ClinicalTrials.Veeva

Menu

Motor Attention Training for Attention Deficit Hyperactivity Disorder (ADHD)

University of Wisconsin (UW) logo

University of Wisconsin (UW)

Status

Enrolling

Conditions

Attention Deficit Hyperactivity Disorder

Treatments

Behavioral: Exercise
Behavioral: Tai Chi

Study type

Interventional

Funder types

Other

Identifiers

NCT02688959
VCRGE\WAISMAN CENTER\WAISMAN (Other Identifier)
2015-0807
A348700 (Other Identifier)
Protocol version 15 July 2024 (Other Identifier)

Details and patient eligibility

About

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

Full description

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.

Enrollment

145 estimated patients

Sex

All

Ages

18 to 23 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • University of Wisconsin-Madison enrolled undergraduate
  • Documented ADHD diagnosis

Exclusion criteria

  • Unable or unwilling to participate in the interventions

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

145 participants in 3 patient groups

Tai Chi
Experimental group
Description:
Participants in this arm will attend 50-minute classes 2 times per week for 8 weeks. The course will emphasize experiential learning with 2 weeks of introductory sessions on gait, posture, and tai chi principles followed by instruction in the 24-form Yang style sequence. Students will be given a video to aid learning outside of class, and maintenance of practice post-intervention.
Treatment:
Behavioral: Tai Chi
Exercise
Active Comparator group
Description:
Participants in the exercise arm will attend 50-minute classes 2 times per week for 8 weeks. The course will emphasize cardio-aerobic fitness training. Students will be given a video to aid practice outside of class, and maintenance of practice post-intervention.
Treatment:
Behavioral: Exercise
Control
No Intervention group
Description:
Participants in the control arm will not attend a class and not be given a video.

Trial contacts and locations

1

Loading...

Central trial contact

Alexander K Converse, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems