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Trial registered on ANZCTR
Registration number
ACTRN12618001089224
Ethics application status
Approved
Date submitted
19/06/2018
Date registered
29/06/2018
Date last updated
21/01/2020
Date data sharing statement initially provided
8/01/2019
Date results provided
21/01/2020
Type of registration
Prospectively registered
Titles & IDs
Public title
SCAMPI – Smoking Cessation App for (Chinese) Male smokers: Pilot Intervention trial
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Scientific title
SCAMPI – Smoking Cessation App for (Chinese) Male smokers: Pilot Intervention trial
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Secondary ID [1]
295249
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None
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Universal Trial Number (UTN)
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Trial acronym
SCAMPI
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Smoking Cessation
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Condition category
Condition code
Mental Health
307406
307406
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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 allocated to intervention group will be offered the full version of SCAMPI programme as a smoking cessation tool. The programme consisted with two parts including SCAMPI WeChat Official Account for sending users quitting messages, as well as SCAMPI mini-programme for helping users to make quitting plan and track their quitting progress. SCAMPI WeChat Official Account will be programmed to send regular quitting tips to participants in intervention group. Participants can review the past messages and read the up-to-date messages whenever they want. The SCAMPI mini-programme will allow participants to create their quitting plan, track their quitting progresses, and evaluate their progresses via doing lung function screening.
Participants will be encouraged to read quitting tips on the SCAMPI WeChat Official Account and use the SCAMPI mini-programme. However, participants can determine the level of usage by their own. Participants are expected to spend 3~5 minutes per week over a 6-week period to provide their smoking statuses to the research team. Notification will be sent through WeChat messages to instruct participants how to take action to provide their smoking statuses. After providing their smoking statuses, participants will be offered with "WeChat Red Pocket" (e-currency). Fix amount of e-currency will be allocated in "WeChat red pocket" and offered by 7 sessions (including baseline assessment and 6 weeks of smoking status data collection). The whole process of the trial will be completely automatic and via social network platform.
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Intervention code [1]
301584
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Behaviour
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Comparator / control treatment
Participants allocated in control group will be offered to have access to a restricted version of the SCAMPI programme. The restricted version will only have the SCAMPI WeChat Official Account for sending users contacts of China smoking cessation service (e.g. Quitline and Smoking Cessation Service). Participants are expected to spend 3~5 minutes per week over a 6-week period to provide their smoking statuses to the research team. Notification will be sent through WeChat messages to instruct participants how to take action to provide their smoking statuses. After providing their smoking statuses, participants will be offered with "WeChat Red Pocket" (e-currency). Fix amount of e-currency will be allocated in "WeChat red pocket" and offered by 7 sessions (including baseline assessment and 6 weeks of smoking status data collection). The whole process of the trial will be completely automatic and via social network platform.
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Control group
Active
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Outcomes
Primary outcome [1]
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The primary outcome of this pilot trial will be participants’ bio-verified 30-day smoking abstinence at 6-week follow-up. At the 6-week time point, researchers will review and analyse participants’ (in both groups) smoking status in the past 30 days to identify their 30-day smoking abstinence at the planned time point. The 30-day smoking abstinence is usually used as the primary outcome measure for smoking cessation intervention trials recommended by the Society for Research on Nicotine and Tobacco (SRNT). Quit failure is defined as any cigarettes smoked in the past 30 consecutive days. This measurement is also known as the 10th level of smoking abstinence in the Chinese Standard for smoking cessation. At the 6-week time point, a Nicotine Cotinine Saliva Test kit will be sent to participants (in both groups) who report themselves with 30-day smoking abstinence to verify their smoking abstinence status.
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Assessment method [1]
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Timepoint [1]
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Assessed weekly after randomisation for 6 weeks
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Secondary outcome [1]
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Participants’ cigarette consumption reduction. Participants who reduce consumption of over 50% from baseline will be counted as successfully achieve smoking reduction. This outcome will be measured based on participants self-reported data through social network platform.
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Assessment method [1]
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Timepoint [1]
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Assessed weekly after randomisation for 6 weeks
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Secondary outcome [2]
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Prolonged smoking abstinence at 6-week follow-up. The prolonged smoking abstinence is defined as participants record no smoking following the first 7 days after the intervention start till the end of the study. The relevant data for measuring this outcome will be self-reported by participants and be collected through social network platform.
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Assessment method [2]
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Timepoint [2]
348428
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Assessed weekly after randomisation for 6 weeks
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Secondary outcome [3]
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7-day smoking abstinence at 4-week – At the 4-week time point, researchers will review and analyse participants’ (in both groups) smoking status in the past 7 days to identify their 7-day smoking abstinence at this time point. 7-day smoking abstinence is defined as not a single cigarette being smoked in the past 7 days. The relevant data for measuring this outcome will be self-reported by participants and be collected through social network platform.
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Assessment method [3]
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Timepoint [3]
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At 4 weeks after randomisation
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Secondary outcome [4]
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7-day smoking abstinence at 6-week – At the 6-week time point, researchers will review and analyse participants’ (in both groups) smoking status in the past 7 days to identify their 7-day smoking abstinence at this time point. 7-day smoking abstinence is defined as not a single cigarette being smoked in the past 7 days. The relevant data for measuring this outcome will be self-reported by participants and be collected through social network platform.
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Assessment method [4]
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Timepoint [4]
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At 6 weeks after randomisation
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Secondary outcome [5]
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Participants’ compliance with SCAMPI programme. Participants’ compliance refers to participants (in both groups) provide their weekly smoking status (self-reported through social network platform) at the end of every week, as well as answering the end-of-trial questionnaires (including VAS for assessing their acceptability and MARS for assessing their satisfaction levels).
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Assessment method [5]
365455
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Timepoint [5]
365455
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Assessed weekly after randomisation for 6 weeks
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Secondary outcome [6]
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Number of times participants visiting SCAMPI programme. At the end of the pilot trial, researchers will review and analyse the frequencies of participants visiting the SCAMPI programme. This data will be available on the server of the programme shown as "frequencies of visit".
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Assessment method [6]
365456
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Timepoint [6]
365456
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Assessed weekly after randomisation for 6 weeks
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Secondary outcome [7]
365457
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Number of times participants interacting with the SCAMPI programme. At the end of the pilot trial, researchers will review and analyse the data of how many times participants (in intervention group) like, comment, forward, post content from SCAMPI programme through their social network accounts.
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Assessment method [7]
365457
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Timepoint [7]
365457
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Assessed weekly after randomisation for 6 weeks
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Secondary outcome [8]
365458
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Participants’ acceptability of using SCAMPI as their smoking cessation tool. Participants’ acceptability (for both groups) of using SCAMPI will be measured by a VAS questionnaire at the end of the pilot trial. Participants’ acceptability to the SCMAPI programme will be asked by questions such as “Did the programme increase your willingness to stop smoking”, and “Did the programme encourage you to look for more stop smoking techniques?”. Each question will be answered by a 5-item scale from “Not at all” to “Very much”.
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Assessment method [8]
365458
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Timepoint [8]
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At 6 weeks after randomisation
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Secondary outcome [9]
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Participants’ satisfaction level of using SCAMPI as their smoking cessation tool. Participants’ satisfaction level (for both groups) of using SCMAPI will be measured by a Mobile Application Rating Scale questionnaire at the end of the pilot trial.
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Assessment method [9]
365459
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Timepoint [9]
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At 6 weeks after randomisation
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Eligibility
Key inclusion criteria
Chinese male smokers will be eligible for inclusion in the study if they indicate at screening that they are smokers (both daily smokers “smoking any types of tobacco products on a daily basis” or occasional smokers “smoking any types of tobacco products occasionally”) between 25-44 years of age; have access to a smartphone; have a WeChat account; process adequate knowledge of Chinese language; and are willing to participate in the study and provide follow-up information at scheduled points of the study.
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Minimum age
25
Years
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Maximum age
44
Years
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Sex
Males
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Can healthy volunteers participate?
No
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Key exclusion criteria
People that do not meet the inclusion criteria will be excluded from the study.
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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)
Randomisation will be performed at the individual level. Participants (N=318) that fulfil entry criteria and have completed baseline assessment will be randomised at a 1:1 ratio to either a intervention group or to a control group. The final randomisation lists will be concealed in the database until the point of randomisation.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
The randomisation sequence will be generated by the trial statistician using block randomisation with variable block sizes of 2 or 4.
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Masking / blinding
Open (masking not 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
control panel for the data in related to the SCAMPI OA usage; (2) Wenjuanxin (it is an online questionnaire that is embed into WeChat OA system) control panel for the data in related to baseline assessment and weekly smoking status; and (3) the lean cloud database for the data in related to SCAMPI mini-programme usage. Extracted data will be entered into an Excel Database, and following cleaning and datalock, exported into SAS (version 9.4) for analysis.
Baseline characteristics
Baseline data collected from all participants will be summarised by occasional smoker and daily smoker. Continuous variables (e.g. average daily cigarette consumption) will be presented as numbers observed, means and standard deviations. Categorical variables (e.g. marital status) will be presented as frequencies and percentages. Since any differences between randomised groups at baseline could only have occurred by chance, no formal significance testing will be conducted.
Outcome relevant data
Primary and secondary outcomes will be first summarised descriptively at identified time points. Generalised linear mixed model will be used to assess the effect of the SCAMPI programme to participants’ smoking cessation outcomes.
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
14/01/2019
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Actual
18/01/2019
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Date of last participant enrolment
Anticipated
14/02/2019
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Actual
29/01/2019
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Date of last data collection
Anticipated
25/03/2019
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Actual
14/03/2019
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Sample size
Target
80
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Accrual to date
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Final
80
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Recruitment outside Australia
Country [1]
10572
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China
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State/province [1]
10572
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Funding & Sponsors
Funding source category [1]
299838
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University
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Name [1]
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University of Auckland
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Address [1]
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261 Morrin Rd, St Johns, Auckland 1072
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Country [1]
299838
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New Zealand
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Primary sponsor type
University
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Name
University of Auckland
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Address
261 Morrin Rd, St Johns, Auckland 1072
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Country
New Zealand
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Secondary sponsor category [1]
299191
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None
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Name [1]
299191
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Address [1]
299191
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Country [1]
299191
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
300715
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University of Auckland Human Participants Ethics Committee (UAHPEC)
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Ethics committee address [1]
300715
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261 Morrin Rd, St Johns, Auckland 1072
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Ethics committee country [1]
300715
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New Zealand
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Date submitted for ethics approval [1]
300715
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20/12/2018
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Approval date [1]
300715
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21/12/2018
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Ethics approval number [1]
300715
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021649
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Summary
Brief summary
This project evaluates a mobile smoking cessation programme, called as “SCAMPI”, which consists of a social network subscription account (SCAMPI WeChat Official Account) and a social network based app (SCAMPI mini-programme). The SCAMPI programme was developed based on the preferred features (functions, user experience and user interface) of its target end--users (Chinese male smokers aged 25 to 44 years). This project will be implemented fully online. The evaluation will be run as a two-arm randomised controlled trial (RCT). After providing e-consents, participants will be randomly allocated to two groups. Participants allocated to intervention group will be offered the full version of SCAMPI programme (3 months intervention) while participants allocated to control group will be offered with restricted version of SCAMPI programme, which provides contact to general Chinese smoking cessation care (including Chinese Quitline and Local smoking cessation clinics). Smoking status of participants from both groups will be measured weekly over a 3-month period. Participants’ prolonged smoking abstinence over the evaluation period will be used to assess the effectiveness of the SCAMPI programme for helping people to quit smoking. At the end of the project, participants will be asked about their satisfaction levels with the SCAMPI programme. Participants from both groups will be offered the SCAMPI programme with free-of-charge for supporting them to quit smoking after the study complete.
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Trial website
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Trial related presentations / publications
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Public notes
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Attachments [1]
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/AnzctrAttachments/375381-SCAMPI Stage 2 Protocol 20180618.docx
(Protocol)
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Attachments [2]
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/AnzctrAttachments/375381-SCAMPI Stage 2 ICF.docx
(Participant information/consent)
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Contacts
Principal investigator
Name
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Prof Chris Bullen
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Address
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National Institute for Health Innovation, 261 Morrin Rd, St Johns, Auckland 1072
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Country
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New Zealand
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Phone
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+64021415267
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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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Jinsong Chen
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Address
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National Institute for Health Innovation, 261 Morrin Rd, St Johns, Auckland 1072
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Country
84583
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New Zealand
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Phone
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+640220951065
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Fax
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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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Jinsong Chen
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Address
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National Institute for Health Innovation, 261 Morrin Rd, St Johns, Auckland 1072
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Country
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New Zealand
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Phone
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+640220951065
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Fax
84584
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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
All participants in this study will be anonymised.
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What supporting documents are/will be available?
No Supporting Document Provided
Doc. No.
Type
Citation
Link
Email
Other Details
Attachment
902
Study protocol
375381-(Uploaded-27-12-2018-15-57-29)-Study-related document.docx
903
Informed consent form
375381-(Uploaded-27-12-2018-16-06-38)-Study-related document.docx
904
Ethical approval
375381-(Uploaded-27-12-2018-16-06-52)-Study-related document.pdf
905
Ethical approval
375381-(Uploaded-27-12-2018-16-09-11)-Study-related document.pdf
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
Mobile Social Network-Based Smoking Cessation Intervention for Chinese Male Smokers: Pilot Randomized Controlled Trial.
2020
https://dx.doi.org/10.2196/17522
N.B. These documents automatically identified may not have been verified by the study sponsor.
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