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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03195244
Other study ID # AT&ASD
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 12, 2017
Est. completion date April 12, 2022

Study information

Verified date April 2022
Source Panhandle Eye Group, LLP
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To compare the efficacy of one-on-one versus group-based aquatic therapy on the social interactions, behaviors and physical activities of children with autism spectrum disorders (ASDs).


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date April 12, 2022
Est. primary completion date April 12, 2022
Accepts healthy volunteers No
Gender All
Age group 3 Years to 17 Years
Eligibility Eligibility criteria: - DSM-V diagnosis of Autism Spectrum Disorder or DSM-IV diagnosis of Asperger's syndrome or high functioning atypical autism or pervasive development disorder - not otherwise specified or else the typical clinical findings and suspicion of an ASD - Treatment naïve to prior aquatic therapy Exclusion criteria: - Not willing to undergo an investigational treatment - Unable to cooperate well enough to safely participate in aquatic therapy under the protocol guidelines - Known allergies to pool chemicals - Other significant co-morbidities which may include (but is not limited to): severe cerebral palsy with low motor function, advanced pulmonary disease, home oxygen requirement, spina bifida with low motor function, permanent feeding tubes, poorly controlled seizure disorder, chronic indwelling urinary catheters or any condition causing severe cognitive impairment

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Aquatic Physical Therapy
Swim Whisperer's Aquatic Therapy Sessions

Locations

Country Name City State
United States Turn Center Amarillo Texas

Sponsors (1)

Lead Sponsor Collaborator
Sloan W. Rush, MD

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in PedsQL Score Survey Baseline and 10 weeks after intervention
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