| identifier: | SDY292 |
| description: |
The goal of this study was to study informed consent by the living donor. This study used surveys to evaluate the understanding of risk and psychological pressure that living organ donors felt when making the decision to donate. It compared participants' answers across geographic, racial and socio-economic backgrounds.
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| aggregation: |
instance of dataset
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| refinement: |
2 - Complete set of descriptive data and results, as ascertained by ImmPort.
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| availability: |
available with registration
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| primaryPublications: |
21158924 |
| isAbout: |
The first objective of this study is to evaluate the donor's understanding at a point in the donation process where he should possess all the information he is likely to have prior to consenting to donation. The second objective of this study is to evaluate if donors experience influences that result in an act of informed consent that is non-autonomous.
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| authorizations: |
registration required
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| accessURL: |
http://www.clinicaltrials.gov/ct2/show/NCT01742234 https://aspera-immport.niaid.nih.gov:9443/browser?path=SDY292 |
| landingPage: |
http://www.immport.org/immport-open/public/study/study/displayStudyDetail/SDY292 |
| clinical trial: | clinical trial |
| study category: | Transplantation |
| study type: | Observational |
| subject species: | Homo sapiens |
| biosample type: | |
| subject gender: | Both |
| assay type: |
| name: |
Living Donors
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| fullName: |
Maryam Valapour
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| affiliations: |
Cleveland Clinic
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| roles: |
principal investigator
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| name: |
RELIVE Informed Consent Study (RELIVE-03)
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| size: |
636
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| name: |
CLINICAL OUTCOMES OF LIVE ORGAN DONORS - DATA COORDINATING CENTER
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| output: |
The primary endpoints of this study are:
Pressure to donate expressed by donors
Understanding of the process of donor screening expressed by donors
Understanding of medical and psychosocial consequences of organ donation expressed by donors
Center variability in the first three primary endpoints
Ethnic/racial variability in the first three primary endpoints
The secondary endpoints of this study are:
Understanding of short-term medical risks of donation expressed by donors
Understanding of long-term medical risks of donation expressed by donors
Understanding of psychological risks of donation expressed by donors
Understanding that recipients may have variable outcomes expressed by donors
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| studyGroups: |
Kidney Donors: People who will donate a kidney at the University of Minnesota, Mayo Clinic, or University of Alabama
Lung Donors: People who will donate a lung at the Washington University School of Medicine or the University of Southern California
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| description: |
The goal of this study was to study informed consent by the living donor. This study used surveys to evaluate the understanding of risk and psychological pressure that living organ donors felt when making the decision to donate. It compared participants' answers across geographic, racial and socio-economic backgrounds.
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| identifier: |
10.21430/M3G310ZBSI
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| startDate: |
2008-08-01
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| name: |
ImmPort
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| identifier: |
SCR:012804
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| homePage: |
http://www.immport.org |