Background: Potential research participants, particularly those from racial and ethnic groups underrepresented in medical research, often decide to participate based on how they judge people, places, and study protocols as trustworthy. And yet, few studies have explored notions of trustworthiness or determinants of trustworthiness from the perspective of potential medical research participants.
Objective: This paper describes how racially and ethnically diverse potential medical research participants conceptualize what makes researchers, research settings, and research protocols seem trustworthy.
Design: Using a criterion sampling strategy, we recruited African American, Latinx, and White adults for participation in focus groups conducted at a community center servings the Latinx community and at a health clinic that primarily serves the African American community.
Participants: A total of 57 African American, Latinx, and White adults APPROACH: We conducted seven focus groups that explored perceptions and determinants of research, trust, privacy, confidentiality, and research participation. We used a phenomenological thematic analytic approach to explore the determinants of trustworthiness to conduct medical research.
Results: In our effort to identify the factors that affect potential research participants' perspectives on the trustworthiness of medical research, we found three themes: Who is trustworthy to conduct medical research? What influences perceptions of trustworthiness in medical research? And what institutions or settings are trustworthy to conduct medical research?
Conclusions: These findings highlight that one's willingness to participate in research is driven in part by their perception of the trustworthiness of researchers, research institutions, and the information they are given about potential research opportunities. There are important and modifiable determinants of trustworthiness that may facilitate minority participation in research. We found that research, researchers, and research institutions each have things that can be done to increase trustworthiness and minority participation in research.
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http://dx.doi.org/10.1007/s11606-020-05868-1 | DOI Listing |
Int J Med Inform
December 2024
Neurosurgery Department, Hamad General Hospital, Qatar; Department of Clinical Academic Sciences, College of Medicine, Qatar University, Doha, Qatar; Department of Neurological Sciences, Weill Cornell Medicine, Doha, Qatar.
Introduction: Artificial Intelligence is in the phase of health care, with transformative innovations in diagnostics, personalized treatment, and operational efficiency. While having potential, critical challenges are apparent in areas of safety, trust, security, and ethical governance. The development of these challenges is important for promoting the responsible adoption of AI technologies into healthcare systems.
View Article and Find Full Text PDFSci Rep
January 2025
Department of Health Informatics, Institute of Public Health, College of Medicine & Health Sciences, University of Gondar, Gondar, Ethiopia.
United Nations is standing for Sustainable Development Goal (SDG) 6 sets the agenda to address worldwide inequality in accessing safe water and improved sanitation facilities for all by 2030. However, governments in Africa seem unable to address the issue water and of sanitation facilities, since there are problems like increasing costs of sustaining existing water sources and the requirement to deliver new facilities ahead of time. Hence, this study aimed to investigate unimproved water sources and sanitation facilities geographical variation in Ethiopia using EDHS 2019 datasets.
View Article and Find Full Text PDFCommun Med (Lond)
January 2025
School of Electrical and Computer Engineering, Georgia Institute of Technology, Atlanta, GA, 30322, USA.
Background: Adolescent idiopathic scoliosis (AIS) is the most common type of scoliosis, affecting 1-4% of adolescents. The Scoliosis Research Society-22R (SRS-22R), a health-related quality-of-life instrument for AIS, has allowed orthopedists to measure subjective patient outcomes before and after corrective surgery beyond objective radiographic measurements. However, research has revealed that there is no significant correlation between the correction rate in major radiographic parameters and improvements in patient-reported outcomes (PROs), making it difficult to incorporate PROs into personalized surgical planning.
View Article and Find Full Text PDFJ Am Med Dir Assoc
December 2024
Innovation in Dementia and Aging Lab, University of British Columbia, Vancouver, British Columbia, Canada.
Objectives: To explore and understand the sources and experiences of joy in caregiving among formal caregivers in Canadian long-term care (LTC).
Design: A qualitative study with interpretative descriptive design.
Setting And Participants: The participants consisted of 20 formal caregivers from a large public LTC home in British Columbia, Canada, focusing on those with at least 6 months of direct caregiving experience.
Ann Agric Environ Med
December 2024
Department of Hygiene and Dietetics, Jagiellonian University Medical College, Krakow, Poland.
Introduction And Objective: Considering the complexity of medical discourse, the enormous amount of information, including fake news, it becomes increasingly challenging to develop health literacy among the general population and to ensure efficient communication of scientific findings on the effects of health interventions to various types of recipients. We aimed to gain an in-depth understanding of how the various types of audiences perceive various formats for presenting data from Cochrane systematic reviews (SRs).
Material And Methods: We conducted focus group interviews with university employees, students, pharmacists, patients, caregivers, physicians, and nurses.
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