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Experiences Receiving and Delivering Virtual Health Care For Women: Qualitative Evidence Synthesis
J Med Internet Res 2025;27:e68314
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Comparative analyses were conducted using the χ2 test, with a two-sided P value
The study protocol was evaluated by the Mayo Clinic institutional review board and it was determined that it was exempted under 45 CFR 46.102 of the Code of Federal Regulations (2/28/2023). No personally identifying information was collected, and all data were fully anonymous. Study participation was voluntary and survey completion was considered as consent.
JMIR Med Educ 2025;11:e58801
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For hospitalizations that resulted in readmission within 30 days or death within 30 days post-discharge, the patients tended to be older (median age 78, IQR 68-86 years vs 72, IQR 62-82 years), were less likely to be male (290/688, 42.2% vs 2187/4326, 50.6%; P
Table 3 shows results from performance testing of several multivariable predictive models of the composite outcome. The best performing models were TSL (c-statistic=0.685) and TSL plus m RS score at discharge (c-statistic=0.694).
JMIR Med Inform 2025;13:e69102
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Podcasts in Mental, Physical, or Combined Health Interventions for Adults: Scoping Review
J Med Internet Res 2025;27:e63360
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There was no significant difference in requested mode based on HPV vaccine dose or language (desired text messages for initiation reminders (22/39, 56%), versus for completion reminders (26/39, 67%; P=.35), desired text messages for reminders in English (21/28, 75%) versus in Luganda (27/50, 54%; P=.07).
Enrollment flow diagram.
Characteristics of study participants.
a HPV: human papillomavirus.
b KCCA: Kampala Capital City Authority.
JMIR Mhealth Uhealth 2025;13:e63527
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Ethical approval was obtained from the Ethics Committee of the Friedrich-Alexander Universität Erlangen-Nürnberg (April 1, 2020: 47_20 B). The original protocol was amended on March 22, 2022, to also include patients already receiving CDK4/6i therapy, as previously, patients could only be enrolled in the SMILER study at the start of CDK4/6i therapy. This change was implemented to improve study enrollment. All participants provided written informed consent before participation.
JMIR Cancer 2025;11:e64083
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