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Don't Throw Your Heart Away: Patient Study 4

Carnegie Mellon University logo

Carnegie Mellon University

Status

Completed

Conditions

Cardiac Transplant Disorder

Treatments

Other: Stratified Transplant Survival Metric
Other: SRTR Information Format

Study type

Interventional

Funder types

Other

Identifiers

NCT04809051
1 F30 HL152526-01-D

Details and patient eligibility

About

This empirical study tests whether transplant center performance data that reflect center donor acceptance rates influence patients and their family members to evaluate centers with high organ decline rates less favorably than centers with low organ decline rates. 400 transplant patients and family members will be recruited from transplant support group social media websites and randomized to one of four different information presentation conditions. Upon viewing a pair of outcome tables corresponding to their condition, the participants are asked to choose which hospital is higher performing (one hospital with a non-selective "accepting" strategy and one hospital with a more selective "cherrypicking" strategy.

Enrollment

94 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Participants 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 be a pre- or post-transplant patient or family member of the transplant patient

Exclusion criteria

Participants who do not meet the primary criterion of being a pre- or post-transplant patient or family member of the transplant patient.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

94 participants in 4 patient groups

Condition 1: Combined Transplant Pictograph
No Intervention group
Description:
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. The "survival following transplant" metric is displayed as a survival rate pictograph corresponding to all patients at the center who received transplants.
Condition 2: Stratified Transplant Pictograph
Experimental group
Description:
Participants randomized to Condition 2 will view only stratified transplant survival outcome information when making a choice between the two hospitals. The "survival following transplant" metric is displayed as a pair of survival rate pictographs corresponding to two distinct groups of transplant patients at the center: those who received optimal donor organs and those who received adequate donor organs.
Treatment:
Other: Stratified Transplant Survival Metric
Condition 3: Combined Transplant SRTR
Experimental group
Description:
Participants randomized to Condition 3 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. The "survival following transplant" metric is displayed as a quintile score corresponding to all patients at the center who received transplants.
Treatment:
Other: SRTR Information Format
Condition 4: Stratified Transplant SRTR
Experimental group
Description:
Participants randomized to Condition 4 will view only stratified transplant survival outcome information when making a choice between the two hospitals. The "survival following transplant" metric is displayed as a pair of quintile scores corresponding to two distinct groups of transplant patients at the center: those who received optimal donor organs and those who received adequate donor organs.
Treatment:
Other: Stratified Transplant Survival Metric
Other: SRTR Information Format

Trial contacts and locations

1

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Central trial contact

Gretchen Chapman, PhD; Alison E Butler, MS

Data sourced from clinicaltrials.gov

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