Ireland
--:--IST
Recruiting Not applicable

Structured Sensory-Based Occupational Therapy in Children With Autism

NCT07789704 · tracked via the Priya Life Science Turkey tracker
Sponsor
Emre DANSUK
Phase
Not applicable
Started
2026-08-28
Last updated
2026-09-10

Condition(s) studied

Autism Spectrum Disorder

Investigational drug(s) / intervention(s)

Structured Sensory-Based Occupational TherapyIndividualized Home Activity Program

Structured 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.

Individualized 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.

Study 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.

Eligibility

Sex
ALL
Min age
3 Years
Max age
9 Years
Healthy volunteers
Accepted
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

Primary outcome measure(s)

  • Change in Occupational Performance — Baseline and Week 12
    Occupational 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 Performance — Baseline and Week 12
    Satisfaction with occupational performance will be assessed using the satisfaction score of the Canadian Occupational Performance Measure. Higher scores will indicate greater satisfaction.

Trial sites (1)

FacilityCityRegionStatus
Emre Dansuk Istanbul Beykoz Recruiting

More Emre DANSUK trials in Turkey

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07789704 on ClinicalTrials.gov ↗ ← All trials in Turkey