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NCT07582289

Labor Epidural Analgesia and Mother-Infant Bonding After Vaginal Delivery

Sponsor: Ataturk University

View on ClinicalTrials.gov

Summary

This prospective observational cohort study aims to evaluate the association between postpartum recovery quality and mother-infant bonding in women undergoing vaginal delivery. Postpartum recovery quality will be assessed using the Obstetric Quality of Recovery-10 (ObsQoR-10) questionnaire, and mother-infant bonding will be evaluated using the Postpartum Bonding Questionnaire (PBQ). Participants will be grouped according to routine clinical labor analgesia preference: women receiving labor epidural analgesia and women not receiving epidural analgesia. Additional assessments will include postpartum pain intensity, anxiety, depressive symptoms, and birth satisfaction. Baseline psychological assessments will be performed before delivery. The primary postpartum evaluation will be conducted between 6 and 24 hours after delivery. Exploratory follow-up assessments will be performed by telephone during postpartum week 2. The study aims to better understand the relationship between labor analgesia, postpartum recovery, and early mother-infant bonding outcomes after vaginal delivery.

Official title: Association Between Postpartum Recovery Quality Measured by ObsQoR-10 and Mother-Infant Bonding After Vaginal Delivery: The Role of Labor Epidural Analgesia

Key Details

Gender

FEMALE

Age Range

18 Years - 40 Years

Study Type

OBSERVATIONAL

Enrollment

140

Start Date

2026-05-15

Completion Date

2029-06-17

Last Updated

2026-05-12

Healthy Volunteers

No

Interventions

PROCEDURE

Labor Epidural Analgesia

Epidural analgesia administered during labor as part of routine clinical care for pain management during vaginal delivery.

Locations (1)

Ataturk University

Erzurum, Turkey (Türkiye)