Trust

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  Subject Areas on Research

  • "He Needed Just About Everything": Caring for Aging Adults Postincarceration. 
  • A case of scientific misconduct: the cost of bad science 
  • Achieving Entrustable Professional Activities During Fellowship. 
  • Addressing Adultification of Black Pediatric Patients in the Emergency Department: A Framework to Decrease Disparities. 
  • Alarm at the Gate-Health and Social Inequalities are Comorbid Conditions of HIV and COVID-19. 
  • Association of psychosocial factors with leukocyte telomere length among African Americans in the Jackson Heart Study. 
  • Barber-led sexual health education intervention for Black male adolescents and their fathers. 
  • Being Right Isn't Always Enough: NFL Culture and Team Physicians' Conflict of Interest. 
  • Biopiracy: conservationists have to rebuild lost trust. 
  • Building a bridge of trust: collaborative assessment with a person with serious mental illness. 
  • Building trust: Reflecting on the earliest human experience. 
  • Caring for the suffering: meeting the Ebola crisis responsibly. 
  • Challenges and opportunities: recruitment and retention of African Americans for Alzheimer disease research: lessons learned. 
  • Children's Selective Trust in Promises. 
  • Chimpanzees trust conspecifics to engage in low-cost reciprocity. 
  • Clinical Teaching: An Evidence-based Guide to Best Practices from the Council of Emergency Medicine Residency Directors. 
  • Clinical trial recruitment challenges with older adults with cancer. 
  • Conceptualizing trust in community-academic research partnerships using concept mapping approach: A multi-CTSA study. 
  • Data Sharing and Reproducibility of Results-Does It Matter for HIV Nursing? 
  • Data Sharing of Imaging in an Evolving Health Care World: Report of the ACR Data Sharing Workgroup, Part 2: Annotation, Curation, and Contracting. 
  • Developmental trajectories of cortical-subcortical interactions underlying the evaluation of trust in adolescence. 
  • Disclosing conflicts of interest in clinical research: views of institutional review boards, conflict of interest committees, and investigators. 
  • Donor designation: racial and ethnic differences in US nondesignators' preferred methods for disclosing intent to donate organs. 
  • Effect of physician disclosure of specialty bias on patient trust and treatment choice. 
  • Effects of disclosing financial interests on attitudes toward clinical research. 
  • Effects of disclosing financial interests on participation in medical research: a randomized vignette trial. 
  • Enhancing communication between oncologists and patients with a computer-based training program: a randomized trial. 
  • Entrustable Professional Activities: A New Direction for PA Education? 
  • Exploring lack of trust in care providers and the government as a barrier to health service use. 
  • Exploring the "legacy" of the Tuskegee Syphilis Study: a follow-up study from the Tuskegee Legacy Project. 
  • Factors associated with African Americans' enrollment in a national cancer genetics registry. 
  • For the patient. Who trusts healthcare institutions? Results from a community-based sample. 
  • From the editor: Trust and the value paradox in science. 
  • HIV/AIDS-related institutional mistrust among multiethnic men who have sex with men: effects on HIV testing and risk behaviors. 
  • High Psychosocial Burden Relates to Poorer Antiretroviral Treatment Adherence Among Black/African American People with HIV. 
  • Homeless women's experiences of service provider encounters. 
  • How Perceived Structural Racism and Discrimination and Medical Mistrust in the Health System Influences Participation in HIV Health Services for Black Women Living in the United States South: A Qualitative, Descriptive Study. 
  • How Should Clinicians Integrate Mental Health Into Epidemic Responses? 
  • How disclosing HMO physician incentives affects trust. 
  • How to write a guideline: a proposal for a manuscript template that supports the creation of trustworthy guidelines. 
  • Hurdles to herd immunity: Distrust of government and vaccine refusal in the US, 2002-2003. 
  • Impacts of managed care patient protection laws on health services utilization and patient satisfaction with care. 
  • Importance of Participant-Centricity and Trust for a Sustainable Medical Information Commons 
  • Influencing Trust for Human-Automation Collaborative Scheduling of Multiple Unmanned Vehicles. 
  • Institutional distrust among gay, bisexual, and other men who have sex with men as a barrier to accessing pre-exposure prophylaxis (PrEP). 
  • Issues affecting minority participation in research studies of Alzheimer disease. 
  • Knowledge matters: how children evaluate the reliability of testimony as a process of rational inference. 
  • Leave me out: Patients' characteristics and reasons for opting out of a pragmatic clinical trial involving medication adherence. 
  • Listening to Community Partners: Successes and Challenges in Fostering Authentic, Effective, and Trusting Partnerships in the RADx-UP Program. 
  • Measuring trust in medical researchers. 
  • Medical Mistrust in Perinatal Mental Health. 
  • Medical Mistrust, Racism, and Delays in Preventive Health Screening Among African-American Men. 
  • Memory, community and the reasons for living: theological and ethical reflections on suicide and euthanasia. 
  • Mercury, vaccines, and autism: one controversy, three histories. 
  • Moral dilemmas and trust in leaders during a global health crisis. 
  • Must a patient be a "person" to be a patient or my uncle Charlie is not much of a person but he is still my uncle Charlie. 
  • Nursing strategies to support family members of ICU patients at high risk of dying. 
  • On the perpetuation of ignorance: system dependence, system justification, and the motivated avoidance of sociopolitical information. 
  • Optimizing Care for Ugandans with Untreated Abdominal Surgical Conditions. 
  • Patient Preferences for Features of Health Care Delivery Systems: A Discrete Choice Experiment. 
  • Patient preference in primary care provider type. 
  • Patients' perceptions of safety if interpersonal continuity of care were to be disrupted. 
  • Pediatric brain tumor patients: their parents' perceptions of the hospital experience. 
  • Peer Review Matters: Research Quality and the Public Trust. 
  • Perceived Discrimination and Reported Trust and Satisfaction with Providers in African Americans: The Jackson Heart Study. 
  • Perceived discrimination, patient trust, and adherence to medical recommendations among persons with sickle cell disease. 
  • Perceived discrimination, trust in physicians, and prolonged symptom duration before ovarian cancer diagnosis in the African American Cancer Epidemiology Study. 
  • Perceptions of Competence, Strength, and Age Influence Voters to Select Leaders with Lower-Pitched Voices. 
  • Personality Structure Among Centenarians: The Georgia Centenarian Study. 
  • Physician Perspectives on Long-Term Relationships and Friendships with Patients: A National Assessment. 
  • Physician attire in the intensive care unit in Japan influences visitors' perception of care. 
  • Principal/agent theory and decision making in health care. 
  • Public trust in genomic risk assessment for type 2 diabetes mellitus. 
  • Public trust in the long-term care insurance pilot program in China: An analysis of mediating effects. 
  • Race and trust in the health care system. 
  • Realizing the Full Potential of Precision Medicine in Health and Health Care. 
  • Redefining Genomic Privacy: Trust and Empowerment 
  • Reframing Consent for Clinical Research: A Function-Based Approach. 
  • Relationships and betrayal among young women: Theoretical perspectives on adolescent dating abuse 
  • Reply: Can You Trust What You Watch? An Assessment of the Quality of Information in Aesthetic Surgery Videos on YouTube. 
  • Reply: Can You Trust What You Watch? An Assessment of the Quality of Information in Aesthetic Surgery Videos on YouTube. 
  • Restoring trust in research among historically underrepresented communities: A call to action for antiracism research in nursing. 
  • Role of Structural Marginalization, HIV Stigma, and Mistrust on HIV Prevention and Treatment Among Young Black Latinx Men Who Have Sex with Men and Transgender Women: Perspectives from Youth Service Providers. 
  • Role of patient factors, preferences, and distrust in health care and access to liver transplantation and organ donation. 
  • Social capital and hypertension in rural Haitian women. 
  • Stakeholder Perspectives on Creating and Maintaining Trust in Community-Academic Research Partnerships. 
  • Surgical Trainees' Sense of Responsibility for Patient Outcomes: A Multi-institutional Appraisal. 
  • Systematic review and metasummary of attitudes toward research in emergency medical conditions. 
  • Targeted Strategies for Recruitment and Engagement of Latinx Immigrants in Longitudinal Biobehavioral Research. 
  • Task force 6: Code of conduct for staff and volunteer leadership. 
  • Testosterone responses to competition predict decreased trust ratings of emotionally neutral faces. 
  • The effects of collaboration and minimal-group membership on children's prosocial behavior, liking, affiliation, and trust. 
  • The impact of patient-generated contextual data on communication in clinical practice: A qualitative assessment of patient and clinician perspectives. 
  • The influence of relationships on children's and adolescents' participation in research 
  • The need for a transparent, ethical, and successful relationship between academic scientists and the pharmaceutical industry: a view of the Group for the Respect of Ethics and Excellence in Science (GREES). 
  • The role of patient-provider sexual health communication in understanding the uptake of HIV prevention services among Black men who have sex with men. 
  • The unbearable rightness of bedside rationing. Physician duties in a climate of cost containment. 
  • Trauma, mental health, distrust, and stigma among HIV-positive persons: implications for effective care. 
  • Trust in American Medicine: A Call to Action for Health Care Professionals. 
  • Trust in Community-Engaged Research Partnerships: A Methodological Overview of Designing a Multisite Clinical and Translational Science Awards (CTSA) Initiative. 
  • Trust in Managed Care Organizations 
  • Trust in Peer Review. 
  • Trust in automation: integrating empirical evidence on factors that influence trust. 
  • Trust in insurers and access to physicians: associated enrollee behaviors and changes over time. 
  • Trusting our memories: dissociating the neural correlates of confidence in veridical versus illusory memories. 
  • Understanding Ethical Issues of Research Participation From the Perspective of Participating Children and Adolescents: A Systematic Review. 
  • Using central IRBs for multicenter clinical trials in the United States. 
  • Views of older adults on patient participation in medication-related decision making. 
  • What I don’t know won’t hurt you: The relation between professed ignorance and later knowledge claims. 
  • What do transplant physicians think about palliative care? A national survey study. 
  • Who trusts healthcare institutions? Results from a community-based sample. 
  • Why Consistency in Practice Will Build Trust in Palliative Care. 
  • Why Physicians Should Oppose Assisted Suicide. 
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  Keywords of People

  • Bradford, Daniel William, Professor of Psychiatry and Behavioral Sciences, Psychiatry, Child & Family Mental Health & Community Psychiatry
  • Olsen, Maren Karine, Professor of Biostatistics & Bioinformatics, Biostatistics & Bioinformatics