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Skip search results from other journals and go to results- 1105 Journal of Medical Internet Research
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All collected samples are stored at –80 °C before being batched and shipped to the United States for analysis.
Families complete a self-administered questionnaire upon enrollment to collect baseline demographics and clinical characteristics.
JMIR Res Protoc 2025;14:e70575
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Reference 13: Controlling high blood pressure(https://www.qualityforum.org/Projects/c-d/Cardiovascular_Endorsement_and_Maintenance
JMIR Med Inform 2025;13:e70752
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Summary of study activities.
a Hb A1c: hemoglobin A1c.
b CRP: C-reactive protein.
c OGTT: oral glucose tolerance test.
At the first visit, a full medical history will be taken by a trained clinician including past medical history and surgical history. Outcomes of previous pregnancies will be recorded including outcome of the pregnancy, gestation, pregnancy complications, and (if relevant) birthweight and neonatal complications. Current medications including dose, and dosing schedule will be recorded.
JMIR Res Protoc 2025;14:e72542
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The primary objective was to examine the difference in self-reported influenza vaccination rates in three groups: (1) people with diabetes who received the intervention using a previously published approach (group A), (2) people with diabetes who received an adapted digital intervention (group B) and (3) people with diabetes who received no intervention (group C or control).
J Med Internet Res 2025;27:e68936
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We examined all contexts along the data pipeline, from population-level breast cancer screening to diagnostic biopsies and surgical treatments, clinical pathology, and specimen accessioning through the biobanking platform, where it may be stored for future use in –80 °C freezers or distributed fresh for next-generation biobanking applications such as patient-derived organoids, multi-omics, and high-throughput testing.
JMIR Bioinform Biotech 2025;6:e70463
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To comply with local regulations in Switzerland regarding clinical trials involving human subjects, this study design is classified as risk category C [28-30].
Therefore, both Swissmedic (the Swiss authority responsible for the authorization and supervision of therapeutic products) and the local ethics committee must review and approve the research protocol. Since both applications require a significant investment, a grant request will be submitted prior to applying to these two institutions.
JMIR Res Protoc 2025;14:e62659
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(C) Private LLMs: EHR data can be shared with a local hospital LLM, and prompt entry with question curation can be used to gain oncologic insights. EHR: electronic health record.
This study was approved by the Institutional Review Board of the Icahn School of Medicine at Mount Sinai (no. 22‐00347). Informed consent was waived given the retrospective nature of the study. To ensure confidentiality of patient data, only authorized research study personnel were permitted access to patient data.
JMIR Form Res 2025;9:e64544
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