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Project 3 Example: Human-AI Collaboration Tester (HAICT) Exp. 7

Project 3 Example: Human-AI Collaboration Tester (HAICT) Exp. 7

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05272189
Enrollment
12
Registered
2022-03-09
Start date
2020-01-01
Completion date
2025-11-04
Last updated
2026-01-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Computer Aided Diagnosis, Decision Making

Keywords

Signal detection, VIsual Perception, BESH

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.

Detailed description

This text is the text of the pre-registration for the HAICT 7 experiment as described on the Open Science Framework. https://osf.io/hngu4/ NOTE: This study is representative of studies conducted in Project 3 of this grant. There are multiple experiments in the bundle of experiments represented by Project 3 but it is not possible to register a bundle of studies on CT.gov. NOTE: Since the pronoun comment is advisory, we will leave it for now. Human-AI Collaboration Tester (HAICT) Exp. 7 (lightly edited from OSF) 1. Data collection. Have any data been collected for this study already? (Yes/No) yes 2. Hypothesis. What's the main question being asked or hypothesis being tested in this study? Background: In a variety of search experiments, both basic and clinical, the data have been consistent with a situation where the variability of the signal (or target) is greater than the variability of the noise (distractors). The classic sign of this is a zROC function with a slope \< 1 - typically around 0.6. A slope of 1.0 is indicative of an equal variance 2AFC task. For the HAICT task that we have been testing, we would expect equal variance, but we think it would be worth checking so we will systematically vary prevalence which will shift criterion. That will sweep out an ROC curve that we can examine. We will also test the Second Reader faux-AI in order to determine if low prevalence makes Second Reader worse. * (H1): We expect to replicate the finding that human criteria become more conservative as prevalence declines. * (H2): We predict that the slope of the resulting zROC will be 1.0. * (H3): We hypothesize that low prevalence will make Second Reader AI less effective because the positive predictive value of its comments will be low. 1. Dependent variable. Describe the key dependent variable(s) specifying how they will be measured. The main dependent variables of interest are accuracy (and the signal detection derivatives of accuracy, d' and c), reaction time, and subjective ratings on the survey following each block. 2. Conditions. How many and which conditions will participants be assigned to? This series of experiments investigates 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). We have developed a paradigm called the Human-AI Collaboration Tester (HAICT) that allows for efficient testing of interactions between a human and a simulated AI. The observers' task in all conditions is to give a 2AFC decision about whether a stimulus is "bad" or "not bad." To use language roughly mimicking a medical diagnosis, each stimulus is referred to as a "case." Observers are asked to make a 2AFC decision about arrays of colored shapes. The decision is made based on the predominant color of the case. The number of elements of each color are drawn from one of two normal distributions, one for positive (bad) stimuli and the other for negative (not bad) stimuli. The results from previous HAICT experiments (3 and 4) showed that human performance in the Second Reader condition drops off significantly at low prevalence. Performance in the Second Reader condition was better than Baseline when the prevalence of bad cases was 50% but was significantly worse than Baseline when prevalence was only 10%. In this experiment, we manipulate the prevalence of "bad" cases in the Second Reader and Baseline conditions. Four different prevalence rates will be tested - 10%, 33%, 67%, and 90%. Observers will complete 8 blocks (2 AI rules x 4 prevalence rates), and block order is random. AI rules to be tested: 1. Baseline - No AI input. Observer classifies each case as "bad" or "not" bad on their own. 2. Second Reader - The observer makes an initial decision about every case. The AI silently classifies stimuli using a conservative criterion (c = 0.5). The logic for the conservative criterion is that the second reader is being used to cut down on false positive responses and so it is intended to question positive human responses that might be marginal. If the observer and AI disagree, then the AI informs the human observer. The observer is then given a chance to either change their response or go with their first opinion. As in Experiments 1-5, the AI d-prime is fixed at 2.2. Feedback is known to increase the prevalence effect, so feedback will be given in both the practice and the test trials. Observers will complete 20 practice trials and 200 test trials in each block. Immediately after each block is completed, observers will be shown a summary of their performance. After the Second Reader blocks, they will also be asked to answer three subjective questions about the usefulness of the AI (see "Files" for more details). 3. Analyses. Specify exactly which analyses you will conduct to examine the main question/hypothesis. First, we summarize the number of hits, true negatives, misses, and false alarms in each block. From this, we can calculate the accuracy, the positive predictive value, sensitivity (d-prime), and the criterion for each observer under each of the different conditions. Given measures of performance at 4 levels of prevalence, we can estimate the ROC curve (pHit x pFA) and the zROC function (zHit x zFA). We will test the hypothesis that the slope of the zROC is equal to 1 (the consequence of an equal variance 2AFC task). 4. More analyses. Any secondary analyses? We will look to see if the observers' subjective opinions about the AI are correlated with variables such as the empirical d-prime, or the positive predictive value. 5. Sample size. How many observations will be collected or what will determine sample size? No need to justify decision, but be precise about exactly how the number will be determined. We will test 12 observers. This is consistent with the sample sizes of previous experiments. 6. Other. Is there anything else that you would like to pre-register? (e.g., data exclusions, variables collected for exploratory purposes, unusual analyses planned?) N/A

Interventions

BEHAVIORALSimulated Second Reader AI

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

BEHAVIORALTarget Prevalence

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

Sponsors

Brigham and Women's Hospital
Lead SponsorOTHER
National Cancer Institute (NCI)
CollaboratorNIH

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Masking description

Participants are naive to the purposes of the study but they are not blinded to the conditions.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* \- All welcome to enroll on line

Exclusion criteria

* Must pass the Ishihara color vision screening test * 20/25 vision (with correction)

Design outcomes

Primary

MeasureTime frameDescription
D'Data are collected within a session of about an hour.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.
CriterionData are collected within a session of about an hour.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.

Secondary

MeasureTime frameDescription
Reaction TimeData are collected within a session of about an hour.This is the measure of how long it takes to make a response.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORJeremy M Wolfe, PhD

Brigham and Women's Hospital

Baseline characteristics

Characteristic
Age, Continuous31 years
STANDARD_DEVIATION 9
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
12 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
Race (NIH/OMB)
Asian
1 Participants
Race (NIH/OMB)
Black or African American
4 Participants
Race (NIH/OMB)
More than one race
0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
White
7 Participants
Sex: Female, Male
Female
7 Participants
Sex: Female, Male
Male
5 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
0 / 12
other
Total, other adverse events
0 / 12
serious
Total, serious adverse events
0 / 12

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026