Maternal Expectations on Labor Analgesia and Risk of Postpartum Depression: An Observational Study

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorUniversity of Padova

About this trial

Postpartum Depression (PPD) is defined as the development of depression at any time during the first year after childbirth¹. Its prevalence ranges from 15% to 20%. It can manifest with symptoms such as depressed mood, loss of interest and energy, insomnia, anxiety, and may even lead to suicidal ideation. The consequences are numerous, both physical and psychological, with long-term repercussions on the mother-infant bond, family dysfunction, and the development of emotional and cognitive disorders in children. The etiology of PPD is multifactorial, but numerous recent studies have focused on the role of labor pain and its management with labor analgesia techniques. The aim of the present study is therefore to assess whether there is a difference in the incidence of PPD between parturients whose expectations regarding labor analgesia were met ('expectations met' group) versus those whose expectations were unmet.

Eligibility criteria

Qualifiers

Signed informed consent

Planned vaginal delivery (spontaneous or induced)

Pregnancy

Age > 18 years

Disqualifiers

Allergy to local anesthetics

Language barrier

Contraindications to labor analgesia

Delivery by Cesarean section

Trial design

Treatments tested in this trial

  • Epidural analgesia
  • Spinal analgesia for labour pain
  • No neuraxial analgesia

Treatment groups

3,640 Participants
are divided into 2 treatment groups

Sponsors and collaborators