Madison, Wisconsin 53705

  • Attention Deficit Hyperactivity Disorder

Purpose:

The investigators will perform a feasibility/pilot trial of two non-pharmacological interventions for ADHD in college students.


Study summary:

College students diagnosed with ADHD will be randomized to three arms of approximately 8 weeks duration: (1) standard care plus a tai chi class, (2) standard care plus an exercise class, and (3) standard care alone. The exercise class will control for the social and motor components of tai chi training. The investigators will determine methodological parameters relevant to a subsequent full scale trial including recruitment and retention rates, acceptance of randomization, adherence to the interventions, and variance in outcome measures. The primary clinical outcome measure of this pilot randomized controlled trial (RCT) will be pre- to post-intervention change in inattention, i.e. the Inattentive Symptoms subscale of the Conners Adult ADHD Rating Scale self-report long form (CAARS-S:L, see Interviews etc. "Converse_S_L"). Secondary measures to be explored will include self- and informant-report, neurocognitive measures, psychophysiological measures, and academic performance. Practice time will be assessed daily and follow-up self-report of ADHD symptoms will be gathered monthly for 3 months beyond the end of the intervention.


Criteria:

Inclusion Criteria: - University of Wisconsin-Madison enrolled undergraduate - Documented ADHD diagnosis Exclusion Criteria: - Unable or unwilling to participate in the interventions


NCT ID:

NCT02688959


Primary Contact:

Principal Investigator
Alexander K Converse, PhD
University of Wisconsin, Madison

Alexander K Converse, PhD
Phone: 608 265 6604
Email: adhd@bi.wisc.edu


Backup Contact:

N/A


Location Contact:

Madison, Wisconsin 53705
United States

Alexander K Converse, PhD
Phone: 608-265-6604
Email: adhd@bi.wisc.edu

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: August 02, 2021

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