Patient Perspectives in Cardiovascular Research: A Qualitative Study of Barriers, Trust, and Strategies for Inclusive

Stephanie Niño de Rivera1, Niurka Suero-Tejeda2, Rhonda Monroe3

  • 1Weill Cornell Medicine, New York, NY (S.N.d.R., B.R., M.F.L.G.).

Insights

To improve cardiovascular clinical trial diversity, patient feedback highlights the need for clear communication and trust. Addressing barriers like complex language and historical mistrust is key for inclusive recruitment strategies.

Area of Science:

  • Cardiovascular Research
  • Health Equity
  • Clinical Trial Recruitment

Background:

  • Cardiovascular disease disproportionately affects women, Black, and Hispanic patients.
  • These populations are underrepresented in clinical trials.
  • Understanding patient perspectives is crucial for inclusive recruitment.

Purpose of the Study:

  • To identify barriers and facilitators to clinical trial participation among underrepresented groups.
  • To inform inclusive recruitment strategies for the RECHARGE trial.
  • To enhance representation in cardiovascular research.

Main Methods:

  • Qualitative study using focus groups and interviews with Black and Hispanic adults.
  • Interviews guided by the Social-Ecological Model.
  • Analysis using directed content analysis and constant comparative approach.

Main Results:

  • Barriers included complex materials, medical jargon, and mistrust of randomization.
  • Societal barriers included limited outreach and lack of culturally appropriate materials.
  • Facilitators included trust in providers, family involvement, and clear, multilingual communication.

Conclusions:

  • Transparent, accessible communication and trust are vital for increasing representation.
  • Engaging trusted healthcare providers and community outreach are critical for equity.
  • Tailoring recruitment strategies to patient needs can advance cardiovascular research.
Abstract

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