Objective To describe patient perspectives on recruitment and retention in clinical trials.
Study Design and Setting Systematic review of qualitative studies that reported the …

Alzheimer's disease and Alzheimer's disease-related dementias (AD/ADRD)
disproportionally affect Hispanic and Latino populations, yet Hispanics/Latinos are …

Artificial Intelligence (AI) represents a significant milestone in health care's digital
transformation. However, traditional health care education and training often lack digital …

As the clinical trial landscape for patients with disorders of consciousness (DoC) expands,
consideration of associated ethical challenges and opportunities is of ever-increasing …

Objective Dissemination of research findings is central to research integrity and promoting
discussion of new knowledge and its potential for translation into practice and policy. We …

This qualitative review explores how established citizen science models can inform and
support meaningful engagement of public in health research in Australia. In particular, with …

Background Slow recruitment and poor retention jeopardize the reliability and statistical
power of clinical trials, delaying access to effective interventions and increasing costs, as …

Background There is an ethical imperative to offer the results of trials to those who
participated. Existing research highlights that less than a third of trials do so, despite the …

Objective Returning aggregate study results is an important ethical responsibility to promote
trust and inform decision making, but the practice of providing results to a lay audience is not …

Background Community engagement is central to the conduct of health-related research
studies as a way to determine priorities, inform study design and implementation, increase …