Validation of the Chinese ObsQoR-11

Validation of the Chinese Version of the Obstetric Quality of Recovery Scoring Tool (ObsQoR-11) at Early and Intermediate Phases After Elective Caesarean Delivery: a Multicentre Observational Trial

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT04349215

Enrollment

319

Registered

2020-04-16

Start date

2020-03-09

Completion date

2022-03-10

Last updated

2022-03-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cesarean Delivery

Keywords

Cesarean delivery,the Obstetric Quality of Recovery-11 score, Chinese

Brief summary

Investigation of post-cesarean recovery among Taiwanese pregnant women.

Detailed description

Improving postpartum quality of recovery is important particularly for women undergoing cesarean delivery. This is because cesarean delivery is associated with significant postoperative pain and risks of anesthesia-related adverse effects. To improve the quality of recovery after a cesarean delivery, the first step is to find out the most relevant perioperative factors. In response to this problem, experts including anesthesiologists, obstetricians and midwives from University College London Hospital, Royal Free Hospital, London as well as Stanford University established a set of 11-item questionaire related to postpartum recovery, namely the Obstetric Quality of Recovery-11 score (ObsQoR-11), with a total score of 110. The latest systemic review in 2020 also confirmed that this questionnaire is the best option for recovery assessment after cesarean delivery. However, for women undergoing cesarean delivery in Taiwan, it is still unknown whether this questionnaire is representative or not. Therefore, this study aims to include women undergoing elective cesarean delivery from three hospitals in Taiwan.

Interventions

None listed

Study design

Observational model

CASE_ONLY

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Age

20 Years to 55 Years

Healthy volunteers

Inclusion criteria

1. age\>= 20 yr 2. elective cesarean delivery Exclusion: emergent surgery

Design outcomes

Primary

Measure	Time frame	Description
Validation of the Chinese ObsQoR-11 score	5 days	To validate the Chinese ObsQoR-11 at 24 hour and 96 hour after cesarean delivery

Secondary

Measure	Time frame	Description
Assessment of reliability, acceptability, and responsiveness of the Chinese ObsQoR-11	5 days	Perform analysis of reliability, acceptability, and responsiveness test for the Chinese ObsQoR-11

Countries

Taiwan

Outcome results