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Matching Treatments to Cognitive Deficits in Offenders With Substance Use Disorders

NCT06981351, Not applicable, Recruiting, The Mind Research Network

Trial 10

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

FieldValueSource
TitleMatching Treatments to Cognitive Deficits in Offenders With Substance Use DisordersClinicalTrials.gov
NCT numberNCT06981351ClinicalTrials.gov
StatusRecruitingClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment288 participants, estimatedClinicalTrials.gov
Lead sponsorThe Mind Research NetworkClinicalTrials.gov
ConditionsAntisocial BehaviorClinicalTrials.gov
InterventionsAttention to Context (ATC) training, Affective Cognitive Control (ACC) trainingClinicalTrials.gov
First posted2025-05-20ClinicalTrials.gov
Last updated2026-08-17ClinicalTrials.gov

Registered outcomes 10

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

ListOutcomeTime frameDescriptionSource
PrimaryCognitive task performance - StroopFrom enrollment to end of treatment at six weeksStroop task. Performance is quantified by number of correct responses (0 - 100)%.ClinicalTrials.gov
PrimaryCognitive task performance - Lexical Decision MakingFrom enrollment to end of treatment at six weeksLexical Decision Making task. Performance is quantified by number of correct responses (0 - 100%).ClinicalTrials.gov
PrimaryCognitive task performance - Delay DiscountingFrom enrollment to end of treatment at six weeksDelay Discounting task. Performance is quantified quantified by calculating where the answers place the respondent amid reference discounting curves. Range 0.0-0.5.ClinicalTrials.gov
PrimaryFunctional MRI - Go/NoGo task performanceChange assessed from enrollment to end of treatment at six weeksFunctional MRI task performance (Go/NoGo task). Performance is quantified by the number of 'false alarms' (responding to the NoGo stimulus). Range 0-39.ClinicalTrials.gov
PrimaryFunctional MRI - Go/Nogo brain responseActivity assessed during MRI scan. Change assessed from enrollment to end of treatment at six weeksChange (i.e. increased or decreased) in functional brain response (Blood Oxygen Level Dependent/BOLD) in region of interest (anterior cingulate) assessed using Statistical Parametric Mapping (SPM).ClinicalTrials.gov
PrimaryReal-World Outcomes - Substance use (TLFB)From enrollment to six months post-release from incarcerationSubstance use. Assessed using the timeline follow back (TLFB) - calendar recording dates of use for stimulant drugs.ClinicalTrials.gov
PrimaryReal-World Outcomes - Substance use (ASE)From enrollment to six months post-release from incarcerationSubstance use. Assessed using the Abstinence Self Efficacy scale (higher scores indicate greater difficulty with abstinence). Range 0-4.ClinicalTrials.gov
PrimaryReal-World Outcomes - Substance use (DUDIT)From enrollment to six months post-release from incarcerationSubstance use. Assessed using the Drug Use Disorders Identification test (higher scores indicate more/severe substance use). Range 0-44.ClinicalTrials.gov
PrimaryReal-World Outcomes - Criminal behaviorFrom enrollment to six months post-release from incarcerationCriminal behavior. Assessed using the Crime Inventory - records the number of instances of criminal behaviorClinicalTrials.gov
PrimaryRisky Impulsive Self-Destructive BehaviorFrom enrollment to six months post-release from incarceration
The RISQ questionnaire measures risky, impulsive, and self-destructive behaviors in 8 domains (aggression, self-harm, gambling, impulsive spending/driving, impulsive eating, risky sex, illegal behavior, and alcohol use). For each behavior, respondents note the number of times they have engaged in the behavior in their lifetime. Higher scores indicate more severe risky, impulsive, and self destructive behavior.
ClinicalTrials.gov

Outcomes 0

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

TypeOutcomeTime framePopulationUnitsMeasured asSource

Results by group 0

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

OutcomeGroupCategoryValueSpreadUnitsSource

Participant flow 0

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

PeriodMilestoneGroupParticipantsUnits countedSource

Adverse events 0

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

TypeEventOrgan systemGroupAffectedAt riskEventsSource

Adverse event totals 0

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource

Papers 0

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource

Trial comparisons 0

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

ComparisonSource

Tests 4

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

TestNamed asSource
Delay DiscountingPrimary outcomeConductCognition
Go/No-Go TaskPrimary outcomeConductCognition
Lexical Decision TaskPrimary outcomeConductCognition
Stroop Color-Word TestPrimary outcomeConductCognition

Source 4

FieldValueSource
Releasetrials-2026-11-12-0.3.0ClinicalTrials.gov
Release manifest SHA-2564a570df2e7274cee2d4fa2959402fab41880e2cd412e4b590390035fbea69391ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov

The same record as JSON

Release trials-2026-11-12-0.3.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.