Cohort of Patients Suffering From Major Depressive Episode With Evaluation of Sleep, Circadian Rhythms and Psychiatric Disorders

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorAssistance Publique - Hôpitaux de Paris

About this trial

Despite international efforts to identify biomarkers of depression, none has been transferred to clinical practice, neither for diagnosis, evolution, nor therapeutic response. This led us to build a French national cohort (through the clinical and research network named SoPsy within the French biological psychiatry society (AFPBN) and sleep society (SFRMS)), to better identify markers of sleep and biological rhythms and validate more homogeneous subgroups of patients, but also to specify the manifestations and pathogeneses of depressive disorders.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Individuals with depressive episode characterized according to the DSM-5 criteria regardless of the associated characteristics and comorbidities.

Adult and child

Affiliated to a social security

Disqualifiers

don't understand or read french

Medical condition incompatible with administration of questionnaire

impossibility to give informed decision (subject in an emergency condition, etc.)

Trial population

The entry point for the cohort is any patient with a major depressive episode, in order to integrate the maximum variance in terms of manifestations, and thus to be able to contrast the different clinical pictures according to the biomarkers of sleep and biological rhythms. The aim of this cohort is to pool the efforts of this network and to homogenise the assessments, in order to characterise more precisely and in a standardised manner the alterations in sleep and rhythms in depressive disorders, according to the different subtypes of disorder.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

amount of REM sleep

during the polysomnography, amount of REM sleep (in minutes)

Time frame
at inclusion

Secondary outcomes

1

duration of the first stage of REM sleep

Time frame
at inclusion
2

duration of the first episode of N3

Time frame
at inclusion
3

latency of the first episode of N3

Time frame
at inclusion
4

duration of N1 slow-wave sleep

Time frame
at inclusion

Other outcomes

Sponsors and contacts

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