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CompletedNCT04663672

Efficacy of Targeted Memory Reactivation for Enhancing Exposure Therapy

Placebo-Controlled, Randomized, Double-Blind Study of the Efficacy of Targeted Memory Reactivation for Enhancing Exposure Therapy

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
158 (actual)
Sponsor
University of Texas at Austin · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This study evaluates whether a scent applied during exposure therapy and during subsequent sleep will increase the durability of treatment effects for individuals with fear of spiders, contamination, and enclosed spaces.

Detailed description

Newly acquired memories encoded during wakefulness are spontaneously re-activated during sleep, resulting in synaptic potentiation and strengthening of the re-activated traces. Targeted memory reactivation (TMR) typically involves a period of initial learning in the presence of an olfactory or auditory contextual cue, coupled with later presentation of the cue during sleep to ostensibly facilitate memory reactivation and consolidation. Numerous studies have found evidence of improved task performance subsequent to cue-induced neuronal replay, however application of TMR to treatment of naturally acquired, clinically significant fear has been limited. The present study will will provide a rigorous test of TMR's efficacy as an augmentative strategy for exposure therapy. It is hypothesized that participants who sleep in the presence of the same odor that they are exposed to during exposure therapy will exhibit reduced fear at follow up, relative to participants who sleep in the presence of a different odor, or a non-odorous control.

Conditions

Interventions

TypeNameDescription
OTHERExperimental ScentParticipants will sleep in the presence of the exposure scent, delivered by an Airwick Essential Oils diffuser
OTHERControl ScentParticipants will sleep in the presence of a novel scent, delivered by an Airwick Essential Oils diffuser
OTHERNo-Scent ControlParticipants will sleep in the presence of an odorless control vehicle, delivered by an Airwick Essential Oils diffuser
BEHAVIORALIn-Vivo ExposureParticipants will receive 40 minutes of in-vivo exposure therapy to feared targets in the presence of a distinctive exposure scent.

Timeline

Start date
2019-01-29
Primary completion
2020-03-01
Completion
2020-03-01
First posted
2020-12-11
Last updated
2020-12-11

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04663672. Inclusion in this directory is not an endorsement.

Efficacy of Targeted Memory Reactivation for Enhancing Exposure Therapy (NCT04663672) · Clinical Trials Directory