Managing work flow in high enrolling trials: The development and implementation of a sampling strategy in the PREPARE trial. Academic Article uri icon

Overview

abstract

  • INTRODUCTION: Pragmatic trials in comparative effectiveness research assess the effects of different treatment, therapeutic, or healthcare options in clinical practice. They are characterized by broad eligibility criteria and large sample sizes, which can lead to an unmanageable number of participants, increasing the risk of bias and affecting the integrity of the trial. We describe the development of a sampling strategy tool and its use in the PREPARE trial to circumvent the challenge of unmanageable work flow. METHODS: Given the broad eligibility criteria and high fracture volume at participating clinical sites in the PREPARE trial, a pragmatic sampling strategy was needed. Using data from PREPARE, descriptive statistics were used to describe the use of the sampling strategy across clinical sites. A Chi-square test was performed to explore whether use of the sampling strategy was associated with a reduction in the number of missed eligible patients. RESULTS: 7 of 20 clinical sites (35%) elected to adopt a sampling strategy. There were 1539 patients excluded due to the use of the sampling strategy, which represents 30% of all excluded patients and 20% of all patients screened for participation. Use of the sampling strategy was associated with lower odds of missed eligible patients (297/4545 (6.5%) versus 341/3200 (10.7%) p < 0.001). CONCLUSIONS: Implementing a sampling strategy in the PREPARE trial has helped to limit the number of missed eligible patients. This sampling strategy represents a simple, easy to use tool for managing work flow at clinical sites and maintaining the integrity of a large trial.

authors

  • Al-Thani, Asma Ali
  • Pogorzelski, David
  • Nguyen, Uyen
  • McKay, Paula
  • Thabane, Lehana
  • Camara, Megan
  • Ramsey, Lolita
  • Seymour, Rachel
  • Goodman, J Brett
  • McGee, Sheketha
  • Fraifogl, Joanne
  • Hudgins, Andrea
  • Tanner, Stephanie L
  • Bhandari, Mohit
  • Slobogean, Gerard P
  • Sprague, Sheila

publication date

  • January 23, 2021

Identity

PubMed Central ID

  • PMC7873628

Scopus Document Identifier

  • 85101219304

Digital Object Identifier (DOI)

  • 10.1016/j.conctc.2021.100730

PubMed ID

  • 33605946

Additional Document Info

volume

  • 21