Effects of Mifepristone on Biomarkers of Metabolic Function and Neuropsychological Performance Among Middle-Aged and Older Individuals



Status:Completed
Conditions:Depression, Depression
Therapuetic Areas:Psychiatry / Psychology
Healthy:No
Age Range:50 - 70
Updated:1/27/2018
Start Date:October 2013
End Date:February 2017

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The purpose of this study is to study the effect of cortisol,a stress hormone in the body, on
memory and attention in people with a history of depression, but who are not in the midst of
a current depressive episode.

Cortisol may affect parts of the brain associated with memory and attention directly. It may
also indirectly affect the brain by controlling how much insulin the body makes. Insulin is
thought to impact cognition by changing the amount of sugar available in certain parts of the
brain.

The investigators are studying this question by giving patients a medication, called
Mifepristone, which reduces cortisol's effect on the brain. The investigators will compare
results from several groups of people, including differences between men and women, and
between those with and without insulin resistance.

The specific aims of this study are threefold:

1. To evaluate the association between glucose utilization and neuropsychological
performance on tests of verbal memory and attention among patients with a history of
depression, but who are euthymic, at baseline;

2. To evaluate changes in neuropsychological test performance among patients with a history
of depression and who have insulin resistance who are treated with open-label
mifepristone and,

3. To explore interactions between changes in patients' glucose tolerance profiles and
changes in verbal memory and attention. An exploratory aim is to explore the interaction
of changes in cortisol awakening response and changes in verbal memory and attention
within subjects with and without IGT, as well as the potential mediating effects of
gender.

Inclusion Criteria:

- Ages 50-70

- History of depression, not currently depressed.

Exclusion Criteria:

- History of type 1 or type 2 diabetes.

- Use of a medication that interacts with Mifepristone.
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