Pilot Study of Pharmaceutical and Behavioral Interventions to Treat Anxiety Disorders
Status:
Completed
Trial end date:
2015-01-01
Target enrollment:
Participant gender:
Summary
The aim of this project is to create fear conditioning paradigm within which the relative
strengths of various novel pharmacological and behavioral interventions can be tested. These
interventions are intended to reduce the fearfulness associated with fear conditioning by
blocking a memory process known as reconsolidation. In fear conditioning, a "conditioned"
stimulus (CS) is paired with an aversive "unconditioned" stimulus (US) such as an electric
shock, until presentation of the CS alone comes to elicit a fear conditioned response (CR).
The investigators hypothesize that by using a more highly prepared CS (i.e. video of
spiders); more sensitive subjects (individuals with stronger acquired CRs); and additional
experimental probes for the presence of the latent CR, the investigators may develop a normal
human paradigm that is not plagued by previously observed floor effects (i.e. intervention is
100% effective), within which both the established techniques of propranolol and delayed
extinction will produce significant, but only partial, CR reduction. This would leave room to
test and compare potentially more powerful candidate reconsolidation-blocking or
memory-updating interventions. To achieve these aims, subjects will undergo a four-day fear
conditioning and delayed extinction protocol. Skin conductance response data will be gathered
across the different phases of the experiment.