Centre Hospitalier CHARLES PERRENS
Bordeaux, New Aquitaine, 33076, France
Location status: Recruiting
Location contact
Anne-Laure SUTTER DALLAY, Prof Md PhD
PRINCIPAL_INVESTIGATOR
Helen SAVARIEAU
CONTACT
Marine GALLET, MD
CONTACT
NCT Number: NCT07008183
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.
Interested in participating?
Request Info18 year and older
Female
Interventional
Not applicable
Bordeaux, New Aquitaine, 33076, France
Location status: Recruiting
Anne-Laure SUTTER DALLAY, Prof Md PhD
PRINCIPAL_INVESTIGATOR
Helen SAVARIEAU
CONTACT
Marine GALLET, MD
CONTACT
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients who volunteer to take part in the research will complete self-questionnaires before their appointment with the psychiatrist.
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
Time frame: 1 day
Time frame: 1 day
the level of perceived stress by self report score>=14 characterize a high level of perceived stress
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
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
Contact information is provided by the study sponsor or research team.
Anne-Laure SUTTER DALLAY, Prof, MD, PhD
CONTACT
Helen SAVARIEAU
CONTACT
Centre Hospitalier Charles Perrens, Bordeaux
Other Gov
Acronym: DYP
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.
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