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Skip search results from other journals and go to results- 813 Journal of Medical Internet Research
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The University of Tokyo Hospital
Mitsui Memorial Hospital
Meiji Yasuda Life Insurance Company Tokyo Hospital
Kobe University Hospital
Akita University Hospital
Tokai University Hospital
Okayama Saiseikai General Hospital
Sawaki Internal Medicine and Diabetes Clinic
Yokota Medical Clinic
Aikawa Comprehensive Internal Medicine Clinic
Yokohama Rosai Hospital
To detect a 0.3% difference in the primary outcome (change in Hb A1c), assuming an SD of 0.41% (the average observed in 2 prior studies [17,61]), and to achieve
JMIR Res Protoc 2025;14:e64023
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Reference 60: The AUDIT alcohol consumption questions (AUDIT-C): an effective brief screening test for
J Med Internet Res 2025;27:e65452
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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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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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deal: samen werken aan duurzame zorg [Article in Dutch](https://www.rvo.nl/sites/default/files/2024-12/C-
J Med Internet Res 2025;27:e67538
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The PROMIS website also gives the mean and SD of the T-score metric (mean 50, SD 10). Power calculations for this primary hypothesis were performed using the SAS procedure PROC GLMPOWER (SAS Version 9.4) [62]. Results indicated that 282 participants after attrition would be needed for 80% power (P
With regard to power for moderation analyses, we ran a sensitivity analysis to compute the smallest effect size our study would be powered to find using 280 given 4 groups (eg, 2 study arms × 2 genders).
JMIR Res Protoc 2025;14:e64449
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t=-00:-01:Race%20and%20Ethnicity)
JMIR Mhealth Uhealth 2025;13:e68242
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