Financial management of large, multi-center trials in a challenging funding milieu

Olivia Lovegreen1, Danielle Riggs2, Myrlene A Staten3

  • 1Research Administration, Department of Medicine, Tufts Medical Center, 800 Washington St, Boston, MA, 02111, USA. olovegreen@tuftsmedicalcenter.org.

Trials
|May 5, 2018
PubMed
Abstract

Insights

A hybrid funding model for clinical trials effectively manages limited public research funds. This approach ensures trial integrity and conserves resources for participant recruitment and follow-up.

Area of Science:

  • Clinical research funding
  • Public health studies
  • Health economics

Background:

  • Publicly funded clinical trials with public health implications often lack commercial interest.
  • Declining public research funds necessitate innovative financial management models.
  • Governmental and not-for-profit organizations are primary funders for such trials.

Purpose of the Study:

  • To develop and evaluate an alternative funding model for clinical trial sites.
  • To ensure judicious allocation of limited public research funds.
  • To support large-scale clinical trials with public health relevance.

Main Methods:

  • A hybrid financial management model was developed for the Vitamin D and Type 2 Diabetes (D2d) study.
  • The model included a Core reimbursement component (~40%) and Performance-Based Payments (~60%).
  • Underperforming sites transitioned to Performance-Based Payments only, with resource reallocation based on site needs.

Main Results:

  • The hybrid model spent 65% of the award (US$26M) over 4 years, compared to an estimated 83% under traditional cost reimbursement.
  • Recruitment took one year longer than projected, with median enrollment varying significantly across sites.
  • The model allowed for dynamic resource reallocation to meet enrollment goals.

Conclusions:

  • A hybrid financial management approach is feasible for public research funding.
  • This model effectively stewards limited funds while maintaining scientific integrity.
  • The approach conserves resources, enabling trial completion and participant follow-up.

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