Leveraging Social Innovation and Community-Engagement to Reduce Disparities in Outbreak Control Outcomes
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Crowdsourced campaign package, Rapid Response Teams.
- Who it may be relevant to
- Registry conditions: Outbreak Investigation. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Community-Academic Partnerships to Address Disparities Within Rural and Urban Communities
Overview
This study evaluates the impact of an intervention to increase viral transmission behaviors. The intervention will be developed through a crowdsourcing contest.
Detailed description
NPIs that are community-driven and developed in collaboration with diverse partners, including community members, public health agencies, and researchers may offer an acceptable and effective approach to reducing viral transmission and addressing individual and socio-structural barriers that lead to worse virus-related outcomes. Our study goals are to use a crowdsourcing open call to identify exceptional ideas (e.g., messages, videos, communication and dissemination strategies) that promote disease testing and encourage the public to practice the 3 Ws, referred to as health-promotive behaviors.
Interventions
- Behavioral Crowdsourced campaign package
Disease prevention intervention developed using a crowdsourcing process. - Behavioral Rapid Response Teams
Pilot a new hybrid training focused on contact tracing and case investigation.
Primary outcome measures
- Number of participants enrolled as measured by enrollment log [Time frame: Up to 3 years]
- Number of participants rating intervention as acceptable as measured by a post-intervention questionnaire [Time frame: Up to 4 years]
Eligibility criteria
All individuals aged 18+ years are eligible for study participation. Each phase may have additional requirements, including residency in North Carolina, employment at a local health department, etc. Participants must be able to complete study activities independently and have the capacity to consent to study participation.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Case-only
Study locations
United States · 1 center
- Wake Forest University Health Sciences — Winston-Salem
Identifiers
NCT: NCT05123729 · IRB00099888 · 40010565