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Organizational Skills Training for Children With Attention Deficit Hyperactivity Disorder

NYU Langone Health logo

NYU Langone Health

Status

Completed

Conditions

Attention Deficit Disorder With Hyperactivity

Treatments

Behavioral: Contingency management (CM)
Behavioral: Organizational Skills Training

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT00381407
DDTR B2-NDH
R01MH074013 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This study will evaluate the effectiveness of organizational skills training in improving organizational, time management, and planning difficulties in children with attention deficit hyperactivity disorder.

Full description

Attention deficit hyperactivity disorder (ADHD) is one of the most common mental disorders among children. Children with ADHD frequently lack organizational, time management, and planning skills. These deficits can cause impaired functioning in multiple settings, including home, school, and peer relationships. Advancements in treatment options for these deficits, however, have been minimal. Previous research has indicated that organizational skills training (OST) is an effective intervention for improving organizational skills in children with ADHD. Its effectiveness relative to other available treatments is unknown. This study will compare the effectiveness of OST with that of contingency management (CM) and a waitlist condition in improving organizational, time management, and planning skills deficits in children with ADHD.

Participants in this study are randomly assigned to OST, CM, or Wait-List (WL). Participants in the OST and CM groups attend 20 1-hour sessions over 10 weeks. OST trains children to use a variety of techniques for improving their organizational skills. Both children and their parents attend every OST session. CM does not involve skills training. Rather, CM trains parents and teachers to identify desired "end" behaviors and to increase the frequency of these behaviors through the use of a structured reward system. Both children and their parents attend every CM session, but the children's participation will be minimal. Participants assigned to the waitlist condition will have the opportunity to receive their choice of either OST or CM once they have completed the study. All participants attend follow-up visits 1 month post-treatment. Participants assigned to OST and CM attend follow-up visits after 1 and 4 months into their next school grade. School performance, feelings about school, ADHD symptoms, organizational skills, family environment, medication or services received, and use of treatment strategies will be assessed at each follow-up visit.

Enrollment

157 patients

Sex

All

Ages

8 to 11 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Between grades 3 and 5 in school
  • Meets criteria for ADHD, any subtype (a formal diagnosis prior to study entry is not necessary)
  • Meets minimum score requirements on either Conners Parent or Conners Teacher Rating Scales
  • Meets minimum criteria for organizational, time management, and planning deficits, as reported by parent or teacher
  • Estimated IQ is greater than 85, as determined by the Wechsler Abbreviated Scale of Intelligence
  • Has a teacher that is willing to participate
  • Parents' schedule will allow attendance at study visits

Exclusion criteria

  • Attends an all-day special education classroom or works with a para-professional in school
  • Diagnosis of pervasive developmental disorder (PDD), psychosis, bipolar disorder, or post-traumatic stress disorder (PTSD)
  • Current history of significant suicidality or sexual or physical abuse
  • Any other comorbid psychiatric diagnosis or medical condition with significant symptoms that may interfere with study participation (e.g., severe depression, obsessive-compulsive disorder [OCD], or cystic fibrosis)
  • Child's teacher has previously participated in this study

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

157 participants in 3 patient groups

1
Experimental group
Description:
Participants will receive organizational skills training program
Treatment:
Behavioral: Organizational Skills Training
2
Experimental group
Description:
Participants will receive contingency management program
Treatment:
Behavioral: Contingency management (CM)
3
No Intervention group
Description:
Participants will receive wait list condition

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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