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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05791071
Other study ID # Floreo Cortica Protocol
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date February 15, 2023
Est. completion date June 29, 2023

Study information

Verified date June 2023
Source Floreo, Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A Randomized Controlled Phase II study to assess the efficacy of Floreo VR (Virtual reality) Building Social Connections as treatment for social skills in children with Autism Spectrum Disorder (ASD)


Description:

In this randomized controlled phase II study, 30 eligible subjects aged 4-10 years old with documented ASD diagnoses will be enrolled and randomized in a 1:1 ratio intervention vs control group. The Floreo VR Building Social Connections intervention is designed to be administered for 12 weeks, with three treatment visits per week, for a total of 36 treatment visits.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date June 29, 2023
Est. primary completion date June 29, 2023
Accepts healthy volunteers No
Gender All
Age group 4 Years to 10 Years
Eligibility Inclusion Criteria: - Males and females aged 4 years to 10 years 11 months of age (up to 11th birthday at randomization). - Patients or legally authorized representatives must provide written informed consent and be willing and able to comply with study procedures. Participants must provide informed assent as clinically appropriate. - A diagnosis of autism spectrum disorder on the basis of the clinical judgement of a qualified clinician according to DSM-5 criteria, supported by either the Autism Diagnostic Observation Schedule or the Autism Diagnostic Interview-Revised. - Participants must receive ABA therapy at Cortica, with scheduled ABA sessions in clinic at least 3 times per week. - Participants must be able to tolerate VR therapy in the judgement of parent or caregiver and study staff Exclusion Criteria: - A history of photosensitive epilepsy, or photoparoxysmal response on electroencephalogram (EEG) - Active diagnosis of migraine headache or migraine variant (abdominal migraine, cyclic vomiting syndrome), not adequately controlled - History of balance disorder including vertigo, motion sensitivity, or balance disorder - Primary sensory impairment (blindness, deafness) - Motor disorder that would interfere with VR engagement

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Floreo VR Building Social Connections
Floreo's VR platform consists of a VR headset and wireless tethered VR screens (iPhones) and tablets (iPads) that are seamlessly linked in real time, allowing the therapist (or monitor) to set up lessons, change the interactive environment, and provide live verbal and VR-based guidance, feedback, and rewards to users. The lessons that will be implemented in this intervention are aimed at targeting social skills such as communication, joint attention, and social interactions.
Sham
This condition will contain the same VR headset and wireless tethered VR screens (iPhones) and tablets (iPads) as the intervention condition, but instead of social skill lessons, only non-intervention, active VR videos such as underwater fish swimming will be shown.

Locations

Country Name City State
United States Cortica Thousand Oaks California

Sponsors (2)

Lead Sponsor Collaborator
Floreo, Inc. Cortica

Country where clinical trial is conducted

United States, 

References & Publications (1)

Kanne SM, Mazurek MO, Sikora D, Bellando J, Branum-Martin L, Handen B, Katz T, Freedman B, Powell MP, Warren Z. The Autism Impact Measure (AIM): initial development of a new tool for treatment outcome measurement. J Autism Dev Disord. 2014 Jan;44(1):168-79. doi: 10.1007/s10803-013-1862-3. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other AIM sub-domain scores The AIM is a 25-item parent questionnaire targeting sensitivity to change of core ASD symptoms. The questionnaire uses a 2-week recall period with items rated on two corresponding 5-point scales (frequency and impact). The items cover distinct sub-domains of ASD symptoms including Repetitive Behavior, Atypical Behavior, Social Reciprocity, and Peer Interaction. A composite score is also calculated. The AIM takes approximately 30 minutes to complete.
Other Vineland-3 Adaptive Behavior Composite and sub-domain scores The Vineland-3 evaluates adaptive behavior in five different domains: Social, Communication, Daily Living Skills, and Motor. In the context of this study, it will be administered using the Comprehensive Interview Form, for which a parent or caregiver is interviewed by a qualified rater familiar with the instrument. Based on the summarized scores in each domain, an Adaptive Behavior Composite (ABC) is also calculated. Items are scored on a scale of 0 (never), 1 (sometimes), or 2 (usually) for the level at which the child can independently perform a skill. The Vineland-3 Comprehensive Interview Form takes approximately 60-90 minutes to complete
Other Adverse events related to VR use Parents or caregivers will be asked about adverse events at the baseline visit (if this is separate from the screening visit), interim visits 1 and 2, and at the end of study visit. The occurrence or absence of AEs, and a description of any AEs, will be recorded on an Adverse Events Form. 5-10 minutes as needed to fill out AE form
Primary Autism Impact Measure (AIM) Assessment The AIM is a 25-item parent questionnaire targeting sensitivity to change of core ASD symptoms. The questionnaire uses a 2-week recall period with items rated on two corresponding 5-point scales (frequency and impact). The items cover distinct sub-domains of ASD symptoms including Repetitive Behavior, Atypical Behavior, Social Reciprocity, and Peer Interaction. A composite score is also calculated. The AIM takes approximately 30 minutes to complete.
Secondary CARS-2 The CARS-2 is a 15-item rating scale used to identify children with autism and determine overall symptom severity. The scale is completed by a clinician familiar with the assessment of ASD after collecting information by direct interview and observation. The rater will also make use of supplemental collected using an unscored Parent/Caregiver Questionnaire. Only the CARS-2 Standard rating scale will be used for the purposes of this study. The CARS-3 takes approximately 5-10 minutes to complete after the information needed to make the ratings is collected
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