Literature DB >> 27009610

Maximizing Patient Recruitment and Retention in a Secondary Stroke Prevention Clinical Trial: Lessons Learned from the STAND FIRM Study.

Tharshanah Thayabaranathan1, Dominique A Cadilhac2, Velandai K Srikanth3, Sharyn M Fitzgerald4, Roger G Evans5, Joosup Kim6, Richard P Gerraty7, Thanh G Phan6, Christopher F Bladin8, Mark R Nelson9, Judith H Frayne10, Amanda G Thrift11.   

Abstract

BACKGROUND: Recruitment and retention of patients in a clinical trial is important for generalizability and robustness of findings. We aimed to investigate features of a study design that were associated with recruitment and retention in a Phase II and Phase III trial of a secondary prevention program for stroke.
METHODS: Following informed consent in hospital, Phase II participants were randomized to intervention or usual care. Baseline clinical assessments were conducted at home approximately 3 months after discharge. In Phase III study, informed consent was obtained at home. We compared the characteristics of participants recruited and retained to 12 months for both phases. Interviews with study nurses were undertaken in order to ascertain their opinions of features of study design. Triangulation was used to identify the features of study design that nurses thought had improved recruitment and retention.
RESULTS: All 24 eligible participants were recruited to the Phase II pilot study (100% recruitment), with 67% retention at 12 months. In Phase III study, 570 participants were recruited, and 93% of these participants had reached their 12-month assessment (n = 532) and were still participating. Consistent with the greater patient retention in Phase III study, nurses reported that patients' willingness to participate was greater when consent was obtained at home.
CONCLUSION: Following a change in the consent process from hospital to home, more participants continued participation to 12 months. Pilot studies can provide important data to improve study design and better understand potential barriers to recruitment and retention.
Copyright © 2016 National Stroke Association. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Stroke; feasibility study; methodology; patient retention; pilot study; recruitment

Mesh:

Year:  2016        PMID: 27009610     DOI: 10.1016/j.jstrokecerebrovasdis.2016.02.020

Source DB:  PubMed          Journal:  J Stroke Cerebrovasc Dis        ISSN: 1052-3057            Impact factor:   2.136


  4 in total

1.  Distance from Home to Research Center: A Barrier to In-Person Visits but Not Treatment Adherence in a Stroke Trial.

Authors:  Enrique C Leira; Catherine M Viscoli; Linnea A Polgreen; Mark Gorman; Walter N Kernan
Journal:  Neuroepidemiology       Date:  2018-03-23       Impact factor: 3.282

2.  Quality of life after stroke: a longitudinal analysis of a cluster randomized trial.

Authors:  Zhomart Orman; Amanda G Thrift; Muideen T Olaiya; David Ung; Dominique A Cadilhac; Thanh Phan; Mark R Nelson; Velandai K Srikanth; Jason Vuong; Christopher F Bladin; Richard P Gerraty; Sharyn M Fitzgerald; Judith Frayne; Joosup Kim
Journal:  Qual Life Res       Date:  2022-01-24       Impact factor: 4.147

3.  Subject Retention in Prehospital Stroke Research Using a Telephone-Based Physician-Investigator Driven Enrollment Method.

Authors:  Bryant J Rosell; Kristina Shkirkova; Jeffrey L Saver; David S Liebeskind; Sidney Starkman; May Kim-Tenser; Marc Eckstein; Latisha Sharma; Robin Conwit; Scott Hamilton; Nerses Sanossian
Journal:  Cerebrovasc Dis Extra       Date:  2019-07-25

4.  High tech and high touch: Recruitment strategies for enrolling African American stroke survivors in Community Based Intervention under Nurse Guidance after stroke (CINGS) trial.

Authors:  Gayenell S Magwood; Charles Ellis; Joy N J Buie; Stephanie Slan; Leo Bonilha; Robert J Adams
Journal:  Contemp Clin Trials Commun       Date:  2021-09-08
  4 in total

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