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Trial · NCT01067846

Cognitive Enhancement and Relapse Prevention in Cocaine Addiction

NCT01067846, Not applicable, Completed, University of Arkansas; results first posted 2013-11-26

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Cognitive Enhancement and Relapse Prevention in Cocaine Addiction. Trials, record NCT01067846. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01067846

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Cognitive Enhancement and Relapse Prevention in Cocaine Addiction
NCT number
NCT01067846
Status
Completed
Phases
Not applicable
Enrollment
85 participants, actual
Lead sponsor
University of Arkansas
Conditions
Cocaine Addiction
Interventions
Seromycin (D-cycloserine, DCS), Placebo, Computerized Cognitive Behavioral Therapy
First posted
2010-02-12
Last updated
2013-11-26
Results first posted
2013-11-26

Source ClinicalTrials.gov

Registered outcomes2

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryDrug Abstinence During Treatment and at Follow up VisitsParticipants provided urine samples for drug testing during treatment which occurred 3 times per week for 4 weeks, at the end of treatment, and at a 1 and 2 month follow up visitPercentage of the overall number of drug abstinences of participants measured by urine drug testing
PrimaryTreatment Retention - Number of Visits During TreatmentTreatment sessions included 3 visits per week for 4 weeksNumber of treatment visits attended prior to discontinuation of treatment

Outcomes2

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYDrug Abstinence During Treatment and at Follow up VisitsParticipants provided urine samples for drug testing during treatment which occurred 3 times per week for 4 weeks, at the end of treatment, and at a 1 and 2 month follow up visitTotal possible urine samples = 225 per arm. Not all participants stayed in treatment, therefore the total units analyzed will not match the total possible.percentage of drug abstinencesNUMBER
PRIMARYTreatment Retention - Number of Visits During TreatmentTreatment sessions included 3 visits per week for 4 weeksTotal possible sessions attended = 180 per arm. Some participants did not complete all sessions, therefore the units analyzed will not match the total possible.visitsMEAN

Results by group4

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Drug Abstinence During Treatment and at Follow up VisitsDCS and Cognitive Behavioral Therapy12percentage of drug abstinences
Drug Abstinence During Treatment and at Follow up VisitsPlacebo and Cognitive Behavioral Therapy25percentage of drug abstinences
Treatment Retention - Number of Visits During TreatmentDCS and Cognitive Behavioral Therapy10Standard Deviation 3visits
Treatment Retention - Number of Visits During TreatmentPlacebo and Cognitive Behavioral Therapy10Standard Deviation 3visits

Participant flow8

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDDCS and Cognitive Behavioral Therapy29
Overall StudySTARTEDPlacebo and Cognitive Behavioral Therapy30
Overall StudyCompleted 3 Tx SessionsDCS and Cognitive Behavioral Therapy15
Overall StudyCompleted 3 Tx SessionsPlacebo and Cognitive Behavioral Therapy15
Overall StudyCOMPLETEDDCS and Cognitive Behavioral Therapy10
Overall StudyCOMPLETEDPlacebo and Cognitive Behavioral Therapy11
Overall StudyNOT COMPLETEDDCS and Cognitive Behavioral Therapy19
Overall StudyNOT COMPLETEDPlacebo and Cognitive Behavioral Therapy19

Adverse events10

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
othercoughRespiratory, thoracic and mediastinal disordersDCS and Cognitive Behavioral Therapy1291
othercoughRespiratory, thoracic and mediastinal disordersPlacebo and Cognitive Behavioral Therapy0300
otherheadacheNervous system disordersDCS and Cognitive Behavioral Therapy1291
otherheadacheNervous system disordersPlacebo and Cognitive Behavioral Therapy0300
othernauseaGeneral disordersDCS and Cognitive Behavioral Therapy1291
othernauseaGeneral disordersPlacebo and Cognitive Behavioral Therapy0300
othersensation on skinSkin and subcutaneous tissue disordersDCS and Cognitive Behavioral Therapy0290
othersensation on skinSkin and subcutaneous tissue disordersPlacebo and Cognitive Behavioral Therapy1302
otherrash on skinSkin and subcutaneous tissue disordersDCS and Cognitive Behavioral Therapy0290
otherrash on skinSkin and subcutaneous tissue disordersPlacebo and Cognitive Behavioral Therapy1302

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityDCS and Cognitive Behavioral Therapy
Total, all-cause mortalityPlacebo and Cognitive Behavioral Therapy
Total, other adverse eventsDCS and Cognitive Behavioral Therapy329
Total, other adverse eventsPlacebo and Cognitive Behavioral Therapy230
Total, serious adverse eventsDCS and Cognitive Behavioral Therapy029
Total, serious adverse eventsPlacebo and Cognitive Behavioral Therapy030

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants1

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal years
R21DA025243The Clinical and Neural Response of Cocaine Addicts to Combination Treatment withKILTS, CLINTON DUNIV OF ARKANSAS FOR MED SCISNATIONAL INSTITUTE ON DRUG ABUSE2008 to 2009

Trial comparisons1

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

Comparison
DCS and Cognitive Behavioral Therapy vs Placebo and Cognitive Behavioral Therapy: serious adverse events

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT01067846

GET https://conductscience.org/api/trials/v1/NCT01067846/registered