← Eichor
Study identifier: NCT06901713 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Smoking Cessation Program With CBT and Mindfulness Audio Support: A Randomized Controlled Trial

Condition: Smoking Cessation; Tobacco Dependence  ·  Sponsor: Sir Run Run Shaw Hospital

PhaseNA
Planned participants2000
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

This protocol describes a randomized controlled trial evaluating the effectiveness of a smoking cessation program with two intervention methods. One method provides only CBT text messages (Group A), while the other combines CBT text with mindfulness audio (Group B). The study aims to compare the two approaches in reducing smoking frequency, managing cravings, and improving emotional regulation. This study investigates the effects of two different smoking cessation interventions: (1) CBT text-based program alone (Group A), and (2) CBT text combined with mindfulness audio (Group B). The primary outcomes include reductions in smoking frequency and cravings, as well as improvements in emotional regulation and quality of life.

This description comes directly from the study's public registry record.

Talk to the study team

Yanhui Liao  ·  86 18814898844  ·  liaoyanhui@zju.edu.cn

Always discuss trial participation with your own doctor first.

Locations (1)

Sir Run Run Shaw HospitalHangzhou, ChinaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06901713