- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06085157
EMA and Content Analysis for Alcohol Marketing in Hong Kong In-school Adolescents
Snapshot Your Drinking: Ecological Momentary Assessment and Content Analysis for Alcohol Marketing in Hong Kong In-school Adolescents
The proposed study aims to assess adolescents' exposure to alcohol marketing and its effect on drinking attitudes and drinking behaviors.
The three main research questions:
- Is exposure to alcohol marketing associated with drinking attitude (perceive popularity, perceive social approval, positive expectancies)?
- What are the contents of alcohol marketing that establish the brand capital of alcohol beverages in Hong Kong?
- Does the brand capital of alcohol beverages mediate the relationship between (a) exposure to alcohol marketing and drinking attitudes? (b) exposure to alcohol marketing and alcohol consumption?
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study design
The proposed project is a combination of a time-based system-triggered ecological momentary assessment (EMA), which will collect real-time exposure to alcohol marketing and alcohol consumption, and a longitudinal survey. Consented participants will first complete a baseline questionnaire, followed by completing 3 regularly prompted EMA surveys via smartphone application (APP) every day for 21 consecutive days. The EMA will include questions of self-report exposure, brand capital (marketing receptivity and brand recognition), and alcohol consumption. One month after the EMA period, a telephone follow-up will be conducted to understand participants' drinking attitude and alcohol consumption.
Setting and subjects
The inclusion criteria will include (1) aged 13 to 18, (2) studying in secondary schools, (3) own a mobile smartphone with internet access, (4) stay in Hong Kong during the EMA study period, and (5) being able to read and write Chinese. To increase statistical power in analyzing alcohol consumption, we will recruit one-third (about 220) of the participants who are ever drinkers. To avoid seasonal variation in the ad exposure and drinking pattern (i.e. more ads and drinking in festivals), the recruitment will be evenly distributed within a year.
Sample size determination
The sample size calculation is based on the multilevel modelling of the estimated effect of alcohol marketing exposure on alcohol consumption and drinking attitude, and the mediation effect of brand capital (Figure 1 in Appendix 1). The R package simsem, MASS and lavaan were used for sample size calculation with Monte Carlo simulation run for 1000 times. Parameters of the multilevel modeling used for simulation was based on our pilot study, which showed that 210 participants will be needed to reach the threshold of 80% power, the comparative fit index and the Tucker Lewis Index larger than 0.90, the standardized root mean square residual less than 0.08 and the root mean square error of approximation less than 0.05.32 We conservatively assume that one in three students will report any exposure to alcohol marketing, therefore we need 636 (210/0.33) students to join the study. According to our first pilot study, the dropout rate of the EMA was 3.9% (2/51). Hence, 661 participants will be needed.
Recruitment procedures
The investigators will conduct both offline and online recruitment. The investigators have collaborated with the Hong Kong Council on Smoking and Health (COSH) to organize the leadership training (the Smokefree Teen project) annually since 2015. The investigators will promote the study to the secondary school students (n=200) participating in this training camp. The investigators will also send invitation letters to the 451 government and subsidized secondary schools. After receiving the schools' consent to join the study, our research assistant will contact these schools to plan the recruitment methods, including the distribution of recruitment posters and leaflets to the students with the help from the cooperators, organization of talks or recruitment booths to recruit participants in those schools. In addition, online recruitment advertisements will be disseminated in online discussion boards and social media (e.g., Facebook, Instagram) that Hong Kong adolescents usually visit. Volunteer participants can directly contact our research staff via telephone, email or submit an online application form via a Quick Response (QR) code. First, all volunteer participants will receive a web link for eligibility screening. Then our research assistant will contact eligible students via a phone call, and invite them for a face-to-face or virtual meeting via WhatsApp or Zoom. If they choose virtual meeting, the research assistant will mail a package including an invitation letter, consent form, and a pre-stamped return envelope, and request them to send back the signed consent form with the participant's and parent's signature. Afterwards, the research assistant will assist them in completing the baseline questionnaire, app installation and using the app in the virtual meeting. If participants choose the face-to-face meeting, the research assistant will complete all study procedures in the meeting, and request the participants to send their parent's signed consent after the meeting. Our second pilot study found that both virtual and face-to-face meeting are feasible in secondary school students.
EMA App
An EMA app will be developed in both iPhone operating system (IOS) and Android platform to administer the regular prompts automatically. Our research assistant will assist participants to install the EMA App in their own smartphone after obtaining study consent. To protect the privacy of participants, no personal information will be collected via the app. Participants only need to impute a 5-digit case number (such as last 5 digits of phone number) as an identifier. Participants will use the App to complete 3 time-based EMA each day for 21 consecutive days. Two systematic reviews on the length of the study period of EMA in the underage showed that compliance can be optimal when participants were prompted to complete about 3 EMA per day within 1 week or more. Once the App is installed and logged in, the participants will be asked to choose a start date for the 21-day EMA study. To facilitate the EMA on school days when they cannot use smartphone all the time, participants can create custom schedule of the 3 EMA prompts. The time gap between any two prompts must be longer than 3 hours to capture more information within the participants' waking hours. The first, second, and third prompt must range from 11:00 am and 1:00 pm, 4:00 pm to 6:00 pm, and 9:00 pm to 11:00 pm, respectively. All data will be uploaded to our server at home office immediately after each EMA completion for further analysis. Only the project administrators can access the datasets in the server with login name and password.
Follow-up
To reduce reactive effect from EMA, all participants will be followed up via telephone 1 month after completing the EMA survey. The survey includes drinking attitude and alcohol consumption. Participants are also requested to rate their satisfaction on EMA App, frequency and content of the EMA survey by a 5-point Likert scale at the follow up.
Consent
Participation in the study is voluntary. The recruitment staff will first explain the project's details to the potential subjects who agree to join the study before seeking consent. The potential subjects will be assured that they can withdraw from the study anytime without any prejudice, and all the information will be kept confidential and results will be reported in an aggregate format. For participants who choose to complete the recruitment procedures virtually, a research assistant will mail them a package including an invitation letter, consent form, and a pre-stamped return envelope, and request that they send back the signed consent form with the theirs and their parent's signature. For participants who choose to complete the recruitment procedures face-to-face, the research assistant will obtain their signed consent in the meeting, and request that they send their parent's signed consent after the meeting.
Statistical analysis
In the 1st research question, ordered logistic regression will be used to examine the association between alcohol marketing exposure from EMA and drinking attitudes from the follow-up survey. In the 2nd research question, descriptive statistics about the themes of alcohol marketing content will be computed. Structural equation modeling will be conducted to examine the research question 3a and 3b. In research question 3a, we will use alcohol marketing exposure and brand capital from EMA, and drinking attitude from 1-month follow-up in the model. In research question 3b, We will use alcohol marketing exposure, brand capital, and alcohol consumption from the EMA in the model. To avoid reversal causality between alcohol marketing exposure and alcohol consumption in research question 3b, the lagged alcohol consumption will be regressed on the alcohol marketing exposure in the previous EMA. In models for 3a and 3b, autocorrelation will be detected and controlled for in this model. 95% confidence interval will be estimated by using bootstrapping with size 10,000. Chi-square (χ2), root mean square error of approximation (RMSEA), comparative Fit Index (CFI), and Tucker-Lewis Index (TLI) will be used to evaluate model fit. Rules of thumb guidelines are that p-value for χ2>0.05, RMSEA≤.05, CFI≥0.95, and TLI≥0.95 represent a good fitting model. All data analysis will be conducted by using R (version 1.3.1073). All significant tests were two-sided with a 5% level of significance.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Yee Tak Derek Cheung, Dr.
- Phone Number: 3917 6652
- Email: derekcheung@hku.hk
Study Locations
-
-
-
Hong Kong, Hong Kong
- LKS Faculty of Medicine
-
Contact:
- Cheung Yee Tak Derek, PhD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- aged 13 to 18
- studying in secondary schools
- own a mobile smartphone with internet access
- stay in Hong Kong during the EMA study period
- being able to read and write Chinese.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Ecological momentary assessment (EMA)
a repeated real-time data collection in real-world environment and allows modeling of within-person processes and temporal dynamics.
|
a smartphone application for self-documentation of drinking pattern
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Exposure to alcohol marketing and content analysis
Time Frame: 3-week EMA period
|
Alcohol marketing includes alcohol advertisement and promotion of drinking culture. If they report any exposure, they will be asked about (1) channels of exposure, (2) types of alcohol beverages, (3) whether they like it or not (e.g., negative, neutral, positive), (4) characters shown in the advertisement (e.g., beautiful young men/women, businessmen etc.), (5) drinking context (e.g., celebrate success, lunch/dinner, gathering, sports, etc.), and (6) tone of the commercial (e.g., humor, relaxation, masculinity, friendship, others, etc. |
3-week EMA period
|
|
Exposure to alcohol marketing and content analysis
Time Frame: 1 month follow-up
|
Alcohol marketing includes alcohol advertisement and promotion of drinking culture. If they report any exposure, they will be asked about (1) channels of exposure, (2) types of alcohol beverages, (3) whether they like it or not (e.g., negative, neutral, positive), (4) characters shown in the advertisement (e.g., beautiful young men/women, businessmen etc.), (5) drinking context (e.g., celebrate success, lunch/dinner, gathering, sports, etc.), and (6) tone of the commercial (e.g., humor, relaxation, masculinity, friendship, others, etc. |
1 month follow-up
|
|
Perceived popularity
Time Frame: 1 month follow-up
|
Participants' perceived popularity will be measure by rating their agreement to (1 = strongly disagree to 5 = strongly agree) the statements including "Most teenagers drink alcohol," "Most teenagers I know drink alcohol," and "Most students in my grade drink alcohol (Cronbach'a α = 0.79)
|
1 month follow-up
|
|
Perceived social approval
Time Frame: 1 month follow-up
|
Subjects will be assessed by rating their agreement from strongly agree (score 5) to strongly disagree (score 1) including "Drinking alcohol in a social gathering with friends is appropriate?"
"Alcohol drinking is a necessary part of celebration", and "There is no health risk to me from drinking".
|
1 month follow-up
|
|
Positive expectancies
Time Frame: 1 month follow-up
|
The 8 items of positive expectancies of drinking will be measured at 1 month follow-up.
Participants will judge how likely (1= very unlikely to 5=very likely) it is that having three or four drinks of any alcohol will lead to positive consequences (feel relaxed, feel happy, feel friendly, feel confident, feel outgoing, have fun, feel easy with expressing feelings, and feel more at ease around people).
(Cronbach's α = 0.90).
|
1 month follow-up
|
|
Marketing receptivity
Time Frame: 1 month follow-up
|
Participants who report exposure to alcohol marketing will be asked to rate their receptivity from 1 (strongly disagree) to 5 (Strongly agree) by 5 statements: (1) I like the ad; (2) I feel the main actors in the ads are attractive; (3) I feel the ad is creative.
(4) The ad content/branding suits my personal image/status; and (5) Drinking is portrayed as a positive behavior.
|
1 month follow-up
|
|
Brand recognition
Time Frame: 1 month follow-up
|
Participants will see five pictures of alcohol marketing with the brand name removed.
Participants will be asked whether or not they have seen the advertised product and write down the advertised brand name.
Brand names will be documented in each EMA when participants report exposure to alcohol marketing.
|
1 month follow-up
|
|
Alcohol consumption
Time Frame: Baseline
|
Alcohol Use Disorder Identification Test (AUDIT) will be used to measure the participants' alcohol consumption in the past month.42
On the 3rd EMA per day during the EMA period, participants will be asked "Have you drunk during the past 24 hours?"
If the answer is yes, they will be asked the types and amount of alcohol beverages and the time that they have consumed those alcohol beverages.
The responses can be processed with the participant's weight and sex to calculate estimated blood alcohol content (eBAC) values indicating intoxication.
|
Baseline
|
|
Alcohol consumption
Time Frame: 1 month follow-up
|
Alcohol Use Disorder Identification Test (AUDIT) will be used to measure the participants' alcohol consumption in the past month.42
On the 3rd EMA per day during the EMA period, participants will be asked "Have you drunk during the past 24 hours?"
If the answer is yes, they will be asked the types and amount of alcohol beverages and the time that they have consumed those alcohol beverages.
The responses can be processed with the participant's weight and sex to calculate estimated blood alcohol content (eBAC) values indicating intoxication.
|
1 month follow-up
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Yee Tak Derek Cheung, Dr., The University of Hong Kong
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- GRF Alcohol
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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