ResProt JMIR Res Protoc JMIR Research Protocols 1929-0748 JMIR Publications Toronto, Canada v14i1e83839 41004799 10.2196/83839 Corrigenda and Addenda Corrigenda and Addenda Correction: Gamification of Incentive Spirometry in Trauma Patients: Protocol for a Prospective, Observational Feasibility Study Al-Dhoon Areen MD 1
Department of Neurology Atrium Health Wake Forest Baptist Medical Center 1 Medical Center Blvd Winston Salem, NC, 27157 United States 1 3364050740 areendhoon@gmail.com
https://orcid.org/0009-0005-3412-9368 Grimes Arthur MD 2 https://orcid.org/0000-0002-3435-8890 Goldstein Carma MD 3 https://orcid.org/0000-0003-0241-1180 Spronk Peter MD, PhD, EDIC 4 https://orcid.org/0000-0003-3319-8706 Martin R Shayn MD, MBA 3 https://orcid.org/0000-0003-0037-3950 Sarwal Aarti MD 5 https://orcid.org/0000-0002-4578-8378 Department of Neurology Atrium Health Wake Forest Baptist Medical Center Winston Salem, NC United States Department of Surgery, College of Medicine University of Oklahoma Oklahoma, OK United States Department of Surgery, Faculty of Medicine Atrium Health Wake Forest Baptist Medical Center Winston Salem, NC United States Department of Intensive Care, Expertise Center for Intensive Care Rehabilitation Apeldoorn Gelre Hospitals Apeldoorn The Netherlands Division of Neurocritical Care, Faculty of Medicine Virginia Commonwealth University Richmond, VA United States Corresponding Author: Areen Al-Dhoon areendhoon@gmail.com 2025 26 9 2025 14 e83839 9 9 2025 10 9 2025 ©Areen Al-Dhoon, Arthur Grimes, Carma Goldstein, Peter Spronk, R Shayn Martin, Aarti Sarwal. Originally published in JMIR Research Protocols (https://www.researchprotocols.org), 26.09.2025. 2025

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 https://www.researchprotocols.org/2025/1/e75871

In “Gamification of Incentive Spirometry in Trauma Patients: Protocol for a Prospective, Observational Feasibility Study” (JMIR Res Protoc 2025;14(1):e75871) the authors made two clarifications.

The Results section in the Abstract has been changed from:

The study was approved by the institutional review board of Atrium Health Wake Forest Baptist Medical Center and was registered at ClinicalTrials.gov. However, no participants were ever enrolled, as the OmniFlow partners did not supply the device for the study. Despite this, it remains a potentially beneficial tool, and future studies may confirm its benefits once the device becomes available.

to

The study was approved by the institutional review board and registered on ClinicalTrials.gov. Due to an unexpected delay in the initiation of the project, no patients were enrolled.

The Results section in the main body of the paper has been changed from:

The study was approved by the institutional review board and registered on ClinicalTrials.gov. However, no participants were enrolled, as the OmniFlow devices were never delivered. Despite initial agreements, the device supplier became unresponsive and failed to fulfill the shipment. Multiple attempts to reestablish contact were unsuccessful. This unexpected barrier highlights the importance of reliable vendor partnerships when implementing novel therapeutic technologies in clinical research.

to

The study was approved by the institutional review board and registered on ClinicalTrials.gov. Due to an unexpected delay in the initiation of the project, no patients were enrolled.