Surveying Healthcare Workers in Nursing Roles

Last registered on November 02, 2022

Pre-Trial

Trial Information

General Information

Title
Surveying Healthcare Workers in Nursing Roles
RCT ID
AEARCTR-0010335
Initial registration date
November 02, 2022

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
November 02, 2022, 5:07 PM EDT

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

Locations

Region

Primary Investigator

Affiliation
Harvard Business School

Other Primary Investigator(s)

PI Affiliation
PI Affiliation
PI Affiliation

Additional Trial Information

Status
In development
Start date
2022-11-04
End date
2023-02-01
Secondary IDs
Prior work
This trial does not extend or rely on any prior RCTs.
Abstract
We employ an online randomized survey experiment to estimate (i) how nurse experience affects job efficiency and quality of patient care and (ii) how bankruptcy status affects reservation wages and willingness to work at a facility.
External Link(s)

Registration Citation

Citation
Antill, Samuel et al. 2022. "Surveying Healthcare Workers in Nursing Roles." AEA RCT Registry. November 02. https://doi.org/10.1257/rct.10335-1.0
Experimental Details

Interventions

Intervention(s)
The first stage of the experiment estimates how nursing staff tenure and experience may affect the quality of healthcare provider care and patient outcomes. The study will elicit beliefs from real healthcare workers about the importance of on-the-job experience for delivering high-quality care. Participants are randomly assigned with equal probability into two conditions regarding the experience level of a hypothetical nurse. We measure how beliefs about relative quality of care received by patients change when we exogenously vary the amount of experience a hypothetical nurse has.

The second stage estimates beliefs about how healthcare provider financial conditions affect worker departures and reservation wages. Participants are randomized into five conditions about the financial health of a hypothetical facility. We measure how required wages and willingness to work at a hypothetical facility change when we exogenously vary information about the firm's financial health.
Intervention Start Date
2022-11-04
Intervention End Date
2023-02-01

Primary Outcomes

Primary Outcomes (end points)
In the first stage of the experiment, the primary outcomes are the time a hypothetical nurse takes to complete a task and the likelihood a hypothetical nurse makes a mistake or a patient has a bad outcome. We truncate both of these values such that answers below 1 are replaced with the value 1 instead. This corresponds to 1 minute to complete a task or a 1% chance of a mistake or bad outcome.
In the second stage of the experiment, the primary outcomes are the likelihood the participant would search for another job if working at a hypothetical facility, the reservation wage the participant would require to stay at that facility, and the participant's beliefs about the fraction of workers at the hypothetical facility that would voluntarily leave.
Primary Outcomes (explanation)

Secondary Outcomes

Secondary Outcomes (end points)
Our secondary outcomes are answers to direct questions about how a facility's financial health affects workers' willingness to work at that facility and questions about how staff tenure impacts quality of care.
Secondary Outcomes (explanation)

Experimental Design

Experimental Design
Participants are randomly assigned with equal probability into two conditions regarding the experience level of a hypothetical nurse. We measure how beliefs about relative quality of care received by that nurse's patients change when we exogenously vary the amount of experience the hypothetical nurse has.

Next, participants are randomly assigned into five conditions describing the financial health of a hypothetical facility. We measure how each participant's willingness to work at the facility and reservation wage required to work at that facility change with the financial health of the facility.
Experimental Design Details
Randomization Method
We conduct our experiment using a Qualtrics study. Qualtrics features a computerized randomization method, which we use to randomize participants into the treatment conditions described above.
Randomization Unit
We randomize at the participant level.
Was the treatment clustered?
No

Experiment Characteristics

Sample size: planned number of clusters
We exclude individuals that fail attention checks. Additionally, we exclude individuals that have never worked in the healthcare industry at a skilled nursing facility as an RN, LPN, or CNA. We also exclude participants who do any of the following: (i) report a probability above 100, (ii) report a time to complete a task above 4 hours, (iii) report a historical wage greater than $100 per hour, or (iv) give answers that are self contradictory as explained in our analysis plan. We will continue to run the experiment until either (i) we have at least 240 completed surveys that meet these criteria or (ii) we have continuously run our survey through February 1, 2023 without reaching 240 complete surveys that meet these criteria. Because of our filters, and because of the nature of our online-survey vendor, we cannot precisely control the number of participants or end date of our experiment.
Sample size: planned number of observations
We exclude individuals that fail attention checks. Additionally, we exclude individuals that have never worked in the healthcare industry at a skilled nursing facility as an RN, LPN, or CNA. We also exclude participants who do any of the following: (i) report a probability above 100, (ii) report a time to complete a task above 4 hours, (iii) report a historical wage greater than $100 per hour, or (iv) give answers that are self contradictory as explained in our analysis plan. We will continue to run the experiment until either (i) we have at least 240 completed surveys that meet these criteria or (ii) we have continuously run our survey through February 1, 2023 without reaching 240 complete surveys that meet these criteria. Because of our filters, and because of the nature of our online-survey vendor, we cannot precisely control the number of participants or end date of our experiment.
Sample size (or number of clusters) by treatment arms
We exclude individuals that fail attention checks. Additionally, we exclude individuals that have never worked in the healthcare industry at a skilled nursing facility as an RN, LPN, or CNA. We also exclude participants who do any of the following: (i) report a probability above 100, (ii) report a time to complete a task above 4 hours, (iii) report a historical wage greater than $100 per hour, or (iv) give answers that are self contradictory as explained in our analysis plan. We will continue to run the experiment until either (i) we have at least 240 completed surveys that meet these criteria or (ii) we have continuously run our survey through February 1, 2023 without reaching 240 complete surveys that meet these criteria. Because of our filters, and because of the nature of our online-survey vendor, we cannot precisely control the number of participants or end date of our experiment.

In the first stage, participants are randomized, with equal probability, into two groups regarding the experience level of a hypothetical nurse. If we have exactly 240 participants, this implies ~120 participants per group.

In the second stage, participants are randomized into a control group or one of four treatment groups. Each group sees different information about a hypothetical facility. We randomly assign one-third of participants to Control. We randomly assign the remaining participants with equal probability to one of the four treatment groups. We thus allocate participants as follows: Control, one-third (~80 participants); Treatment 1, one-sixth (~40 participants), Treatment 2, one-sixth (~40 participants), Treatment 3 , one-sixth (~40 participants), Treatment 4, one-sixth (~40 participants). Most of our analysis combines treatments 1 and 2 together into one condition and treatments 3 and 4 together in one condition. See our analysis plan for details. Note that because of our filters, and because of the nature of our online-survey vendor, we cannot precisely control the number of participants or end date of our experiment. In particular, it is very likely we will not end up with exactly 240 participants so these distributions are approximate.
Minimum detectable effect size for main outcomes (accounting for sample design and clustering)
IRB

Institutional Review Boards (IRBs)

IRB Name
Harvard University-Area Committee on the Use of Human Subjects
IRB Approval Date
2022-09-07
IRB Approval Number
IRB22-1066
IRB Name
The UCLA Office of the Human Research Protection Program
IRB Approval Date
2022-09-14
IRB Approval Number
IRB#22-001483
Analysis Plan

Analysis Plan Documents

NurseSurvey_AnalysisPlan_Nov2.pdf

MD5: 02c20b076303387bcf875ce4c3964278

SHA1: 68778c694bab89a7e39bcfb48d6230657d4c47ae

Uploaded At: November 02, 2022

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