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Don't Throw Your Heart Away: Layperson Study 1

Not Applicable
Completed
Conditions
Cardiac Transplant Disorder
Interventions
Other: Total Survival
Other: Stratified Transplant Survival
Registration Number
NCT04133831
Lead Sponsor
Carnegie Mellon University
Brief Summary

Publicly available outcome assessments for transplant programs do not make salient that some programs tend to reject many of the hearts they are offered, whereas other programs accept a broader range of donor offers. The investigators use empirical studies to test whether transplant center performance data (i.e. transplant and waitlist outcome statistics) that reflect center donor acceptance rates influence laypersons to evaluate centers with high organ decline rates less favorably than centers with low organ decline rates. 1000 lay participants will be recruited from Amazon Mechanical Turk and randomized to one of five different information presentation conditions. Participants will be given an introduction to the donor organ match process, then asked to view the table of transplant outcomes corresponding to the condition they were randomized to. Each participant is asked to choose between two hospitals: one hospital with an non-selective, "accepting" strategy (takes all donor heart offers), and one hospital with a more selective, "cherrypicking" strategy (tends to reject donor offers that are less than "excellent" quality).

Detailed Description

Publicly available outcome assessments for transplant programs do not make salient that some programs tend to reject many of the hearts they are offered, whereas other programs accept a broader range of donor offers. The investigators use empirical studies to test whether transplant center performance data (i.e. transplant and waitlist outcome statistics) that reflect center donor acceptance rates influence laypersons to evaluate centers with high organ decline rates less favorably than centers with low organ decline rates. 1000 lay participants will be recruited from Amazon Mechanical Turk and randomized to one of five different information presentation conditions:

1. Condition 1 ("baseline" condition): view only combined transplant survival (e.g. transplant survival rate not stratified by number and quality of donor hearts accepted at each center)

2. Condition 2: view combined transplant survival + total survival (e.g. overall survival rate at each center, computed from survival rates of both transplant and waitlist patients)

3. Condition 3: view only stratified transplant survival (e.g. transplant survival rate stratified into patients who received excellent donor organs and patients who received less than optimal donor organs)

4. Condition 4: view stratified transplant survival + total survival

5. Condition 5: view only total survival

Participants will be given an introduction to the donor organ match process, then asked to view the table of transplant outcomes corresponding to the condition they were randomized to. Each participant is asked to choose between two hospitals: one hospital with an non-selective, "accepting" strategy (takes all donor heart offers), and one hospital with a more selective, "cherrypicking" strategy (tends to reject donor offers that are less than "excellent" quality). In order to identify the decision process that underlies this choice pattern, the investigators will examine a putative mediator. Specifically, participants will be asked to rate the extent to which they considered patients' chances of getting an excellent heart, avoiding a less-than-optimal heart, and getting any type of heart when making their choice between the two hospitals.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
1019
Inclusion Criteria

Participants who are already qualified mTurk workers with Worker Accounts meeting the above criteria will be asked to participate if they confirm the following inclusion criteria in the consent form.

  1. 18 years of age or older
  2. must read and understand the information in the consent form
  3. must want to participate in the research and continue with the survey
  4. must live in United States
Exclusion Criteria
  1. Participants on mTurk will not be allowed to participate if they fail to pass the initial "bot screening", a multiple-choice question that asks, "What phone number should you dial when there is an emergency?" The obvious correct response in this screening question is "911", so participants who select one of the incorrect responses (i.e. "1-800-ANTIBOT", "1-877-MTURKER", "123") are filtered out and not allowed to complete the survey.
  2. Participants on mTurk will be allowed to participate, but excluded from data analysis, if they submit a nonsense response to the free-response question which reads, "In your own words, why do you think patients should choose the hospital you picked?" This question takes place after the participant has viewed the choice stimuli and selected their response. If participants input nonsense in the text response box, they will be permitted to complete the survey and paid, but filtered out from the data analysis.

Study & Design

Study Type
INTERVENTIONAL
Study Design
FACTORIAL
Arm && Interventions
GroupInterventionDescription
Condition 5: Total onlyTotal SurvivalParticipants randomized to Condition 5 will view only total survival outcome information when making a choice between the two hospitals.
Condition 2: Combined plus TotalTotal SurvivalParticipants randomized to Condition 2 will view combined transplant survival and total survival outcome information when making a choice between the two hospitals.
Condition 3: Stratified onlyStratified Transplant SurvivalParticipants randomized to Condition 3 will view only stratified transplant survival outcome information when making a choice between the two hospitals.
Condition 4: Stratified plus TotalTotal SurvivalParticipants randomized to Condition 4 will view stratified transplant survival and total survival outcome information when making a choice between the two hospitals.
Condition 4: Stratified plus TotalStratified Transplant SurvivalParticipants randomized to Condition 4 will view stratified transplant survival and total survival outcome information when making a choice between the two hospitals.
Primary Outcome Measures
NameTimeMethod
Hospital Choice1 day

The outcome variable will be a measure of binary choice between two hospitals: one with a selective donor-heart acceptance strategy and one with a non-selective donor heart acceptance strategy.

Participants will respond to the question "Which Hospital is a better choice for patients? Please click on one of the two tables below to indicate which hospital is the better choice." Participants will choose been two outcome tables featuring the selective and non-selective hospital (counterbalanced, such that each of the two choices is equally likely to be presented at top of the choice scenario in each condition). The number of participants that choose each hospital will be the measured outcome variable used in analyses.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Carnegie Mellon University

🇺🇸

Pittsburgh, Pennsylvania, United States

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