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Completed

NCT Number: NCT05508672

Community-Centered eHealth Smoking Cessation Intervention(CCeSCI)

Recent findings regarding why Chinese male smokers are reluctant to quit have offered insight for a possible new solution. Consistent with the Cognitive Dissonance Theory, "smoking rationalization beliefs" are a set of beliefs by smokers to rationalize their smoking behavior and avoid quitting. These beliefs have been well studied by global researchers, and a "smoking rationalization beliefs" scale was recently developed and validated for Chinese male smokers. The six dimensions of these beliefs are: smoking functional beliefs, risk generalization beliefs, social acceptability beliefs, safe smoking beliefs, self-exempting beliefs, and quitting is harmful beliefs. Studies on smoking rationalization in China have primarily been observational. Investigators propose to develop a Community-Centered eHealth Smoking Cessation Intervention (CCeSCI). The trinity of CCeSCI are the triangular unity of "smoking rationalization beliefs" framework, the non-physician community workers, and the eHealth technologies. The latter two were previously proven effective in interventional studies (including three conducted by the PI) but not yet widely used in smoking cessation. With the adoption of smoking rationalization beliefs framework aiming to address the cognitive causes of phycological addition to smoking and supported by the community-based behavioral interventions and the use of eHealth, CCeSCI is designed to overcome previous challenges with the principles of people-centeredness, convenience, and personalization.

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Key information

Conditions

Smoking Cessation Behavior Health Behavior Lifestyle, Healthy

Age range

25 year–64 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Shanghai Qingpu Patriotic Hygiene and Health Promotion Guidance Center

Shanghai, Shanghai Municipality, 201700, China

About this study

Investigators will firstly evaluate the feasibility of CCeSCI. Once CCeSCI is ready to deploy, investigators will recruit 60 smokers (male, 25-64 years old) in two communities in Qingpu to conduct a pilot non-blinded randomized controlled trial. They will be randomized in a 1:1 ratio into either the intervention group to receive CCeSCI or the control group to receive the traditional "smoking is harmful" education video. Investigators will also use qualitative research methods (one on one interviews) to conduct process evaluations at 4th, 8th, and 12th weeks according to the RE-AIM (Reach, Effectiveness, Adoption, Implementation, Maintenance) framework. At the end of the 12th week after the participants joined the RCT, saliva samples will be collected by community workers and quitting outcomes will be biochemically verified by a third party lab.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male, current cigarette smokers who are willing to quit
  • Citizens who currently reside in Qingpu District, Shanghai, China
  • Age 25-64
  • Smoking index greater than or equal to 100 (smoking index = average number of cigarettes smoked per day × years of smoking)
  • Able to understand mandarin Chinese
  • Willing to provide informed consent to participate in the study

Exclusion criteria

  • Ever or currently on pharmacologic treatments, including various forms of NRT formulations such as gum, transdermal patch, nasal spray, oral inhaler, lozenge, Bupropion, Varenicline and newly emerged precision medicine
  • Currently participating in other individual-based cessation program(s), such as psychological counseling, behavioral therapy etc.
  • Currently under treatment of life-threatening medical conditions or critically ill
  • Unable to make commitment of a consecutive 4-hour video viewing
  • Plan to move out of the community in the next 3 month

Treatment and study plan

Community-Centered eHealth Smoking Cessation Intervention (CCeSCI)

Other

We will equip CCeSCI with both core eHealth features and provider-side intervention. Patients assigned to the intervention group will receive a series of online interactive and personalization technologies, including an algorithm-based video curriculum with auto-texting, backstage monitoring system etc. Besides, the patients will also have the face-to-face meetings with community health workers. Provider-side intervention includes training for community workers, WeChat group discussion, and performance-based incentives. The training aims to provide essential skills for community workers so that they can provide face-to-face meetings with smokers during the first 3 months of quitting to prevent or revert relapse in a timely and proactive manner.

Traditional "smoking is harmful" education

Other

In the control group, the participants will receive traditional "smoking is harmful" education video, which is recorded by the clinical physicians.

Primary outcomes

  1. Biochemically verified continuous smoking abstinence at 3 month

    Time frame: 3 month

    Investigators will use cotinine to measure the smoking abstinence. Cotinine is a good biomarker for nicotine with a longer half-life (16-18h), and lab test for saliva is highly sensitive, convenient, and cost-effective. measured by cotinine saliva tests (<10ng•mL-1)

Secondary outcomes

  1. Fagerstrom Test For Nicotine Dependence (FTND) Score

    Time frame: Change from baseline to 3-month follow up

    Investigators will use the Fagerström Test for Nicotine Dependence as a standard instrument for assessing the intensity of physical addiction to nicotine. In scoring the Fagerstrom Test for Nicotine Dependence, the three yes/no items are scored 0 (no) and 1 (yes). The three multiple-choice items are scored from 0 to 3. The items are summed to yield a total score of 0-10. A higher score means more dependence on nicotine.

  2. Patient Health Questionnaire-9

    Time frame: Change from baseline to 3-month follow up

    Investigators will use PHQ-9 as a 9-question instrument to screen for depression. The scale ranges from 0 to 27. Total scores of 5, 10, 15, and 20 represent cutpoints for mild, moderate, moderately severe, and severe depression, respectively. Higher score indicates severe depression

  3. Self-reported 7-day point smoking status

    Time frame: 3-month follow up

    self-reported 7-day point prevalence of abstinence (not even a puff of smoke, for the last 7 days) at 3 months

  4. Self-reported continuous abstinence at 3 month

    Time frame: 3-month follow up

    not even a puff of smoke, for the last 3 months

  5. Self-reported average number of cigarettes

    Time frame: Change from baseline to 3-month follow up

    Investigators will count the number of cigarettes at 3 month

  6. Smoking Rationalization Scale

    Time frame: Change from baseline to 3-month follow up

    Investigators will use Smoking Rationalization Scale to measure smokers' thoughts about smoking. The scale comprised 26 items (e.g., "Smoking is good for inspiration and active thinking.") and was divided into 6 dimensions including smoking functional beliefs, risk generalization beliefs, social acceptability beliefs, safe smoking beliefs, self-exempting beliefs and quitting is harmful beliefs. Participants responded on a 5-point Likert scale (1 = completely disagree, 5 = completely agree). Higher scores indicated a higher level of smoking rationalization beliefs.

  7. Questionnaire about community health workers' Knowledge, Attitude and Practices (KAP)

    Time frame: 3-month follow up

    The knowledge, attitude, and practices (KAPs) survey provides a design to evaluate existing programs and to identify effective strategies for behavior change in society. The first section was related to knowledge, and this section had some questions where 1 point was assigned to the correct answer and 0 points were assigned to the wrong answer. A higher score demonstrated good knowledge. The second section was on attitude and had some questions on a 5-point Likert scale as strongly disagree = 1, disagree = 2, uncertain = 3, agree = 4, and strongly agree = 5. A higher score demonstrated a good attitude. The last part of the questionnaire was composed of questions related to the practice, and each question was scored as "yes" (1-point), "no" (0-point), and "sometimes" (0-point). A higher score indicated good practice.

  8. Weight in kilograms

    Time frame: Change from baseline to 3-month follow up

    Investigators will measure the participants' heights

  9. Blood Pressure

    Time frame: Change from baseline to 3-month follow up

    Investigators will measure the participants' both systolic and diastolic blood pressure

  10. Waist Circumference

    Time frame: Change from baseline to 3-month follow up

    Investigators will measure the waist circumference of the participants

Sponsors and collaborators

Lead sponsor

Duke Kunshan University

Other

Registry information

Official study title

Community-Centered eHealth Smoking Cessation Intervention Based on the "Smoking Rationalization Beliefs" Framework for Chinese Male Smokers

Important dates

Study start
2023
Primary completion
2023
Study completion
2023
First posted
Aug 19, 2022
Registry last updated
Feb 28, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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