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JMIR Publications is the leading ehealth publisher, advancing progress in the health, engineering and social sciences to ultimately help people to live happier and healthier lives using technology.
JMIR Publications helps innovators in the health technology space to collaborate and to disseminate their innovations, ideas, and research results to the widest possible audience.
JMIR Publications is a rapidly growing innovative academic publisher. It builds on the success of JMIR (Journal of Medical Internet Research), which started in 1998 as a small independent open access project hosted at a university, which subsequently grew into the most influential journal in medical informatics (ranked #1 by Impact Factor by Thomson Reuters for three years, JIF>5.0) and health services research.
Pioneer in #openaccess and #openscience, JMIR Publications is now also publishing a superjournal JMIRx as overlay journal on top of preprint servers. Source
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| Language | English |
| Country | Canada |
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Recent Articles
Search ArticlesAssessment Instruments for Social Anxiety in Oral and Public Communication Among Health Sciences Students: Protocol for a Scoping Review
Study Design Research Question and the Population, Concept, and Context Model Table 1. Definition of the guiding question.
Evaluation of a Digital Intervention for Monitoring and Improving Medication Adherence Among Real-World e-Consumers of HIV Preexposure Prophylaxis in China: Protocol for a Randomized Controlled Trial
Study Design Population Sample Size Planning Randomization and Blinding Figure 1. Flowchart of recruitment and follow-up procedures of the study. PrEP: preexposure prophylaxis. Control and Intervention Description Real-Time Monitoring Figure 2. PLP Camp screenshots of the adherence recording journey from the user end. Table 1. Criteria for risk classification of preexposure prophylaxis (PrEP) nonadherence in the Real-Time Monitoring and Precision Intervention for HIV PrEP Adherence trial.
Cost-Effectiveness Analysis of Age-Specific N-Terminal Pro-B-Type Natriuretic Peptide Thresholds for Heart Failure Diagnosis in China: Protocol for a Markov Model–Based Study
Model Overview Target Population and Diagnostic Strategies Decision Tree Markov Model Structure Figure 1. Final model structure of the diagnostic decision tree and Markov pathways. FN: false negative; FP: false positive; HF: heart failure; NT-proBNP: N-terminal pro-B-type natriuretic peptide; TN: true negative; TP: true positive.
Repetitive Transcranial Magnetic Stimulation as a Cognitive Rehabilitation Approach for Veterans With Parkinson Disease and Mild Cognitive Impairment: Protocol for a Randomized Sham-Controlled Trial
Background and Rationale Objectives Participants, Interventions, and Outcomes Study Setting Eligibility Criteria Table 1. Defining mild cognitive impairment in Parkinson disease (PD-MCI)a.
Comparative Outcomes of a Pediatric Walking Rehabilitation Robot Combined With Repetitive Transcranial Magnetic Stimulation in Children With Spastic Cerebral Palsy: Protocol for a Prospective Observational Study
Background Study Objective and Hypothesis Study Design Figure 1. Flowchart. CP: Cerebral palsy; rTMS: repetitive transcranial magnetic stimulation. Figure 2. Schedule of enrollment, intervention, and assessment. Participants Textbox 1. Inclusion and exclusion criteria.
A Metacognitive Intervention for Children and Adolescents in Neuropediatric Care (Mio-Training): Protocol for a Randomized Controlled Trial
Design and Setting of the Study Figure 1. Study flow chart. T0: screening; T1: first assessment (before intervention or waiting period); T2: second assessment (immediately after intervention or waiting period); T3: third assessment (12 weeks after intervention or waiting period). Participants Overview Cancer Survivors Children and Adolescents With ADHD Healthy Controls Ethical Considerations Intervention Figure 2. Prototype of the Mio-Training app.
Four-Week vs Six-Week Antibiotic Therapy in the Management of Nonsurgically Treated Diabetic Foot Osteomyelitis: Protocol for a Multicentric, Single-Blind Randomized Clinical Trial
Trial Design Ethical Considerations Characteristics of the Groups and Interventions Randomization and Group Allocation Methodology Table 1. List of the allowed antibiotic treatments (empirical or targeted).
Evaluating Client-Centered Counseling Approaches to Improve Contraceptive Uptake at Family Planning Centers in Rawalpindi, Pakistan: Protocol for a Pilot Cluster-Randomized Trial
Study Framework Figure 1. Conceptual framework of the study. Study Aim Study Design Study Setting Study Timeline Figure 2. SPIRIT (Standard Protocol Items: Recommendations for Interventional Trials) timeline of the study. GATHER: greet, ask, tell, help, explain, return.
Correction: Challenges in Developing a Patient-Reported Symptom-Based Risk Stratification System for Suspected Head and Neck Cancer: Protocol for a Qualitative Case Study
JMIR Res Protoc 2026;15:e100038 doi:10.2196/100038 In “Challenges in Developing a Patient-Reported Symptom-Based Risk Stratification System for Suspected Head and Neck Cancer: Protocol for a Qualitative Case Study” [], the authors noted one error. has been replaced with the file attached to this notice. The correction will appear in the online version of the paper on the JMIR Publications website, together with the publication of this correction notice.
Evaluation of the Efficacy of Human Papillomavirus Screening Compared With Cytology Screening in Pregnant Women: Protocol for a Prospective Multicenter Trial
Figure 1. Current cervical cancer screening protocol in Japan. In the human papillomavirus (HPV) testing protocol, HPV-negative cases are scheduled for another HPV test in 5 years. HPV-positive cases undergo cervical cytology. For cases positive for HPV and atypical squamous cells of undetermined significance (ASC-US), colposcopy with or without cervical biopsy is performed immediately.