Quality of Recovery After Childbirth
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age21-50
SponsorKK Women's and Children's Hospital
About this trial
In this proposed study, the investigators hope to assess the quality of recovery after delivery in a local population that would take into account physiological and psychological parameters to better understand the recovery process after delivery. The investigators will identify risk factors, especially those that are modifiable and associated with a poorer ObsQoR score and hence a poor quality of recovery after delivery. This data may then be used to educate women and manage expectations in the postpartum period, and help develop potential therapeutic interventions.
Eligibility criteria
Qualifiers
Aged 21-50 years old;
Able to read and understand written Chinese;
Primiparous and having singleton pregnancy;
Delivered via spontaneous vaginal delivery, or elective cesarean delivery;
Disqualifiers
Failed neuraxial analgesia in those receiving elective cesarean delivery;
General anaesthesia;
Intrapartum cesarean delivery;
Women whose infants have died;
Trial design
Treatments tested in this trial
- Not listed
Trial groups
No trial groups listed
Sponsors and collaborators
Source ClinicalTrials.gov