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NCT01948674 Clinical Trial

Cognitive Stimulation in Adolescents

Substance Use Disorders Clinical Trial

Official title:
Cognitive Training in Adolescents During Treatment for Substance Use Disorders

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01948674
Other study ID # NA_00080023
Secondary ID R21DA034942
Status Completed
Phase Phase 2
First received September 17, 2013
Last updated August 22, 2016
Start date October 2013
Est. completion date August 2015

Study information
Verified date August 2016
Source Johns Hopkins University
Contact n/a
Is FDA regulated No
Health authority United States: Federal GovernmentUnited States: Institutional Review Board
Study type Interventional

Clinical Trial 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.

Recruitment information / eligibility
Status Completed
Enrollment 87
Est. completion date August 2015
Est. primary completion date August 2015
Accepts healthy volunteers No
Gender Both
Age group 14 Years to 21 Years
Eligibility 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

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Behavioral:
• Computerized tasks
The study will compare the effects of different methods of computerized mental stimulation. The intervention involves 25 sessions involving computerized cognitive tasks.

Locations
Country Name City State
United States Mountain Manor Treatment Center Baltimore Maryland

Sponsors (2)
Lead Sponsor Collaborator
Johns Hopkins University National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary working memory (change from baseline) expected within 2 weeks after intervention No
Secondary timeline follow back (change from baseline) expected within 2 weeks after intervention No
Secondary delay discounting (change from baseline) expected within 2 weeks after intervention No
Secondary Stroop (change from baseline) expected within 2 weeks after intervention No
Secondary reading comprehension (change from baseline) expected within 2 weeks after intervention No
Secondary emotion regulation (change from baseline) expected within 2 weeks after intervention No
Secondary Go-No Go (change from baseline) expected within 2 weeks after intervention No
Secondary Global Appraisal of Individual Needs (change from baseline) expected within 2 weeks after intervention No
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