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ID
Source
Brief title
Health condition
Depression, Prevention,Relapse, fMRI
Depressie, preventie, terugval, fMRI
Sponsors and support
Hersenstichting Nederland (HS), Fellowship F2014(1)-21
Intervention
Outcome measures
Primary outcome
Testing whether preventive cognitive therapy in remitted patients results in increased prefrontal control and whether this increased prefrontal control results in a decrease in attentional biases and increase in emotion regulation capacity.
Secondary outcome
Predict individual treatment succes in remitted depressed patients based on neurocognitive measures.
Translate neurocognitive principles to clinically usefull measures to predict and monitor individual preventive cognitive therapy success.
Background summary
Major depressive disorder (MDD) is the most prevalent psychiatric disorder, characterized by at least one life disrupting depressive episode and high risk for relapse after recovery (40% within 2 years). Risk for relapse and chronic-MDD increases dramatically with the number of previous episodes. Therefore, preventing relapse in the remitted phase is a major, but largely overlooked opportunity in treating MDD. Preventive cognitive therapy (CT), a psychological therapy aiming at improving emotion regulation skills, in remitted-MDD has been successful in lowering relapse-risk, though not in all patients. Mechanisms underlying preventive-CT are unclear, hindering clinicians in predicting for whom preventive-CT is warranted. Reliable predictors of preventive-treatment success are currently lacking, yet urgently needed. Clearly, accurate prediction of preventive-success contributes to effective preventive-treatment allocation and lower relapse-rates. In this research, we hypothesize that the capacity of the brain’s prefrontal cortex to regulate emotional information is crucial for understanding and predicting preventive-CT-success. The main objective of this study is to understand the neurocognitive mechanisms of preventive-CT by studying neurophysiological (i.e. brain responsivity as measured with functional Magnetic Resonance Imaging and autonomic nervous system reactivity as measured from pupil dilation) and cognitive processes associated with attentional processing and regulation of emotional information. Secondarily, this study aims to identify neurophysiological and neurocognitive predictors of individual preventive-CT success. As routinely performing neuroimaging investigations for predicting treatment-success is clinically not feasible, a third aim of this study is to validate the pupil dilation-response (an autonomic index previously linked to emotion regulation-success and associated brain activation) as reflector of brain-activation during emotion regulation in remitted-MDD, for use in innovative non-imaging, brain-informed prediction and monitoring of preventive-CT success.
Study objective
We hypothesize that the capacity of the brain’s prefrontal cortex to regulate emotional information is crucial for understanding and predicting preventive-CT-success.
Study design
Screening: with the SCID-I, the IDS-SR , the DART
First phase: Questionnaires, computer tasks, fMRI-scan
Second phase: Preventive cognitive therapy (8x 45 mins)
Third phase: 3 months after 1st phase, similar as 1st phase.
Fourth phase: questionnaires, 1,5 year after 1st phase,
Intervention
Protocolised Preventive Cognitive Therapy
M.J. van Tol
Ant. Deusinglaan 2
Groningen 9713 AW
The Netherlands
050 3616405
m.j.van.tol@umcg.nl
M.J. van Tol
Ant. Deusinglaan 2
Groningen 9713 AW
The Netherlands
050 3616405
m.j.van.tol@umcg.nl
Inclusion criteria
between 18 - 60 years of age
current remission (>2 months; according to criteria in DSM IV)
>2 major depressive episodesin past 5 years
recency of last episode < 2years
currently not using any anti-depressant medication (>4 weeks)
Exclusion criteria
current major depressive episode
current use of anti-depressant medication
neurological problems
drug abuse
use of psychotropic medication other than frequent use of benzodiazepine
anu other current DSM IV Axis-I diagnosis, as objectified with the SCID-I
MRI contra indications
Design
Recruitment
IPD sharing statement
Followed up by the following (possibly more current) registration
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
NTR-new | NL5219 |
NTR-old | NTR5368 |
CCMO | NL53205.042.15 |
OMON | NL-OMON47768 |