A randomized controlled trial of a smoking cessation smartphone application with a carbon monoxide checker

被引:60
作者
Masaki, Katsunori [1 ]
Tateno, Hiroki [1 ,2 ]
Nomura, Akihiro [3 ,4 ,5 ]
Muto, Tomoyasu [3 ,6 ]
Suzuki, Shin [6 ]
Satake, Kohta [3 ,6 ]
Hida, Eisuke [7 ]
Fukunaga, Koichi [1 ]
机构
[1] Keio Univ, Dept Med, Div Pulm Med, Sch Med, Tokyo, Japan
[2] Saitama City Hosp, Dept Internal Med, Saitama, Japan
[3] CureApp Inst, Nagano, Japan
[4] Kanazawa Univ iCREK, Innovat Clin Res Ctr, Kanazawa, Ishikawa, Japan
[5] Kanazawa Univ, Dept Cardiovasc Med, Grad Sch Med Sci, Kanazawa, Ishikawa, Japan
[6] CureApp Inc, Tokyo, Japan
[7] Osaka Univ, Dept Biostat & Data Sci, Grad Sch Med, Osaka, Japan
关键词
RECEPTOR PARTIAL AGONIST; VARENICLINE; DEPENDENCE; QUESTIONNAIRE; BUPROPION; THERAPY; PLACEBO;
D O I
10.1038/s41746-020-0243-5
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Evidence of the long-term efficacy of digital therapies for smoking cessation that include a smartphone application (app) is limited. In this multi-center randomized controlled trial, we tested the efficacy of a novel digital therapy for smoking cessation: the "CureApp Smoking Cessation (CASC)" system, including a CASC smartphone app, a web-based patient management PC software for primary physicians, and a mobile exhaled carbon monoxide (CO) checker. A total of 584 participants with nicotine dependence were recruited from October 2017 to January 2018, and allocated 1:1 to the CASC intervention group or the control group. Both groups received a standard smoking cessation treatment with pharmacotherapy and counseling for 12 weeks. Meanwhile, the intervention group used the CASC system, and the control group used a control-app without a mobile CO checker, each for 24 weeks. The primary outcome was the biochemically validated continuous abstinence rate (CAR) from weeks 9 to 24. The main secondary outcome was an extended CAR from weeks 9 to 52. Except for 12 participants who did not download or use the apps, 285 participants were assigned to the intervention group, and 287, to the control. CAR from weeks 9 to 24 in the intervention group was significantly higher than that in the control group (63.9% vs. 50.5%; odds ratio [OR], 1.73; 95% confidence interval [CI], 1.24 to 2.42; P = 0.001). The CAR from weeks 9 to 52 was also higher in the intervention group than that in the control group (52.3% vs. 41.5%; OR, 1.55; 95% CI, 1.11 to 2.16; P = 0.010). No specific adverse events caused by the CASC system were reported. Augmenting standard face-to-face counseling and pharmacotherapy with a novel smartphone app, the CASC system significantly improved long-term CARs compared to standard treatment and a minimally supportive control app.
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页数:7
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