Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
ID07008183

Perinatal Thymic Dysregulation: Characterization of Perinatal Mood Episodes

Led by Centre Hospitalier Charles Perrens, Bordeaux · Updated on 2025-12-01

200

Participants Needed

1

Research Sites

21 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research focuses on mood episodes occurring during the perinatal period, a time when women are more vulnerable to psychological issues. The study aims to improve the diagnosis and treatment of mood episodes such as depression and hypomania, which often go unrecognized. It addresses the complexity of mood symptoms that can appear during pregnancy or shortly after childbirth, emphasizing the need for better clinical evaluation and management during this critical time. Participants in this study will complete self-questionnaires before their psychiatric appointments to systematically evaluate mood episode criteria and explore related contextual factors. The study integrates this process into routine clinical care to standardize assessments of mood episodes, including depressive and hypomanic symptoms. The study uses established scales such as the Edinburgh Postnatal Depression Scale and the Multidimensional Assessment of Thymic Scale to measure symptoms and related risk factors. Participants' involvement includes completing self-report questionnaires that assess mood symptoms and risk factors like perceived stress and social support. Researchers will use these assessments to better understand mood episode characteristics during the perinatal period. The study monitors participants during their first psychiatric consultation related to the current pregnancy or postpartum period, with data collected on one day to describe mood symptoms and contextual influences.

CONDITIONS

Brief Title

Perinatal Thymic DYsregulation: Characterization of Perinatal Mood Episodes

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women over 18 years old
  • Currently pregnant or have given birth less than a year ago
  • Attending first psychiatric consultation related to this pregnancy
  • Good command of the French language
  • Affiliated to the social security system
  • Provided consent to participate in the study
Not Eligible

You will not qualify if you...

  • Women who gave birth more than a year ago
  • Currently under psychiatric care
  • Under court protection

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - 1 day

Participants complete self-questionnaires and attend a psychiatric consultation to characterize mood episodes using various assessment scales.

1 visit (in-person)

Trial Site Locations

Total: 1 location

1

Centre Hospitalier CHARLES PERRENS

Bordeaux, New Aquitaine, France, 33076

Actively Recruiting

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Research Team

A

Anne-Laure SUTTER DALLAY, Prof, MD, PhD

H

Helen SAVARIEAU

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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