Menu
Recruiting NCT07203105

GAINS Expert Guiding Technology to Coach Life Skill Teaching

No phase Interventional GAINS Expert Guiding Technology to Coach Life Skill Teaching

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: GAINS expert guiding technology to coach life skill teaching.
Who it may be relevant to
Registry conditions: GAINS Expert Guiding Technology to Coach Life Skill Teaching. Basic parameters: 3 years — 10 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Based on proven techniques in operant conditioning, the expert behavior guiding functionality in GAINS to teach life skills will be evaluated. Behavior practitioners will develop task analyses that break down complex life skills into simpler component steps and then enter these tasks into the GAINS system. In a similar way to navigation systems for drivers, GAINS will provide behavioral navigation for caregivers implementing ABA therapy programs. Using the GAINS app on a tablet or smartphone, caregivers will receive automatically updated visual and audio behavioral guidance, that includes what to do, when to do it, and detailed step-by-step guidance on how to execute ABA therapy programs.

Interventions

  • Behavioral GAINS expert guiding technology to coach life skill teaching
    GAINS expert guiding technology to coach life skill teaching

Primary outcome measures

  • Child independent life skill performance [Time frame: 60 days]

Eligibility criteria

Inclusion criteria

  • Only children ages 3 through 10 years who present with Autism Spectrum Disorder (ASD) will be recruited for this study.

Exclusion criteria

  • No individuals will be excluded or included based on race, ethnicity, or gender

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Treatment

Study locations

United States · 1 center
  • University of Arkansas — Fayetteville

Identifiers

NCT: NCT07203105 · 1R43MH130298-01 · 1R43MH130298-01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗