Information Domain | (Phase 1) | (Phase 2) | (Phase 3) |
---|---|---|---|
 | Community profile tool (document and internet based) | Key informant perspective (interview guide) | Community members perspective (focus group guide) |
Basic community descriptions | Demographic information | n/a | n/a |
Leadership | Basic contact information | Formal and informal leadership; economic and political structures | n/a |
Community programs | Contact information, addresses, organizational information | Description of activities, quality, cultural relevance, integration of services, community awareness and access; interacting medical traditions | Lived experience of the health issues in the community, cultural context, program quality, perspectives on self-management, cultural perspectives; interacting medical traditions |
Local understanding of the health issue | n/a | Perceived importance and quality of local health data on the issue | Pathways to access to health information |
Resources and planning | Basic descriptions of funders and initiatives | Implications of funding streams and planned initiatives | n/a |
Perceived fit of the intervention with community objectives | n/a | Past experiences with similar interventions, potential challenges and facilitators | Context of culture and community, challenges and facilitators; medical traditions |
Infrastructure and technology | Basic descriptions | Community comfort, use of technology, barriers | Community comfort, level of use in the community and with different groups |
Readiness for community-based research | n/a | Quality of community experience with research; community expectations; competency and learning requirements for researchers | Quality of community experience with research; community expectations; competency and learning requirements for researchers; experience of past oppression |