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Participants (n=106) are being recruited from the University of Washington Medicine Multiple Sclerosis Center, a comprehensive, interdisciplinary center that provides specialty care (including neurology, rehabilitation medicine, and psychology) for >3000 patients with MS per year. All clinic patients are offered opportunities to participate in clinical research through a coordinated research registry recruitment effort that is a standard element of the clinic’s patient flow.
JMIR Res Protoc 2025;14:e72213
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Usability interview participant demographics (N=15).
We assessed the number of participants who reported each identified usability challenge (Table 3). Five frequently observed challenges were noted; 2 were related to content in the toolkit: participants had difficulty interpreting instructions and participants had difficulty condensing content from the full consent document into the visual KI template.
JMIR Form Res 2025;9:e76740
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Clinical and demographic data of the study participants enrolled in the usability study of limb-worn wearable devices for monitoring PD motor function and blood pressure in Ireland in the period 2021-2023 (N=6).
a MDS-UPDRS: Movement Disorder Society - Unified Parkinson’s Disease Rating Scale.
b6-CIT: 6-Item Cognitive Impairment Test.
JMIR Form Res 2025;9:e73423
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Initial interviews were held using Microsoft Teams with VHR super users (N=15) across 5 specialty services. Representative snowball sampling was used, through the on-site virtual health resource center, to recruit clinical champion participants based on their knowledge and proactive integrated use of VHRs, as identified by their clinical team members within each specialty care service.
J Med Internet Res 2025;27:e81414
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Descriptions of the 8 studies included in the pooled analysis of parent-reported race and ethnicity of child participants (N=8087).
a Study names have been deidentified to protect participant privacy and unpublished data.
b MA: Massachusetts; CA: California; KY: Kentucky; MS: Mississippi; SC: South Carolina; RI: Rhode Island.
The institutional review board of Tufts University exempted this study from review because it was deemed not human participant research.
JMIR Public Health Surveill 2025;11:e65660
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Exact statistical methods to estimate 95% CIs will be used in cases of small cell counts or analysis of continuous measures where n
Primary study end points evaluated in both studies include intervention acceptability and appropriateness assessed via survey measures. The additional primary end point of intervention feasibility will be evaluated in study 1. Descriptive statistics will be calculated for primary outcomes among intervention arm participants.
JMIR Res Protoc 2025;14:e76442
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