Study of the Collaborative Life Skills Program
Completed · Not applicable
Conditions studied: Attention Deficit Hyperactivity Disorder Symptoms
In brief
This study tests the effectiveness of a newly developed integrated school-home behavioral intervention for behaviors related to Attention Deficit Hyperactivity Disorder (ADHD). The intervention is implemented by school-based mental health professionals within school settings.
Key facts
- Study ID
- NCT01686724
- Run by
- University of California, San Francisco
- People needed
- 504
- Starts
- 2012-09-01
- Expected to finish
- 2016-06-01
- Last updated by the study team
- 2019-06-18
Who can join
Age: 7 and older, up to 11. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Attending a participating school and in 2-5th grade
- Referral by LSP as a child with apparent ADHD-related problems
- ≥ 6 symptoms (item score ≥ 2) of Inattention or Hyperactivity-Impulsivity on the pooled parent and teacher Child Symptom Inventory
- ≥ 3 on the Impairment Rating Scale by parent and teacher (cross-situational impairment)
- FSIQ or VIQ ≥ 80 (necessary for cognitive demands of the child skills curriculum)
- Caretaker consents to participate in treatment, child assents to participate
You may not qualify if…
- Presence of conditions that are incompatible with this study's treatment.
- severe visual or hearing impairment,
- severe language delay,
- psychosis,
- pervasive developmental disorder
- Parent or child does not read or speak English or does not read or speak Spanish for our Spanish language implementation of CLS (inability to complete assessment measures or participate in group treatments).
- Child is in an all-day special education classroom (children in these classrooms are frequently receiving intensive behavior modification programs such that the intervention would be expected to require modification for use in these settings)
- Children taking psychotropic medication for any reason other than to treat ADHD
- Children planning to change (start or stop) psychotropic medication
- Children who have changed a regimen of psychotropic medication (started or stopped) within 30 days prior to screening
Where it is running
- University of California San Francisco — San Francisco, California, United States
Full record on ClinicalTrials.gov
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