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ASDNCT07699692

A Sensory-Profile Framework for Differentiated Swim Instruction in Autistic Children

A study testing sensory-based instruction and standard instruction in people with ASD, run by Genesis Indep Research at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Autistic children drown at one-hundred sixty times the rate of their neurotypical peers: a public health crisis that the adapted learning field has only addressed by demonstrating that standard swimming instruction sometimes works for autistic children. Read more about this study

Who is it for?
Ages 3 to 16 months
Conditions the study is for
ASD
What is being tested?
sensory-based instruction and standard instruction
Could I receive a placebo?
No, everyone receives an active treatment
How many people
95 participants
Where
1 siteUnited States
Study dates
15 Oct 2025to 25 May 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 3 to 16 months
  • All sexes
  • No healthy volunteers
  • Child

Who may be able to join

  • ASD

Who cannot join

  • Neurotypical

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Genesis

    Louisville, Kentucky, 40299

Other trials in United States

About this study

Official title: A Sensory-Profile Framework for Differentiated Swim Instruction in Autistic Children: A Randomized Controlled Study With Nonverbal Learner Findings

Autistic children drown at one-hundred sixty times the rate of their neurotypical peers: a public health crisis that the adapted learning field has only addressed by demonstrating that standard swimming instruction sometimes works for autistic children. This study presents a three-profile framework (sensory-seeking/hyposensitive, sensory-avoidant/hypersensitive, variable/mixed) founded in sensory processing literature, based on ~950 lessons to 65 autistic children (ages 3-15) to determine why this disjunction exists, and how swim instructors can fix it.

Conditions
ASD
Being tested
sensory-based instruction, standard instruction
Keywords
autism, asd, swim, instruction, learning, neurotypical, aquatics, sensory, sensory profile
Medical subject headings
Autistic Disorder, Child Development Disorders, Pervasive

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • sensory-based instructionBehavioural

    This study provided sensory-based instruction to children with ASD to increase aquatics-based learning efficiency

  • standard instructionBehavioural

    standard swim instruction with no neurological accommodations

Study groups in NCT07699692
Study groupRoleWhat they receive
sensory-profile frameworkExperimentalProfile 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.
Receives: Behavioral: sensory-based instruction
controlActive comparatorNormal non-sensory-based instruction for the autistic children
Receives: Behavioral: standard instruction

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. (1) lessons to 5-meter unassisted float/kick;

    Measured: 10 lessons for each participant; 10-14 weeks

  2. (2) percentage of sessions ending 10+ minutes early due to apparent dysregulation;

    Measured: 10 lessons for each participant; 10-14 weeks

  3. (3) week-4 composite trust score (1-10 score: 10=highest);

    Measured: 10 lessons for each participant; 10-14 weeks

  4. (4) technique corrections accepted per session without protest.

    Measured: 10 lessons for each participant; 10-14 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted13 Jul 2026
  2. Study start15 Oct 2025
  3. Primary completion15 Apr 2026
  4. Study completion25 May 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Single group
Masking
Double blind
Who is masked
Care provider, Outcomes assessor
Enrolment
95 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07699692
Sponsor's protocol ID
IRB00014585
Status last verified
Jul 2026
First submitted
27 Jun 2026
Last updated
13 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing sensory-based instruction and standard instruction in people with ASD, run by Genesis Indep Research at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 13 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

(1) lessons to 5-meter unassisted float/kick; (time frame: 10 lessons for each participant; 10-14 weeks). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Jul 2026.

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