LearningRx Cognitive Training for ADHD

NCT ID: NCT02917109

Last Updated: 2018-02-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

3 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-09-30

Study Completion Date

2017-12-31

Brief Summary

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The purpose of this investigation is to conduct a series of case studies on the impact of LearningRx cognitive training on cognitive skills, brain structure, and daily functioning for participants with ADHD.

Detailed Description

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Using a multiple baseline design across cases with start point randomization, the proposed study will examine the outcomes from LearningRx one-on-one cognitive training across domains on standardized measures used to monitor treatment effectiveness for ADHD.

Conditions

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Attention Deficit Hyperactivity Disorder (ADHD)

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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LearningRx cognitive training

The intervention is a 60-hour, clinician-delivered cognitive training program.

Group Type EXPERIMENTAL

LearningRx cognitive training

Intervention Type BEHAVIORAL

A clinician will deliver three 90-minute cognitive training sessions per week for 14 weeks. There are 16 different categories of leveled training procedures sequenced in intensity and difficulty for a total of 530 training tasks.

Interventions

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LearningRx cognitive training

A clinician will deliver three 90-minute cognitive training sessions per week for 14 weeks. There are 16 different categories of leveled training procedures sequenced in intensity and difficulty for a total of 530 training tasks.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Age 15-22 previously diagnosed with ADHD
* High school students or college students with a prior diagnosis of ADHD living in the greater Colorado Springs area

Exclusion Criteria

* No braces, metal implants, or claustrophobia that would contraindicate magnetic resonance imaging
Minimum Eligible Age

15 Years

Maximum Eligible Age

22 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Gibson Institute of Cognitive Research

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Christina Ledbetter, PhD

Role: PRINCIPAL_INVESTIGATOR

Gibson Institute of Cognitive Research

Amy L Moore, PhD

Role: STUDY_DIRECTOR

Gibson Institute of Cognitive Research

Locations

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Gibson Institute of Cognitive Research

Colorado Springs, Colorado, United States

Site Status

Countries

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United States

Other Identifiers

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GICR-0916-A

Identifier Type: -

Identifier Source: org_study_id

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