Trial Review

The ANZCTR website will be unavailable from 1pm until 3pm (AEDT) on Wednesday the 30th of October for website maintenance. Please be sure to log out of the system in order to avoid any loss of data.

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been endorsed by the ANZCTR. Before participating in a study, talk to your health care provider and refer to this information for consumers
Trial registered on ANZCTR


Registration number
ACTRN12622000901707p
Ethics application status
Not yet submitted
Date submitted
16/06/2022
Date registered
24/06/2022
Date last updated
27/01/2023
Date data sharing statement initially provided
24/06/2022
Type of registration
Prospectively registered

Titles & IDs
Public title
The effect of a text-message based intervention on adolescent e-cigarette use
Scientific title
A randomised controlled trial to examine the potential effect of a text-message based intervention on e-cigarette use in adolescents who have never used e-cigarettes
Secondary ID [1] 307373 0
Nil known
Universal Trial Number (UTN)
Trial acronym
Linked study record
This trial has been replaced by trial ACTRN12623000079640.

Health condition
Health condition(s) or problem(s) studied:
E-cigarette use 326683 0
Condition category
Condition code
Public Health 323923 323923 0 0
Health promotion/education
Mental Health 323979 323979 0 0
Addiction

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
A randomised controlled trial design will be used to test the effectiveness of a theory-based intervention to prevent e-cigarette use among adolescents aged 14 to 17 years in New South Wales, Australia.

Adolescents allocated to the intervention group will receive a 12-week theory-based intervention to prevent e-cigarette use. The intervention will consist of a library of text messages targeting adolescent e-cigarette use developed following extensive consultation with parents and adolescents via focus groups, semi-structured interviews and online surveys, in addition to consultation with researchers and experts from the field of e-cigarettes and tobacco. The messages will target constructs within the Theory of Planned Behaviour (i.e. attitudes, subjective norms and perceived behavioural control), a theory frequently employed to guide the development of text-message based interventions to prevent and address adolescent tobacco use. The messages will be plain-text and will be sent to adolescents to target factors (I.e. barriers and enablers) associated with adolescent e-cigarette use, aligned to each of the Theory of Planned Behaviour constructs.

Adolescents allocated to the intervention group will receive two text messages per week for one school term (12 weeks). The length of each text message will be 1-2 sentences. Analytics automatically captured by the text-message program used to disseminate the messages (e.g. read receipts) will be used to monitor adherence to the intervention.
Intervention code [1] 323801 0
Prevention
Intervention code [2] 323802 0
Behaviour
Comparator / control treatment
Adolescents allocated to the control group will receive the text-messages following the completion of all outcome measures (i.e. at 6 months after enrolment).
Control group
Active

Outcomes
Primary outcome [1] 331730 0
Adolescent intentions to use e-cigarettes will be assessed in an online or telephone survey conducted by a trained research assistant. Validated survey items outlined by O’Brien et al. (2022) will be used to assess adolescent intentions to use e-cigarettes.
Timepoint [1] 331730 0
Assessed at follow-up (12 weeks and 6-months post intervention commencement)
Secondary outcome [1] 410885 0
Adolescent ever-use of e-cigarettes, defined as any lifetime use of e-cigarettes, will be assessed via an online or telephone survey conducted by a trained research assistant. To aid comparisons of the effect of e-cigarette policies and interventions, Pearson et al. (2018) recommends for eight core constructs of e-cigarette use to be assessed. As such, adolescents that report e-cigarette ever-use at follow-up will be asked additional survey items (recommended by Pearson et al. (2018)) to assess the remaining constructs, including: frequency of e-cigarette use; former daily use; relative perceived harm; device type; primary flavour preference; presence of nicotine within the e-cigarettes; and primary reason for use.
Timepoint [1] 410885 0
Assessed at follow-up (12 weeks and 6-months post intervention commencement)
Secondary outcome [2] 410886 0
Acceptability of the text-message intervention (defined as the perception amongst adolescents that the intervention is agreeable, palatable or satisfactory) will be assessed in an online or telephone survey with adolescents allocated to the intervention group. Survey items to assess acceptability will be based on validated items developed by Weiner et al. (2017)
Timepoint [2] 410886 0
Assessed at follow-up (12 weeks post-intervention commencement)
Secondary outcome [3] 411093 0
Appropriateness of the text-message intervention (defined as the perceived fit, relevance or compatibility of the intervention for adolescents) will be assessed in an online or telephone survey with adolescents allocated to the intervention group. Survey items to assess appropriateness will be based on validated items developed by Weiner et al. (2017).
Timepoint [3] 411093 0
Assessed at follow-up (12 weeks post-intervention commencement)

Eligibility
Key inclusion criteria
Adolescents aged between 14 to 17 years, located within New South Wales, Australia, who have never used e-cigarettes will be eligible to participate.
Minimum age
14 Years
Maximum age
17 Years
Sex
Both males and females
Can healthy volunteers participate?
Yes
Key exclusion criteria
None

Study design
Purpose of the study
Prevention
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Participants will be recruited via multiple methods, including social media (e.g. Facebook and Instagram) using paid advertising targeting adolescents. Potentially eligible participants will be encouraged to complete an Expression of Interest online form accessible via the targeted advertisements to indicate their (and parental) consent to participate. A research assistant, blind to group allocation will conduct a short telephone call to confirm participant eligibility. Following recruitment and confirmation of eligibility, an independent statistician will randomly allocate adolescents to either the intervention or control condition.
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Following recruitment, an independent statistician will randomise adolescents, using a computerised random number function, stratified by the geographic and socio-economic location in a 1:1 (intervention: control) ratio using random block sizes of between 2-6.
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?


The people assessing the outcomes
The people analysing the results/data
Intervention assignment
Parallel
Other design features
Phase
Not Applicable
Type of endpoint/s
Efficacy
Statistical methods / analysis
Descriptive statistics will be used to describe adolescent characteristics, acceptability and appropriateness of the text-message intervention.

Analyses of trial outcomes will be undertaken under an intention to treat framework. For the primary trial outcome (intentions to use e-cigarettes) between group differences will be assessed using logistic regression. The model will include a term for treatment group (intervention vs control) and pre-specified covariates prognostic of the outcome. We will employ multiple imputation for any missing data in the event that participants withdraw from the study and request that their data is not used. All statistical tests will be 2 tailed with alpha of 0.05.

Recruitment
Recruitment status
Withdrawn
Reason for early stopping/withdrawal
Other reasons/comments
Other reasons
This trial is being replaced by trial ACTRN12623000079640.
Date of first participant enrolment
Anticipated
31/01/2023
Actual
Date of last participant enrolment
Anticipated
31/03/2023
Actual
Date of last data collection
Anticipated
30/09/2023
Actual
Sample size
Target
144
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
NSW

Funding & Sponsors
Funding source category [1] 311655 0
University
Name [1] 311655 0
University of Newcastle
Country [1] 311655 0
Australia
Primary sponsor type
University
Name
University of Newcastle
Address
University Drive
Callaghan NSW 2308
Country
Australia
Secondary sponsor category [1] 313100 0
Government body
Name [1] 313100 0
Hunter New England Population Health
Address [1] 313100 0
Locked Bag 10
Wallsend NSW 2287
Country [1] 313100 0
Australia

Ethics approval
Ethics application status
Not yet submitted
Ethics committee name [1] 311111 0
University of Newcastle Human Research Ethics Committee
Ethics committee address [1] 311111 0
Ethics committee country [1] 311111 0
Australia
Date submitted for ethics approval [1] 311111 0
01/10/2022
Approval date [1] 311111 0
Ethics approval number [1] 311111 0

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 119978 0
Prof Luke Wolfenden
Address 119978 0
Hunter New England Population Health
Locked Bag 10
Wallsend, NSW Australia 2287
Country 119978 0
Australia
Phone 119978 0
+61 2 49246472
Fax 119978 0
Email 119978 0
[email protected]
Contact person for public queries
Name 119979 0
Courtney Barnes
Address 119979 0
Hunter New England Population Health
Locked Bag 10
Wallsend, NSW Australia 2287
Country 119979 0
Australia
Phone 119979 0
+61 2 49246678
Fax 119979 0
Email 119979 0
[email protected]
Contact person for scientific queries
Name 119980 0
Courtney Barnes
Address 119980 0
Hunter New England Population Health
Locked Bag 10
Wallsend, NSW Australia 2287
Country 119980 0
Australia
Phone 119980 0
+61 2 49246678
Fax 119980 0
Email 119980 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment
No individual participant data for this trial will be available as ethics approval does not cover this. If a request for individual participant data is made and appropriate ethics approvals obtained, such data may be made available in the future.


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
No additional documents have been identified.