All Stories

  1. Pain in women: relevance of history of iron deficiency
  2. Associations Between Lifetime Histories of Iron Deficiency, Anxiety, Depression
  3. Reducing risk of bias in interventional studies during their design and conduct: a scoping review
  4. Identifying and counteracting fraudulent responses in online recruitment for health research
  5. Conceptualising, operationalising and utilising equity, diversity and inclusion in clinical trials
  6. Data sharing policies across health research globally: Cross-sectional meta-research study
  7. Quality of systematic reviews and meta-analyses in dermatology
  8. Service needs of people from culturally and linguistically diverse backgrounds
  9. Quality of randomized controlled trials and systematic reviews in pediatric surgery
  10. Cord clamping at preterm birth
  11. Responsibilities for receiving and using individual participant data
  12. Umbilical cord clamping at preterm birth
  13. Quality of randomised controlled trials, systematic reviews and meta-analyses in paediatric surgery: a cross-sectional analysis
  14. Quality of randomised controlled trials, systematic reviews and meta-analyses in paediatric surgery: a cross-sectional analysis
  15. Processing individual participant data from randomised trials
  16. Biopsychosocial sequelae of chronically painful injuries sustained in motor vehicle accidents
  17. Electrical injury
  18. The landscape of COVID-19 trials in Australia
  19. Data sharing—trialists' plans at registration, attitudes, barriers and facilitators
  20. International representation of authors, editors and research in neurology journals
  21. Health and support service needs of individuals with disability
  22. On Lessons Learned in The Gambia
  23. The reporting quality of published randomised controlled trial protocols since the SPIRIT statement
  24. Is retrospective assessment of health-related quality of life valid?
  25. Why unidimensional pain measurement prevails in the pediatric acute pain context
  26. Prevalence of trial registration varies by study characteristics and risk of bias
  27. Data quality audit of a clinical quality registry: a generic framework and case study
  28. Chronic widespread pain and fibromyalgia syndrome: life-course risk markers in young people
  29. The Modern Medical Student Manual: a book review