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NCT02856061 · ClinicalTrials.gov registry record · NA

Tracking Intervention Effects With Eye Tracking

A NA study, sponsored by Yale University.

Completed
Registry status
NA
Development phase
76
Enrollment target

NCT02856061: Completed NA study, sponsored by Yale University.

NCT02856061 is a NA study that has completed, run by Yale University. The registered enrollment target is 76 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02856061, a NA study, has completed, sponsored by Yale University.

COMPLETED
Registry status
NA
Development phase
76 participants
Enrollment target

Study Summary

This pilot study examines concurrent and predictive relationships between eye tracking and clinical outcomes during a 16-week behavioral intervention (PRT) for children with ASD. Eye tracking will be comprised of both laboratory-based measures (using a commercial eye-tracking system) as well as home-based measures (using tablet-based eye tracking systems). The major goals of this study are both to improve our understanding of the potential role of eye tracking in clinical trials and to advance technologies that may further improve the sensitivity, robustness, accessibility, and ultimate utility of eye tracking methodologies.

Primary Outcome

A comprehensive laboratory eye-tracking battery will be administered to participants before, at midpoint, and at the end of a 16-week period to assess change over the course of treatment.

Interventions

  • BEHAVIORAL Pivotal Response Treatment

Trial Details

FieldValue
Enrollment Target 76 participants
Start Date 2016-01
Est. Completion 2018-03
Phase NA
Yale University

1,492 total trials

What the finished NCT02856061 record still lists

NCT02856061 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 76 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).

The record links to 0 conditions, and to 1 intervention - of which Pivotal Response Treatment is the first listed.

NCT02856061 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02856061 about?

NCT02856061 is a clinical study titled "Tracking Intervention Effects With Eye Tracking". This pilot study examines concurrent and predictive relationships between eye tracking and clinical outcomes during a 16-week behavioral intervention (PRT) for children with ASD. Eye tracking will be comprised of both laboratory-based measures (using a commercial eye-tracking system) as well as home...

What is the current status of trial NCT02856061?

This trial is currently completed. It is a NA study. The enrollment target is 76 participants. The study started on 2016-01. Estimated completion is 2018-03.

What interventions are being tested in trial NCT02856061?

The interventions under investigation include: Pivotal Response Treatment (BEHAVIORAL).

Who is sponsoring clinical trial NCT02856061?

This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02856061's enrollment target sits among peer trials

76 1062nd of 2000 higher than 932 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02856061, the US trial registry maintained by the National Library of Medicine. NCT02856061 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.