Acoustic Startle Reduction In Cocaine Dependence
2 other identifiers
observational
144
1 country
1
Brief Summary
Chronic cocaine administration leads to changes in brain function that persist long after the acute withdrawal phase. The acoustic startle response (ASR) is a well characterized reflexive response to a sudden acoustic stimulus. The ASR is mediated by a simple 3-synapse subcortical circuit; it is modulated in part by brain areas and neurotransmitters associated with cocaine administration. Our initial study and subsequent replication reveals a profound diminution of the ASR in cocaine-dependent subjects after a brief period of abstinence. Our preliminary findings indicate that first degree relatives of cocaine-dependent subjects also have reduced startle compared to healthy controls. The findings of low ASR in rats and humans during cocaine washout and low ASR in family members suggests there may be both a trait and state component of the startle reductions we have reported. The central objectives of this proposal are to dissect this finding with regard to its development and persistence in early and later phases of cocaine abstinence in humans; to ascertain whether startle reduction and its potential normalization during later abstinence is a predictor of clinical course in human subjects with cocaine dependence; and to examine whether startle reduction is, at least in part, a vulnerability trait for the development of cocaine dependence. This latter Aim will be carried out in humans by testing siblings of cocaine-dependent subjects. Cocaine dependence is an enormous public health problem. The significance of this work lies in the potential for the ASR reduction to serve as a reliable, easily repeatable biological measure of cocaine-induced brain changes that may enhance outcome prediction so that tailored treatments may be directed at those patients most vulnerable to relapse, given the restriction of resources for available for substance abuse treatment.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Sep 2006
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2006
CompletedFirst Submitted
Initial submission to the registry
February 1, 2007
CompletedFirst Posted
Study publicly available on registry
February 2, 2007
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 19, 2011
CompletedStudy Completion
Last participant's last visit for all outcomes
July 19, 2011
CompletedAugust 7, 2019
August 1, 2019
4.9 years
February 1, 2007
August 5, 2019
Conditions
Outcome Measures
Primary Outcomes (1)
Acoustic startle magnitude
Magnitude of acoustic startle response as measured by electromyography of eyeblink.
at baseline
Study Arms (3)
1
Cocaine dependent subjects
2
Healthy controls
3
Siblings of cocaine dependent subjects
Interventions
acoustic startle testing: listening to sounds through headphones while the eyeblink component of the acoustic startle reflex is recorded with small surface electrodes
Eligibility Criteria
Subjects with cocaine dependence who are entering substance abuse treatment; siblings of these subjects; and healthy controls
You may qualify if:
- Cocaine dependent subjects:
- males or females,
- age 18-80,
- with a DSM-IV diagnosis of cocaine dependence,
- a usage history characterized by a minimum of 1 year of at least $50 per day or weekly binges of at least $200 of cocaine use.
You may not qualify if:
- current clinically significant medical illness (including HIV, because of possible confound of neurological involvement),
- current or past neurological illness, and no history of head trauma with loss of consciousness ≥ 5 minutes because of the possible confound of neurological damage to startle-modulating brain areas,
- other Axis I psychiatric disorder currently or in the previous three months with the exception of substance induced disorders as determined by SCID,
- history of schizophrenia, schizoaffective disorder, posttraumatic stress disorder, or bipolar disorder,
- known hearing impairments (intact hearing will be insured by brief audiology screening),
- dependence on other drugs or alcohol within the previous 6 months, as confirmed by ASI.
- Healthy controls:
- males or females,
- age 18-80.
- history of any Axis I psychiatric illness or history of treatment as determined by SCID Axis I,
- substance dependence or abuse history by ASI and SCID,
- no current clinically significant medical illness (including HIV),
- current or past neurological illness, or history of head trauma with loss of consciousness ≥ 5 minutes because of the possible confound of neurological damage to startle-modulating brain areas,
- known hearing impairments (intact hearing will be insured by brief audiology screening),
- Axis I disorder, including substance dependence, in first degree family member.
- +9 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Emory Universitylead
- National Institute on Drug Abuse (NIDA)collaborator
Study Sites (1)
Atlanta Veterans Adminstration Medical Center
Decatur, Georgia, 30033, United States
Biospecimen
Blood and extracted DNA
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Erica Duncan, MD
Emory University / Atlanta VA
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor
Study Record Dates
First Submitted
February 1, 2007
First Posted
February 2, 2007
Study Start
September 1, 2006
Primary Completion
July 19, 2011
Study Completion
July 19, 2011
Last Updated
August 7, 2019
Record last verified: 2019-08
Data Sharing
- IPD Sharing
- Will not share