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NCT07504224 · ClinicalTrials.gov registry record · NA

ASD Wearables Feasibility Study

A NA study, sponsored by Rady Pediatric Genomics & Systems Medicine Institute.

Completed
Registry status
NA
Development phase
40
Enrollment target

NCT07504224 is a NA study that has completed, run by Rady Pediatric Genomics & Systems Medicine Institute. The registered enrollment target is 40 participants.

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The verdict

NCT07504224, a NA study, has completed, sponsored by Rady Pediatric Genomics & Systems Medicine Institute.

COMPLETED
Registry status
NA
Development phase
40 participants
Enrollment target

Study Summary

The goal of this clinical study is to evaluate and compare the feasibility of wearable device use among pediatric participants with autism spectrum disorder (ASD) across four different wearable device form factors: a wristband, headband, adhesive patch, and finger ring. Rather than investigating health or clinical outcomes associated with wearable device use, the study focuses on comparative assessment of device types to determine which forms are most acceptable and practical for this population. The study explores factors that may influence feasibility, including comfort, wearability, sustained use, and participant and caregiver engagement. The main questions the study aims to answer are: * Were adolescents with ASD able to tolerate wearing the assigned device for the full two-week study period? * Did adolescents with ASD and their caregivers consider the wearable device to be comfortable and usable? * Were there any unanticipated factors that affected the feasibility of wearable device use among youth with ASD? Researchers will compare data collected across device groups to determine (1) which form factor performed most effectively in real-world settings, and (2) which design characteristics are most important to consider when developing or selecting wearable devices intended for safe, acceptable, and sustained use in adolescent ASD populations. Adolescent participants and their caregivers will: * Be asked to complete four research visits (two in-person and two virtual video visits) * Complete multiple questionnaires (caregivers), assessments (adolescents) and two semi-structured interviews * Wear the assigned wearable device, as instructed, for a two-week trial: either a headband, wristband, adhesive patch, or finger ring

Interventions

  • DEVICE 14-Day Device Monitoring

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2024-07-15
Est. Completion 2026-01-06
Phase NA

What the Registry Record Tells You About NCT07504224

The ClinicalTrials.gov registry entry for NCT07504224 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Rady Pediatric Genomics & Systems Medicine Institute, which has 6 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which 14-Day Device Monitoring is the first listed.

NCT07504224 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT07504224 about?

NCT07504224 is a clinical study titled "ASD Wearables Feasibility Study". The goal of this clinical study is to evaluate and compare the feasibility of wearable device use among pediatric participants with autism spectrum disorder (ASD) across four different wearable device form factors: a wristband, headband, adhesive patch, and finger ring. Rather than investigating hea...

What is the current status of trial NCT07504224?

This trial is currently completed. It is a NA study. The enrollment target is 40 participants. The study started on 2024-07-15. Estimated completion is 2026-01-06.

What interventions are being tested in trial NCT07504224?

The interventions under investigation include: 14-Day Device Monitoring (DEVICE).

Who is sponsoring clinical trial NCT07504224?

This trial is sponsored by Rady Pediatric Genomics & Systems Medicine Institute, which has 6 total clinical trials registered on ClinicalTrials.gov.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.