• Bess Site Staff Questionnaire

  • The aim of this short questionnaire is to find out how well you think BESS has been going at your site. This includes what you think is working well and perhaps what isn’t working so well. We will use these findings, alongside data collected from parents to inform season three of BESS. Please note that by completing this survey you are giving permission for your responses to be included in the BESS trial. All information will be held by the University of Liverpool Qualitative team, anonymised and stored securely in compliance with the 2018 Data Protection Act and GDPR guidelines.
  • Background Information

  • 4. Are you involved in clinical care of children?
  • 5. How have you been involved in the BESS study (please tick all that apply)

  • Training

  • 6. Who provided your BESS training (please tick all that apply)

  • 7. Overall how would you rate the BESS site training from the trial team?
  • 8. Overall how would you rate the BESS site training from your site team?
  • 9. Do you think the BESS site training could be improved?
  • Process and acceptability

  • 10. Do you think the screening process could be improved?
  • 11. Do you think the randomisation process could be improved?
  • 12. Have you experienced any difficulties with the randomisation and intervention allocation system? (e.g. problems with accessing or using the system, allocated vials not being available)
  • 13. Have you experienced any difficulties in adhering to the protocol (e.g. blinding, delivering the allocation)
  • 14. Have you experienced any logistical problems with the BESS study?  (E.g. staff availability, delays, missed eligible patients)
  • 15. Did you find the case report form easy to use?
  • 16. Did you find the consent form easy to use?
  • 17. How acceptable do you think administering the intervention (surfactant) to patients is?
  • 18. How acceptable do you think administering the placebo (sham) to patients is?
  • 19. Overall how acceptable do you find the BESS study?
  • Consent and comments

  • 20. How acceptable did you find seeking informed consent before randomisation in BESS?
  • 21. Have you chosen not to approach any parents of eligible children to seek consent for trial participation?
  • 22. How have parents responded to the BESS consent discussion?
  • 23. Have any of the parents you have approached declined consent for their child’s participation in Bess
  • Should be Empty: