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Don't Throw Your Heart Away: Layperson Study 1

Don't Throw Your Heart Away: Layperson Study 1

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04133831
Enrollment
1019
Registered
2019-10-21
Start date
2019-11-15
Completion date
2020-04-30
Last updated
2026-04-23

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

Conditions

Cardiac Transplant Disorder

Keywords

Heart Transplant, Transplant Survival, Applied Ethics, Decision Psychology, Human Behavior

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.

Interventions

OTHERTotal Survival

The overall or "total" survival rate at each center is displayed in the table of outcome statistics. Total survival is computed from survival rates of both transplant and waitlist patients: \[(number of patients surviving after transplant at end of year + number of patients alive on waitlist at end of year)\] / \[number of patients alive on waitlist at start of year\].

The transplant survival rate in the table of outcome statistics is stratified into two groups: (i) patients who received excellent donor organs and (ii) patients who received less than optimal donor organs. Stratified transplant survival is computed from survival rates of transplant patients who received each quality category of organ. excellent transplant survival = \[number of patients surviving after transplant with excellent organ\]/\[number of patients for whom excellent organ was accepted for transplant\] marginal transplant survival = \[number of patients surviving after transplant with marginal organ\]/\[number of patients for whom marginal organ was accepted for transplant\]

Sponsors

Carnegie Mellon University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Subject)

Eligibility

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

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.

Design outcomes

Primary

MeasureTime frameDescription
Hospital Choice1 dayThe 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

MeasureTime frameDescription
Mediator of Hospital Choice1 dayParticipants responded to the question, "There are many reasons why one transplant hospital might outperform another. Which reasons were most important in your decision? Please move the slider to indicate how much you considered each of the reasons below (0=reason was not important, 100=reason was extremely important). Patients were more likely to receive any type of donor heart at the hospital I picked.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORAlison E Butler, BS

Carnegie Mellon University

Participant flow

Participants by arm

ArmCount
Condition 1: Combined Only
Participants randomized to baseline (control) arm Condition 1 will view only combined transplant survival outcome information (e.g. transplant survival rate not stratified by number and quality of donor hearts accepted at each center) when making a choice between the two hospitals.
183
Condition 2: Combined Plus Total
Participants randomized to Condition 2 will view combined transplant survival and total survival outcome information when making a choice between the two hospitals. Total Survival: The overall or total survival rate at each center is displayed in the table of outcome statistics. Total survival is computed from survival rates of both transplant and waitlist patients: \[(number of patients surviving after transplant at end of year + number of patients alive on waitlist at end of year)\] / \[number of patients alive on waitlist at start of year\].
194
Condition 3: Stratified Only
Participants randomized to Condition 3 will view only stratified transplant survival outcome information when making a choice between the two hospitals. Stratified Transplant Survival: The transplant survival rate in the table of outcome statistics is stratified into two groups: (i) patients who received excellent donor organs and (ii) patients who received less than optimal donor organs. Stratified transplant survival is computed from survival rates of transplant patients who received each quality category of organ. excellent transplant survival = \[number of patients surviving after transplant with excellent organ\]/\[number of patients for whom excellent organ was accepted for transplant\] marginal transplant survival = \[number of patients surviving after transplant with marginal organ\]/\[number of patients for whom marginal organ was accepted for transplant\]
192
Condition 4: Stratified Plus Total
Participants randomized to Condition 4 will view stratified transplant survival and total survival outcome information when making a choice between the two hospitals. Total Survival: The overall or total survival rate at each center is displayed in the table of outcome statistics. Total survival is computed from survival rates of both transplant and waitlist patients: \[(number of patients surviving after transplant at end of year + number of patients alive on waitlist at end of year)\] / \[number of patients alive on waitlist at start of year\]. Stratified Transplant Survival: The transplant survival rate in the table of outcome statistics is stratified into two groups: (i) patients who received excellent donor organs and (ii) patients who received less than optimal donor organs. Stratified transplant survival is computed from survival rates of transplant patients who received each quality category of organ. excellent transplant survival = \[number of patients surviving after transplant with excellent organ\]/\[number of patients for whom excellent organ was accepted for transplant\] marginal transplant survival = \[number of patients surviving after transplant with marginal organ\]/\[number of patients for whom marginal organ was accepted for transplant\]
209
Condition 5: Total Only
Participants randomized to Condition 5 will view only total survival outcome information when making a choice between the two hospitals. Total Survival: The overall or total survival rate at each center is displayed in the table of outcome statistics. Total survival is computed from survival rates of both transplant and waitlist patients: \[(number of patients surviving after transplant at end of year + number of patients alive on waitlist at end of year)\] / \[number of patients alive on waitlist at start of year\].
241
Total1,019

Baseline characteristics

CharacteristicCondition 1: Combined OnlyCondition 2: Combined Plus TotalCondition 3: Stratified OnlyCondition 4: Stratified Plus TotalCondition 5: Total OnlyTotal
Age, Categorical
<=18 years
1 Participants0 Participants0 Participants0 Participants0 Participants1 Participants
Age, Categorical
>=65 years
1 Participants2 Participants2 Participants2 Participants2 Participants9 Participants
Age, Categorical
Between 18 and 65 years
181 Participants192 Participants190 Participants207 Participants239 Participants1009 Participants
Race (NIH/OMB)
American Indian or Alaska Native
2 Participants2 Participants1 Participants0 Participants1 Participants6 Participants
Race (NIH/OMB)
Asian
9 Participants7 Participants10 Participants11 Participants11 Participants48 Participants
Race (NIH/OMB)
Black or African American
13 Participants10 Participants14 Participants19 Participants16 Participants72 Participants
Race (NIH/OMB)
More than one race
6 Participants11 Participants9 Participants10 Participants13 Participants49 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
2 Participants0 Participants0 Participants0 Participants0 Participants2 Participants
Race (NIH/OMB)
Unknown or Not Reported
9 Participants10 Participants17 Participants12 Participants10 Participants58 Participants
Race (NIH/OMB)
White
142 Participants154 Participants141 Participants157 Participants190 Participants784 Participants
Region of Enrollment
United States
183 participants194 participants192 participants209 participants241 participants1019 participants
Sex/Gender, Customized
Sex/Gender (customized)
Female
82 Participants97 Participants87 Participants102 Participants119 Participants487 Participants
Sex/Gender, Customized
Sex/Gender (customized)
Male
97 Participants90 Participants96 Participants106 Participants115 Participants504 Participants
Sex/Gender, Customized
Sex/Gender (customized)
Unknown/Other
4 Participants7 Participants9 Participants1 Participants7 Participants28 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
EG003
affected / at risk
EG004
affected / at risk
deaths
Total, all-cause mortality
0 / 1830 / 1940 / 1920 / 2090 / 241
other
Total, other adverse events
0 / 1830 / 1940 / 1920 / 2090 / 241
serious
Total, serious adverse events
0 / 1830 / 1940 / 1920 / 2090 / 241

Outcome results

Primary

Hospital Choice

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.

Time frame: 1 day

ArmMeasureCategoryValue (COUNT_OF_PARTICIPANTS)
Condition 1: Combined OnlyHospital ChoiceProportion choosing non-selective center64 Participants
Condition 1: Combined OnlyHospital ChoiceProportion choosing selective center119 Participants
Condition 2: Combined Plus TotalHospital ChoiceProportion choosing selective center69 Participants
Condition 2: Combined Plus TotalHospital ChoiceProportion choosing non-selective center125 Participants
Condition 3: Stratified OnlyHospital ChoiceProportion choosing selective center29 Participants
Condition 3: Stratified OnlyHospital ChoiceProportion choosing non-selective center163 Participants
Condition 4: Stratified Plus TotalHospital ChoiceProportion choosing non-selective center192 Participants
Condition 4: Stratified Plus TotalHospital ChoiceProportion choosing selective center17 Participants
Condition 5: Total OnlyHospital ChoiceProportion choosing selective center17 Participants
Condition 5: Total OnlyHospital ChoiceProportion choosing non-selective center224 Participants

Source: ClinicalTrials.gov · Data processed: Apr 24, 2026