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RECRUITING NA

Family-Implemented Treatment on the Behavioral Inflexibility of Children With Autism

NCT05125003 · View on ClinicalTrials.gov ↗

Study Summary

The overall goal of this project is to determine whether a new form of family-based treatment for repetitive and inflexible behaviors, delivered using videoconferencing technology, can counter any negative effects of those behaviors, but also improve positive outcomes for young children with ASD.

Interventions

  • BEHAVIORAL FITBI
  • BEHAVIORAL Parental Education

Study Locations (1)

Kansas

  • Juniper Gardens Children's Project — Kansas City

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2022-04-01
Est. Completion 2026-03-31
Phase NA

Sponsor

University of Kansas

23 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05125003

The ClinicalTrials.gov registry entry for NCT05125003 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Kansas, which has 23 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Autism Spectrum Disorder appearing as the primary indexed condition, and to 2 interventions — of which FITBI is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05125003 reports 1 study location spanning 1 distinct geographic area — top geographies include Kansas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05125003 about?

NCT05125003 is a clinical study titled "Family-Implemented Treatment on the Behavioral Inflexibility of Children With Autism". The overall goal of this project is to determine whether a new form of family-based treatment for repetitive and inflexible behaviors, delivered using videoconferencing technology, can counter any negative effects of those behaviors, but also improve positive outcomes for young children with ASD.

What is the current status of trial NCT05125003?

This trial is currently recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2022-04-01. Estimated completion is 2026-03-31.

What conditions does trial NCT05125003 study?

This clinical trial studies the following conditions: Autism Spectrum Disorder, Repetitive Compulsive Behavior. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05125003?

The interventions under investigation include: FITBI (BEHAVIORAL), Parental Education (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05125003?

This trial is sponsored by University of Kansas, which has 23 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05125003 being conducted?

This trial has 1 study location across Kansas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial