Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07008183

Perinatal Thymic DYsregulation: Characterization of Perinatal Mood Episodes

The perinatal period is recognized as a time of heightened psychological vulnerability. This research aims to improve the diagnosis and therapeutic management of mood episodes occurring during this time. It is integrated into routine clinical care and seeks to standardize the evaluation of criteria used to characterize mood episodes, while also exploring relevant contextual factors.

Traditionally, clinical attention has focused on postnatal depression; however, increasing evidence highlights the presence of hypomanic symptoms-such as distractibility, reduced need for sleep, tachypsychia, and irritability-during the postpartum period. These symptoms may coexist with depressive features, resulting in complex clinical presentations that are often difficult to recognize and manage. Consequently, many cases go undiagnosed and untreated.

Current research has largely concentrated on depressive episodes (perinatal depression), with less emphasis on manic, hypomanic, or mixed episodes indicative of bipolar disorder. A systematic evaluation of hypomanic symptoms occurring alongside depressive symptoms in the postpartum period could refine clinical diagnosis and support more targeted and effective therapeutic interventions.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women over 18 years old
  • Pregnant or having given birth less than a year ago
  • First psychiatric consultation for the pregnancy concerned.
  • Good command of the French language.
  • Participant affiliated to the social security system
  • Participant who has given her consent to take part in the study.

Exclusion criteria

  • Women who gave birth more than a year ago.
  • Participant under psychiatric care
  • Participant under court protection

Treatment and study plan

Self-questionnaires

Other

Patients who volunteer to take part in the research will complete self-questionnaires before their appointment with the psychiatrist.

Primary outcomes

  1. Detailed description of the Edinburg Postnatal (EPDS) scale

    Time frame: 1 day

    A sensitivity analysis will be carried out on the group of patients with an EPDS score greater than 12, and a comparison between these patients and patients with an EPDS score equal to or less than 12 will also be carried out

  2. Detailed description of Multidimensional Assessment of Thymic (MAThyS) scale

    Time frame: 1 day

Secondary outcomes

  1. Association of the risk factors Perceived Stress Scale (PSS) will be assessed by self-report

    Time frame: 1 day

    the level of perceived stress by self report score>=14 characterize a high level of perceived stress

  2. Association of the risk factors Medical Outcomes Study -Social Support Survey (MOS-SSS) will be assessed by self-report

    Time frame: 1

    the level of perceived social support by self-report scale scores can range from 19 to 95, with a median score of 57

  3. Association of the risk factors Perceived Professional Social Support (QSSP-P) will be assessed by self-report

    Time frame: 1

    the level of perceived social support in the professional by self-report. scale scores pcan range from 12 to 120, with a median score of 66

Study contacts

Contact information is provided by the study sponsor or research team.

Anne-Laure SUTTER DALLAY, Prof, MD, PhD

CONTACT

[email protected]

+33 556561782

Helen SAVARIEAU

CONTACT

[email protected]

+33556563556

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Charles Perrens, Bordeaux

Other Gov

Registry information

Acronym: DYP

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jun 6, 2025
Registry last updated
Dec 1, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.