Working Memory Training in College Students With Attention-Deficit Hyperactivity Disorder/Learning Disabilities
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|ClinicalTrials.gov Identifier: NCT01154686|
Recruitment Status : Unknown
Verified June 2010 by University of Toronto.
Recruitment status was: Recruiting
First Posted : July 1, 2010
Last Update Posted : July 1, 2010
The overall objective of the current study is to determine whether computerized Working Memory (WM) training will enhance WM capacity in college students with Attention Deficit Hyperactivity Disorder (ADHD)/Learning Disabilities (LD). There are also three additional objectives. The first is to determine whether improvements in WM will generalize to secondary outcome tasks, such as inhibitory control and planning. The second objective is to examine whether WM training will also ameliorate ADHD symptoms of inattention and hyperactivity. The last objective is to investigate whether improvements will be maintained at a two month follow-up period.
It is expected that the computerized WM training program will enhance WM capacity in college students with ADHD. In addition, it is believed that these increases in WM capacity will also lead to improvements in other executive functions. It is also hypothesized that WM training will lead to a reduction in ADHD symptomology. Lastly, these improvements should be maintained at three month follow-up.
|Condition or disease||Intervention/treatment||Phase|
|Attention Deficit Disorder||Behavioral: Cogmed||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||30 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Working Memory Training in College Students With ADHD/LD|
|Study Start Date :||September 2009|
|Estimated Primary Completion Date :||September 2010|
|Estimated Study Completion Date :||September 2010|
- Paced Auditory Serial Addition Test (auditory verbal working memory measure) [ Time Frame: within 120 days ]
- Cognitive Failures Questionnaire [ Time Frame: within 120 days ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01154686
|Contact: Rachel Gropper, MA||(416) firstname.lastname@example.org|
|University of Toronto||Recruiting|
|Toronto, Ontario, Canada|
|Contact: Rachel Gropper, MA|
|Principal Investigator:||Rachel Gropper, MA||University of Toronto|