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School-Based Sensory Processing and Daily Living Skills-Focused Occupational Therapy Program

Ç

Çankırı Karatekin University

Status

Not yet enrolling

Conditions

Autism Spectrum Disorder (ASD)
Intellectual Disability, Variable

Treatments

Behavioral: Task-Oriented Activities of Daily Living Training
Behavioral: Sensory Preparation Using Proprioceptive, Vestibular, and Tactile Input
Behavioral: Family Education and Written Home Program
Behavioral: Individual School-Based Occupational Therapy Sessions
Behavioral: Generalization and Classroom-Based Sensory Support Strategies

Study type

Interventional

Funder types

Other

Identifiers

NCT07326267
2529c9d3ba6d4dce

Details and patient eligibility

About

This study aims to develop and evaluate a school-based occupational therapy program focused on sensory processing and activities of daily living for children with Autism Spectrum Disorder and Intellectual Disability. Sensory processing difficulties often affect school participation, behavior regulation, and independence in daily tasks. Although occupational therapy interventions have shown benefits in clinical settings, evidence for their use in schools is limited.

The trial will take place at Vali Ayhan Çevik Special Education School and will enroll students aged 6 to 14 years. Participants will be randomly assigned to either an intervention group or a control group. The intervention group will receive weekly 50-minute occupational therapy sessions for 10 to 12 weeks, including sensory preparation, task-oriented practice, and strategies to support everyday skills. The control group will receive family education, a written home program, and routine school observation.

Outcomes will be assessed at baseline, after the intervention, and at 4 to 6-week follow-up. The main outcome is change in Goal Attainment Scaling scores, which reflect progress toward individualized goals. Additional measures include functional ability, sensory processing, and demographic and clinical information. The study will also monitor feasibility and how closely the program is delivered as planned.

This research is expected to provide evidence on the feasibility and effects of a standardized occupational therapy program in a school setting and to support the use of similar approaches in educational contexts.

Full description

This project aims to develop and evaluate a School-Based Occupational Therapy Program focused on Sensory Processing and Activities of Daily Living (ADL) through a randomized controlled feasibility trial. Children with Autism Spectrum Disorder (ASD) and Intellectual Disability (ID) frequently experience sensory processing difficulties that adversely affect school participation, behavioral regulation, and independence in ADLs. Although the effectiveness of sensory-based and ADL-focused occupational therapy interventions has been demonstrated in clinical settings, evidence regarding their standardized, high-fidelity implementation within school environments remains limited.

The study will be conducted at Vali Ayhan Çevik Special Education School and will include students aged 6-14 years. Using a two-arm, parallel-group randomized controlled design, participants will be randomly allocated (1:1) to either an intervention group or a control group. The intervention group will receive once-weekly, 50-minute occupational therapy sessions over 10-12 weeks, comprising sensory preparation, task-oriented ADL practice, and generalization activities. The control group will receive family education, a written home program, and routine school observation. Outcome assessments will be conducted at baseline (T0), post-intervention (T1), and follow-up (T2; 4-6 weeks).

The primary outcome measure will be the Goal Attainment Scaling (GAS) T-score, reflecting progress toward individualized, occupation-based goals. Secondary outcomes will include the Pediatric Disability Assessment Inventory (PEDI), Sensory Profile, and a Pediatric Information Form capturing demographic and clinical routine data. Feasibility indicators-such as attendance rate, data completeness, and classroom micro-protocol utilization-as well as intervention fidelity measures, including session checklists and secondary rater/video-based evaluations, will be systematically monitored.

Expected outcomes include clinically meaningful improvements in GAS scores and ADL-related indicators in the intervention group, alongside enhanced sensory equipment infrastructure and the development of teacher micro-protocols to strengthen institutional capacity. This study aims to address a significant gap in the literature on school-based occupational therapy in Türkiye by providing a feasible, standardized, and replicable intervention model for special education settings.

Enrollment

40 estimated patients

Sex

All

Ages

6 to 14 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Regular school attendance (Anticipated ability to attend at least 70% of the planned intervention sessions during the study period);
  • Written informed consent obtained from the family;
  • Formal diagnosis of Autism Spectrum Disorder or Intellectual Disability, documented by an official disability report;
  • Presence of observable difficulties in sensory processing and activities of daily living (ADL), verified through the student's Individualized Education Program (IEP) records;
  • Ability to partially follow single-step basic instructions, as documented in the IEP records;
  • Willingness of families and teachers to participate in follow-up assessments (T2 and beyond).

Exclusion criteria

  • Uncontrolled epilepsy or other medical conditions that may interfere with participation or safety during sessions.
  • Medical contraindications to modalities such as swinging or deep pressure or severe musculoskeletal limitations preventing participation in task-oriented ADL practice.
  • Being in a period of severe acute behavioral crisis;
  • Concurrent participation in occupational therapy or special education programs for ≥2 hours per week that would compromise data interpretation;
  • Presence of severe visual or hearing impairments that would substantially limit the child's ability to perceive sensory stimuli, follow task instructions, or validly engage in assessment procedures;
  • Inability to maintain family and/or teacher collaboration throughout the intervention period;
  • Inconsistent school attendance during the intervention period (e.g., prolonged absenteeism);
  • Insufficient language comprehension to engage with basic task instructions even with support.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

40 participants in 2 patient groups

School-Based OT (Sensory + ADL)
Experimental group
Description:
Participants receive a structured, school-based individual occupational therapy program targeting sensory processing and activities of daily living.
Treatment:
Behavioral: Generalization and Classroom-Based Sensory Support Strategies
Behavioral: Individual School-Based Occupational Therapy Sessions
Behavioral: Family Education and Written Home Program
Behavioral: Task-Oriented Activities of Daily Living Training
Behavioral: Sensory Preparation Using Proprioceptive, Vestibular, and Tactile Input
Family Education and Home Program
Active Comparator group
Description:
Participants receive family education and a written home program without individualized occupational therapy intervention.
Treatment:
Behavioral: Family Education and Written Home Program

Trial contacts and locations

0

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Central trial contact

Feyza Şengül, Res. Asst.; Ceyhun Türkmen, associate professor

Data sourced from clinicaltrials.gov

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