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A Mobile App (Joint Effort) to Support Cannabis Use Self-Management and Reinforce the Use of Protective Behavioral Strategies: Development Process and Usability Testing

A Mobile App (Joint Effort) to Support Cannabis Use Self-Management and Reinforce the Use of Protective Behavioral Strategies: Development Process and Usability Testing

This study aimed to develop Joint Effort, a mobile app prototype designed to support CU self-management and reinforce PBS use among young adults, and to assess its usability. IM is a rigorous, theory- and evidence-based approach that emphasizes the role of research and theory in the intervention development process [32]. Our process was based on IM and a co-design approach.

José Côté, Patricia Auger, Gabrielle Chicoine, Jinghui Cheng, Sylvie Cossette, Guillaume Fontaine, Christine Genest, Shalini Lal, Judith Lapierre, M Gabrielle Pagé, Marc-André Maheu-Cadotte, Geneviève Rouleau, Billy Vinette, Didier Jutras-Aswad

JMIR Form Res 2025;9:e71924

Integrating Mobile Health App Data Into Electronic Medical or Health Record Systems and Its Impact on Health Care Delivery and Patient Health Outcomes: Scoping Review

Integrating Mobile Health App Data Into Electronic Medical or Health Record Systems and Its Impact on Health Care Delivery and Patient Health Outcomes: Scoping Review

Patient involvement in the development and implementation of m Health apps and its integration into EMR/EHR systems ensures that m Health apps and the integration are tailored to their needs, preferences, and concerns, thereby enhancing usability, engagement, and trust [18,23,24,26,31]. The integration of m Health app data into EMR/EHR systems provides significant benefits in several key areas [12,14,16,21,29].

Jialing Lin, Shona Marie Bates, Luke N Allen, Michael Wright, Limin Mao, Michael Kidd

JMIR Mhealth Uhealth 2025;13:e66650

Evaluating the User Experience and Usability of Game-Based Cognitive Assessments for Older People: Systematic Review

Evaluating the User Experience and Usability of Game-Based Cognitive Assessments for Older People: Systematic Review

Although this is not in itself an assessment of usability, it revealed an important usability finding: a lack of digital experience did not impact overall cognitive performance scores in a sample of older game users with low digital literacy and experience. A potential reason for this result may be the cautious and simplistic design of the SASG interface, which supported usability for the target cohort.

Rhys Mantell, Ye In Jane Hwang, Matthew Dark, Kylie Radford, Michael Kasumovic, Lauren Monds, Peter W Schofield, Tony Butler, Adrienne Withall

JMIR Aging 2025;8:e65252

Feasibility of a 12-Week, Therapist-Independent, Smartphone-Based Biofeedback Treatment for Episodic Migraine in Adults: Single-Center, Open-Label, 1-Armed Trial

Feasibility of a 12-Week, Therapist-Independent, Smartphone-Based Biofeedback Treatment for Episodic Migraine in Adults: Single-Center, Open-Label, 1-Armed Trial

The purpose of this study is to assess the feasibility, usability, and safety of 12 weeks of daily use of a home-based biofeedback system as a preventative in adults with episodic migraine. The findings of the study are intended to lead to refinements in the feasibility and usability of Cerebri (version 0.1.0; Nordic Brain Tech AS) and guide study design choices for a future randomized controlled trial. The study was a single-center, open-label, one-armed interventional trial conducted at St.

Amalie Christine Poole, Ingunn Grøntveit Winnberg, Melanie Rae Simpson, Anker Stubberud, Kjersti Grøtta Vetvik, Marte-Helene Bjørk, Lise Rystad Øie, Petter Holmboe, Alexander Olsen, Erling Tronvik, Tore Wergeland

JMIR Hum Factors 2025;12:e59622

The Effect of a Mobile App (eMOM) on Self-Discovery and Psychological Factors in Persons With Gestational Diabetes: Mixed Methods Study

The Effect of a Mobile App (eMOM) on Self-Discovery and Psychological Factors in Persons With Gestational Diabetes: Mixed Methods Study

Finally, we will evaluate the acceptance and usability of the e MOM app. This study is a secondary analysis of e MOM GDM RCT [20], where the intervention arm used the e MOM app with a CGM and activity bracelet for 1 week per month and a digital food diary for 3 days of this week (referred to as the ‘app week’ later in this paper), from gestational weeks 24-28 to delivery. The e MOM GDM study was conducted between February 2021 and December 2022 in Helsinki, Finland.

Sini Määttänen, Saila Koivusalo, Hanna Ylinen, Seppo Heinonen, Mikko Kytö

JMIR Mhealth Uhealth 2025;13:e60855

Extended Reality Biofeedback for Functional Upper Limb Weakness: Mixed Methods Usability Evaluation

Extended Reality Biofeedback for Functional Upper Limb Weakness: Mixed Methods Usability Evaluation

After completing all 3 tasks, participants filled out the system usability scale (SUS) questionnaire for each task. The SUS is a 10-item questionnaire yielding a score from 0 to 100, where higher scores indicate better perceived usability. We chose the SUS because it is a well-established, quick tool for usability assessment, suitable even for small samples [26]. Participants also provided written free-text feedback on their experience with each task and the overall platform.

Anirban Dutta, Katerina Hatjipanagioti, Matthew Alexander Newsham, Lewis Leyland, Lindsey Rickson, Alastair Buchanan, Ildar Farkhatdinov, Jacqueline Twamley, Abhijit Das

JMIR XR Spatial Comput 2025;2:e68580

Usability Evaluation of an Electrically Powered Orthopedic Exerciser: Focus Group Interview and Satisfaction Survey Study

Usability Evaluation of an Electrically Powered Orthopedic Exerciser: Focus Group Interview and Satisfaction Survey Study

Usability issues in medical devices can directly affect patient safety and treatment outcomes, often arising from deficiencies in UI design [12]. To mitigate such risks, the International Electrotechnical Commission (IEC) introduced the IEC 62366 standard, which emphasizes the integration of usability engineering throughout the device development process, distinguishing between formative and summative evaluations [13-15].

Seojin Hong, Hyun Choi, Hyosun Kweon

JMIR Hum Factors 2025;12:e60607

Supporting Medication Adherence in Pediatric Patients Undergoing Hematopoietic Stem Cell Transplant Using the BMT4me mHealth App: Mixed Methods Usability Study

Supporting Medication Adherence in Pediatric Patients Undergoing Hematopoietic Stem Cell Transplant Using the BMT4me mHealth App: Mixed Methods Usability Study

Data are from a longitudinal mixed methods study to assess the usability of a newly developed m Health intervention for pediatric post-HCT medication management. The study was conducted at a large Midwestern children’s hospital from September 2021 to January 2023.

Mariam Kochashvili, Parishma Guttoo, Emre Sezgin, Ahna Pai, Rajinder Bajwa, Wendy Landier, Cynthia Gerhardt, Micah Skeens

JMIR Cancer 2025;11:e66847

Framing the Human-Centered Artificial Intelligence Concepts and Methods: Scoping Review

Framing the Human-Centered Artificial Intelligence Concepts and Methods: Scoping Review

The interaction of users with innovation prototypes not only accelerates the identification of usability issues, highlighting improvement opportunities, but also strengthens the capacity of researchers to define cost and benefits evaluation methods that are propaedeutic to identify the return of investments also in terms of economic benefit.

Roberta Bevilacqua, Tania Bailoni, Elvira Maranesi, Giulio Amabili, Federico Barbarossa, Marta Ponzano, Michele Virgolesi, Teresa Rea, Maddalena Illario, Enrico Maria Piras, Matteo Lenge, Elisa Barbi, Garifallia Sakellariou

JMIR Hum Factors 2025;12:e67350

Co-Designed Digital Device for Tracking Rehabilitation Dosage in a Clinical Environment After Stroke: Mixed Methods Validity and Feasibility Study

Co-Designed Digital Device for Tracking Rehabilitation Dosage in a Clinical Environment After Stroke: Mixed Methods Validity and Feasibility Study

This pilot study, conducted in 2 phases, evaluated the digital dose tracker, co-designed by users, by assessing its feasibility, validity, and usability. Phase 1 focused on a usability study (n=9) conducted in a research setting. Phase 2 involved a clinical trial to assess the trackers’ feasibility and validity (n=15). The primary outcome for Phase 1 was usability, measured by the System Usability Scale (SUS) and Intrinsic Motivation Inventory (IMI).

Fiona Boyd, Gillian Sweeney, Mark Barber, Elaine Forrest, Mark Dunlop, Andrew Kerr

JMIR Rehabil Assist Technol 2025;12:e68129