- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01948674
Cognitive Stimulation in Adolescents
August 22, 2016 updated by: Matthew Johnson, Johns Hopkins University
Cognitive Training in Adolescents During Treatment for Substance Use Disorders
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.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
87
Phase
- Phase 2
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Maryland
-
Baltimore, Maryland, United States, 21229
- Mountain Manor Treatment Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
14 years to 21 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: computerized tasks- adaptive
|
The study will compare the effects of different methods of computerized mental stimulation.
The intervention involves 25 sessions involving computerized cognitive tasks.
|
|
Active Comparator: computerized tasks - nonadaptive
|
The study will compare the effects of different methods of computerized mental stimulation.
The intervention involves 25 sessions involving computerized cognitive tasks.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
working memory (change from baseline)
Time Frame: expected within 2 weeks after intervention
|
expected within 2 weeks after intervention
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
timeline follow back (change from baseline)
Time Frame: expected within 2 weeks after intervention
|
expected within 2 weeks after intervention
|
|
delay discounting (change from baseline)
Time Frame: expected within 2 weeks after intervention
|
expected within 2 weeks after intervention
|
|
Stroop (change from baseline)
Time Frame: expected within 2 weeks after intervention
|
expected within 2 weeks after intervention
|
|
reading comprehension (change from baseline)
Time Frame: expected within 2 weeks after intervention
|
expected within 2 weeks after intervention
|
|
emotion regulation (change from baseline)
Time Frame: expected within 2 weeks after intervention
|
expected within 2 weeks after intervention
|
|
Go-No Go (change from baseline)
Time Frame: expected within 2 weeks after intervention
|
expected within 2 weeks after intervention
|
|
Global Appraisal of Individual Needs (change from baseline)
Time Frame: expected within 2 weeks after intervention
|
expected within 2 weeks after intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Matthew W Johnson, PhD, Johns Hopkins University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
October 1, 2013
Primary Completion (Actual)
August 1, 2015
Study Completion (Actual)
August 1, 2015
Study Registration Dates
First Submitted
September 17, 2013
First Submitted That Met QC Criteria
September 19, 2013
First Posted (Estimate)
September 23, 2013
Study Record Updates
Last Update Posted (Estimate)
August 24, 2016
Last Update Submitted That Met QC Criteria
August 22, 2016
Last Verified
August 1, 2016
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- NA_00080023
- R21DA034942 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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