Clinical Trials Directory

Trials / Terminated

TerminatedNCT02088047

The Effects of ProFoveate on Reducing Self-Stimulating Behaviors

The Effects of ProFoveate on Reducing Self-Stimulating Behaviors in Children Diagnosed With Autism Spectrum Disorders

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
4 (actual)
Sponsor
University of Arkansas · Academic / Other
Sex
All
Age
10 Years – 17 Years
Healthy volunteers
Accepted

Summary

This study is designed to pilot an intervention technique to reduce the self-stimulating behaviors seen in individuals with autism spectrum disorders using intervention with ProFoveate pellets. Self-stimulating behaviors like hand flapping, eye blinking, and rocking, can interfere with the individual's ability to interact with their peers. Participants will wear the pellets for four week and measures with taken again. Another group of participants will not get the pellets. Both groups will be tested at the beginning and end of the study. Any variations in self-stimulating behaviors will be documented through parent report, Observational data. The investigators hypothesize that they will see changes in self- stimulating behaviors as a result of the strategic placement of the ProFoveate™ pellets on the ears of one group of the participants.

Conditions

Interventions

TypeNameDescription
DEVICEProFoveateProFoveate™ intervention for nystagmus is a management approach comprised of non-magnetic, 1.2 mm spheres that can be made from either stainless steel, gold plated stainless steel or titanium, placed strategically about the face and ears and a set of exercises designed to support improved vision for patients with nystagmus.The spheres (i.e., stimulating press balls or pellets) are supplied in packages of 20 with each sphere supplied on a transparent hypoallergenic adhesive tape approximately 7.6 mm in diameter. Within each package, all spheres are individually contained on a single paper backing measuring approximately 8.5 cm by 1.7 cm. Individual pellets (with adhesive tape) are removed from the backing as needed according to the prescribed treatment regimen.

Timeline

Start date
2014-08-30
Primary completion
2018-10-04
Completion
2018-10-04
First posted
2014-03-14
Last updated
2020-10-09
Results posted
2020-10-09

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02088047. Inclusion in this directory is not an endorsement.