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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03042338
Other study ID # R34MH102499
Secondary ID R34MH102499
Status Completed
Phase N/A
First received
Last updated
Start date March 31, 2017
Est. completion date July 31, 2018

Study information

Verified date June 2018
Source Florida State University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Feasibility study of Central Executive Training (CET) for ADHD. The goal of the current project is to develop and assess the feasibility, acceptability, engagement, and usability of a novel, central executive (CE) working memory training intervention.


Description:

The goal of the core study is to develop a central executive training (CET) intervention for children with attention-deficit/hyperactivity disorder (ADHD) and examine its feasibility, acceptability, engagement, and usability. This will involve early developmental work on software and treatment manuals followed by evaluation of the feasibility of enrolling, retaining, and treating ADHD children with CET. An evidence-informed intervention targeting central executive functioning in children with ADHD has the potential to result in clinically significant improvements in ADHD symptoms relative to extant behavioral treatments and capacity-based (short-term memory) training interventions. The long-term goal is to develop an efficacious and acceptable CET intervention with the potential for generalized improvements in, or normalization of, ADHD-related impairments in peer, family, and academic functioning.


Recruitment information / eligibility

Status Completed
Enrollment 54
Est. completion date July 31, 2018
Est. primary completion date July 31, 2018
Accepts healthy volunteers No
Gender All
Age group 8 Years to 13 Years
Eligibility Inclusion Criteria: - Children ages 8-12 with principal ADHD diagnoses (via K-SADS) - parent Behavior Assessment System for Children (BASC) Attention Problems or Hyperactivity subscale or ADHD-5 in clinical/borderline range based on age and gender - teacher BASC Attention Problems or Hyperactivity subscale or ADHD-5 scale in clinical/borderline range based on age and gender. Exclusion Criteria: - gross neurological, sensory, or motor impairment, history of a seizure disorder, or psychosis, bipolar disorders, substance use, or intellectual disability disorders - non-English speaking child or parent

Study Design


Related Conditions & MeSH terms

  • Attention Deficit Disorder with Hyperactivity
  • Attention Deficit Hyperactivity Disorder

Intervention

Behavioral:
CET: Central Executive Training
CET: Central Executive Training
CET: Comparison Executive Training
CET: Comparison Executive Training

Locations

Country Name City State
United States Florida State University Tallahassee Florida

Sponsors (3)

Lead Sponsor Collaborator
Florida State University National Institute of Mental Health (NIMH), National Institutes of Health (NIH)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Kaufman Test of Educational Achievement-3 (KTEA3) Reading Comprehension Growth scale value (GSV) Approximately 15 minute task administered during a 3 hour follow-up testing session occurring 2-4 months after last intervention session (variable time frame to account for school breaks)
Other NIH List Sorting Assessing feasibility of this test as possible primary outcomes for follow-up trial Approximately 15 minute task administered during a 3 hour follow-up testing session occurring 2-4 months after last intervention session (variable time frame to account for school breaks)
Other Teacher ADHD symptom ratings (ADHD-5 rating scale) Teacher questionnaire requiring approximately 15 minutes to complete, mailed to teacher within 2 weeks of child's last intervention session
Other Inhibition test Stop-signal and go/no-go scores will be combined via weighted average (factor score). Divergent validity (expected to improve more in comparison condition than experimental condition). Approximately 10 minute task administered during a 3 hour post-treatment testing session occurring within 2 weeks of last intervention session
Other Kaufman Test of Educational Achievement-3 (KTEA3) Listening Comprehension Growth scale value (GSV) Approximately 15 minute task administered during a 3 hour follow-up testing session occurring 2-4 months after last intervention session (variable time frame to account for school breaks)
Other Kaufman Test of Educational Achievement-3 (KTEA3) Math Concepts and Applications Growth scale value (GSV) Approximately 15 minute task administered during a 3 hour follow-up testing session occurring 2-4 months after last intervention session (variable time frame to account for school breaks)
Other Kaufman Test of Educational Achievement-3 (KTEA3) Reading Fluency Growth scale value (GSV) Approximately 15 minute task administered during a 3 hour follow-up testing session occurring 2-4 months after last intervention session (variable time frame to account for school breaks)
Other Kaufman Test of Educational Achievement-3 (KTEA3) Math Fluency Growth scale value (GSV) Approximately 15 minute task administered during a 3 hour follow-up testing session occurring 2-4 months after last intervention session (variable time frame to account for school breaks)
Primary Rapport visuospatial/phonological working memory test Outcome: stimuli correct Approximately 10 minute task administered during a 3 hour post-treatment testing session occurring within 2 weeks of last intervention session
Secondary Parent-reported ADHD symptoms (ADHD-5 rating scale) Parent questionnaire requiring approximately 15 minutes to complete, administered to parent while child is completing the 3 hour post-treatment testing session occurring within 2 weeks of last intervention session
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