Major Depressive Disorder Clinical Trial
Official title:
Hypersomnia in Major Depressive Disorder
Background: MDD is a common mental disorder with significant morbidities and mortalities.
Recent local data suggested that depressive disorders have a prevalence of over 12% in
females and nearly 7 % in males in Hong Kong general adult population. Other than insomnia,
patients with MDD often complained another sleep symptom - hypersomnia (defined as daytime
sleepiness or excessive sleep). Interestingly, when compared to insomnia, there is much far
less research on the role of hypersomnia in MDD. However, there are available data suggested
that hypersomnia is associated with greater treatment-resistance, more recurrence, and
increased suicidality, suggesting a need to investigate this problem in MDD patients.
Objective: To investigate the prevalence and determine characteristics of hypersomnia amongst
major depressive disorder.
Design: 2-phase study design Setting: A case-control study Participants: Patients with a
history of Major Depressive Disorder from out-patient clinics in New Territories East
Cluster.
Main outcome measures: Daytime sleepiness measured by MSLT, actigraphy and self-reported
questionnaire (ESS), sleep duration as measured by sleep diary and actigraphy.
Background
Significance of hypersomnia in depressive illness
Sleep disturbances are observed in up to 90% of depressed patients. Both insomnia, defined
clinically as difficulty initiating and/or maintain sleep, and hypersomnia, defined as
excessive daytime sleepiness (EDS) and/or excessive sleep duration, are key symptoms in the
diagnostic criteria of depression. A sizeable number of studies have demonstrated clear
associations between insomnia and poorer depressive outcomes. These include greater
depressive symptom severity, poorer treatment response and increased risk of suicidal
ideations and attempts. Persistent insomnia complaints following remission of major
depressive episodes (MDE) have also been found to be associated with greater risk of
recurrence, poorer overall functioning and quality of life. Compared to insomnia, there is
much less research on the role of hypersomnia in depressive illness.
Studies so far have suggested a prognostic significance. Hypersomnia in depressed subjects
amongst a mix of mood disorders have been linked to greater treatment-resistance, depressive
relapse, higher suicidal ideations and increased risk of suicide; while hypersomnia
complaints amongst general populations have predicted the risk of incident depression. More
recently, studies of depressed individuals amongst a mix of mood disorders had further found
that the concurrence of insomnia and hypersomnia was associated with worse symptomatology
compared to patients with insomnia or hypersomnia alone. These studies also found that the
concurrence of insomnia and hypersomnia had greater associations with bipolar spectrum
features, which builds on from previous findings suggesting that hypersomnia itself may be a
clinical marker for undetected or subsequent diagnosis of bipolar II disorders in depressed
patients.
Knowledge gaps in the understanding of hypersomnia in major depression
Despite its prognostic implications, there is currently a lack of studies investigating
potential determinants or clinical correlates of hypersomnia in major depressive disorder
(MDD). MDD is one of the commonest diagnoses encountered in the outpatient setting, and may
be distinct in its determinants and outcomes compared to other mood disorders. Existing
studies on hypersomnia in depression have predominantly included subjects from a mix of mood
disorders; thus, a gap exists to extend the scope of understanding on hypersomnia amongst
unipolar depression.
Due to the lack of standardized definitions, even amongst contemporary classifications, there
is little clarity as to which aspect of hypersomnia - i.e. whether EDS or excessive sleep
duration, or in combination - is related to poorer depressive outcomes. Moreover, little is
known about what severity of "excessive" daytime sleepiness and sleep duration may be of
clinical significance. Most studies of hypersomnia in mood disorders have used crude
definitions, predominantly in form of single yes/no questions, to define hypersomnia. Despite
the availability of validated questionnaires such as the Epworth Sleepiness Scale (ESS) that
could help quantify EDS, or the use of sleep diaries that may help determine an individual's
average sleep duration, limited studies of hypersomnia in MDD have employed these tools. The
variability in definitions have also resulted in a large range of reported prevalence -
between 8.9% to 78% of hypersomnia in MDD samples. In order to generate more clinically
useful data, it may be helpful to "deconstruct" hypersomnia into EDS and prolonged sleep
duration, to quantify them using validated or clinically-relevant measures, and further
analyze their associations with potential determinants and depressive outcomes.
Theoretically, a myriad of factors can contribute to EDS or prolonged sleep duration. These
include physical-health related factors, such as the use of sedative medications, the
presence of medical illnesses and sleep-related breathing disorders; also sleep-related
factors, such as the need for shift-work, the presence of insomnia or other sleep-behavioral
disturbances, or the presence of circadian-disorders or particular chronotype preferences.
Psychiatric factors, such as increased anxiety, somatic complaints and perceived fatigue
levels, may also be related to EDS or prolonged sleep duration. So far, no studies have
simultaneously examined this range of factors and their potential associations with
hypersomnia complaints in MDD. Whether these factors mediate or act synergistically with
hypersomnia to influence depressive outcomes remain to be elucidated.
A limitation that many hypersomnia studies have faced is the lack of objective measures used
to corroborate subjective measures of EDS or sleep duration. The mean sleep latency test
(MSLT) is currently regarded as the gold standard objective measure for EDS, while
polysomnography (PSG) and wrist actigraphy has been useful in validating sleep diary data.
However, the costs, expertise and time required to conduct these tests have limited their
use. A study involving the use of both subjective and objective measures of EDS or sleep
duration, in addition to a thorough analysis of the potential determinants and clinical
correlates, may provide valuable information on the clinical profiles of hypersomnia patients
and shed light on areas for further research and management.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05537558 -
Precision Medicine for the Prediction of Treatment (PROMPT) Response (PROMPT)
|
||
Terminated |
NCT02192099 -
Open Label Extension for GLYX13-C-202, NCT01684163
|
Phase 2 | |
Completed |
NCT03142919 -
Lipopolysaccharide (LPS) Challenge in Depression
|
Phase 2 | |
Recruiting |
NCT05547035 -
Identification of Physiological Data by a Wearable Monitor in Subjects Suffering From Major Depression Disorders
|
N/A | |
Terminated |
NCT02940769 -
Neurobiological Effects of Light on MDD
|
N/A | |
Recruiting |
NCT05892744 -
Establishing Multimodal Brain Biomarkers for Treatment Selection in Depression
|
Phase 4 | |
Recruiting |
NCT05537584 -
SMART Trial to Predict Anhedonia Response to Antidepressant Treatment
|
Phase 4 | |
Active, not recruiting |
NCT05061706 -
Multicenter Study of Lumateperone as Adjunctive Therapy in the Treatment of Patients With Major Depressive Disorder
|
Phase 3 | |
Completed |
NCT04479852 -
A Study of the Safety and Efficacy of SP-624 in the Treatment of Adults With Major Depressive Disorder
|
Phase 2 | |
Recruiting |
NCT04032301 -
Repeated Ketamine Infusions for Comorbid PTSD and MDD in Veterans
|
Phase 1 | |
Recruiting |
NCT05527951 -
Enhanced Measurement-Based Care Effectiveness for Depression (EMBED) Study
|
N/A | |
Completed |
NCT03511599 -
Cycloserine rTMS Plasticity Augmentation in Depression
|
Phase 1 | |
Recruiting |
NCT04392947 -
Treatment of Major Depressive Disorder With Bilateral Theta Burst Stimulation
|
N/A | |
Recruiting |
NCT05895747 -
5-HTP and Creatine for Depression R33 Phase
|
Phase 2 | |
Recruiting |
NCT05273996 -
Predictors of Cognitive Outcomes in Geriatric Depression
|
Phase 4 | |
Recruiting |
NCT05813093 -
Interleaved TMS-fMRI in Ultra-treatment Resistant Depression
|
N/A | |
Recruiting |
NCT05135897 -
The Neurobiological Fundaments of Depression and Its Relief Through Neurostimulation Treatments
|
||
Enrolling by invitation |
NCT04509102 -
Psychostimulant Augmentation of Repetitive TMS for the Treatment of Major Depressive Disorder
|
Early Phase 1 | |
Recruiting |
NCT06026917 -
Assessing Dopamine Transporter Occupancy in the Patients With Depression Brain With Toludesvenlafaxine Hydrochloride Extended-Release Tablets Using 11C-CFT Positron Emission Tomography (PET)
|
Phase 4 | |
Recruiting |
NCT06145594 -
EMA-Guided Maintenance TMS for Depression
|
N/A |