Development and Validation of the Paediatric Scale for Quality of Recovery in the Post-Anaesthesia Care Unit

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age2-17
SponsorMahidol University

About this trial

This project aims to develop and test a new questionnaire to measure how well children recover in the post-anaesthesia care unit (PACU). Currently, children in PACU are mainly assessed using discharge readiness criteria, but these do not fully capture the child's recovery experience or overall wellbeing. Participants will be children aged 2-17 years having elective procedures requiring anaesthesia or sedation, and their parents/caregivers where proxy reporting is needed for younger children. The study will be conducted in stages, including interviews to identify important aspects of recovery, expert review of draft questions, testing of question clarity and acceptability, and field testing of the questionnaire in PACU at planned time points during recovery. Clinical information routinely collected as part of care, such as pain scores, nausea vomiting, airway or oxygen events, and length of stay in PACU, will also be examined to assess how well the questionnaire performs. The expected outcome is a child-centred, practical, and reliable PACU recovery measure that can be used in clinical care, quality improvement, and future research.

Eligibility criteria

Qualifiers

Children aged 8-17 years for self-report version

Parents/caregivers of children aged 2-7 years for proxy-report version

Elective surgery/procedure under anaesthesia

Planned recovery in PACU

Disqualifiers

Unable to communicate in the prespecified site language (Thai - in Siriraj Hospital site)

Urgent or emergency surgery/procedure

Not planned to recover in PACU, including planned direct transfer from theatre to ICU

Developmental delay or other condition limiting comprehension for interview participation or questionnaire completion

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

200 Participants
are grouped into 2 trial groups

Sponsors and collaborators

Mahidol University

Lead sponsor

Murdoch Childrens Research Institute

Collaborator