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Co-Designing a Web-Based and Tablet App to Evaluate Clinical Outcomes of Early Psychosis Service Users in a Learning Health Care Network: User-Centered Design Workshop and Pilot Study

Kathleen E Burch, Valerie L Tryon, Katherine M Pierce, Laura M Tully, Sabrina Ereshefsky, Mark Savill, Leigh Smith, Adam B Wilcox, Christopher Komei Hakusui, Viviana E Padilla, Amanda P McNamara, Merissa Kado-Walton, Andrew J Padovani, Chelyah Miller, Madison J Miles, Nitasha Sharma, Khanh Linh H Nguyen, Yi Zhang, Tara A Niendam

JMIR Hum Factors 2025;12:e65889

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Identification and Categorization of the Distinct Purposes Underpinning the Use of Digital Health Care Self-Monitoring: Qualitative Study of Stakeholders in the Health Care Ecosystem

Mattias Elg, Daan Kabel, Ida Gremyr, Jesper Olsson, Jason Martin, Frida Smith

J Med Internet Res 2025;27:e58264

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Impact of a 6-Week Postpartum Text Messaging Program (Essential Coaching for Every Mother) at 6 Months: Follow-Up Study to a Randomized Controlled Trial

Justine Dol, Marsha Campbell-Yeo, Megan Aston, Douglas McMillan, Amy K Grant

JMIR Pediatr Parent 2025;8:e62841

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Considering Theory-Based Gamification in the Co-Design and Development of a Virtual Reality Cognitive Remediation Intervention for Depression (bWell-D): Mixed Methods Study

Mark Hewko, Vincent Gagnon Shaigetz, Michael S Smith, Elicia Kohlenberg, Pooria Ahmadi, Maria Elena Hernandez Hernandez, Catherine Proulx, Anne Cabral, Melanie Segado, Trisha Chakrabarty, Nusrat Choudhury

JMIR Serious Games 2025;13:e59514

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Engaging End Users to Inform the Design and Social Marketing Strategy for a Web-Based Sexually Transmitted Infection/Blood-Borne Virus (STI/BBV) Testing Service for Young People in Victoria, Australia: Qualitative Study

Ethan T Cardwell, Teralynn Ludwick, Shanton Chang, Olivia Walsh, Megan Lim, Rachel Podbury, David Evans, Christopher K Fairley, Fabian Y S Kong, Jane S Hocking

J Med Internet Res 2025;27:e63822

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Treatment of Substance Use Disorders With a Mobile Phone App Within Rural Collaborative Care Management (Senyo Health): Protocol for a Mixed Methods Randomized Controlled Trial

Tyler S Oesterle, Nicholas L Bormann, Margaret M Paul, Scott A Breitinger, Benjamin Lai, Jamie L Smith, Cindy J Stoppel, Stephan Arndt, Mark D Williams

JMIR Res Protoc 2025;14:e65693

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Dying in Darkness: Deviations From Data Sharing Ethics in the US Public Health System and the Data Genocide of American Indian and Alaska Native Communities

For example, Megan Doerr argues that building or establishing a “social license” for collecting and using data can be more appropriate and protective than deidentification [47]. A social license represents the informal permission of a community to engage in a specific activity [48,49]. In public health contexts, a social license can legitimize the collection, use, or sharing of data about relevant communities.

Cason D Schmit, Meghan Curry O’Connell, Sarah Shewbrooks, Charles Abourezk, Fallon J Cochlin, Megan Doerr, Hye-Chung Kum