e.g. mhealth
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Skip search results from other journals and go to results- 10 JMIR Research Protocols
- 4 JMIR Formative Research
- 3 JMIR mHealth and uHealth
- 3 Journal of Medical Internet Research
- 2 JMIR Public Health and Surveillance
- 1 Iproceedings
- 1 JMIR Medical Education
- 1 JMIR Mental Health
- 1 JMIR Rehabilitation and Assistive Technologies
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Unintended Prolonged Opioid Use: Protocol for a Case-Controlled Trial
It also did not perform prospective assessment of several factors important to evaluate the proposed conceptual framework.
In this research project, 3 Clinical and Translational Science Awards (CTSA) programs (Mayo Clinic, University of Michigan, and Yale University) leveraged the conceptual framework for UPOU to investigate how the patient characteristics, practice environment characteristics, and opioid prescriber characteristics facilitate or impede UPOU.
JMIR Res Protoc 2025;14:e72032
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We thus performed an exploratory, prospective, open-label, parallel, single-center, randomized controlled trial (RCT) to investigate the effectiveness of CGM on short-term, in-hospital mortality among frail and critically ill patients with COVID-19.
This is an exploratory, prospective, open-label, parallel, single-center RCT.
J Med Internet Res 2025;27:e67012
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This monocentric, prospective, interventional, open-label, controlled, two-arm feasibility study was conducted at the university hospital Klinikum rechts der Isar (MRI) of the Technical University of Munich (TUM), Germany, in 2021.
JMIR Form Res 2024;8:e57608
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This is a prospective noninterventional clinical trial planned in accordance with the principles of evidence-based medicine using the PICO (patient, problem, or population; investigated condition; comparison; and outcome) criteria. The study procedure is outlined in Figure 1.
Flowchart of participants with suspected preeclampsia (PE) in the trial. Eligible pregnant women will be enrolled, and consecutive urine samples will be collected at each visit.
JMIR Res Protoc 2024;13:e54026
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A prospective randomized controlled trial was conducted at 2 tertiary hospitals in South Korea (the Department of Otolaryngology, Seoul National University Hospital and the Department of Otolaryngology, The Catholic University of Korea, Seoul St. Mary’s Hospital) from August 2020 to November 2022. The inclusion criteria were (1) acquired symmetrical, sensorineural, and mild-to-moderate hearing loss; (2) current use of a smartphone; and (3) no previous experience with hearing amplification.
JMIR Mhealth Uhealth 2023;11:e46911
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This study had a prospective observational design. Participants were involved in the study for a duration of 4 months, with data collection taking place at 2 time points during this period: within the month preceding their scheduled TKA and 3 months (12 weeks) following the TKA procedure. Figure 1 outlines the participants’ timeline for this study and the number of participants recruited and excluded at each stage.
Participant timeline. TKA: total knee arthroplasty.
JMIR Res Protoc 2023;12:e48801
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This prospective study was approved by the medical ethics committee of MUMC+ (Ref. No. 2019-1261).
Patients with premenopausal endometriosis aged ≥18 years, diagnosed by physical examination, imaging techniques, or laparoscopy, were recruited at the outpatient gynecology department at MUMC+, a tertiary referral center, between December 2019 and November 2020. Furthermore, patients were recruited by advertisement on the website of the Dutch Endometriosis Foundation.
JMIR Form Res 2023;7:e29480
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This is a substudy of a larger prospective cohort study (Universal Trial Number U1111-1216-8678) undertaken and reported according to the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) checklist [22] and registered prospectively on March 6, 2018, at the Australia New Zealand Clinical Trials Registry (ACTRN12618000337279). The results of the larger study have been published elsewhere [21].
JMIR Form Res 2022;6(11):e29713
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This research combines a retrospective study of analytical sensitivity and specificity with a prospective accuracy observational study. In the prospective part of the study, approximately 200 individuals testing positive for SARS-Co V-2 and 200 individuals testing negative for SARS-Co V-2 by routine SARS-Co V-2 testing will be subsequently retested with each RAT, with RT-PCR on deep oropharyngeal cavity swabs as the reference method.
JMIR Res Protoc 2022;11(5):e35706
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