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Spousal perceptions and their role in promoting breast cancer screening: a focus group study.
BMJ Open
March 2025
Genome Institute of Singapore (GIS), Agency for Science, Technology and Research (A*STAR), Singapore
Objectives: To explore husbands' views on breast cancer screening, risk-based screening and their role in influencing their wives' health-seeking behaviours.
Design: Qualitative focus group discussion (FGD) supplemented by quantitative data from a cohort study using a structured questionnaire.
Setting: This study was conducted in a community-based setting, with participants recruited online through non-profit organisations via social media and email.
Barriers to conversations about deceased organ donation among adults living in the UK: a systematic review with narrative synthesis.
BMJ Open
March 2025
Institute for Health Research, University of Bedfordshire Faculty of Health and Social Sciences, Luton, UK.
Objectives: To explore the barriers to conversations about deceased organ donation among adults living in the UK.
Design: Systematic review with narrative synthesis.
Data Sources: PubMed, MEDline via OVID, APA PsycInfo via EBSCO, Web of Science via Clarivate and Scopus via Elsevier, covering studies that were published between January 2006 and December 2023.
Research quality and dissemination of paediatric randomised controlled trials with and without patient and family engagement: systematic review.
BMJ Open
March 2025
Division of Paediatric Medicine and Paediatric Outcomes Research Team (PORT), The Hospital for Sick Children, Toronto, Ontario, Canada.
Objectives: Authentic patient and family engagement in child health research is defined as researchers working in partnership with patients and families on all aspects of the research process, including refining the research question, tailoring the intervention, devising study procedures and disseminating study findings. While there is good evidence of a positive impact of patient engagement on the research process, on research teams and on patient partners, there are few empirical data on the impact of patient and family engagement on research quality and dissemination. We conducted a systematic review to compare research quality and dissemination metrics for paediatric randomised controlled trials (RCTs) that engaged patients and families in the research process with trials that did not.
View Article and Find Full Text PDFCommunication attributes modify the anxiety risk associated with problematic social media use: Evidence from a prospective diary method study.
Addict Behav
March 2025
Department of Epidemiology, New York University School of Global Public Health, New York, United States; Department of Social and Behavioral Science, New York University School of Global Public Health, New York, United States.
Purpose: Social media use in younger people has shown mixed associations with mental health. We hypothesized that communication types during social media use might alter the relationship between problematic social media use (PSMU) and anxiety over time. We aimed to identify how four dimensions of communication influence the link between PSMU and anxiety.
View Article and Find Full Text PDFPublic spheres or echo chambers? Nonprofit E-advocacy and civic engagement on harm reduction policy in the U.S.
Int J Drug Policy
March 2025
Department of Social Work, Yonsei University, Seoul, South Korea.
This study examines how social media platforms shape drug policy advocacy by analyzing stakeholder engagement surrounding supervised consumption sites in New York City. While research has explored organizational use of social media for advocacy, less attention has focused on patterns of civic engagement and dialogue. Analyzing messages and comments from two opposing organizations-OnPoint NYC and Harlem East Block Association-over 24 months (2022-2023), we investigate whether social media-based drug policy advocacy creates public spheres for diverse dialogue or echo chambers of like-minded individuals.
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