Influence of Clinical Research Investigator Fraud on Clinical Trial Participation

Purnachandra Garimella1,2, Irwin G Martin1

  • 11 School of Health Sciences, Eastern Michigan University, Ypsilanti, MI, USA.

Insights

Knowledge of clinical investigator fraud discourages participation in clinical trials. Even among educated individuals, learning about misconduct reduced willingness to join studies, impacting patient recruitment efforts.

Area of Science:

  • Medical Ethics
  • Clinical Research Management
  • Public Health Policy

Background:

  • Increasing disqualifications/restrictions of clinical research investigators by the US Food and Drug Administration (FDA).
  • Public surveys reveal challenges in clinical trial participation and public perception of research.

Purpose of the Study:

  • To investigate the impact of clinical investigator fraud or misconduct on public willingness to participate in clinical trials.

Main Methods:

  • An electronic survey was distributed to faculty at Eastern Michigan University.
  • Survey results were analyzed to assess the influence of awareness of investigator fraud on participation intent.

Main Results:

  • 81% of respondents expressed willingness to participate or had participated in clinical trials.
  • Exposure to a case of investigator fraud discouraged approximately 25% of willing respondents.
  • Geographic proximity of the fraud case did not significantly correlate with its impact on respondents.

Conclusions:

  • Awareness of clinical investigator fraud can significantly deter potential participants.
  • Further research is needed to understand the broader impact and duration of this effect on patient recruitment for clinical studies.

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