About this trial
The goal of this clinical trial is to learn if an 8-week, community-based pickleball program can improve sensory-motor function and reduce the severity of core autism symptoms in adults ages 18-45 with autism spectrum disorder (ASD) who can participate independently without a caregiver.
The main questions it aims to answer are:
1. Does participating in the pickleball program improve sensory-motor function (including visual-motor integration and proprioceptive bias), measured using the HaptiKart task and a pickleball skill assessment? 2. Does participating in the pickleball program reduce core autism symptom severity, measured by the Social Responsiveness Scale, 2nd edition (SRS-2)?
Researchers will compare an early-start pickleball group to a delayed-start control group (who continues usual activities at first) to see if the pickleball program leads to greater improvements in sensory-motor outcomes and ASD symptom severity.
Participants will:
* Complete an in-person baseline visit at a local public library to provide written consent, complete surveys (SRS-2, PROMIS Depression and Sleep measures, and WHOQOL-BREF), and complete a video game-based sensory-motor assessment (HaptiKart). * Be randomly assigned to either start pickleball classes immediately or after an initial delay period. * Attend pickleball classes twice per week for 8 weeks (90 minutes per class; 16 sessions total), led by trained instructors at community indoor court facilities. * Continue their usual activities during periods when they are not assigned to pickleball classes. * Complete a brief pickleball skill assessment during the intervention period at their first and last class. * Complete follow-up assessments after each phase of the study to repeat surveys and sensory-motor testing. * Participants will also wear a small activity monitor (ActiGraph) during pickleball sessions to measure in-class physical activity levels, and complete brief online check-ins about safety/injury and program feedback during the intervention period.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Aged 18-45 years
Clinical diagnosis of autism spectrum disorder (ASD)
Able to participate in group-based activities without caregiver support
Able to understand English and independently communicate without assistance
Disqualifiers
Clinical diagnosis of intellectual disability (ID)
Does not have normal or corrected-to-normal vision
Actively participating in a racquet sport ≥1 time per week
Use of mobility aids
Trial design
Parallel
Treatments tested in this trial
Pickleball Program (Community-Based)
BehavioralGroup-based beginner-friendly pickleball classes delivered in community indoor court facilities. Sessions occur twice per week for 8 weeks (16 sessions total), approximately 90 minutes per session, led by trained instructors.
Treatment groups
Trial outcomes
Primary outcomes
Sensory-Motor Function (HaptiKart task outcomes)
Sensory-motor integration and proprioceptive bias measured using the HaptiKart videogame task.
Autism Symptom Severity (SRS-2 Total Score)
Core autism symptom severity measured by the Social Responsiveness Scale, 2nd edition (SRS-2), adult self-report, total score. The SRS-2 consists of 65 items rated on a 4-point Likert scale (1 = not true; 4 = almost always true). Raw total scores range from 0 to 195. Higher scores indicate greater severity of autism-related social impairment.
Secondary outcomes
Depression Symptoms (PROMIS Depression)
Self-reported depressive symptoms measured using the Patient-Reported Outcomes Measurement Information System (PROMIS) Emotional Distress-Depression-Short Form. (8-item version). Items are rated on a 5-point Likert scale (1 = never to 5 = always). Raw summed scores range from 8 to 40. Raw scores are converted to standardized PROMIS T-scores (mean = 50, standard deviation = 10) using established scoring tables. Higher T-scores indicate greater depressive symptom severity. T-scores will be used for primary analyses.
Sleep-Related Impairment
Self-reported sleep disturbance and sleep-related impairment measured using Patient-Reported Outcomes Measurement Information System (PROMIS) Sleep-Related Impairment - Short Form 8a. The instrument includes 8 items rated on a 5-point Likert scale. Raw summed scores range from 8 to 40. Raw scores are converted to standardized PROMIS T-scores (mean = 50, standard deviation = 10) using published scoring tables. Higher T-scores indicate greater sleep-related impairment (worse daytime functioning related to poor sleep). T-scores will be used for primary analyses.
Sleep Disturbance
Sleep disturbance will be measured using the Patient-Reported Outcomes Measurement Information System (PROMIS) Sleep Disturbance-Short Form 8b. The instrument includes 8 items rated on a 5-point Likert scale. Raw summed scores range from 8 to 40. Raw scores are converted to standardized PROMIS T-scores (mean = 50, standard deviation = 10) using published scoring tables. Higher T-scores indicate greater sleep disturbance (worse perceived sleep quality). T-scores will be used for primary analyses.
Quality of Life (WHOQOL-BREF)
Quality of life will be measured using the World Health Organization Quality of Life-BREF (WHOQOL-BREF). The WHOQOL-BREF contains 26 items rated on a 5-point Likert scale and yields four domain scores: Physical Health, Psychological Health, Social Relationships, and Environment. Raw domain scores are transformed to a 0-100 scale according to WHO scoring guidelines. Higher scores indicate better quality of life. Domain scores will be analyzed as continuous outcomes.
Other outcomes
Pickleball Skill Performance
Pickleball performance measured using a structured ball-return assessment with coach fed-ball trials and scored for accuracy and paddle contact quality.
Physical Activity During Sessions (ActiGraph)
Physical activity level during pickleball sessions measured using wearable accelerometry (ActiGraph).
Sponsors and contacts
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