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Clinical Trials/NCT01948674
NCT01948674
Completed
Phase 2

Cognitive Training in Adolescents During Treatment for Substance Use Disorders

Johns Hopkins University1 site in 1 country87 target enrollmentOctober 2013

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Substance Use Disorders
Sponsor
Johns Hopkins University
Enrollment
87
Locations
1
Primary Endpoint
working memory (change from baseline)
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this study is to see if computer tasks that challenge the brain (cognitively stimulating tasks) can improve memory and other types of thinking in adolescents and young adults who are being treated for substance use problems. The study will compare the effects of different versions of the computer tasks.

Registry
clinicaltrials.gov
Start Date
October 2013
End Date
August 2015
Last Updated
9 years ago
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Matthew Johnson

Associate Professor

Johns Hopkins University

Eligibility Criteria

Inclusion Criteria

  • age 14-21
  • Diagnosis of substance use disorder (SUD) by DSM-IV criteria with marijuana as primary substance of abuse
  • eligible for intensive outpatient treatment

Exclusion Criteria

  • Untreated psychiatric disorder that might make participation hazardous
  • Any condition associated with severe cognitive impairment

Outcomes

Primary Outcomes

working memory (change from baseline)

Time Frame: expected within 2 weeks after intervention

Secondary Outcomes

  • timeline follow back (change from baseline)(expected within 2 weeks after intervention)
  • emotion regulation (change from baseline)(expected within 2 weeks after intervention)
  • delay discounting (change from baseline)(expected within 2 weeks after intervention)
  • reading comprehension (change from baseline)(expected within 2 weeks after intervention)
  • Global Appraisal of Individual Needs (change from baseline)(expected within 2 weeks after intervention)
  • Stroop (change from baseline)(expected within 2 weeks after intervention)
  • Go-No Go (change from baseline)(expected within 2 weeks after intervention)

Study Sites (1)

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