Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID04332783

Isolating and Mitigating Sequentially Dependent Perceptual Errors in Clinical Visual Search

Led by University of California, Berkeley · Updated on 2026-02-03

10120

Participants Needed

1

Research Sites

69 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating how visual serial dependencies (VSDs) affect the accuracy of lesion detection and diagnosis in remote store-and-forward teledermatology. This method, which allows clinicians to review dermatological images remotely, is widely used but may be impacted by the way prior image viewings influence current observations. The study aims to establish, identify, and reduce the negative impact of VSDs on clinical judgments in this setting to improve diagnostic accuracy. Participants, including both clinicians and non-clinicians, will take part in computer-based psychophysical experiments involving the visual search, detection, localization, and categorization of medical images of skin lesions. These experiments use continuous report match-to-sample and forced-choice discrimination tasks, with images presented in different orders, locations, and timing intervals to analyze sequential effects in perception and decision making. Each participant will spend 30 to 60 minutes undergoing psychophysical testing to assess serial dependence in their perceptual judgments. The study measures discrimination accuracy and signal detection metrics across trials. Observers will complete all conditions of the assigned experiment, with the goal of developing guidelines to mitigate negative serial effects and improve remote teledermatology accuracy. Participation involves no drug use and includes healthy adults with normal or corrected vision.

CONDITIONS

Brief Title

Isolating and Mitigating Sequentially Dependent Perceptual Errors in Clinical Visual Search

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Subjects must have normal or corrected to normal vision with contacts or glasses.
Not Eligible

You will not qualify if you...

  • Subjects may not be under the age of 18 to participate.
  • Subjects may not participate if they are blind.

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (remote or in-person)

Outpatient Treatment

Duration - 30 to 60 minutes per session

Participants complete computer-based psychophysical experiments involving visual search, detection, localization, and categorization of medical images to assess sequential perceptual biases.

1 session of 30-60 minutes

Trial Site Locations

Total: 1 location

1

University of California, Berkeley

Berkeley, California, United States, 94720

Actively Recruiting

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Research Team

K

Katrina Wolters, BA

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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