- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02747459
Sensory Supported Swimming for Children With ASD (SSS)
Sensory Supported Swimming-Swimming and Water Safety for Children With Autism Spectrum Disorder
The purpose of Sensory Supported Swimming is to provide a sustainable, low cost recreational swim program for children with ASD. A secondary purpose is to train general recreation providers and swim instructors to meet the unique needs of children. Specific aims include both program development and research aims as described below.
Specific Aims:
1. Provide more opportunities for families of children with ASD to access a recreational swim program at low cost. (program development) 2. Increase the capacity of swim instructors and general recreation providers working with children with ASD. (Research) 3. Increase physical activity for children with ASD in a way that is a good match for their individual sensory needs. (Research) 4. Increase safety among children with ASD in and around the water so they and their families can swim safely. (Research) 5. Transition swimmers with ASD from a learn-to-swim program to an inclusive swim team. (Program Development) Hypotheses
- The Sensory Supported Swim Program will increase physical activity of children with ASD.
- The Sensory Supported Swim Program will increase safety of children with ASD in and around the water.
- The Sensory Supported Swim Program will increase the capacity of general recreation providers and swim instructors to serve children with ASD.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Kansas
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Kansas City, Kansas, United States, 66160
- University of Kansas Medical Center
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Autism diagnosis (any autism spectrum diagnosis)
- Order of response
Exclusion Criteria:
- Children with sensory impairments (i.e., blindness, deafness)
- Based on the discretion of the program directors, participants that display aggressive or harmful behaviors may be excluded for safety purposes
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: SSS Intervention
Sensory Supported Swimming-eight, 30 minute lessons
|
A swimming and water safety program for children with autism spectrum disorders.
Individualized instruction utilizing evidence-based teaching methods and sensory modifications.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Skill Acquisition Form
Time Frame: 8 weeks
|
This outcome measure was created for the study to measure changes in swimming and water safety skills.
The skill acquisition form is supplemented with weekly progress notes.
|
8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Instructor Survey
Time Frame: 16 weeks
|
Instructors are surveyed at least annually to determine if Sensory Supported Swimming is increasing their competence to serve children with autism spectrum disorders
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16 weeks
|
|
Parent Survey
Time Frame: 16 weeks
|
Parents of program participants are surveyed at least annually to determine if Sensory Supported Swimming is increasing children's physical activity and safety around water
|
16 weeks
|
|
Program Records
Time Frame: 8 weeks
|
demographics forms, enrollment & attendance records
|
8 weeks
|
Collaborators and Investigators
Investigators
- Principal Investigator: Lisa Mische Lawson, PhD, University of Kansas Medical Center
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 13124
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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