NCT07292649 Maternal Expectations on Labor Analgesia and Risk of Postpartum Depression: An Observational Study
| NCT ID | NCT07292649 |
| Status | Recruiting |
| Phase | — |
| Sponsor | University of Padova |
| Condition | Postpartum Depression (PPD) |
| Study Type | OBSERVATIONAL |
| Enrollment | 3,640 participants |
| Start Date | 2026-01-08 |
| Primary Completion | 2029-01 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 3,640 participants in total. It began in 2026-01-08 with a primary completion date of 2029-01.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
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
Inclusion Criteria: * Signed informed consent * Planned vaginal delivery (spontaneous or induced) * Pregnancy * Age \> 18 years Exclusion Criteria: * Allergy to local anesthetics * Language barrier * Contraindications to labor analgesia * Delivery by Cesarean section * Known history of psychiatric disorders (including major depression)
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07292649 clinical trial?
This trial is open to female participants only, aged 18 Years or older, studying Postpartum Depression (PPD). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07292649 currently recruiting?
Yes, NCT07292649 is actively recruiting participants. Contact the research team at fabrizia.calabrese@aopd.veneto.it for enrollment information.
Where is the NCT07292649 trial being conducted?
This trial is being conducted at Padova, Italy.
Who is sponsoring the NCT07292649 clinical trial?
NCT07292649 is sponsored by University of Padova. The trial plans to enroll 3,640 participants.
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