InterventionNCT07070154
Evaluating the Efficacy of a Text Messaging-based Shisha Smoking Cessation Intervention
A study testing text-messaging based intervention in people with Intervention and Control, run by The University of Hong Kong at 1 site in Hong Kong.
Trial summary
The goal of this study is to evaluate the efficacy of a culture specific text-messaging based shisha smoking cessation intervention for young adults in Hong Kong. Participants in the intervention group will receive smartphone text messaging-based intervention and support that contained personalised messages with both… Read more about this study
- Who is it for?
- Ages 18 to 35 yearsHealthy volunteers can take part
- Conditions the study is for
- Intervention, Control
- What is being tested?
- text-messaging based intervention
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 100 participants
- Where
- 1 siteHong Kong
- Study dates
- 20 Jul 2025to Jul 2026
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 35 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- young adults aged 18 to 35 years who are interested in quitting shisha
- smoked shisha within the 30 days at the time of enrolment (current smoker)
- smoked for more than twelve times in 12 months (i.e., on a monthly basis)22
- able to read and communicate in Chinese or English
- agree to utilise his/her own personal mobile or smartphone to send and receive messages
Who cannot join
- scored 10 (''have already quitted'') on Contemplation Ladder assessment at baseline
- unable to provide consent
- unable to read and communicate in Chinese or English
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Hong Kong1 site
Room 212, New Clinical Building, Queen Mary Hospital, 102 Pokfulam Road
Hong Kong, 0000000
Johnson Kai Chun Law, MSc, +85266703003, u3009145@connect.hku.hk
Johnson Kai Chun Law, MSc
About this study
Official title: Evaluating the Efficacy of a Text Messaging-based Shisha Smoking Cessation Intervention for Young Adults in Hong Kong: A Randomised Controlled Pilot Trial
The goal of this study is to evaluate the efficacy of a culture specific text-messaging based shisha smoking cessation intervention for young adults in Hong Kong. Participants in the intervention group will receive smartphone text messaging-based intervention and support that contained personalised messages with both text and visual elements over 6 weeks under a manualised programme. Participants in the control group will only receive a leaflet about the health risks of shisha smoking (the exact identical contents received by the participants in the intervention group at a session).
All participants will complete a self-administered questionnaire at baseline, 6th- and 12th-week on their self-reported shisha abstinences, knowledge on risk, readiness to quit and attitudes on shisha smoking
Read the detailed description
Shisha smoking becomes the most prevalent form of tobacco use among university students in Hong Kong. The World Health Organisation (WHO) has urged healthcare professionals, policy makers and researchers to establish cultural-specific preventing and controlling strategies for shisha smoking to address this uprising public health threat. To date, only limited researches have been conducted focusing on reducing shisha use. Medications, like varenicline and bupropion, do not outweigh behavioural intervention alone for shisha smoking cessation. Early interventions adopting from traditional tobacco smoking cessation interventions were unsuccessful in lowering the smoking rates since these interventions were unable to cover the unique features of shisha smoking, such as the social dimension, the intermittent smoking patterns and the positive attitudes towards shisha. Though a Cochrane review and meta- analysis conducted in 2022 supported the use of behavioural intervention to promote shisha abstinence (risk ratio = 3.19, 95% CI: 2.17-4.69), the level of evidence remained unsatisfactory as there were only 9 interventional studies included. The authors further suggested that more interventional studies with the use of e-health behavioural interventions for shisha smoking cessation might enhance the robustness on its efficacies.
There are strong cultural differences for the practice of shisha smoking. For example, shisha smoking is a religiously acceptable culture that deeply ingrained in Middle Eastern countries whereas it is more of a social activity in Hong Kong. In fact, culture-based shisha cessation strategies showed preliminary promising results in reducing shisha smoking. For instance, an Iranian study which recruited 212 shisha-exclusive women to evaluate the effectiveness of a 4-month in-person educational program revealed that the programme had significantly increased shisha abstinence rates, health knowledge, self-efficacy, and intention to quit when compared to the control group. A recent randomised controlled trial adopting a 6-week smoker-tailored mobile messaging intervention among 319 young adults in the US demonstrated promising results in shisha abstinence and reduced the frequency of use last up to 6 months. Up-to-date, there is no Chinese- or Hong Kong-culture based shisha smoking intervention programme available. Thus, the development of a culture specific shisha cessation interventional program for shisha smokers in Hong Kong is deemed necessary.
In short, shisha smoking is common in Hong Kong especially among youth and young adults despite its hazardous effects being similar to cigarette smoking. A growing amount of evidence has supported the use of shisha-specific behavioural interventions to address this public health threat. With the recommendation from WHO on the culture specific interventions for shisha smoking cessation but a lack of such cessation intervention in the East Asian region, there is an utmost urgent need to develop and research on a shisha smoking cessation intervention for young adults in Hong Kong.
In light of such contexts, we developed a culture specific smartphone text messaging-based shisha smoking cessation intervention for young adults in Hong Kong using the well-structured intervention mapping method. Intervention mapping is an iterative process that is commonly used to develop, implement and evaluate theory-based health or behavioural interventions. It has been widely adopted to design and implement behavioural interventions in shisha smoking and cigarette smoking cessation studies. Based on the shisha smoker's individual characteristics, the developed text messaging-based intervention contains personalised messages with both text and visual elements emphasising the negative impacts of shisha smoking. Supported by previous overseas and local studies using mHealth intervention, together with the high penetration rates of smartphone use in Hong Kong and the openness to mobile health interventions, smartphone instant messaging applications, such as WhatsApp, Telegram and Signal, will be the powerful and effective delivery modes for this text messaging-based shisha smoking cessation intervention among Hong Kong young adults.
The current randomised controlled pilot trial aims to evaluate the efficacy of the culture specific text-messaging based shisha smoking cessation intervention for young adults in Hong Kong. It is hypothesised that participants randomly allocated to the intervention can achieve higher shisha abstinence, which maintain through the three months follow-up study period than the participants in the control group. For secondary outcomes, it is hypothesised that participants in the intervention group will have lowered level of dependency, increased knowledge on risk, improved readiness to quit, and more negative attitudes on shisha smoking during the study period.
Methods Design This study will be a 3-month, prospective, 2-arm, randomised controlled pilot trial. Participants will be assessed in three timepoints: baseline, 6th-, and 12th- week. The proposed study duration will be 2 years starting from 1st December, 2024 to 30th November, 2026. The trial will be conducted in accordance with the Good Clinical Practice and the CONSORT eHealth checklist.
The newly systematically developed smartphone text-messaging based shisha smoking cessation intervention targeted for young adults in Hong Kong has never been tested. The uncertainties such as shisha smokers' acceptability and usability, or the feasibility of the intervention should be examine using a smaller sample size before scaling up to a full trial. Therefore, the current study aimed to evaluate the intervention as a pilot study.
Randomisation and blinding Consented participants will be randomised into either the intervention or the control group on a 1:1 ratio, according to the sequences from the computer-generated random number by a researcher who is independent from the recruitment and the delivery of the intervention. Allocation concealment will be performed using sealed opaque envelopes with a card inside outlining the group allocation. As shisha smoking is often a social activity, if a group of shisha smokers are recruited at the same time, the whole group will be allocated to the same treatment group to minimise the spill-over effect between the two treatment arms.
Single-blind design will be adopted for this study. To achieve effective blinding, only the outcome assessors will be blinded to the treatment arms. Blinding will not be applied to the researcher who is responsible to delivers the interventions for the two treatment arms. Though consented participants will be strongly advised not to discuss their interventions allocated between themselves, full blinding will not be employed to the participants in this study. This is because shisha is often a social activity, hence participants might still have a chance to communicate with each other, leading to the potential observational bias on the study results.
Participants A convenience sample of 100 young adult shisha smokers in Hong Kong will be recruited through local universities' email invitations, snowballing from the recruited participants and outreaching to high prevalent areas that young people smoke shisha. With references to a similar 3-month pilot randomised controlled trial in the UK that had 67 young adult shisha smokers completed the study, and assuming 30% drop-out rate, 100 young adult shisha smokers shall be appropriate to evaluate the efficacy of this novel smartphone text-messaging based intervention in this pilot study.
Procedures After eligible participants completing the informed consents and baseline assessments, they will be randomly allocated into either the intervention or the control group. For the intervention group, except for the first face-to-face encountering with the participants for informed consents and baseline assessments. The researcher will follow the intervention manual and deliver the relevant customised information and personalised messages (in Chinese or English) to the participants via their preferred smartphone text- messaging applications, such as WhatsApp, WeChat, Signal, etc. commencing on every preceding Thursday (2 days before weekend). All intervention sessions will be delivered by a researcher who will be provided with a 1-day training workshop and will be assessed by the research team before implementing the intervention. Weekly meeting will be held with the research team to monitor the progress to ensure treatment integrity and to ensure the single-blinding nature of this study. For the control group, except for the first face-to-face encountering with the participants for informed consents and baseline assessments, the researcher will only provide a leaflet about the health risks of shisha smoking in either Chinese or English to them.
Both groups will be followed-up for 3 months. Outcome assessments and data will be collected from all participants at baseline, 6th-, and 12th-week follow-up via telephone call or face-to-face interview in a research room at the University of Hong Kong. The assessments will include a self-administered (or self- reported) questionnaire booklet, and the structured interview using the Structured Clinical Interview for Diagnostic and Statistical Manual of Mental Disorders, fifth version (SCID-5). Each assessment takes around 30 minutes.
Statistical Analyses Data entry and analyses will be performed using IBM Statistical Package for the Social Sciences (SPSS), with a significance of p = 0.05. Intention to treat analysis will be adopted in this trial, missing data will be handled by the last observation carried forward approach from the 6th week follow-up onwards.
Baseline demographic characteristics, treatment adherence rate, shisha smoking, and other tobacco product smoking behaviours will be summarised with descriptive statistics in overall and by treatment condition. Between group differences will be compared by nonparametric tests, such as Pearson's chi-squared and likelihood ratio tests at baseline.
Generalised linear mixed models will be performed to explore the comparisons within and between treatment conditions for all outcome measures, including the percentage of participants who achieves shisha abstinence, the average days and smoking session (1-hour per session), frequency and duration of shisha smoking, and the mean scores and standard deviations from risk knowledges, attitudes towards shisha smoking, CL and SCID-5. Cox regression model will be conducted to determine the between group abstinence duration by hazard ratio.
- Conditions
- Intervention, Control
- Being tested
- text-messaging based intervention
- Keywords
- shisha smoking, text-messaging based, cessation intervention, mHealth
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
text-messaging based interventionBehavioural
The 6-week, culture specific, text-messaging based cessation intervention for young adults in Hong Kong consists of 6 sessions: 1) Programme overview, 2) Psychoeducation on the health risks, 3) Social support, 4) Stress management, 5) Craving and withdrawal symptoms management, and 6) Summary and relapse prevention.
| Study group | Role | What they receive |
|---|---|---|
| Intervention | Experimental | Participants will receive smartphone text messaging-based intervention and support that contained personalised messages with both text and visual elements over 6 weeks under a manualised programme. The contents of the messages within the intervention is developed based on the results of a Delphi study that identified 32 behaviour change techniques by 46 tobacco/ substance use control policy experts and mental health professionals in Hong Kong. Receives: Behavioral: text-messaging based intervention |
| Control | No intervention | Participants in the control group will only receive a leaflet about the health risks of shisha smoking in either Chinese or English. The information of the leaflet will be with the exact identical contents on the leaflet received by the participants in the intervention group at Session 2. |
What is being measured
The primary outcome is the main question the study is designed to answer.
shisha abstinences
To compare the self-reported shisha abstinences between intervention and control group to evaluate the efficacy of the culture specific text-messaging based shisha smoking cessation intervention. Shisha abstinence is determined by self-reported last use 1) in the past 7 days using the Timeline Followback Method for active use, 2) in the past 30 days to determine current use, and 3) in the past 90 days to determine early remission in accordance with the criteria from the Diagnostic and Statistical Manual for Mental Disorders, 5th Edition.
Measured: From enrollment, 6-week (after treatment) and 12-week follow-up
Secondary outcomes (4)
Level of dependency
To compare the level of dependency between participants in intervention and control group during the study by using the diagnostic criteria from the Diagnostic and Statistical Manual of Mental Disorders, fifth version on Other Substance Use Disorder under Structured Clinical Interview for Diagnostic and Statistical Manual of Mental Disorders, fifth version. Participants will be classified as having no (0-1), mild (2-3), moderate (4-5), or severe (6-11) substance (shisha) use disorder. The minimum score ranged from 0 to 11.
Measured: From enrolment, 6-week (after treatment) and 12-week follow-up
Knowledge on risk
To compare the knowledge on risk between participants in intervention and control group during the study period by using a self-designed 10-item multiple choice questions (True/ False/ Do not know). Each correct answer will have 1 score, the score ranged from 0 to 10, with higher score indicates better knowledge.
Measured: From enrolment, 6-week (after treatment) and 12-week follow-up
Readiness to quit
To compare the readiness to quit between participants in intervention and control group during the study period using The Contemplation ladder. This measurement is a valid tool consists of 11 rungs ranging from 0 = 'no thought about quitting' to 10 = 'have already quitted', representing 5 stages of change in readiness for cigarette smoking and substance use control.
Measured: From enrolment, 6-week (after treatment) and 12-week follow-up
Attitudes on shisha smoking
To compare the attitudes towards shisha smoking between participants in intervention or control group during the study period by self-designed a 14-item, 5-point Liker scale (ranging from 1 = Strongly disagree to 5 = Strongly agree), the score ranged from 14 to 70, higher score represents more positive attitude towards shisha smoking.
Measured: From enrolment, 6-week (after treatment) and 12-week follow-up
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Jul 2025
- Study start20 Jul 2025 (estimated)
- Primary completionMay 2026 (estimated)
- Study completionJul 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for InterventionStudies of the same condition, open and under way.
- More trials run by The University of Hong KongThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Health services research
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Who is masked
- Participant, Outcomes assessor
- Enrolment
- 100 participants (estimated)
Sponsor and investigators
- Lead sponsor
- The University of Hong Kong
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Johnson Kai Chun LAW, The University of Hong Kong
- Investigators
- Johnson Kai Chun Law, MSc, Principal investigator, The University of Hong Kong
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07070154
- Sponsor's protocol ID
- SSCI-E
- Status last verified
- Jul 2025
- First submitted
- 18 Jun 2025
- Last updated
- 17 Jul 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: The dataset without personal identifiers and contact information will be available upon reasonable request.
Study at a glance
From the registry record, last updated by the sponsor on 17 Jul 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Evaluating the Efficacy of a Text Messaging-based Shisha Smoking Cessation Intervention for Young Adults in Hong Kong: A Randomised Controlled Pilot Trial
- ClinicalTrials.gov ID
- NCT07070154
- Acronym / sponsor ID
- SSCI-E
- Conditions
- Intervention, Control
- Keywords
- shisha smoking, text-messaging based, cessation intervention, mHealth
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 100 participants (estimated)
- Lead sponsor
- The University of Hong KongUniversity, hospital or other
- Study start
- 20 Jul 2025 (estimated)
- Primary completion
- May 2026 (estimated)
- Study completion
- Jul 2026 (estimated)
- First posted
- 17 Jul 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this study is to evaluate the efficacy of a culture specific text-messaging based shisha smoking cessation intervention for young adults in Hong Kong. Participants in the intervention group will receive smartphone text messaging-based intervention and support that contained personalised messages with both text and visual elements over 6 weeks under a manualised programme. Participants in the control group will only receive a leaflet about the health risks of shisha smoking (the exact identical contents received by the participants in the intervention group at a session).
All participants will complete a self-administered questionnaire at baseline, 6th- and 12th-week on their self-reported shisha abstinences, knowledge on risk, readiness to quit and attitudes on shisha smoking
Detailed description
Shisha smoking becomes the most prevalent form of tobacco use among university students in Hong Kong. The World Health Organisation (WHO) has urged healthcare professionals, policy makers and researchers to establish cultural-specific preventing and controlling strategies for shisha smoking to address this uprising public health threat. To date, only limited researches have been conducted focusing on reducing shisha use. Medications, like varenicline and bupropion, do not outweigh behavioural intervention alone for shisha smoking cessation. Early interventions adopting from traditional tobacco smoking cessation interventions were unsuccessful in lowering the smoking rates since these interventions were unable to cover the unique features of shisha smoking, such as the social dimension, the intermittent smoking patterns and the positive attitudes towards shisha. Though a Cochrane review and meta- analysis conducted in 2022 supported the use of behavioural intervention to promote shisha abstinence (risk ratio = 3.19, 95% CI: 2.17-4.69), the level of evidence remained unsatisfactory as there were only 9 interventional studies included. The authors further suggested that more interventional studies with the use of e-health behavioural interventions for shisha smoking cessation might enhance the robustness on its efficacies.
There are strong cultural differences for the practice of shisha smoking. For example, shisha smoking is a religiously acceptable culture that deeply ingrained in Middle Eastern countries whereas it is more of a social activity in Hong Kong. In fact, culture-based shisha cessation strategies showed preliminary promising results in reducing shisha smoking. For instance, an Iranian study which recruited 212 shisha-exclusive women to evaluate the effectiveness of a 4-month in-person educational program revealed that the programme had significantly increased shisha abstinence rates, health knowledge, self-efficacy, and intention to quit when compared to the control group. A recent randomised controlled trial adopting a 6-week smoker-tailored mobile messaging intervention among 319 young adults in the US demonstrated promising results in shisha abstinence and reduced the frequency of use last up to 6 months. Up-to-date, there is no Chinese- or Hong Kong-culture based shisha smoking intervention programme available. Thus, the development of a culture specific shisha cessation interventional program for shisha smokers in Hong Kong is deemed necessary.
In short, shisha smoking is common in Hong Kong especially among youth and young adults despite its hazardous effects being similar to cigarette smoking. A growing amount of evidence has supported the use of shisha-specific behavioural interventions to address this public health threat. With the recommendation from WHO on the culture specific interventions for shisha smoking cessation but a lack of such cessation intervention in the East Asian region, there is an utmost urgent need to develop and research on a shisha smoking cessation intervention for young adults in Hong Kong.
In light of such contexts, we developed a culture specific smartphone text messaging-based shisha smoking cessation intervention for young adults in Hong Kong using the well-structured intervention mapping method. Intervention mapping is an iterative process that is commonly used to develop, implement and evaluate theory-based health or behavioural interventions. It has been widely adopted to design and implement behavioural interventions in shisha smoking and cigarette smoking cessation studies. Based on the shisha smoker's individual characteristics, the developed text messaging-based intervention contains personalised messages with both text and visual elements emphasising the negative impacts of shisha smoking. Supported by previous overseas and local studies using mHealth intervention, together with the high penetration rates of smartphone use in Hong Kong and the openness to mobile health interventions, smartphone instant messaging applications, such as WhatsApp, Telegram and Signal, will be the powerful and effective delivery modes for this text messaging-based shisha smoking cessation intervention among Hong Kong young adults.
The current randomised controlled pilot trial aims to evaluate the efficacy of the culture specific text-messaging based shisha smoking cessation intervention for young adults in Hong Kong. It is hypothesised that participants randomly allocated to the intervention can achieve higher shisha abstinence, which maintain through the three months follow-up study period than the participants in the control group. For secondary outcomes, it is hypothesised that participants in the intervention group will have lowered level of dependency, increased knowledge on risk, improved readiness to quit, and more negative attitudes on shisha smoking during the study period.
Methods Design This study will be a 3-month, prospective, 2-arm, randomised controlled pilot trial. Participants will be assessed in three timepoints: baseline, 6th-, and 12th- week. The proposed study duration will be 2 years starting from 1st December, 2024 to 30th November, 2026. The trial will be conducted in accordance with the Good Clinical Practice and the CONSORT eHealth checklist.
The newly systematically developed smartphone text-messaging based shisha smoking cessation intervention targeted for young adults in Hong Kong has never been tested. The uncertainties such as shisha smokers' acceptability and usability, or the feasibility of the intervention should be examine using a smaller sample size before scaling up to a full trial. Therefore, the current study aimed to evaluate the intervention as a pilot study.
Randomisation and blinding Consented participants will be randomised into either the intervention or the control group on a 1:1 ratio, according to the sequences from the computer-generated random number by a researcher who is independent from the recruitment and the delivery of the intervention. Allocation concealment will be performed using sealed opaque envelopes with a card inside outlining the group allocation. As shisha smoking is often a social activity, if a group of shisha smokers are recruited at the same time, the whole group will be allocated to the same treatment group to minimise the spill-over effect between the two treatment arms.
Single-blind design will be adopted for this study. To achieve effective blinding, only the outcome assessors will be blinded to the treatment arms. Blinding will not be applied to the researcher who is responsible to delivers the interventions for the two treatment arms. Though consented participants will be strongly advised not to discuss their interventions allocated between themselves, full blinding will not be employed to the participants in this study. This is because shisha is often a social activity, hence participants might still have a chance to communicate with each other, leading to the potential observational bias on the study results.
Participants A convenience sample of 100 young adult shisha smokers in Hong Kong will be recruited through local universities' email invitations, snowballing from the recruited participants and outreaching to high prevalent areas that young people smoke shisha. With references to a similar 3-month pilot randomised controlled trial in the UK that had 67 young adult shisha smokers completed the study, and assuming 30% drop-out rate, 100 young adult shisha smokers shall be appropriate to evaluate the efficacy of this novel smartphone text-messaging based intervention in this pilot study.
Procedures After eligible participants completing the informed consents and baseline assessments, they will be randomly allocated into either the intervention or the control group. For the intervention group, except for the first face-to-face encountering with the participants for informed consents and baseline assessments. The researcher will follow the intervention manual and deliver the relevant customised information and personalised messages (in Chinese or English) to the participants via their preferred smartphone text- messaging applications, such as WhatsApp, WeChat, Signal, etc. commencing on every preceding Thursday (2 days before weekend). All intervention sessions will be delivered by a researcher who will be provided with a 1-day training workshop and will be assessed by the research team before implementing the intervention. Weekly meeting will be held with the research team to monitor the progress to ensure treatment integrity and to ensure the single-blinding nature of this study. For the control group, except for the first face-to-face encountering with the participants for informed consents and baseline assessments, the researcher will only provide a leaflet about the health risks of shisha smoking in either Chinese or English to them.
Both groups will be followed-up for 3 months. Outcome assessments and data will be collected from all participants at baseline, 6th-, and 12th-week follow-up via telephone call or face-to-face interview in a research room at the University of Hong Kong. The assessments will include a self-administered (or self- reported) questionnaire booklet, and the structured interview using the Structured Clinical Interview for Diagnostic and Statistical Manual of Mental Disorders, fifth version (SCID-5). Each assessment takes around 30 minutes.
Statistical Analyses Data entry and analyses will be performed using IBM Statistical Package for the Social Sciences (SPSS), with a significance of p = 0.05. Intention to treat analysis will be adopted in this trial, missing data will be handled by the last observation carried forward approach from the 6th week follow-up onwards.
Baseline demographic characteristics, treatment adherence rate, shisha smoking, and other tobacco product smoking behaviours will be summarised with descriptive statistics in overall and by treatment condition. Between group differences will be compared by nonparametric tests, such as Pearson's chi-squared and likelihood ratio tests at baseline.
Generalised linear mixed models will be performed to explore the comparisons within and between treatment conditions for all outcome measures, including the percentage of participants who achieves shisha abstinence, the average days and smoking session (1-hour per session), frequency and duration of shisha smoking, and the mean scores and standard deviations from risk knowledges, attitudes towards shisha smoking, CL and SCID-5. Cox regression model will be conducted to determine the between group abstinence duration by hazard ratio.
Study design
- Primary purpose
- Health services research
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Intervention | Experimental | Behavioral: text-messaging based interventionParticipants will receive smartphone text messaging-based intervention and support that contained personalised messages with both text and visual elements over 6 weeks under a manualised programme. The contents of the messages within the intervention is developed based on the results of a Delphi study that identified 32 behaviour change techniques by 46 tobacco/ substance use control policy experts and mental health professionals in Hong Kong. |
| Control | No intervention | –Participants in the control group will only receive a leaflet about the health risks of shisha smoking in either Chinese or English. The information of the leaflet will be with the exact identical contents on the leaflet received by the participants in the intervention group at Session 2. |
Who may qualify
- Ages
- 18 to 35 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (5 listed)
- young adults aged 18 to 35 years who are interested in quitting shisha
- smoked shisha within the 30 days at the time of enrolment (current smoker)
- smoked for more than twelve times in 12 months (i.e., on a monthly basis)22
- able to read and communicate in Chinese or English
- agree to utilise his/her own personal mobile or smartphone to send and receive messages
Key exclusion criteria (3 listed)
- scored 10 (''have already quitted'') on Contemplation Ladder assessment at baseline
- unable to provide consent
- unable to read and communicate in Chinese or English
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| text-messaging based interventionThe 6-week, culture specific, text-messaging based cessation intervention for young adults in Hong Kong consists of 6 sessions: 1) Programme overview, 2) Psychoeducation on the health risks, 3) Social support, 4) Stress management, 5) Craving and withdrawal symptoms management, and 6) Summary and relapse prevention. | Behavioural | Intervention |
Primary outcome
shisha abstinences
Time frame: From enrollment, 6-week (after treatment) and 12-week follow-up
To compare the self-reported shisha abstinences between intervention and control group to evaluate the efficacy of the culture specific text-messaging based shisha smoking cessation intervention. Shisha abstinence is determined by self-reported last use 1) in the past 7 days using the Timeline Followback Method for active use, 2) in the past 30 days to determine current use, and 3) in the past 90 days to determine early remission in accordance with the criteria from the Diagnostic and Statistical Manual for Mental Disorders, 5th Edition.
4 secondary outcomes
Level of dependency
Time frame: From enrolment, 6-week (after treatment) and 12-week follow-up
Knowledge on risk
Time frame: From enrolment, 6-week (after treatment) and 12-week follow-up
Readiness to quit
Time frame: From enrolment, 6-week (after treatment) and 12-week follow-up
Attitudes on shisha smoking
Time frame: From enrolment, 6-week (after treatment) and 12-week follow-up
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 17 Jul 2025.
- Individual participant dataSharing planned: Yes. The dataset without personal identifiers and contact information will be available upon reasonable request.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Johnson Kai Chun Law, MSc principal investigator
The University of Hong Kong
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing text-messaging based intervention in people with Intervention and Control, run by The University of Hong Kong at 1 site in Hong Kong.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 17 Jul 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Hong Kong. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Johnson Kai Chun Law, MSc (+85266703003, u3009145@connect.hku.hk), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
shisha abstinences (time frame: From enrollment, 6-week (after treatment) and 12-week follow-up). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Jul 2025.