NCT05272189

Brief Summary

The study is one part of a "bundle" of experiments that constitute Project Three of a National Eye Institute grant. Project Three includes a series of experiments that investigate how changing the input from a simulated AI can affect the decisions made by human observers in a two-alternative forced choice task (like the decision to recall a woman for further examination in mammography). HAICT 7, the experiment described here, investigates how changing prevalence affects human performance when AI is used as a Second Reader.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
12

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jan 2020

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2020

Completed
2.1 years until next milestone

First Submitted

Initial submission to the registry

February 18, 2022

Completed
19 days until next milestone

First Posted

Study publicly available on registry

March 9, 2022

Completed
2.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2024

Completed
1.3 years until next milestone

Study Completion

Last participant's last visit for all outcomes

November 4, 2025

Completed
3 months until next milestone

Results Posted

Study results publicly available

January 20, 2026

Completed
Last Updated

January 20, 2026

Status Verified

December 1, 2025

Enrollment Period

4.6 years

First QC Date

February 18, 2022

Results QC Date

December 4, 2025

Last Update Submit

December 29, 2025

Conditions

Keywords

Signal detectionVIsual PerceptionBESH

Outcome Measures

Primary Outcomes (2)

  • D'

    D' (d-prime) is the signal detection theory measure of the level of performance on a task. It is computed by calculating the proportion of true positive responses =(true positive trials)/(true positive + false negative trials) = p(TP) and by calculating the proportion of false positive responses =(false positive trials)/(false positive + true negative trials) = p(FP). These values are transformed into 'z-scores' (for example, using NORMSINV in Excel to calculate the inverse of the standard normal distribution). D' is defined as Z(TP)-Z(FP). Its range is from 0 for cases where no signal can be discriminated from the noise, to \~4.0. The upper limit is not defined, but 4 would mean that and observer is essentially perfect at discriminating signal from noise.

    Data are collected within a session of about an hour.

  • Criterion

    Criterion, like D' (see above) is calculated from z(TP) and z(FP). Criterion ( c ) = (z(TP)+z(FP))/-2. A value of zero means that the observer is equally likely to make a positive (e.g. 'target present') response as a negative (absent) response. Positive values mean that the observer is more likely to say "absent" (a "conservative" criterion). Negative values mean the observer is more likely to say "present" (a "liberal" criterion). Liberal and conservative have no political connotations in this case. Criterion values almost always fall between -2 and 2.

    Data are collected within a session of about an hour.

Secondary Outcomes (1)

  • Reaction Time

    Data are collected within a session of about an hour.

Study Arms (1)

Experiment

EXPERIMENTAL

All participants are tested in all conditions of this experiment.

Behavioral: Simulated Second Reader AIBehavioral: Target Prevalence

Interventions

In this experiment, in some conditions, the participant makes their decision in the presence of information about a simulated artificial intelligence decision.

Experiment

The frequency with which targets are presented varies from 10% to 90%

Also known as: Base Rate
Experiment

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • \- All welcome to enroll on line

You may not qualify if:

  • Must pass the Ishihara color vision screening test
  • /25 vision (with correction)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Visual Attention Lab / Brigham and Women's Hospital

Boston, Massachusetts, 02215, United States

Location

Results Point of Contact

Title
Jeremy M Wolfe, Professor and Principle Investigator
Organization
Brigham & Women's Hospital

Study Officials

  • Jeremy M Wolfe, PhD

    Brigham and Women's Hospital

    PRINCIPAL INVESTIGATOR

Publication Agreements

PI is Sponsor Employee
Yes

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Masking Details
Participants are naive to the purposes of the study but they are not blinded to the conditions.
Purpose
BASIC SCIENCE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

February 18, 2022

First Posted

March 9, 2022

Study Start

January 1, 2020

Primary Completion

August 1, 2024

Study Completion

November 4, 2025

Last Updated

January 20, 2026

Results First Posted

January 20, 2026

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will share

De-identified raw data will be posted on the experiment's OSF page and will also be available on request to the PI.

Shared Documents
STUDY PROTOCOL, SAP, ICF
Time Frame
Materials will be available when requested
Access Criteria
essentially unrestricted
More information

Locations