![]() |
Current
|
Our research program focuses mainly on examining the cognitive causes, correlates, and origins of depression. The current focus of the lab is on understanding the cognitive features of high-risk individuals. This research primarily examines the cognitive mechanisms of risk in adults, but also assesses processes linked to the possible developmental origins of cognitive risk. Specific projects have assessed information processing under conditions thought to elicit vulnerability, and have also examined the early experiences of vulnerable individuals that might predispose them to risk for later depression. For example, we have examined how problems in parental bonding and attachment are related to dysfunctional cognition in depression risk, and have also assessed dysfunctional information processing in high-risk children under affect-linked conditions. The lab has also begun to possible mechanisms linking depression risk to health problems.
Publication references, and some PDF files, from our research can be found on the Publications page.
Current Projects
Pupil Dilation, Emotional Information
and Depression Vulnerability
This study is designed to examine whether people who are vulnerable to
depression are more likely to attend to negative information, and to ruminate
about this information, in comparison to people who have never been depressed.
Attention is assessed through pupil dilation, which serves as a peripheral
measure of depth of information processing.
Pupil Dilation
in Dysphoria
Studies that
have assessed sustained pupil dilation, an indicator of cognitive and emotional
processing, have demonstrated that individuals with major depression process
emotional, specifically negative, information for longer than nondepressed
individuals. Individuals experiencing dysphoria (a negative affective
syndrome that characterizes depressive states, but which is usually less
severe, less enduring, and not exclusively related to depression) have performed
similarly to depressed individuals on certain cognitive tasks. Thus, the current
study is comparing sustained pupil dilation in dysphoric versus nondysphoric
individuals during a valence identification task to determine whether this
correlate of depression exists in individuals who have never experienced a major
depressive episode. If dysphoric individuals exhibit greater sustained
processing of emotional information than nondysphoric individuals, it might
suggest that this factor contributes to cognitive vulnerability to depression.
Cardiovascular Reactivity Project
Although depression is known to be associated with
cardiovascular problems, it is unclear if vulnerability to depression may be
associated with risk, as indicated by cardiovascular reactivity (CVR). In
response to a negative mood state, heart rate and blood pressure are measured in
both vulnerable and not vulnerable participants.
Back to the Cognitive-Clinical Lab main page