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NIH Sep 30, 1991 | R01
How Much Information about the Risk of Cystic Fibrosis Do Couples Want to Know?
Institution: University of Pennsylvania
FOA Number: RFA-HG-91--01
Abstract
To complement his theoretical work, Dr. Asch will also be leading a project to assess the amount of information that couples desire about the risk of CF. The appropriate timing of CF carrier screening, as well as the amount that should be performed, will be investigated. The research team will analyze the decision-making processes of couples who are offered CF carrier testing one partner at a time. In the event of a negative result for the first partner, the team will determine whether or not the couple chooses to have the second partner tested. In this way, the team will determine the utility of obtaining less than the maximum information available from screening. (Member of Cystic Fibrosis Studies Consortium--CFSC)
FUNDING AGENCY:
Funder:
NIHInstitute:
NATIONAL HUMAN GENOME RESEARCH INSTITUTEFunding Type:
R01Project Number:
R01HG000616Start Date:
Sep 30, 1991End Date:
Aug 31, 1995PROJECT TERMS:
Cystic Fibrosis, Decision Making, disease /disorder proneness /risk, gene mutation, Genetic Counseling, genetic disorder diagnosis, health care model, Judgment, Motivation, preference, Prenatal Diagnosis, Questionnaires, Self Concept