The correlation between quality of recovery and parturient outcomes after Cesarean delivery: a cohort study.
Hon Sen Tan, Chin Wen Tan, Rehena Sultana...
https://pubmed.ncbi.nlm.nih.gov/39134784Actively Recruiting
Age: 21Years - 50Years
FEMALE
ID04989894
Investigating the Quality of Recovery After Childbirth Using ObsQoR-10 in Chinese and Malay-Speaking Women
Led by KK Women's and Children's Hospital · Updated on 2024-10-09
122
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating the quality of recovery after childbirth, focusing on both physical and psychological factors. They aim to validate the Chinese and Malay versions of the ObsQoR-10 questionnaire, which measures recovery aspects such as pain, comfort, control, ability to care for the baby, mobility, and hygiene. This study will identify modifiable risk factors linked to poorer recovery scores to better understand postpartum recovery and help manage expectations and develop future interventions. The study will begin with a pre-test of the translated questionnaires in a small group of patients, followed by recruitment of 112 women on the first postpartum day to complete the ObsQoR-10 and other related questionnaires assessing mood, anxiety, and pain. The participants will have delivered either by spontaneous vaginal delivery or elective cesarean section and will be assessed shortly after delivery. Participants will be involved mainly on postpartum day 1, completing the questionnaires initially and again after 60 minutes to measure changes in recovery scores. Additional correlations with health status, pain, breastfeeding confidence, depressive symptoms, and length of hospital stay will be evaluated. The study focuses on female participants aged 21 to 50 years and will continue through the postpartum period, aiming to provide comprehensive data on recovery quality after childbirth.
CONDITIONS
Brief Title
Quality of Recovery After Childbirth
Who Can Participate
Age: 21Years - 50Years
FEMALE
Eligibility Criteria
You may qualify if you...
- Aged 21-50 years old
- Able to read and understand written Chinese
- First pregnancy with a single baby
- Delivered via spontaneous vaginal delivery or elective cesarean delivery
- Pregnancy at or beyond 38 weeks gestation
You will not qualify if you...
- Failed neuraxial analgesia during elective cesarean delivery
- General anaesthesia used
- Cesarean delivery performed during labor
- Infant has died
- Mother or baby requires intensive care after delivery
- Assisted or operative vaginal delivery
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
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2
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Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Diagnostic Evaluation
Duration - 1 day postpartum
Participants complete the Chinese or Malay translated ObsQoR-10 questionnaire and other related questionnaires to assess quality of recovery after childbirth.
1 visit (in-person)
Long-term Monitoring
Duration - 7 days postpartum
Participants are assessed on recovery parameters including breastfeeding self-efficacy and postnatal depressive symptoms.
1 follow-up visit (in-person)
Trial Site Locations
Total: 1 location
1
KK Women's and Children's Hospital
Singapore, Singapore
Actively Recruiting
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Research Team
B
Ban Leong Sng
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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