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Skip search results from other journals and go to results- 262 JMIR Research Protocols
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This protocol has been registered in the OSF Registries (osf.io/m58zj/). As per the JBIs’ recommendation, a critical appraisal will not be assessed because the purpose of a scoping review is to describe the extent of available evidence in the field [28].
JMIR Res Protoc 2025;14:e76796
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To assess adherence to the Feelee manual and study protocol, clinicians complete a brief questionnaire following each treatment session during the intervention phase.
The primary outcome measure is collected daily through a short self-report questionnaire on the adolescents’ smartphones. Participants received a notification on their smartphones after 3 PM to complete the questionnaire before the end of the day.
JMIR Res Protoc 2025;14:e64756
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A clear scoping review question informs the inclusion criteria, supports protocol development, enhances the efficiency of the literature search, and provides a structured foundation for the review [66]. The main research question that will guide the scoping review is as follows: What interventions are used to optimize the influence of resilience and job satisfaction and minimize the influence of occupational stress on early retirement?
JMIR Res Protoc 2025;14:e72089
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This exploratory study protocol has been approved by the Ethical Board Committee of the Hospital Clínico San Carlos (23/799-E). The study will be conducted in accordance with the Declaration of Helsinki and Good Clinical Practice (GCP) guidelines. All participants provided their written informed consent to participate in this study. Participant confidentiality will be maintained throughout the study. All data will be anonymized during processing and stored securely.
JMIR Res Protoc 2025;14:e73383
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An experienced therapist will perform the intervention protocol. This protocol is based on the SPIRIT (Standard Protocol Items: Recommendations for Interventional Trials) guidelines (checklist provided in Multimedia Appendix 1).
The recruitment, intervention, and follow-up phase will be 2 years, followed by 6 months of data analysis. Patient recruitment will start in January 2023 and the trial will be completed by July 2025.
JMIR Res Protoc 2025;14:e66531
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Severe noncompliance with protocol as judged by the investigator.
The investigator judges it necessary due to medical reasons.
Female participants who become pregnant should immediately discontinue study drug administration and will be discontinued from the study (female participants with childbearing potential are excluded from the study).
JMIR Res Protoc 2025;14:e63588
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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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