Background: Although moral distress is increasingly recognized as an important problem that threatens the integrity of health care providers and health care systems, few reliable and valid measures of moral distress are currently in use in research or clinical practice. This article describes the development and testing of a revised measure of moral distress, the…
AJOB Primary Research Template
Write in a clean editor, then format for AJOB Primary Research in one click — DocuGuru applies the official Taylor & Francis template with author–year references and exports a submission-ready PDF plus the editable LaTeX source. Free to start.
About the AJOB Primary Research format
AJOB Primary Research is a peer-reviewed journal published by Taylor & Francis, covering Ethics in Clinical Research, Ethics in medical practice, Patient Dignity and Privacy.
| Publisher | Taylor & Francis |
|---|---|
| Reference style | Author–year (Chicago, T&F) Author–year — (Smith, 2023) in the text Smith, Ada, Ben Jones, and Cara Lee. 2023. "A Representative Article Title." AJOB Primary Research 12 (3): 45–58.
Formats any DOI in AJOB Primary Research style. No sign-up. |
| Publishes research in | Ethics in Clinical Research Ethics in medical practice Patient Dignity and Privacy Ethics and Legal Issues in Pediatric Healthcare Medical Malpractice and Liability Issues |
| ISSN | 2150-7716 |
| h-index | 22 |
| i10-index | 50 |
| Total citations | 2,059 |
| Top institutions publishing here | University of Washington |
| Journal website | www.tandfonline.com |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
Papers published in AJOB Primary Research per year
Citation impact of AJOB Primary Research by publication year
Citations each year’s papers have accumulated so far — the most recent years are still building up.
Most-cited papers in AJOB Primary Research
BACKGROUND: Recruiting and retaining human participants in cancer clinical trials is challenging for many investigators. Although we expect participants to identify and weigh the benefits and burdens of research participation for themselves, it is not clear what burdens adult cancer participants perceive in relation to benefits. We identify key attributes and develop an initial conceptual…
BACKGROUND: To promote effective genome-scale research, genomic and clinical data for large population samples must be collected, stored, and shared. METHODS: We conducted focus groups with 45 members of a Seattle-based integrated healthcare delivery system to learn about their views and expectations for informed consent in genome-scale studies. RESULTS: Participants viewed information about study purpose,…
Little analysis has been made of ethical challenges encountered by health care professionals (HCPs) participating in humanitarian aid work. This is a qualitative study drawing on Grounded Theory analysis of 20 interviews with health care professionals who have provided humanitarian assistance. We collected the stories of ethical challenges reported by expatriate HCPs who participated in…
BACKGROUND: Parental decision making is a critical component in the provision of palliative and end-of-life care, yet factors that parents perceive as influencing this process, when they are making decisions for their children, have not been well characterized. METHODS: As part of a mixed-methods cohort study, we interviewed 73 parents of 50 pediatric patients who…