All Stories

  1. Quality of systematic reviews and meta-analyses in dermatology
  2. Service needs of people from culturally and linguistically diverse backgrounds
  3. Quality of randomized controlled trials and systematic reviews in pediatric surgery
  4. Cord clamping at preterm birth
  5. Responsibilities for receiving and using individual participant data
  6. Umbilical cord clamping at preterm birth
  7. Quality of randomised controlled trials, systematic reviews and meta-analyses in paediatric surgery: a cross-sectional analysis
  8. Quality of randomised controlled trials, systematic reviews and meta-analyses in paediatric surgery: a cross-sectional analysis
  9. Processing individual participant data from randomised trials
  10. Biopsychosocial sequelae of chronically painful injuries sustained in motor vehicle accidents
  11. Electrical injury
  12. The landscape of COVID-19 trials in Australia
  13. Data sharing—trialists' plans at registration, attitudes, barriers and facilitators
  14. International representation of authors, editors and research in neurology journals
  15. Health and support service needs of individuals with disability
  16. On Lessons Learned in The Gambia
  17. The reporting quality of published randomised controlled trial protocols since the SPIRIT statement
  18. Is retrospective assessment of health-related quality of life valid?
  19. Why unidimensional pain measurement prevails in the pediatric acute pain context
  20. Prevalence of trial registration varies by study characteristics and risk of bias
  21. Data quality audit of a clinical quality registry: a generic framework and case study
  22. Chronic widespread pain and fibromyalgia syndrome: life-course risk markers in young people
  23. The Modern Medical Student Manual: a book review