Focus Group
Phase
Focus groups were
held with constituents of the Community Based Organizations. The focus
group participants were African Americans and Latinos broadly representative
in age and socio-economic status. The focus group members developed
a "menu" of issues of concern relating to the development and application
of genetics knowledge and technology. The Community Advisory Board reviewed
all educational materials used at the start of the focus groups and
those used in dialogue sessions.
Community Dialogue
Phase
During this phase,
twelve dialogue groups of 10-20 participants each met over a period
of months for six times. CBOs recruited participants and hosted the
dialogue sessions, and the Community Advisory Board assisted in the
selection of dialogue facilitators.
The objectives
of this phase were to: 1) open up community discussion about those issues
identified in the focus groups; and 2) allow community members to transform
their moral and ethical concerns into a consensus on general values
and desirable policies pertaining to the issues discussed. Participants
were educated about the genetic concepts and participated in dialogues
about the topics chosen by the focus group participants.
Reports on the
key concerns, and recommendations of each group were reviewed and approved
by each group for accurate representation, and quotations preserve the
authentic voice of participants.
Policy Phase
After completion
of all community-based dialogues, the project team, with members of
the Community Advisory Board, researched and wrote position papers on
the seven topics that were of greatest concern to the great majority
of the dialogue groups. They then planned and held briefings for legislators
and their staff in Michigan and Washington, D.C.
Dissemination
Phase
In addition to
the dissemination efforts at the state and nation legislative levels,
outcomes of the renewal project, including final policy recommendations
and the evaluation reports, are being publicly disseminated through
the peer-reviewed literature as well as presented at key conferences
and meetings. The project aims to reach policy-makers, health care providers
and organizations, and consumers.
Contacting
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Last updated 02/22/02
Copyright © 2002 Communities
of Color & Genetics Policy Project