Sensory Intervention for Children With Autism

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Description

Greater than 80% of children with autism spectrum disorder (ASD) experience sensory differences that make it difficult for them to fully participate in meaningful everyday activities. In this research study, we will use MRI and behavioral methods to assess how sensory interventions might change sensory brain structures, allowing us to better predict which sensory interventions might work best for whom.

Targeted Conditions

Study Overview

Start Date
January 16, 2024
Completion Date
June 26, 2025
Enrollment
40
Date Posted
February 7, 2024
Accepts Healthy Volunteers?
No
Gender
Male

Locations

Full Address
University of Florida
Gainesville, Florida 32610, United States

Eligibility

Minimum Age (years)
6
Maximum Age (years)
9
Eligibility Criteria
Inclusion Criteria: Male children 6 years, 0 months to 8 years, 6 months of age with a diagnosis of autism spectrum disorder (ASD) will qualify for inclusion. Our inclusion age ensures all study participants will complete intervention/control conditions and be retested before they turn 9 years of age. Additional inclusion criteria include:

The families of children will have access to transportation to attend intervention sessions 2 times per week for 16-weeks.
Children who qualify will be verbal, and will speak and understand English. The native language of caregivers can include Spanish.
Children who qualify will have sensorimotor delays as assessed by the study team using the standardized, norm-referenced assessments described in this research proposal (z-scores on 3 of 5 tests -1.0 or lower).

Exclusion Criteria: Children younger than 6 years of age or older than 8 years, 6 months of age will be excluded. Additional exclusion criteria include:

Female children
Auditory hyperresponsivity as assessed during screening procedures.
Medical co-morbidities such as extreme prematurity (less than 28 weeks), blindness, deafness, cerebral palsy, Down Syndrome, tuberous sclerosis, or head-injury with loss of consciousness.
History of individual occupational therapy services in a clinical setting that includes sensory equipment.
Non-removable metal in the head or body (e.g. dental fillings & braces, metal pins, screws or plates).
Children unable to complete neurocognitive or sensorimotor testing.
Children unsuccessful in 3 mock scanning sessions during baseline testing.

Study Contact Info

Study Contact Name
Stefanie Bodison
Study Contact Email
Study Contact Phone

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Other Details

FDA Regulated Drug?
No
FDA Regulated Device?
No
NCTid (if applicable)
NCT06246487