [3]
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145 Studley Road
Heidelberg
VIC 3084
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Country [3]
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Australia
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Other collaborator category [4]
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Hospital
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Name [4]
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Barwon Health
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Address [4]
260620
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The Geelong Hospital
Bellerine Street
Geelong VIC 3220
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Country [4]
260620
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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The Alfred Ethics Committee
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Ethics committee address [1]
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The Alfred Hospital 55 Commercial Road Melbourne Victoria 3004
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
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Approval date [1]
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02/03/2012
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Ethics approval number [1]
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314/11
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Ethics committee name [2]
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Austin Health Human Research Ethics Committee
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Ethics committee address [2]
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Research Ethics Unit Henry Buck Building Austin Hospital
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Ethics committee country [2]
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Australia
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Date submitted for ethics approval [2]
286937
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Approval date [2]
286937
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07/02/2012
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Ethics approval number [2]
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H2011/04438
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Ethics committee name [3]
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Barwon Health Human Research Ethics Committee
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Ethics committee address [3]
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Barwon Health Ryrie Street Geelong
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Ethics committee country [3]
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Australia
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Date submitted for ethics approval [3]
286938
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Approval date [3]
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24/01/2012
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Ethics approval number [3]
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11/91
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Summary
Brief summary
"GIVE UP FOR GOOD" (Copyright) is a research study, evaluating the effectiveness of a pharmacist-led multidisciplinary system change smoking cessation intervention for smokers admitted to Victorian hospitals. Approximately 200 smokers will be recruited from each of three participating Victorian hospitals (The Alfred, Austin Health & Barwon Health). Participants will have an equal chance of being randomly allocated to either the intervention or usual care (control) group. Participants randomized to "Give up for Good" program will receive a series of smoking cessation counseling sessions by a specially trained pharmacist over the course of at least three sessions. The first during the hospital stay, second on discharge or immediately after the discharge and third within one month post-discharge. All smoking cessation medications during the hospital stay and for at least one week after discharge will be provided free of charge. When participants are discharged from hospital, the pharmacist will communicate with the participant's General Practitioner and community pharmacist about further smoking cessation support. Participants randomized to usual care group receive the current routine care provided by the hospital. All the participants will be followed up for a period of 12 months. All measurements at baseline, discharge, 1 month, 6 months and 12 months will be performed by a Research Assistant blinded to group allocation. The main outcome measures are abstinence from smoking on discharge, and 1 month, 6 months and 12 months post-discharge.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Dr Dr Johnson George
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Address
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Faculty of Pharmacy and Pharmaceutical Sciences
Centre for Medicine Use and Safety
Monash University (Parkville Campus)
381 Royal Parade,
Parkville
VIC 3052
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Country
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Australia
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Phone
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+61-3-9903 9178
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Dr Johnson George
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Address
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Faculty of Pharmacy and Pharmaceutical Sciences
Centre for Medicine Use and Safety
Monash University (Parkville Campus)
381 Royal Parade, Parkville
VIC 3052
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Country
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Australia
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Phone
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+61-3-9903 9178
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Fax
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+61-3-9903 9629
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Email
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[email protected]
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Contact person for scientific queries
Name
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Dr Johnson George
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Address
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Faculty of Pharmacy and Pharmaceutical Sciences
Centre for Medicine Use and Safety
Monash University (Parkville Campus)
381 Royal Parade, Parkville
VIC 3052
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Country
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Australia
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Phone
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+61-3-9903 9178
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Fax
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+61-3-9903 9629
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Email
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
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What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
Source
Title
Year of Publication
DOI
Embase
Quitting experiences and preferences for a future quit attempt: A study among inpatient smokers.
2015
https://dx.doi.org/10.1136/bmjopen-2014-006959
Embase
Hypnotherapy for smoking cessation.
2019
https://dx.doi.org/10.1002/14651858.cd001008.pub3
N.B. These documents automatically identified may not have been verified by the study sponsor.
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