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Gen AI Powered Behavioral Support Plus Chewing Gum Intervention for Construction Workers Who Smoke

2026年6月14日 更新者:Prof. Wang Man-Ping、The University of Hong Kong

Build to Quit 「築建無煙」: Gen AI Powered Behavioral Support Plus Chewing Gum Intervention for Construction Workers Who Smoke: A Pragmatic, Pilot, Cluster Randomized Controlled Trial

The goal of this pilot trial is to learn if 1-week NRT sampling, 3-week chewing gum, and 12-week chatbot-delivered instant messaging support works to help smoking cessation in construction workers who smoke. It will also learn about the feasibility, acceptability, and preliminary effectiveness of delivering the comprehensive intervention in construction settings. The main questions it aims to answer are:

  1. Will the integrated intervention, comprising NRT sampling, chewing gum, and chatbot-delivered instant messaging support, show feasibility, acceptability, and appropriateness for delivery in construction worksite settings?
  2. Will participants who receive the comprehensive intervention have a higher validated abstinence rate than those who receive NRT sampling alone?

Researchers will compare the integrated intervention, comprising NRT sampling, chewing gum, and chatbot-delivered instant messaging support, to the standard care group (NRT sampling alone) to see if the integrated intervention works to promote smoking cessation.

Participants in the intervention group will receive:

  1. AWARD advice and brief video
  2. 1-week NRT sampling
  3. 3-week chewing gum
  4. 12-week chatbot-based instant messaging support (via WhatsApp)

調査の概要

詳細な説明

Hong Kong has achieved a sustained reduction in daily cigarette smoking, from 23.3% in the early 1980s to 8.5% in 2025. However, the current prevalence remains above the Government's Towards 2025 target of 7.8%, indicating the need for continued and targeted cessation efforts. The construction industry represents a particularly important setting for intervention, as recent legislative amendments to designate construction sites as no-smoking areas have further strengthened the policy basis for promoting smoke-free worksites.

Construction workers (CWs) are a high-priority population for smoking cessation because they have consistently higher smoking prevalence than many other occupational groups and the general population. In Hong Kong, a workplace health study found that 45% of construction workers were daily smokers, nearly twice the prevalence among office clerks/professionals. For CWs, smoking may compound existing occupational health risks by increasing susceptibility to respiratory and cardiovascular diseases in a physically demanding and dust-exposed work environment.

This study proposes a comprehensive worksite-targeted smoking cessation intervention model for CWs who smoke in Hong Kong, integrating NRT sampling, chewing gum support, and chatbot-delivered instant messaging. NRT is an evidence-based pharmacotherapy for reducing nicotine withdrawal symptoms and supporting smoking abstinence, and has been widely used in community-based cessation interventions. For CWs, short-term NRT sampling may provide immediate access to evidence-based pharmacological support, reduce early withdrawal symptoms, and lower the initial barrier to treatment uptake in a worksite setting. Chewing gum may complement NRT sampling by serving as a low-cost behavioral substitute for smoking, particularly by replacing the hand-to-mouth and oral routines associated with cigarette use. Chatbot-delivered instant messaging support can further extend the intervention beyond the worksite by providing 24/7 support, reminders for NRT and chewing gum use, and real-time assistance during cravings or high-risk smoking situations.

研究の種類

介入

入学 (推定)

200

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

  • 名前:Man Ping Wang, PhD
  • 電話番号:+852 3917 6636
  • メール:mpwang@hku.hk

研究連絡先のバックアップ

研究場所

    • Hong Kong
      • Hong Kong、Hong Kong、香港、999077
        • Hong Kong Council on Smoking and Health (COSH)
        • コンタクト:
          • Fung Wong
          • 電話番号:+852 2180 5186
        • 副調査官:
          • Tai Hing Lam, MD
        • 副調査官:
          • Tzu Tsun Luk, PhD
        • 副調査官:
          • Xiaoyun Xie, MPH
        • 副調査官:
          • Mengyao Li, Mphil
        • 副調査官:
          • Ziqiu Guo, PhD
        • 副調査官:
          • Yilan Wu, Mphil

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  1. Hong Kong residents aged 18 or above
  2. Smoke at least one cigarette per day in the preceding 3-month
  3. Able to communicate in Cantonese (including reading and writing Chinese)
  4. Saliva cotinine 30 ng/ml or above
  5. Intent to quit / reduce smoking
  6. Have instant messaging tool (WhatsApp) installed
  7. Able to use instant messaging tool (e.g., WhatsApp) for communication.

Exclusion Criteria:

  1. Smokers who are participating in other smoking cessation programmes
  2. Smokers who are using any smoking cessation medication
  3. Smokers who are presenting with the following oral diseases, including recent oral surgery or tooth extraction, unstable dentures, significant tooth mobility or advanced periodontal disease, temporomandibular pain or dysfunction, or painful oral mucosal lesions

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:ヘルスサービス研究
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:独身

武器と介入

参加者グループ / アーム
介入・治療
実験的:介入群
内容としては、禁煙のメリット、喫煙と病気、禁煙方法、禁断症状への対処法、禁煙宣言などが含まれます。
賞のアドバイスには、喫煙の歴史についての質問、高いリスクについて警告し、禁煙するようにアドバイスし、喫煙者を喫煙した禁煙サービス(紹介カード付き)に紹介し、再度行うことが含まれます。
内容は、簡単な情報と、既存の禁煙サービス、連絡方法、動機付け情報、強力なサポートメッセージまたはスローガンのハイライトで構成されています。
The contents of the leaflet include (1) highlights of the absolute risk of death due to smoking; (2) the whole list of diseases caused by active and secondhand smoking; (3) ten horrible pictorial warnings of health consequences of smoking and second-hand smoking in one page to maximize the impacts; (4) benefits of SC and (5) simple messages to encourage participants to quit smoking.
Participants in both group will receive a 1-week supply of free nicotine gum (2 mg or 4 mg). The dosage of nicotine gum will be guided by participants' daily cigarette consumption, in accordance with recommendations from the Department of Health. Research assistants will explain the benefits of NRT for smoking cessation, provide instructions on the correct use of nicotine gum, encourage participants to continue using nicotine gum after completing the free sample where appropriate, and advise participants to reduce smoking or make a quit attempt when using NRT.
Participants in the intervention group will receive 6 packs of chewing gum at baseline (2 packs per week). Chewing gum will be presented as a practical strategy to replace the hand-to-mouth and oral routines associated with smoking, particularly during work breaks, after meals, in other smoking-related situations at construction sites, or when participants are unwilling to use nicotine gum.
Participants in the intervention group will receive 12 weeks of instant messaging support delivered by the LLM-based chatbot accessible via WhatsApp platform. The chatbot, powered by Claude model (or more advanced model available) using prompt-engineering and agent-based techniques, will deliver theory-based and structured intervention alongside freeform, on-demand support. The structured intervention session deploys the 5As model (Ask, Advise, Assess, Assist, and Arrange follow-up) and 5Rs model (Relevance, Risks, Rewards, Roadblocks, Repetition), as used in our previous telephone-counselling trials and recommended by WHO for brief SC intervention.
Participants in both groups will receive a brief motivational video (15-second) via WhatsApp. The video will feature a construction worker who successfully quit smoking in our previous trial, providing a relatable peer role model for participants. The video will welcome participants to the programme, encourage them to make a quit attempt, and promote early use of nicotine gum as a practical strategy for managing cravings and supporting smoking cessation.
アクティブコンパレータ:対照群
内容としては、禁煙のメリット、喫煙と病気、禁煙方法、禁断症状への対処法、禁煙宣言などが含まれます。
賞のアドバイスには、喫煙の歴史についての質問、高いリスクについて警告し、禁煙するようにアドバイスし、喫煙者を喫煙した禁煙サービス(紹介カード付き)に紹介し、再度行うことが含まれます。
内容は、簡単な情報と、既存の禁煙サービス、連絡方法、動機付け情報、強力なサポートメッセージまたはスローガンのハイライトで構成されています。
The contents of the leaflet include (1) highlights of the absolute risk of death due to smoking; (2) the whole list of diseases caused by active and secondhand smoking; (3) ten horrible pictorial warnings of health consequences of smoking and second-hand smoking in one page to maximize the impacts; (4) benefits of SC and (5) simple messages to encourage participants to quit smoking.
Participants in both group will receive a 1-week supply of free nicotine gum (2 mg or 4 mg). The dosage of nicotine gum will be guided by participants' daily cigarette consumption, in accordance with recommendations from the Department of Health. Research assistants will explain the benefits of NRT for smoking cessation, provide instructions on the correct use of nicotine gum, encourage participants to continue using nicotine gum after completing the free sample where appropriate, and advise participants to reduce smoking or make a quit attempt when using NRT.
Participants in both groups will receive a brief motivational video (15-second) via WhatsApp. The video will feature a construction worker who successfully quit smoking in our previous trial, providing a relatable peer role model for participants. The video will welcome participants to the programme, encourage them to make a quit attempt, and promote early use of nicotine gum as a practical strategy for managing cravings and supporting smoking cessation.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
生化学的に検証された禁欲
時間枠:6ヶ月間のフォローアップ
呼気COレベル<4ppmおよび唾液コチニンレベル≦30ng/mlとして定義されます。
6ヶ月間のフォローアップ

二次結果の測定

結果測定
メジャーの説明
時間枠
生化学的に検証された禁欲
時間枠:3ヶ月のフォローアップ
呼気COレベル<4ppmおよび唾液コチニンレベル≦30ng/mlとして定義されます。
3ヶ月のフォローアップ
自己報告された7日間のポイントの有病率禁止
時間枠:3か月と6か月のフォローアップ
フォローアップの前に7日間でパフを吸わなかった喫煙者
3か月と6か月のフォローアップ
自己報告された削減
時間枠:1、2、3、および6か月のフォローアップ
ベースラインの少なくとも50%の減少によって定義されたタバコ数
1、2、3、および6か月のフォローアップ
禁煙サービスの自己報告された使用
時間枠:1、2、3、および6か月のフォローアップ
1、2、3、および6か月のフォローアップでの禁煙サービスの使用。
1、2、3、および6か月のフォローアップ
Family well-being
時間枠:3- and 6-month follow-ups
Family well-being will be assessed using the 3H scale, which measures perceived family health, happiness, and harmony on a 0-10 scale.
3- and 6-month follow-ups
Perceived family happiness
時間枠:3- and 6-month follow-ups
Perceived family happiness will be measured using a single-item self-reported family happiness scale ranging from 0 to 10.
3- and 6-month follow-ups

その他の成果指標

結果測定
メジャーの説明
時間枠
Recruitment rate
時間枠:Baseline
Defined as the number of participants divided by the number of eligible smokers
Baseline
Retention rate
時間枠:1-, 2-, 3- and 6-month follow-ups
Defined as the number of participants who completed the follow-up divided by the number of participants
1-, 2-, 3- and 6-month follow-ups
Acceptability of NRT sampling
時間枠:1-, 2-, 3- and 6-month follow-ups
Acceptability of NRT sampling will be assessed through 4 brief items (score range from 0 to10) on perceived usefulness for craving relief, perceived side effects, willingness to continue using NRT after the free sample, and overall satisfaction with the NRT gum.
1-, 2-, 3- and 6-month follow-ups
Acceptability of chewing gum
時間枠:1-, 2-, 3- and 6-month follow-ups
Acceptability of chewing gum will be assessed through 3 brief items (score range from 0 to 10) on perceived usefulness for behavioral substitution, perceived fit with construction worksite routines, and willingness to continue using chewing gum as a cessation aid.
1-, 2-, 3- and 6-month follow-ups
Self-reported adverse events
時間枠:1-, 2-, 3- and 6-month follow-ups
Self-reported adverse events related to nicotine gum and chewing gum will be assessed using a binary question: "Have you experienced any adverse events when using nicotine gum or chewing gum?"
1-, 2-, 3- and 6-month follow-ups
Chatbot usability
時間枠:3-month follow-up
Chatbot usability will be evaluated using the 11-item Bot Usability Scale (BUS), which assesses perceived effectiveness, efficiency, and satisfaction. The score of the Bot Usability Scale ranges from 0 to 100, with the higher score indicating more usability of the chatbot.
3-month follow-up

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Man Ping Wang, PhD、The University of Hong Kong

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年6月20日

一次修了 (推定)

2027年5月31日

研究の完了 (推定)

2027年6月30日

試験登録日

最初に提出

2026年6月9日

QC基準を満たした最初の提出物

2026年6月9日

最初の投稿 (実際)

2026年6月15日

学習記録の更新

投稿された最後の更新 (実際)

2026年6月17日

QC基準を満たした最後の更新が送信されました

2026年6月14日

最終確認日

2026年6月1日

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