Abstract

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.

Details

Title
A randomized controlled trial of a smoking cessation smartphone application with a carbon monoxide checker
Author
Masaki Katsunori 1   VIAFID ORCID Logo  ; Tateno Hiroki 2 ; Nomura Akihiro 3 ; Muto Tomoyasu 4   VIAFID ORCID Logo  ; Suzuki, Shin 5 ; Satake Kohta 4   VIAFID ORCID Logo  ; Hida Eisuke 6 ; Fukunaga Koichi 1 

 Keio University School of Medicine, Division of Pulmonary Medicine, Department of Medicine, Tokyo, Japan (GRID:grid.26091.3c) (ISNI:0000 0004 1936 9959) 
 Keio University School of Medicine, Division of Pulmonary Medicine, Department of Medicine, Tokyo, Japan (GRID:grid.26091.3c) (ISNI:0000 0004 1936 9959); Saitama City Hospital, Department of Internal Medicine, Saitama, Japan (GRID:grid.26091.3c) 
 CureApp Institute, Karuizawa, Nagano, Japan (GRID:grid.26091.3c); Kanazawa University (iCREK), Kanazawa, Innovative Clinical Research Center, Ishikawa, Japan (GRID:grid.9707.9) (ISNI:0000 0001 2308 3329); Kanazawa University Graduate School of Medical Sciences, Kanazawa, Department of Cardiovascular Medicine, Ishikawa, Japan (GRID:grid.9707.9) (ISNI:0000 0001 2308 3329) 
 CureApp Institute, Karuizawa, Nagano, Japan (GRID:grid.9707.9); CureApp, Inc, Tokyo, Japan (GRID:grid.9707.9) 
 CureApp, Inc, Tokyo, Japan (GRID:grid.9707.9) 
 Osaka University Graduate School of Medicine, Department of Biostatistics and Data Science, Osaka, Japan (GRID:grid.136593.b) (ISNI:0000 0004 0373 3971) 
Publication year
2020
Publication date
Dec 2020
Publisher
Nature Publishing Group
e-ISSN
23986352
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2528863548
Copyright
© The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.