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The Quality of Recovery-15 Survey After Cardiac Surgery

NCT05602298 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 160

Last updated 2022-11-02

No results posted yet for this study

Summary

Patient reported outcomes are becoming increasingly recognized as an important metric to determine efficacy of interventions following recovery after cardiac surgery. Quality of Recovery 15 survey is a tool that attempts to measure patients' recovery across several different domains (i.e physical, emotional and social). This tool has been validated extensively in the post operative patient population, but these studies contained only small numbers of cardiac surgery patients. This population faces unique challenges to recovery such as a longer duration of mechanical ventilation, ICU and hospital LOS, delirium, significant pain in the first 24-48 hours and post operative arrhythmias. This study aims to validate the QoR 15 in this population exclusively to determine if it is feasible, valid, reliable and responsive in this unique population.

Conditions

  • Cardiac Disease
  • Surgery
  • Surgery-Complications
  • Cardiac Valve Disease
  • Cardiac Complication
  • Cardiac Event

Interventions

OTHER

Quality of Recovery 15 survey

QOR 15 is a patient reported outcomes measure (PROM) tool used as a global measure of patient recovery after surgery and anesthesia. It uses fifteen questions to assess various domains of patient health: pain, physical comfort, physical independence, psychological support, and emotional state.

Sponsors & Collaborators

  • University of British Columbia

    lead OTHER

Principal Investigators

  • Alana Flexman · University of British Columbia

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-08-04
Primary Completion
2023-02-01
Completion
2023-05-01

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05602298 on ClinicalTrials.gov