search
Back to results

Retrain Your Brain in Children/Adolescents With Bipolar Disorder: A Pilot Study (COGFLEX)

Primary Purpose

Bipolar Disorder, Pediatric Bipolar Disorder, Childhood-onset Bipolar Disorder

Status
Unknown status
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
COGFLEX-skill building levels
COGFLEX-control condition
Sponsored by
Bradley Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bipolar Disorder focused on measuring bipolar disorder, child, adolescent

Eligibility Criteria

7 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 7-17 years old
  • bipolar disorder type I preferred (at least 1 week of mania)

Exclusion Criteria:

  • no implanted metal (no braces, no cochlear implants)
  • can not have full Diagnostic and Statistical Manual 4th Edition (DSM-IV) autistic disorder
  • no active drug/alcohol abuse/dependence

Sites / Locations

  • Bradley HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

COGFLEX-skill building levels

COGFLEX-control condition

Arm Description

In the R33, children will be randomized to receive either COGFLEX with skill-building levels or just baseline/non-probabilistic trials. All children will play COGFLEX twice per week for 8-weeks.

In the R33, children will be randomized to receive either COGFLEX with skill-building levels or the control condition--which is just baseline/non-probabilistic trials. All children will play COGFLEX twice per week for 8-weeks.

Outcomes

Primary Outcome Measures

Change in functional magnetic resonance imaging (fMRI) brain activation
We will compare functional magnetic resonance imaging (fMRI) brain activation from week 1 (before intervention starts) to week 8 (after intervention is complete).

Secondary Outcome Measures

Change in Clinician global Impression Improvement-Irritability
Clinician global Impression Improvement-Irritability

Full Information

First Posted
September 20, 2013
Last Updated
January 16, 2018
Sponsor
Bradley Hospital
Collaborators
National Institute of Mental Health (NIMH)
search

1. Study Identification

Unique Protocol Identification Number
NCT01954680
Brief Title
Retrain Your Brain in Children/Adolescents With Bipolar Disorder: A Pilot Study
Acronym
COGFLEX
Official Title
COGFLEX: Pilot Translational Intervention of Pediatric Bipolar Disorder
Study Type
Interventional

2. Study Status

Record Verification Date
January 2018
Overall Recruitment Status
Unknown status
Study Start Date
August 2013 (undefined)
Primary Completion Date
September 2018 (Anticipated)
Study Completion Date
September 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Bradley Hospital
Collaborators
National Institute of Mental Health (NIMH)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The main aim of this study is to test a new, non-medication computer-based potential treatment for bipolar disorder in children and adolescents. In the study, children and adolescents with bipolar disorder will come to our lab at Bradley Hospital 2-times per week for 8-weeks to "play" a custom computer "game" designed to retrain the brain--to build a skill that my work has shown is impaired in children/adolescents with bipolar disorder. Before and after this 8-week trial, children will have a special magnetic resonance imaging (MRI) scan. This is a test of feasibility--meaning we want to see if the 8-week trial results in brain changes. If it does, we will conduct a second study to see if it improves how bipolar children function--i.e., if it helps their illness.
Detailed Description
Prior studies have shown that "computer assisted cognitive remediation"--meaning using computer "games" to build up a skill that has been shown to be impaired in a specific disorder--can result in improvement in psychiatric illnesses--including schizophrenia. This will be the first National Institute of Mental Health (NIMH)-funded study to use this "retrain your brain" approach in children and adolescents with bipolar disorder. During this study, we are seeking 40 children and adolescents with bipolar disorder to: come to our lab at Bradley Hospital in East Providence R.I. twice per week (each lasting 1 hour) to "play" a special computer game for a total of 8 weeks to have a special MRI before and after this 8-week trial to see if our "game" improves brain activity it does NOT matter if your child is already on medications--they can continue during this study all children/adolescents with bipolar disorder are welcome--as long as they do NOT have implanted metal (no braces, no cochlear implants, etc) because of magnetic resonance imaging (MRI) safety. This is a test of feasibility--meaning we want to see if the 8-week trial results in brain changes. If it does, we will conduct a second study to see if it improves how bipolar children function--i.e., if it helps their illness.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bipolar Disorder, Pediatric Bipolar Disorder, Childhood-onset Bipolar Disorder
Keywords
bipolar disorder, child, adolescent

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Model Description
R21 phase was an open phase 1a trial for feasibility and acceptability with enrollment goal including intervention development of 20. R33 phase enrollment goal of 40 including double-blind placebo-controlled randomized trial of 2 versions of video game potential intervention.
Masking
ParticipantCare ProviderOutcomes Assessor
Masking Description
Neither participant nor independent evaluator knows group assignment in R33 phase randomized controlled trial.
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
COGFLEX-skill building levels
Arm Type
Experimental
Arm Description
In the R33, children will be randomized to receive either COGFLEX with skill-building levels or just baseline/non-probabilistic trials. All children will play COGFLEX twice per week for 8-weeks.
Arm Title
COGFLEX-control condition
Arm Type
Experimental
Arm Description
In the R33, children will be randomized to receive either COGFLEX with skill-building levels or the control condition--which is just baseline/non-probabilistic trials. All children will play COGFLEX twice per week for 8-weeks.
Intervention Type
Behavioral
Intervention Name(s)
COGFLEX-skill building levels
Other Intervention Name(s)
COGFLEX is a computer assisted cognitive remediation
Intervention Description
COGFLEX--in English-- is a computer game designed to build up a specific skill that our work has shown is impaired in children and adolescents with bipolar disorder). In the R33, children will be randomized to receive either COGFLEX with skill-building levels or COGFLEX-control condition which is just baseline/non-probabilistic trials. All children will play COGFLEX twice per week for 8-weeks. This same approach has shown great success in many psychiatric disorders including schizophrenia. This is the first such study in children/adolescents with bipolar disorder.
Intervention Type
Behavioral
Intervention Name(s)
COGFLEX-control condition
Intervention Description
In the R33, the control condition will be the same COGFLEX "game"--but just baseline/non-probabilistic trials. All children will play COGFLEX twice per week for 8-weeks.
Primary Outcome Measure Information:
Title
Change in functional magnetic resonance imaging (fMRI) brain activation
Description
We will compare functional magnetic resonance imaging (fMRI) brain activation from week 1 (before intervention starts) to week 8 (after intervention is complete).
Time Frame
Change from week 1 to week 8
Secondary Outcome Measure Information:
Title
Change in Clinician global Impression Improvement-Irritability
Description
Clinician global Impression Improvement-Irritability
Time Frame
Change from week 1 to week 8

10. Eligibility

Sex
All
Minimum Age & Unit of Time
7 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 7-17 years old bipolar disorder type I preferred (at least 1 week of mania) Exclusion Criteria: no implanted metal (no braces, no cochlear implants) can not have full Diagnostic and Statistical Manual 4th Edition (DSM-IV) autistic disorder no active drug/alcohol abuse/dependence
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Daniel Dickstein, M.D.
Organizational Affiliation
Bradley Hospital/Alpert Medical School of Brown University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Bradley Hospital
City
East Providence
State/Province
Rhode Island
ZIP/Postal Code
02915
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
PediMIND Program
Phone
401-432-1600
Email
pedimind@gmail.com
First Name & Middle Initial & Last Name & Degree
Daniel Dickstein, M.D.

12. IPD Sharing Statement

Learn more about this trial

Retrain Your Brain in Children/Adolescents With Bipolar Disorder: A Pilot Study

We'll reach out to this number within 24 hrs