This randomized controlled trial evaluates the effectiveness of a 16-week structured sensory-motor integration exercise program compared to conventional therapy (Applied Behavior Analysis and massage therapy) in improving sensory processing abilities and balance in children aged 6-12 years diagnosed with Autism Spectrum Disorder (ASD). Outcomes are measured using the Short Sensory Profile and Berg Balance Scale at baseline and after 16 weeks of intervention. Findings aim to demonstrate the clinical utility of sensory-motor integration exercises in enhancing functional outcomes for children with ASD.

Children with Autism Spectrum Disorder often experience significant sensory processing issues and motor coordination challenges, particularly balance deficits. This study evaluates a sensory-motor integration intervention aimed at improving sensory modulation and motor abilities. Participants aged 6 to 12 years are randomized into two groups: an intervention group participating in structured sensory-motor exercises (64 sessions, 4 times weekly, 45 minutes per session), and a control group receiving conventional therapy (primarily Applied Behavior Analysis and massage therapy). Outcomes are assessed using standardized measures: the Short Sensory Profile (SSP) for sensory processing and the Berg Balance Scale (BBS) for balance, at baseline and immediately following the intervention period.

Inclusion Criteria:

• Age 6-12 years
• Diagnosed with Autism Spectrum Disorder (DSM-5 criteria)
• Mild-to-moderate ASD severity (CARS score ≤ 39.5)
• Ability to participate in structured sessions

Exclusion Criteria:

• Significant physical impairments or medical conditions affecting participation
• Recent (within 6 months) participation in sensory integration therapy

De-identified individual participant data (IPD) collected during the trial will be shared, including baseline characteristics, Short Sensory Profile (SSP) scores, and Berg Balance Scale (BBS) outcomes. No personally identifiable information will be shared.

IPD and supporting documents will be made available beginning 6 months after publication of the primary results and will remain accessible for at least 5 years.

Qualified researchers and healthcare professionals can request access to the data for scientific purposes. Requests should include a brief research proposal and data use agreement. Access will be granted through a secure platform or upon direct request to the principal investigator.