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Development of the Better Research Interactions for Every Family (BRIEF) intervention to support recruitment for
Elliott Mark Weiss1,2, Megan M Gray3, Linda K Ko4
1Treuman Katz Center for Pediatric Bioethics and Palliative Care, Seattle Children's Research Institute, 4800 Sand Point Way NE, M/S FA.2.113 Neonatology, Seattle, WA, 98105, USA. emweiss@uw.edu.
Insights
Improving neonatal clinical trial recruitment is crucial. The Better Research Interactions for Every Family (BRIEF) Intervention was developed to enhance parent experiences and reduce participation disparities in neonatal research.
Area of Science:
- Neonatal clinical trials
- Clinical trial recruitment
- Health disparities
Background:
- Neonatal clinical trial recruitment faces significant challenges, leading to biased research populations and reduced generalizability.
- Low enrollment rates in neonatal studies disproportionately affect minoritized populations.
- A critical need exists for interventions to improve recruitment strategies in neonatal research.
Purpose of the Study:
- To develop an intervention to improve the recruitment experience for parents in neonatal clinical trials, with a focus on minoritized populations.
- To increase participation in neonatal clinical trials and decrease disparities in research engagement.
- To create a research team-facing intervention to optimize recruitment processes.
Main Methods:
- Intervention Mapping (IM) framework was utilized for systematic intervention development.
- Stakeholder engagement included parent and expert panels to guide intervention components.
- Key determinants of enrollment were identified, and relevant behavior change theories were integrated.
Main Results:
- The Better Research Interactions for Every Family (BRIEF) Intervention was developed, including pre-work and an in-person session.
- The intervention targets research team members to improve recruitment practices.
- A pilot study was identified, and a multi-stage evaluation plan was created.
Conclusions:
- The developed intervention, BRIEF, offers a structured approach to enhance recruitment in neonatal clinical trials.
- This methodology can guide the development of similar interventions in other research contexts.
- The study provides a model for improving research team-based recruitment strategies.
Background:
Recruitment for neonatal clinical trials can be particularly challenging. Low enrollment rates bias the research population and decrease generalizability of findings. We identified a critical need for an intervention to improve how researchers recruit for neonatal clinical trials. Working within the US neonatal research context, we developed the Better Research Interactions for Every Family (BRIEF) Intervention, which had two overarching goals: to improve the recruitment experience for all parents, focusing on minoritized populations, and to increase participation, focusing on decreasing disparities in research participation.
Methods:
We used intervention mapping (IM) to guide all steps of intervention development. IM is a planning framework that provides a systematic process and detailed protocol for step-by-step decision-making for intervention development, implementation, and evaluation.
Results:
We performed IM's six steps. In step 1, we convened two stakeholder groups, a parent panel and an expert panel, who provided guidance through development of all BRIEF components. Through a recent systematic review, empirical data collected by our team, and consultations with the panels, we identified key determinants (barriers and facilitators) of low enrollment rates and research team members as change agents. In step 2, we iteratively refined our list of key factors to include and linked determinants of behavior changes to these performance objectives. In step 3, we chose three theories (social cognitive theory, theory of information processing, and the trans-theoretical model), methods from identified practical applications suitable for the population (research team members) and the context (busy research NICU teams). In step 4, we developed and refined the intervention components, including self-guided pre-work and a single in-person session. In step 5, we identified the Darbepoetin plus slow-release intravenous iron trial as our partner study in which to pilot BRIEF. In step 6, we developed a multi-stage evaluation plan that included five distinct levels of outcomes.
Conclusions:
This manuscript shares our rationale and processes for the creation of a research team member-facing intervention aiming to improve recruitment processes for neonatal clinical trials. Our approach can inform those aiming to improve recruitment for neonatal clinical trials and those who may be considering use of IM within similar contexts.
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