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Beliefs in Misinformation About COVID-19 and the Russian Invasion of Ukraine Are Linked: Evidence From a Nationally Representative Survey Study

Beliefs in Misinformation About COVID-19 and the Russian Invasion of Ukraine Are Linked: Evidence From a Nationally Representative Survey Study

The cross-sectional survey was completed by members of the Czech National Panel [37] as a part of a longitudinal study [38], using the standardized computer-assisted web interviewing method. Participation was voluntary, with financial compensation. The mean completion time of the survey was approximately 11 minutes, and participants were informed in advance about the length.

Dominika Grygarová, Marek Havlík, Petr Adámek, Jiří Horáček, Veronika Juríčková, Jaroslav Hlinka, Ladislav Kesner

JMIR Infodemiology 2025;5:e62913

Engagement With and Use of Health Information on Social Media Among US Latino Individuals: National Cross-Sectional Survey Study

Engagement With and Use of Health Information on Social Media Among US Latino Individuals: National Cross-Sectional Survey Study

For example, the National Association of Latino Elected and Appointed Officials’ 2022 National Latino Voter tracking poll reported that 76% of Latino survey respondents were exposed to news that abortion is now illegal in the United States and that individuals can be imprisoned for seeking abortion services [15].

Yonaira M Rivera, Kathryna Corpuz, Tahilin Sanchez Karver

J Med Internet Res 2025;27:e59387

Associations of Wearable Activity Tracker Use With Physical Activity and Health Outcomes in Patients With Cancer: Findings from a Population-Based Survey Study

Associations of Wearable Activity Tracker Use With Physical Activity and Health Outcomes in Patients With Cancer: Findings from a Population-Based Survey Study

We analyzed the Health Information National Trends Survey–Surveillance, Epidemiology, and End Results (HINTS-SEER) dataset. The Health Information National Trends Survey (HINTS) is a nationally representative survey that examined the knowledge, attitudes, and usage of cancer- and health-related information by American adults [14].

Weijiao Zhou, Shaomei Shang, Youmin Cho

J Med Internet Res 2024;26:e51291

Inequities in Technology Access and Digital Health Literacy Among Patients With Dermatologic Conditions: Cross-Sectional Analysis of the National Health Interview Survey

Inequities in Technology Access and Digital Health Literacy Among Patients With Dermatologic Conditions: Cross-Sectional Analysis of the National Health Interview Survey

Using the National Health Interview Survey (NHIS), we sought to identify factors associated with low levels of TA and DHL among people with dermatologic conditions [3]. All NHIS respondents provided oral consent prior to participation, which was voluntary. The Instituional Review Board of the Boston Children’s Hospital reviewed and exempted this study since it does not include human subjects research as defined in federal regulations (45 CFR 46.102; IRB-P00036281).

Danny Linggonegoro, Kathryn Williams, Madeline Hlobik, Jennifer Huang

JMIR Dermatol 2024;7:e51511

Impact of the COVID-19 Pandemic on People Living With Rare Diseases and Their Families: Results of a National Survey

Impact of the COVID-19 Pandemic on People Living With Rare Diseases and Their Families: Results of a National Survey

We compared the monthly number of self-reported COVID-19 cases with the number expected based on data reported by the New York Times [68], computed by multiplying the national monthly infection rate by the number of respondents who were at risk of acquiring a COVID-19 infection during that month. The cases reported in the New York Times database are a mix of laboratory-confirmed cases and cases meeting the state-determined diagnostic criteria.

Maurizio Macaluso, Marc E Rothenberg, Thomas Ferkol, Pierce Kuhnell, Henry J Kaminski, David W Kimberlin, Michael Benatar, Mirna Chehade, The Principal Investigators of the Rare Diseases Clinical Research Network – Cycle 4

JMIR Public Health Surveill 2024;10:e48430

A Call to Reconsider a Nationwide Electronic Health Record System: Correcting the Failures of the National Program for IT

A Call to Reconsider a Nationwide Electronic Health Record System: Correcting the Failures of the National Program for IT

In April 2005, the NHS Connecting for Health Agency (CFH) was established to implement the National Programme for IT (NPf IT). Its goal was to propel NHS England into the 21st century by creating 7 nationwide IT services, including a secure NHSmail system and an electronic prescription service. Although many of these services have now been incorporated into everyday practice, the program’s primary objective was never realized: to establish a single nationwide database of electronic health records (EHRs).

James Seymour Morris

JMIR Med Inform 2023;11:e53112

The Australian Genetic Heart Disease Registry: Protocol for a Data Linkage Study

The Australian Genetic Heart Disease Registry: Protocol for a Data Linkage Study

Here we report a protocol for the linkage of Australian Genetic Heart Disease (AGHD) Registry participants [12,13] with state-wide hospitalization, emergency department and mortality registries, and the national mortality registry to establish a rich and comprehensive data resource to examine the health care use of individuals with a genetic heart disease and their families for the first time.

Alexandra Butters, Bianca Blanch, Anna Kemp-Casey, Judy Do, Laura Yeates, Felicity Leslie, Christopher Semsarian, Lee Nedkoff, Tom Briffa, Jodie Ingles, Joanna Sweeting

JMIR Res Protoc 2023;12:e48636