Endogenous Information Acquisition in Candidate Evaluation

Last registered on March 09, 2023

Pre-Trial

Trial Information

General Information

Title
Endogenous Information Acquisition in Candidate Evaluation
RCT ID
AEARCTR-0010969
Initial registration date
February 17, 2023

Initial registration date is when the trial was registered.

It corresponds to when the registration was submitted to the Registry to be reviewed for publication.

First published
February 21, 2023, 10:31 AM EST

First published corresponds to when the trial was first made public on the Registry after being reviewed.

Last updated
March 09, 2023, 5:45 AM EST

Last updated is the most recent time when changes to the trial's registration were published.

Locations

Region

Primary Investigator

Affiliation
Harvard Business School

Other Primary Investigator(s)

PI Affiliation
University of Florida
PI Affiliation
University of Florida

Additional Trial Information

Status
In development
Start date
2023-03-09
End date
2023-03-20
Secondary IDs
Prior work
This trial does not extend or rely on any prior RCTs.
Abstract
This project examines how decision-makers acquire and use information in their evaluation decisions. Using a controlled experiment, we explore how individuals assess candidates given noisy signals of quality and how they choose to acquire additional (costly) information about the candidate’s quality before making a final decision. In particular, we ask whether candidate gender impacts evaluator decisions about whether to seek out more information before making a decision. Do evaluators require fewer positive signals to decide that a male candidate is above-the-bar compared to the number of signals they would need to make that same determination for a female candidate? How many negative signals are required before a candidate is rejected, and does this depend on candidate gender? In addition, by comparing across two randomly-assigned treatments, one in which additional information is provided exogenously and one in which decision-makers choose when to acquire more information, we ask whether the endogeneity of information acquisition amplifies discriminatory outcomes.
External Link(s)

Registration Citation

Citation
Coffman, Katherine, Scott Kostyshak and Perihan Saygin. 2023. "Endogenous Information Acquisition in Candidate Evaluation." AEA RCT Registry. March 09. https://doi.org/10.1257/rct.10969-2.0
Experimental Details

Interventions

Intervention(s)
Intervention Start Date
2023-03-09
Intervention End Date
2023-03-20

Primary Outcomes

Primary Outcomes (end points)
We will have three primary outcome measures:
1. The final classification a decision-maker provides for a candidate: this is the incentivized classification that the decision-maker provides for each candidate that they are assigned. The decision-maker can classify each candidate as either “above-the-bar” or “below-the-bar.” For decision-makers in the exogenous treatment, the final classification occurs after receiving 5 quality signals for a candidate. For decision-makers in the endogenous treatment, the final classification is made when the decision-maker chooses to stop acquiring additional signals and provide a classification (so after anywhere between 0 – 5 signals are observed). We will compare these final classifications across treatment and candidate gender and assess accuracy rates.
2. The final evaluation a decision-maker provides for a candidate: the incentivized likelihood of being “above-the-bar” that the decision-maker provides for each candidate that they are assigned. After each quality signal that the decision-maker views, the decision-maker is asked to provide an incentivized estimate of the likelihood that the candidate they are assessing is “above-the-bar.” For decision-makers in the exogenous treatment, the final evaluation occurs after receiving 5 quality signals for a candidate. For decision-makers in the endogenous treatment, the final evaluation is made when the decision-maker chooses to stop acquiring additional signals and provide a classification (so after anywhere between 0 – 5 signals are observed). We will compare these final evaluations across treatment and candidate gender and assess accuracy rates.
3. Number of signals acquired: the number of costly signals purchased by a decision-maker for a given candidate (in the endogenous information treatment). We will compare the number of signals acquired by gender and prior beliefs.
Primary Outcomes (explanation)

Secondary Outcomes

Secondary Outcomes (end points)
In addition to these primary outcome measures, we are also interested in the following secondary outcome measures:
• The initial evaluation a decision-maker provides for a candidate: the incentivized likelihood of being “above-the-bar” that the decision-maker provides for each candidate that they are assigned, prior to viewing any signals.
• The interim evaluations a decision-maker provides for a candidate: the incentivized likelihood of being “above-the-bar” that the decision-maker provides for each candidate that they are assigned after any particular signal.
• Belief revisions: the change in a decision-maker’s estimated likelihood that a candidate is above-the-bar after seeing a positive (or negative) signal of quality.
Secondary Outcomes (explanation)

Experimental Design

Experimental Design
This is an online study conducted on Prolific. The main task of a participant is to classify candidates as above or below-the-bar.

First, we introduce participants to the task of evaluation of candidates. These candidates are past study participants who completed a math and science test and were classified as above or below-the-bar based upon having a test score above a set threshold. We use these past study participants to construct “pools” of candidates for our study participants to assess.

Before assessing candidates, each evaluator (main study participant) is provided with information about the candidate pool from which their candidates are chosen. In particular, they are told the share of male candidates who were above-the-bar (likelihood of a given male candidate being above-the-bar) and the share of female candidates who were above-the-bar.

Evaluators are randomly-assigned to one of four different candidate pools. There are 50 total candidates in each pool. The pools vary in the likelihood of male and female candidates being above-the-bar:

(1) 40-40 pool: 40% of female candidates and 40% of male candidates were above-the-bar
(2) 60-60 pool: 60% of female candidates and 60% of male candidates were above-the-bar
(3) 40-60 pool: 40% of male candidates and 60% of female candidates were above-the-bar
(4) 60-40 pool: 60% of male candidates and 40% of female candidates were above-the-bar

After describing the selected pool to the evaluator, we randomly-draw a candidate from the described pool for the evaluator to assess. Participants see some basic information about this candidate, including their gender and their answers to some (arguably irrelevant) questions (i.e., do you prefer mountain vacations or beach vacations?). Participants provide an incentivized estimated likelihood of that candidate being above-the-bar.

Participants can pay to acquire additional information about the candidate. We refer to these as “signals” – a signal can be either good or bad. The probability with which a good signal is drawn depends upon the true performance of the candidate:
• A candidate who is above-the-bar produces a good signal with probability of 75% and a bad signal with probability of 25%
• A candidate who is below-the-bar produces a good signal with probability of 25% and a bad signal with probability of 75%.

Our primary treatment randomization is whether evaluators can choose whether or not to acquire signals about the candidate. We call this endogenous or exogenous information acquisition:
• Exogenous information acquisition: the evaluator must acquire 5 signals about the candidate before making a classification. After each signal, they provide an updated incentivized likelihood of the candidate being above-the-bar. After acquiring all 5 signals, they make a final binary classification of the candidate, classifying the candidate as either “above-the-bar” or “below-the-bar.”
• Endogenous information acquisition: the evaluator can choose to acquire up to 5 signals about the candidate before making a classification. After each signal, they provide an updated incentivized likelihood of the candidate being above-the-bar. At any point, the evaluator can choose to stop acquiring signals and make a final classification, classifying the candidate as either “above-the-bar” or “below-the-bar.”

Both the random assignment to candidate pools and the random assignment to information treatment is across-participant. All evaluators evaluate 5 candidates from their selected pool, chosen randomly with replacement. They receive no feedback or information on their decision-making until the end of the study.

We will pay 1 out of every 10 participants (randomly-selected) additional incentive pay. For those participants:

At the conclusion of the study, we randomly select one candidate that participant evaluated. For that randomly selected candidate, we pay a bonus of $7 if their final classification of the chosen candidate is correct, and a bonus of $0.50 if they incorrectly classified the randomly-chosen candidate. In addition, we deduct $0.05 from the bonus payment for every signal they acquired for the randomly-chosen candidate in the endogenous treatment. We also randomly select one likelihood slider and pay them an extra $1 if within 10pp of the true likelihood.
Experimental Design Details
Randomization Method
Computer
Randomization Unit
We randomize treatment assignment at the individual level. Randomization by the computer.
Was the treatment clustered?
No

Experiment Characteristics

Sample size: planned number of clusters
3,200 participants
Sample size: planned number of observations
3,200 participants
Sample size (or number of clusters) by treatment arms
400 participants in each of the 4 pools across 2 treatment conditions (exogenous and endogenous information acquisition), for a total of 3,200 participants.
Minimum detectable effect size for main outcomes (accounting for sample design and clustering)
IRB

Institutional Review Boards (IRBs)

IRB Name
Harvard Business School
IRB Approval Date
2023-03-09
IRB Approval Number
IRB23-0306

Post-Trial

Post Trial Information

Study Withdrawal

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Intervention

Is the intervention completed?
No
Data Collection Complete
Data Publication

Data Publication

Is public data available?
No

Program Files

Program Files
Reports, Papers & Other Materials

Relevant Paper(s)

Reports & Other Materials