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Structured Sensory-Based Occupational Therapy in Children With Autism

Effects of Structured Sensory-Based Occupational Therapy on Occupational Performance and Sensory-Motor Outcomes in Children With Autism Spectrum Disorder: A Controlled Clinical Study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07789704
Enrollment
40
Registered
2026-08-27
Start date
2026-08-28
Completion date
2026-11-01
Last updated
2026-09-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Autism Spectrum Disorder

Keywords

Autism Spectrum Disorder, Occupational Therapy, Sensory-Based Intervention, Children

Brief summary

This controlled clinical study will investigate the effects of a 12-week structured sensory-based occupational therapy intervention on occupational performance, sensory processing, gross motor development, and eating behaviors in children with autism spectrum disorder. Forty children aged 3-9 years will be assigned to either an intervention group receiving face-to-face occupational therapy twice weekly or a control group receiving an individualized home program.

Detailed description

This controlled clinical study will evaluate the effects of a structured sensory-based occupational therapy intervention on occupational performance, sensory processing, gross motor development, and eating behaviors in children with autism spectrum disorder. A total of 40 children aged 3-9 years with Level 2 autism spectrum disorder will be assigned to a structured sensory-based occupational therapy group (n=20) or a control group (n=20). The intervention group will receive 40-minute, face-to-face occupational therapy sessions twice weekly for 12 weeks. The sessions will be structured according to each child's sensory and functional needs and will be progressively adapted based on the child's clinical development. The control group will receive individualized home recommendations, which will be monitored weekly using information and visual records provided by caregivers. Assessments will be performed at baseline and after 12 weeks. Occupational performance and satisfaction will be evaluated using the Canadian Occupational Performance Measure, sensory processing using the Dunn Sensory Profile, gross motor development using the Test of Gross Motor Development-Third Edition, and eating behaviors using the Children's Eating Behaviour Questionnaire.

Interventions

BEHAVIORALStructured Sensory-Based Occupational Therapy

The intervention will consist of individualized sensory-based occupational therapy activities addressing tactile, proprioceptive, vestibular, visual-motor, gross motor, feeding-related, and occupational performance needs. It will be delivered face-to-face for 40 minutes, twice weekly, over 12 weeks, and will be progressively adapted according to each child's clinical needs and development.

BEHAVIORALIndividualized Home Activity Program

Caregivers will implement individualized home-based sensory and functional activity recommendations using materials available in the home environment. The program will continue for 12 weeks and adherence will be monitored weekly through caregiver reports and visual records.

Sponsors

Emre DANSUK
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

Because of the nature of the interventions, participants and treating physiotherapists will be aware of the allocated intervention. Outcome assessments will be conducted by an independent physiotherapist who will be blinded to group allocation. Statistical analyses will be performed by a biostatistician who will be blinded to the coded group assignments.

Eligibility

Sex/Gender
ALL
Age
3 Years to 9 Years
Healthy volunteers
Yes

Inclusion criteria

* Children aged 3-9 years * Diagnosis of autism spectrum disorder according to DSM-5 criteria * Level 2 autism spectrum disorder * Residence in Istanbul * Written informed consent provided by a parent or legal guardian

Exclusion criteria

* Presence of an additional neurological, psychiatric, genetic, or developmental diagnosis * Regular medication use that may affect study outcomes * History of epilepsy or seizures * Inability to participate in the assessment or intervention procedures * Participation in another structured sensory-based occupational therapy program during the study period

Design outcomes

Primary

MeasureTime frameDescription
Change in Occupational PerformanceBaseline and Week 12Occupational performance will be assessed using the performance score of the Canadian Occupational Performance Measure. Higher scores will indicate better perceived occupational performance.
Change in Satisfaction with Occupational PerformanceBaseline and Week 12Satisfaction with occupational performance will be assessed using the satisfaction score of the Canadian Occupational Performance Measure. Higher scores will indicate greater satisfaction.

Secondary

MeasureTime frameDescription
Change in Sensory ProcessingBaseline and Week 12Sensory processing will be assessed using the Dunn Sensory Profile. Scale scores will be interpreted according to the instrument's standardized scoring system.
Change in Gross Motor DevelopmentBaseline and Week 12Gross motor development will be assessed using the Test of Gross Motor Development Third Edition, including locomotor and ball skills subscales. Higher scores will indicate better gross motor performance.
Change in Eating BehaviorsBaseline and Week 12Eating behaviors will be assessed using the Children's Eating Behaviour Questionnaire and its subscale scores.

Countries

Turkey (Türkiye)

Contacts

CONTACTEmre Dansuk, PhD
edansuk@medipol.edu.tr05377790434
CONTACTBurak Menek, PhD
PRINCIPAL_INVESTIGATOREmre DANSUK, PhD

Medipol University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 11, 2026