Attention Deficit Hyperactivity Disorder (ADHD) Clinical Trial
— IBBSOfficial title:
Integrated Brain, Body and Social Intervention (IBBS) for Attention Deficit Hyperactivity Disorder (ADHD)
Verified date | January 2018 |
Source | Yale University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The investigators are conducting this randomized trial to determine if IBBS (Integrated
Brain, Body, and Social)intervention is an effective treatment for ADHD (attention Deficit
Hyperactivity Disorder) in two culturally distinct settings; Hamden and New Haven,
Connecticut and Beijing, China. A subgroup of the children in the US will also participate in
an EEG study before and after IBBS and will be compared to a group of typically developing
children.
IBBS combines computer-presented brain exercises with a physical education curriculum, all of
which is designed to be fun, as well as to enhance sustained attention, inhibitory control
and other executive capacities.
IBBS is a school-based program in which groups children (composed of children with ADHD,
children at risk for ADHD, and typically developing children) alternate between a classroom
setting and the gymnasium four days a week for 15 weeks. These mixed age groups will be
composed of children with ADHD, children at-risk for ADHD, and typically developing children.
Although IBBS takes place in a group setting, the computer game component individualizes
instruction to maximize benefit for each child.
During the last year of the grant, we will be introducing a pilot study of an organizational
skills training (OST) that will provide individualized parent and child training for improved
executive functioning in children randomized to the OST plus home-based program.
Status | Completed |
Enrollment | 117 |
Est. completion date | July 2016 |
Est. primary completion date | July 2016 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 5 Years to 10 Years |
Eligibility |
Inclusion Criteria: - Boys and girls between 5 and 10 years of age, inclusive. - Diagnostic and Statistical Manual of Mental Disorders (DSM)-IV Diagnosis of ADHD (definite, probable, possible) based on a best estimate diagnosis using all available information. - IQ of greater or equal to 80 on the Abbreviated IQ Test - Currently not receiving any psychotropic medication or on a stable dose of medication prescribed for ADHD (psychostimulants, alpha agonists, atomoxetine, modafinil) for > 4 weeks. Exclusion Criteria: - English is a secondary language - Current DSM-IV diagnosis requiring alternative treatment, e.g., Major Depression, Bipolar Disorder, Autism Spectrum Disorder, or a psychotic disorder. - Presence of serious behavioral problems (tantrums, aggression, self-injury) for which another treatment is warranted or which could be too disruptive of the group treatment settings. - Significant medical condition or injury identified by school personnel (that would normally identify these issues such as the school nurse, physical education teacher, or child's primary pediatrician) that would prohibit or limit the child's ability to perform the physical activity component of the IBBS (e.g. uncontrolled asthma or a musculoskeletal injury or condition.) - Any restrictions that have been previously identified by the child's pediatrician to school personnel will, of course, be followed. - Children with conditions normally prohibiting exercise will be excluded. |
Country | Name | City | State |
---|---|---|---|
China | Capital Medical University | Beijing | Beijing |
China | Peking University | Beijing | Beijing |
United States | Hamden Public Schools | Hamden | Connecticut |
United States | Department of Psychiatry, Yale University | New Haven | Connecticut |
United States | Yale Child Study Center | New Haven | Connecticut |
Lead Sponsor | Collaborator |
---|---|
Yale University | BeCaid China, Beijing Sport University, C8Sciences, Capital Medical University, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), Hamden Public Schools, Connecticut, Peking University |
United States, China,
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* Note: There are 22 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Improvement in ADHD Severity From Baseline to End of Intervention | ADHD severity was measured by the Swanson, Nolan, and Pelham Rating Scale (SNAP)-IV-ADHD consists of 18 items that closely parallel in wording the diagnostic symptoms for ADHD as they appear in the DSM-IV. The range of scores are from 0 to 54. Higher scores indicate greater ADHD severity . The blinded assessors (Clinicians) used clinical judgement to provide an overall rating, based on all available information from the parents, teachers, and the assessors' own direct interactions with the child on the day of the assessment. | End of intervention is at a maximum of 15 weeks from baseline. | |
Secondary | Overall Improvement | Clinical Global Improvement Scale (CGI-I) - responders vs. non-responders. CGI is a seven point scale with the following anchor point: 1=Very Much Improved, 2=Much Improved, 3=Improved, 4=No change, 5=Minimally worse, 6=Much worse, 7=Very much worse. Participants with a score of 1, 2, or 3 at Endpoint were considered Responders; all others were considered non-responders. | 15 weeks for a total of 60 IBBS sessions vs. treatment as usual (TAU) |
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