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Clinical Trials/NCT00930449
NCT00930449
Completed
N/A

Effects Of A Computerized Working Memory Training Program On Attention, Working Memory, And Academics, In Adolescents With Severe ADHD/LD

The Hospital for Sick Children2 sites in 1 country120 target enrollmentNovember 2008

Overview

Phase
N/A
Intervention
Not specified
Conditions
Attention Deficit Disorder With Hyperactivity
Sponsor
The Hospital for Sick Children
Enrollment
120
Locations
2
Primary Endpoint
Automated Working Memory Assessment Listening Recall
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

Our primary aim is to determine whether a computerized working memory (WM) training program will help students with severe learning and attention problems, in terms of improving their WM. Additional aims are to determine whether the WM training will also result in improvements in the students' concentration and school work, and how long any beneficial effects will last (i.e., whether the students will continue to show improvements once the training program has stopped).

Detailed Description

We have established a collaborative partnership between OISE, HSC, OPDS, and JVS to evaluate the effectiveness of a WM training program when conducted in a school setting. To determine whether the WM training program does improve WM, attention, behaviour, and/or academic achievement, we will compare its effects to those expected to result from two other intervention programs that focus on academic skills only: 1) a computerized software program known to improve math skills (Academy of Math®); and 2) extra, individualized tutoring in an area of academic weakness supervised by a trained and experienced staff person. We will assess WM, related cognitive abilities, ADHD symptoms, academic achievement, before and after intervention, and also at 3- and 6-month follow-up to determine whether any improvements are sustained and increased after the training has finished.

Registry
clinicaltrials.gov
Start Date
November 2008
End Date
January 2012
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Rosemary Tannock

Senior Scientist

The Hospital for Sick Children

Eligibility Criteria

Inclusion Criteria

  • fulltime enrollment at one of the three English-language speaking OPDS schools
  • confirmed diagnosis of a specific LD with or without comorbid ADHD
  • IQ \> 80 (based on WISC-IV)
  • English as the primary spoken language

Exclusion Criteria

  • uncorrected sensory impairments (vision, hearing)
  • severe comorbid mental health disorders requiring medications other than those used for ADHD or intensive treatment
  • severe impairments in oral communication, impeding intelligibility of spoken responses

Outcomes

Primary Outcomes

Automated Working Memory Assessment Listening Recall

Time Frame: 15-20 min

CANTAB Spatial Working Memory

Time Frame: 15-20 min

Secondary Outcomes

  • Wide Range Achievement Test 4 Progress Monitoring Version: word reading, spelling, sentence comprehension, math computation(10-15 min)
  • Teacher - Children's Organizational Skills Scale(5 min/student)
  • Teacher - Strengths and Weakness of ADHD-symptoms and Normal-behavior scale (SWAN)(5 min/student)

Study Sites (2)

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