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Clinical Trials/NCT02444208
NCT02444208CompletedNot Applicable

Randomized Clinical Trial (01): A Feasibility Trial for Inhibitory-Control Training to Reduce Cocaine Use

University of Kentucky1 site in 1 country40 target enrollmentStarted: May 1, 2015Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
40
Locations
1
Primary Endpoint
Stop-Signal Task

Study Overview

Brief Summary

Cocaine abuse is an unrelenting public-health concern. Behavioral therapies are considered the "standard of care" for reducing cocaine use and preventing relapse. However, even with intense behavioral interventions, rates of relapse to cocaine use are discouragingly high (i.e., 60-95% of patients return to drug use). Novel strategies are urgently needed to improve treatment outcomes for cocaine-use disorders. The overarching goal of this project is to assess the feasibility, acceptability and initial efficacy of an innovative cocaine-based inhibitory-control training procedure. This goal will be accomplished through the conduct of a Stage I pilot trial. Cocaine-dependent participants will be enrolled and randomized to receive inhibitory-control training to cocaine or neutral images (N=20/condition). This proposed intervention, cocaine based inhibitory-control training, will be delivered using an innovative computer program which teaches cocaine abusers to inhibit a pre-potent response to cocaine or neutral cues. The primary hypothesis is the proposed procedures are feasible and acceptable to the participants. Feasibility will be assessed by determining time needed to enroll the target sample; adaptive randomization outcomes; participant attendance, completion and adherence to study procedures. Acceptability will be determined using a Treatment Acceptability Questionnaire. The secondary hypothesis is that participants receiving cocaine-based inhibitory-control training will reduce their drug use to a greater extent than their counterparts in the neutral-image condition. Reduced cocaine use will be demonstrated by fewer positive-urine samples using qualitative urinalysis and a reduction in levels of benzoylecgonine as determined by quantitative urinalysis (i.e., ELISA). The third hypothesis is that participants receiving cocaine-based inhibitory-control training will show improved inhibitory control and neurocognitive functioning relative to their counterparts in the neutral-image condition. Improved inhibitory control, impulsivity and cognitive functioning will be demonstrated using a battery of clinical instruments and laboratory tasks. The proposed research is highly innovative in that it will provide critical information regarding the feasibility, acceptability, initial efficacy of cocaine-based inhibitory-control training to reduce drug use and improve inhibitory control and neurocognitive functioning in cocaine-dependent participants. Cocaine-based inhibitory control training is also easy to administer (i.e., 15 minutes), inexpensive, need not be administered by a clinician, and could easily be incorporated into current behavioral or community-based treatment approaches to enhance sustained abstinence, thereby quickly impacting clinical research and practice.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Factorial
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 55 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Recent cocaine use verified by a cocaine-positive urine sample
  • •Meet Cocaine Abuse or Dependence criteria, verified by computerized Structured Clinical Interview for DSM-IV (SCID)
  • •Subjects must be seeking treatment for their cocaine use.
  • •Subjects must have at least 10% errors in response to cocaine go cues on the ABBA Task at baseline

Exclusion Criteria

  • •History of serious physical or psychiatric disease that would interfere with study participation
  • •Current physical or psychiatric disease that would interfere with study participation
  • •Current or past histories of substance abuse or dependence that would interfere with study completion

Arms & Interventions

Cocaine Inhibitory Control Training

Experimental

This group will receive active inhibitory control training.

Intervention: Active Inhibitory Control Training (Behavioral)

Neutral Inhibitory Control Training

Placebo Comparator

This group will receive neutral inhibitory control training.

Intervention: Neutral Inhibitory Control Training (Behavioral)

Outcomes

Primary Outcomes

Stop-Signal Task

Time Frame: 8 weeks after study entry

Response inhibition and response execution will be measured using a stop-signal paradigm using a choice reaction time task that engages participants in responding to go-signals when stop-signals occasionally inform them to inhibit the response.

Secondary Outcomes

  • Self-Reported Cocaine Use(7 days)
  • Retention(8, 9 and 10 weeks after study entry)
  • Protocol Adherence(Three years)
  • Biologically verified cocaine use(72 hours)
  • Recruitment(Three years)
  • Treatment acceptability(8, 9 and 10 weeks after study)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Craig Rush

Professor

University of Kentucky

Study Sites (1)

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