The main objective for this proposal is to investigate the neurophysiology of BDD, and compare irregularities of BDD neurophysiology with OCD neurophysiology.
ID
Source
Brief title
Condition
- Anxiety disorders and symptoms
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
Changes in EEG in response to the task demands.
Secondary outcome
* Y-BOCS (Goodman et al., 1989)
* BDD-YBOCS (Phillips et al., 1997)
* Global assessment of functioning (Hall, 1995)
* Hamilton Scale for Depression (Hamilton, 1960)
* Hamilton Anxiety Scale (Hamilton, 1959)
* Brown Assessment of Beliefs Scale (Eisen et al. 1998)
* Behavioural Inhibition and Activation Scales (Carver & White, 1994)
Background summary
Patients suffering from Obsessive * Compulsive disorder (OCD) and Body
Dysmorphic Disorder (BDD) experience very similar problems. Both diseases are
characterized by recurring intrusive thoughts that cause anxiety and force the
patients to perform compulsive acts that often take hours. The content of the
intrusions is different however; OCD intrusions typically range from fear about
cleaning/contamination, incurring harm and fears to transgress societal mores
(fear to transgress can be oriented on sexual, aggressive or religious topics).
Patients with BDD instead fret over the perceived social rejection considering
certain aspects of their bodily appearance. However, these unrealistic fears
cause both groups of patients avoid the cause of the experienced fear and leads
to compulsively acts when exposed. The striking overlap between phenotypes has
lead researchers to propose that a novel diagnostic category, *Anxiety and
Obsessive-Compulsive spectrum disorders*, should be considered in an updated
version of the DSM (Phillips et al, 2010).
Although the clinical literature suggests that OCD and BDD are very similar
disorders, there is almost no imaging literature to support this hypothesis at
the level of the brain. We know from the functional Magnetic Resonance Imaging
(fMRI) literature that in OCD, the frontostriatal circuitry, comprised of the
basal ganglia, anterior cingulate cortex (ACC; Aouizerate et al., 2004) and
prefrontal cortex show different activity patterns. These brain regions are
associated with action selection, goal directed behaviors and performance
monitoring (Grundler et al., 2009; Harrison et al., 2009; Ridderinkhof et al.,
2004), brain functions that are disturbed in OCD and potentially also disturbed
in BDD. To investigate the rapid, cognitive dynamics we propose using the
electroencephalogram (EEG) to investigate how rapid interactions in brain
activity within the frontostriatal circuitry shapes the pathology in OCD and
BDD.
Study objective
The main objective for this proposal is to investigate the neurophysiology of
BDD, and compare irregularities of BDD neurophysiology with OCD
neurophysiology.
Study design
Observational study with non-invasive measures
Study burden and risks
Using a very basic study design, risk associated with participation can be
considered negligible and the burden can be considered minimal. No
pharmacological nor (otherwise) invasive interventions are applied. No adverse
events are expected. There is no direct benefit for participants.
Meibergdreef 5
Amsterdam 1105 AZ
NL
Meibergdreef 5
Amsterdam 1105 AZ
NL
Listed location countries
Age
Inclusion criteria
* Age range: 18 to 65 years
* For patients: The presence of a primary diagnosis for either BDD or OCD.
* For healthy controls: The absence of psychiatric, neurologic, endocrine problems.
* Predominant right-handedness
Exclusion criteria
* Abnormal hearing or (uncorrected) vision.
* History of neurological/endocrine treatment or current neurological/endocrine treatment.
* Average use of more than 3 alcoholic beverages daily.
* Use of recreational drugs over a period of 72 hours prior to each test session, and use of alcohol within the last 24 hours before each measurement.
* Irregular sleep/wake rhythm (e.g., regular nightshifts or cross timeline travel).
Additional exclusion criteria for Patients
* Currently unstable (due to changes in) SSRI, behavioural treatment, or life-event.
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL41440.018.12 |