- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07699692
A Sensory-Profile Framework for Differentiated Swim Instruction in Autistic Children
A Sensory-Profile Framework for Differentiated Swim Instruction in Autistic Children: A Randomized Controlled Study With Nonverbal Learner Findings
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Kentucky
-
Louisville, Kentucky, United States, 40299
- Genesis
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- ASD
Exclusion Criteria:
- Neurotypical
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: sensory-profile framework
Profile 1: Hyposensitive. Students of this profile pursue full-body pressure because their sensory systems under-register input. The instructional challenge for these children is not entry, but instead channeling that drive for stimulation toward skill acquisition. Yilmaz et al. (2004) documented proprioceptive gains from structured, repetitive swimming, which is precisely the kind of input these children seek but need sensory-based instruction to hone. Profile 2: Hypersensitive. Hypersensitive children are the ones for whom one wrong splash early on might end the lesson. Yet Vonder Hulls et al. (2006) found measurable improvements in touch tolerance following aquatic therapy. Their best mechanism for instruction is controlled and consensual exposure, not forced desensitization. |
This study provided sensory-based instruction to children with ASD to increase aquatics-based learning efficiency
|
|
Active Comparator: control
Normal non-sensory-based instruction for the autistic children
|
standard swim instruction with no neurological accommodations
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
(1) lessons to 5-meter unassisted float/kick;
Time Frame: 10 lessons for each participant; 10-14 weeks
|
10 lessons for each participant; 10-14 weeks
|
|
(2) percentage of sessions ending 10+ minutes early due to apparent dysregulation;
Time Frame: 10 lessons for each participant; 10-14 weeks
|
10 lessons for each participant; 10-14 weeks
|
|
(3) week-4 composite trust score (1-10 score: 10=highest);
Time Frame: 10 lessons for each participant; 10-14 weeks
|
10 lessons for each participant; 10-14 weeks
|
|
(4) technique corrections accepted per session without protest.
Time Frame: 10 lessons for each participant; 10-14 weeks
|
10 lessons for each participant; 10-14 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
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
- IRB00014585
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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