Attention Deficit Hyperactivity Disorder Clinical Trial
Official title:
Home-Based Parent Training in ADHD Preschoolers
The purpose of this research is to evaluate and compare the effectiveness of two parenting
programs in reducing the ADHD symptoms and behavioral problems of preschool children with
ADHD through a controlled study. One program is a home-based parent training intervention
that is designed to enhance the parent-child interaction, constructive parenting skills, and
the child's tolerance for delay. The other intervention is a clinic-based parent training
program that focuses on reducing noncompliance in preschool children and improving parenting
skills.
Both programs consist of private weekly parenting sessions with Clinical Psychologists -
once a week for 8 weeks. The sessions are 1-1.5 hours in length. Both programs use behavior
modification as a means of improving oppositional and non-compliant child behavior. Both
interventions also involve procedures that focus on improving children's attention.
Neither program involves medication, and all families will receive one of the two parenting
programs being evaluated. Study evaluations, as well as participation in the parenting
programs, are provided at no cost to families. Evaluation and parenting sessions can be
scheduled at times convenient to families.
Status | Completed |
Enrollment | 187 |
Est. completion date | November 2014 |
Est. primary completion date | November 2014 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 3 Years to 4 Years |
Eligibility |
Inclusion Criteria: - Age = 3.0 - 4.11 - In preschool program at least 2 half days per week - Meets criteria for ADHD on clinical evaluation / DISC - ADHD severity: > 1.5 SD above mean for age/sex on CTRS-R - ADHD severity: > 1.0 SD above mean for age/sex on CPRS-R Exclusion Criteria: - Current Medication treatment for ADHD - IQ < 70 (Full Scale on WPPSI III) - Pervasive Developmental Disorder - Psychosis - Severe receptive language impairment - Neurological Disorder - Significant medical disorder - Primary caretaker is not able to participate - Non-English speaking primary care taker |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | NYU Child Study Center, One Park Avenue | New York | New York |
Lead Sponsor | Collaborator |
---|---|
New York University School of Medicine |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Conners Teacher Rating Scale | Behavior Rating Scale | Post-Treatment (within one week of the last treatment session / end of the 8 week waiting period) | No |
Secondary | Conners Parent Rating Scale | Behavior Rating Scale | Post-Treatment (within one week of the last treatment session / end of the 8 week waiting period) | No |
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