e.g. mhealth
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Skip search results from other journals and go to results- 4 JMIR Formative Research
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- 1 JMIR mHealth and uHealth
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However, we could not be sure whether the high number of remaining participants were bots or actual participants who did not continue to the next part of the study, although we assumed they were bots.
Yet this scenario presented us with a unique opportunity to attempt to create a bot detection algorithm to distinguish bots from genuine participants in CS2 better using strategies previously recommended in the literature [18,22].
Interact J Med Res 2025;14:e60548
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The platform sends notifications via the Active App to remind study participants to fill out the questionnaires and other prompts; related timestamps are recorded when the notification is delivered when participants start filling out the questionnaires and finish them.
JMIR Form Res 2025;9:e54531
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RQ1: For Black participants, which types of m Health engagement predict ART medication adherence, and through which mediators?
RQ2: For White participants, which types of m Health engagement predict ART medication adherence, and through which mediators?
RQ3: How does the relationship between m Health engagement and ART medication adherence differ between Black and White participants?
Recruitment took place at 2 US health clinics.
J Med Internet Res 2024;26:e57774
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If participants had symptoms, they stated what kind of symptoms they had, whether they took medication, and if they used a specific SCA [17]. If participants used the SCA on a day this was classified as a use-case, if the SCA was not used on a day this was classified as a nonuse case. Participants were asked if the symptoms appeared for the first time. Those who reported symptoms were asked to describe them in open-ended responses.
J Med Internet Res 2024;26:e55161
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This study consists of a total of 11 participants, comprising 7 clinical trial investigators, 2 research assistants, and 2 physicians. In 1 instance, the interview was conducted with 2 individuals simultaneously. The ages of the interviewees ranged from 25 to 34 years (2 participants), 35 to 44 years (4 participants), and 45 to 54 years (4 participants). The average number of years of professional experience in patient recruitment was 10.4 years (range 1-21 years).
JMIR Hum Factors 2024;11:e56872
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Participants received emails with login credentials for registering in the FA+ system. They were further provided with a link to an on-demand tutorial video demonstrating the step-by-step process of installing and logging into the FA+ system. Digital sessions were subsequently arranged for groups of participants (n=1-3). Participants were instructed to verbalize each step they took while using the interface, including tasks such as installation, login, and use of the FA+ system.
JMIR Form Res 2024;8:e53206
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This paper focuses on a comprehensive case review of 2 participants, detailing their passive (ie, obtained via screenomics screenshot capture) and active (ie, obtained via EMA) risk profiles that culminated in suicidal crises and subsequent psychiatric hospitalization.
JMIR Form Res 2024;8:e55999
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The successful implementation of CTs depends on the recruitment of a suitable number of participants who fulfill all EC. Insufficient participant recruitment is the foremost reason for the premature discontinuation of CTs, which raises ethical concerns because participants are exposed to risk, without potential benefits. Furthermore, the extension of the recruitment period is also associated with significant financial costs and is consequently inefficient [6-10].
JMIR Form Res 2024;8:e49347
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Potential participants were recruited through snowball sampling and advertising via email, social media (Facebook and Twitter), hardcopy posters in targeted work environments, and word of mouth. Potential participants were asked to positively enroll via emailing or texting the research team.
JMIR Hum Factors 2022;9(3):e33682
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The participants were a racially and ethnically diverse sample with at least 50% (300/600) identity as people of color or from rural communities. After enrollment, eligible participants assigned to the experimental arm had access to the i Reach web app over 12 months of the study.
JMIR Mhealth Uhealth 2021;9(8):e28232
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