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Skip search results from other journals and go to results- 256 JMIR Research Protocols
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Researchers were able to accommodate many of these adaptations in the final ACTPr EP protocol. Additionally, the values related to Pr EP were in the life areas of relationships, health, intimacy, and life longevity. These values were used to tailor intervention content and as probes for the values section of the intervention. More details on the developmental phase findings can be found in another published study [34].
JMIR Res Protoc 2025;14:e65921
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Clinical Nurse Educators’ Job Satisfaction and Turnover Intentions: Protocol for a Scoping Review
This scoping review protocol was developed following the PRISMA-P (Preferred Reporting Items for Systematic Reviews and Meta-Analyses Protocols) 2015 checklist for systematic review protocols [19] (see Multimedia Appendix 1). The final scoping review will be conducted in accordance with the JBI methodology [20] and the PRISMA-Sc R (Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews).
JMIR Res Protoc 2025;14:e66712
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The study protocol was designed in accordance with the Standard Protocol Items: Recommendations for Interventional Trials (SPIRIT) guidelines (Multimedia Appendix 1) [19].
This is a randomized, controlled, evaluator-blinded trial. Sixty patients were evenly divided into the experimental group and the control group.
All participants were recruited from Guang’anmen Hospital, China Academy of Chinese Medical Sciences.
JMIR Res Protoc 2025;14:e59682
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The protocol was approved by the Institutional Science Committee as well as the non-WMO committee and will adhere to Good Clinical Practice (GCP) regulations.
To be eligible for the study, participants must daily communicate with patients or their relatives as part of their daily duties, speak proficient Dutch (local language) to be able to complete the surveys, and participate in an interview. Nurses leaving the ward within a year were excluded.
JMIR Res Protoc 2025;14:e65795
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This study uses a secret shopper caller protocol design and will be conducted at Wake Forest University School of Medicine and East Carolina University.
Pharmacies are eligible to be included in the study if they are listed on the 2023 list of active licensed pharmacies from Hayes Directories, Inc and have a physical location. Nonretail, compounding, and veterinarian pharmacies will be excluded.
The sample size is 1000 pharmacies from across the United States.
JMIR Res Protoc 2025;14:e64344
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The research team will revise the protocol as appropriate during the review process. Any changes to the protocol will be detailed and justified in the final report.
To determine the eligibility criteria of the articles to be included in the review, the research team will follow the PCC (Population, Concept, Context) framework for scoping reviews by the Joanna Briggs Institute [35]. The inclusion criteria will be as follows.
JMIR Res Protoc 2025;14:e70831
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This protocol adheres to the SPIRIT (Standard Protocol Items: Recommendations for Interventional Trials) 2013 checklist [29].
Study flowchart.
Participants will be recruited from the Obstetrics and Gynecology Hospital of Fudan University, where they will receive routine antenatal care and plan to give birth. Upon admission to the LDU, trained research staff will identify eligible women through a screening process that includes reviewing medical records and conducting brief assessments.
JMIR Res Protoc 2025;14:e63050
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To test for other STIs, blood samples will be processed according to the laboratory protocol to obtain serum. The serum will be stored at 2-8°C until transportation and sent weekly to designated laboratories for testing. The results of all reactive tests will be returned to the respondents through the ART centers for follow-up and treatment.
A linked anonymous testing strategy will be adopted for testing the blood specimens collected during IBBS-PLHIV.
JMIR Res Protoc 2025;14:e58252
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We present a protocol for a randomized controlled clinical trial to validate the clinical efficacy and safety of HH333 in patients with ischemic stroke induced by small-vessel disease. This study aimed to provide a high level of evidence for the efficacy of HH333 in ischemic stroke and ultimately propose a novel alternative for stroke treatment.
JMIR Res Protoc 2025;14:e70953
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This protocol is registered with the International Prospective Register of Systematic Review (PROSPERO) and the review will be conducted and reported following the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-analysis) protocol [20].
We will include all empirical study designs including observational (eg, case control, cohort, and cross-sectional) and experimental studies (randomized controlled trial [RCT], non-RCT, and cluster RCT) to capture all desired outcomes.
JMIR Res Protoc 2025;14:e65807
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