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Cocreating the Visualization of Digital Mobility Outcomes: Delphi-Type Process With Patients
JMIR Form Res 2025;9:e68782
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Reference 9: Advanced life support in obstetrics (ALSO) and post-partum hemorrhage: a prospective intervention Reference 27: Effect of maternal death reviews and training on maternal mortality among cesarean delivery: post-hoc
JMIR Med Educ 2025;11:e54911
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Prerequisites for Cost-Effective Home Blood Pressure Telemonitoring: Early Health Economic Analysis
://www.zorginstituutnederland.nl/over-ons/werkwijzen-en-procedures/adviseren-over-en-verduidelijken-van-het-basispakket-aan-zorg /beoordeling-van-geneesmiddelen/richtlijn-voor-economische-evaluatie) dashboard-arbeidsmarkt/ontwikkeling-cao-lonen/uurloon#:~:text=Als%20we%20kijken%20naar%20gemiddelden,van /Verdiepingsmodule+QALY+en+kwaliteit-van-leven-metingen+%28versie+2024%29.pdf) hospitalization and associated costs for patients with heart failure in Finland: nonrandomized pre-post
JMIR Cardio 2025;9:e64386
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This study was approved by the ethics committee of Klinikum rechts der Isar, Technical University of Munich, before distribution. The approval number is 2023‐146-S-NP. By answering the mandatory questions of the survey and submitting them, the participants provided their consent to the anonymous study. In case they refrained from submitting the answers or refrained from answering specific mandatory questions, their consent was denied. In these cases, data were neither submitted nor recorded in any form.
JMIR Hum Factors 2025;12:e60779
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The studies involving human participants were reviewed and approved by the Ethical Committee of the Medical Faculty, Kiel University, Kiel, Germany; Health Research Authority and Health and Care Research Wales, United Kingdom; Ethik-Kommission der Ärztekammer Westfalen-Lippe und der Westfälischen Wilhelms-Universität, Münster, Germany; and the Medical Ethics Review Committee, Erasmus MC, Netherlands. The patients or participants provided their written informed consent to participate in this study.
JMIR Form Res 2025;9:e65879
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integrative education program and mHealth for Korean children with spina bifida: a quasi-experimental pre-post
Interact J Med Res 2025;14:e66336
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This RCT follows up on a pilot study (N=22) of the same BITT program, which previously demonstrated promising results, including a reduction in PTSD symptoms up to 3 months post treatment [34].
The primary objective of this RCT is to assess the effectiveness of a BITT compared to a waitlist control group (WLCG) in reducing symptoms of PTSD among adolescents aged 12-18 years.
JMIR Res Protoc 2025;14:e66115
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Post hoc comparisons between groups were made using the Tukey test when variances were equal or the Games-Howell test when the assumption of equal variances was violated. Initial power analyses indicated that a minimum of 159 participants were needed to detect moderate effects (with α=0.05 and 80% power). Statistical analyses were conducted using SPSS Statistics (version 29; IBM Corp).
Future analyses will center on longitudinal changes in PROMs and PREMs, using repeated measures and mixed model analyses.
JMIR Form Res 2025;9:e65686
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