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RECRUITING NA

Testing Tactile Aids With Blind Subjects

NCT06237829 · View on ClinicalTrials.gov ↗

Study Summary

The objective of this project is to create richer tactile aids by using materials chemistry to create tactile sensations in tactile aids, as an alternative to traditional physical bumps, lines, or textures. These materials are commonly used in household products, but have not yet been used to enrich tactile aids. Successful outcomes are primarily the accuracy with which low vision or blind subjects identify objects made from tactile coatings versus traditional tactile aids. Other outcomes include time to completion of the task, or the number of distinctive categories that participants can identify.

Conditions Studied

Interventions

  • BEHAVIORAL Single bump acuity
  • BEHAVIORAL Optimal spacing between bumps
  • BEHAVIORAL Improving signal from a single bump with designer materials

Study Locations (1)

Delaware

  • University of Delaware — Newark

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2021-09-01
Est. Completion 2027-12
Phase NA

Sponsor

University of Delaware

159 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06237829

The ClinicalTrials.gov registry entry for NCT06237829 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 Delaware, which has 159 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 Blindness appearing as the primary indexed condition, and to 3 interventions — of which Single bump acuity 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: NCT06237829 reports 1 study location spanning 1 distinct geographic area — top geographies include Delaware. 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 NCT06237829 about?

NCT06237829 is a clinical study titled "Testing Tactile Aids With Blind Subjects". The objective of this project is to create richer tactile aids by using materials chemistry to create tactile sensations in tactile aids, as an alternative to traditional physical bumps, lines, or textures. These materials are commonly used in household products, but have not yet been used to enrich...

What is the current status of trial NCT06237829?

This trial is currently recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2021-09-01. Estimated completion is 2027-12.

What conditions does trial NCT06237829 study?

This clinical trial studies the following conditions: Blindness, Vision, Low. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06237829?

The interventions under investigation include: Single bump acuity (BEHAVIORAL), Optimal spacing between bumps (BEHAVIORAL), Improving signal from a single bump with designer materials (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06237829?

This trial is sponsored by University of Delaware, which has 159 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06237829 being conducted?

This trial has 1 study location across Delaware. 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