Clinical Trials Directory

Trials / Completed

CompletedNCT03335748

the Cogmed Program for Youths With ADHD

Is the Cogmed Program Effective for Youths With ADHD Under Pharmacological Treatment?

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Université du Québec a Montréal · Academic / Other
Sex
All
Age
7 Years – 13 Years
Healthy volunteers
Not accepted

Summary

The primary objective of this study was to examine the effects of the Cogmed training program on working memory among youths 7 to 13 years old, while controlling presence and presentation of ADHD-related comorbidity. A secondary objective was to examine the generalization of effects to ADHD symptoms, non-verbal reasoning, attentional and executive functions, motor impulsivity, reading comprehension, and mathematical reasoning. Participants were under pharmacological treatment for ADHD combined type and a comorbidity. They were randomized into an experimental group that received the Cogmed program and an active control group that received a low-intensity comparison version of the training. They were evaluated at three time points: six weeks prior to intervention onset (T1), immediately prior to onset(T2), and one week following intervention completion (T3).

Detailed description

Participants completed the Cogmed WM training program at home.Each training session lasted from 30 to 45 minutes and was supervised by a parent. For five consecutive weeks, participants had to complete at least five sessions per week.

Conditions

Interventions

TypeNameDescription
OTHERCognitive training Cogmed programCognitive training Cogmed program

Timeline

Start date
2014-02-22
Primary completion
2014-09-22
Completion
2015-09-22
First posted
2017-11-08
Last updated
2017-11-08

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT03335748. Inclusion in this directory is not an endorsement.