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Skip search results from other journals and go to results- 64 JMIR Research Protocols
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Because of the different modes of administration of these treatments, each group receives both an injection and oral tablets. The study therefore comprises three arms: (1) a “toxin” group treated with an injection of botulinum toxin and placebo oral baclofen; (2) a “baclofen” group treated with oral baclofen and an injection of placebo botulinum toxin; and (3) a double “placebo” group treated with placebo oral baclofen and an injection of placebo botulinum toxin.
JMIR Res Protoc 2025;14:e62951
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In “Patient Experiences With a Mobile Self-Care Solution for Low-Complex Orthopedic Injuries: Mixed Methods Study” (JMIR Hum Factors 2025;12:e53074) the authors noted one error.
The ninth author’s name previously appeared as:
Carel Goslings
This has been changed to
J Carel Goslings
The correction will appear in the online version of the paper on the JMIR Publications website, together with the publication of this correction notice.
JMIR Hum Factors 2025;12:e75812
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A study conducted in Australia [11] examined health care professionals’ experiences with the rapid upscaling of telehealth during the pandemic. The study found that telephone consultations were the predominant method of telehealth delivery, while video consultations were less frequently used. Although telehealth improved access to care for vulnerable populations and those in rural areas, it posed challenges for patients with language barriers and limited digital literacy.
J Med Internet Res 2025;27:e68434
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This feasibility study was a community-based participatory research design with 2 phases, namely, a development phase and an implementation phase. The development phase included a 4-month preparation phase, where study staff worked with a community engagement group to modify a working VR randomized controlled trial home-based protocol to a local public high school setting.
JMIR Form Res 2025;9:e65801
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The 10/66 Dementia Research Group study [25] highlights the high cost of dementia for health systems and the negative mental health impacts on women in LMICs, who are often primary caregivers for people with dementia [26]. This underscores the need for further research on dementia diagnosis and care in LMICs and for directing it effectively toward impactful decision-making.
JMIR Res Protoc 2025;14:e60296
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The aim of this study was therefore to explore the experiences of patients with DD to ensure durable adoption and to improve the protocol.
An observational mixed method study was conducted among patients and parents of patients younger than 12 years who sustained low-complex, isolated, stable musculoskeletal injuries parallel to the implementation of DD in 3 Dutch level-2 trauma centers from September 2021 to July 2022 with an inclusion period of 3 months per hospital (Figure 1).
JMIR Hum Factors 2025;12:e53074
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The ED data included information on the patient (age group and sex) and administrative information (ED, date and time of admission, and disposition information).
JMIR Public Health Surveill 2025;11:e66218
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Regular users’ and superusers’ sentiments when replying to each other: To do this, we first identified threads started by regular users and superusers, denoted as TU and TS, and calculated the AVS of replies written by the other group of users. Specifically, we computed , which denotes the average sentiment of regular users in reply to superusers' initiated threads; and , which denotes the average sentiment of superusers in reply to regular users' initiated threads.
J Med Internet Res 2025;27:e56038
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Given these promising results and developments in the field of unsupervised ML techniques, we chose to include new developments in this study.
In particular, we explore in this paper the clustering of a large multidimensional dataset provided by The Maastricht Study. The Maastricht Study is an observational, prospective, population-based, cohort study [17].
JMIR Med Inform 2025;13:e64479
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The trial was stopped early, and we launched a recovery strategy for nonparticipants in the intervention group.
The study received ethical approval from the Ethics Committee of the Bellvitge University Hospital (reference PR042/20), which waived the requirement to obtain the participant’s signature as part of the consent process, as the intervention was a minor variation on the invitation practice. The study was performed under Good Clinical Practice and the Declaration of Helsinki.
JMIR Mhealth Uhealth 2025;13:e64243
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