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Mobile Phone-Based Smoking-Cessation Intervention for Smoking Parents

Effectiveness of AI-powered Mobile Phone-based Interventions in Parental Smoking Cessation

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06570122
Enrollment
300
Registered
2024-08-26
Start date
2024-09-01
Completion date
2025-12-30
Last updated
2024-08-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Smoking Cessation

Brief summary

This study aims to explore the feasibility and preliminary effectiveness of a mobile phone-based intervention tailored specifically for smoking parents.

Detailed description

Parental smoking is associated with numerous adverse outcomes, including exposure to secondhand smoke, heightened risk of respiratory illnesses in children, and an increased likelihood that children will adopt smoking behaviors themselves. Despite awareness of these risks, many parents find it challenging to quit smoking due to stress, lack of support, and time constraints. This randomized controlled trial (RCT) investigates the effectiveness of a mobile phone-based intervention tailored specifically for smoking parents. The intervention group will receive AI-powered chatbot cessation support, while the control group will be provided with brief cessation advice. The study aims to determine whether the AI-driven intervention is more effective in helping parents quit smoking compared to traditional brief advice.

Interventions

5A's (Ask, Advise, Assess, Assist, Arrange) for smokers who are ready to quit, and 5R's (relevance, risks, rewards, roadblocks, and repetition) for smokers who are not ready to quit.

The health warning leaflet provides essential information on the dangers of secondhand and thirdhand smoke. It outlines how exposure to these forms of smoke can harm both smokers and non-smokers, particularly children, by increasing the risk of respiratory illnesses and other health issues.

Participants will receive three months of AI-powered chatbot, equipped with personalized interactions and real-time support, via WeChat.

Sponsors

Beijing Normal University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. aged 18 and above, reside in Zhuhai for the next 6 months 2. smoke at least 1 cigarette or use e-cigarettes daily 3. have a smartphone and a WeChat account, able to use WeChat skillfully

Exclusion criteria

1. Smokers who have communication barrier (either physically or cognitively) 2. Smokers who are currently participating in other SC programmes or services

Design outcomes

Primary

MeasureTime frameDescription
Self-reported 7-day point prevalence quit rate3 and 6 months follow-upSelf-reported 7-day point prevalence quit rate in the two groups
Eligibility ratebaselinethe percentage of eligible smokers out of the total number of smokers screened

Secondary

MeasureTime frameDescription
Consent ratebaselinethe percentage of eligible smokers who agree to participate out of the total number of eligible smokers
Percentage of Participant Engagement with E-Messages and Counselor Chats3 months follow-upThis outcome measures the percentage of participants who engage with the intervention by reading e-messages and responding to counselor chat messages at least once during the 3-month follow-up period.

Countries

China

Contacts

Primary ContactXue Weng
xueweng@bnu.edu.cn3621259

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026