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Clinical Trials/NCT01154686
NCT01154686UnknownNot Applicable

Working Memory Training in College Students With ADHD/LD

University of Toronto1 site in 1 country30 target enrollmentStarted: September 2009Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
30
Locations
1
Primary Endpoint
Paced Auditory Serial Addition Test (auditory verbal working memory measure)

Study Overview

Brief Summary

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.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 35 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Diagnosis of ADHD/Learning Disability
  • registered as a university student (full or part time)
  • registered at accessibilities services
  • taking at least one course

Exclusion Criteria

  • On a leave

Outcomes

Primary Outcomes

Paced Auditory Serial Addition Test (auditory verbal working memory measure)

Time Frame: within 120 days

Secondary Outcomes

  • Cognitive Failures Questionnaire(within 120 days)

Investigators

Sponsor Class
Other

Study Sites (1)

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