2009
DOI: 10.4037/ajcc2009400
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Strategies for Overcoming Site and Recruitment Challenges in Research Studies Based in Intensive Care Units

Abstract: Although enrolling a sufficient number of participants is a challenge for any multisite clinical trial, recruiting patients who are critically ill and receiving mechanical ventilatory support presents additional challenges because of the severity of the patients’ illness and the impediments to their communication. Recruitment challenges related to the research sites, nursing staff, and research participants faced in the first 2 years of a 4-year multisite clinical trial of a patient-directed music intervention… Show more

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Cited by 24 publications
(53 citation statements)
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“…First, recruiting participants who are receiving mechanical ventilatory support for clinical study poses particular challenges (Chlan et al, 2009). Our results are limited by the small size of our sample.…”
Section: Limitationsmentioning
confidence: 88%
“…First, recruiting participants who are receiving mechanical ventilatory support for clinical study poses particular challenges (Chlan et al, 2009). Our results are limited by the small size of our sample.…”
Section: Limitationsmentioning
confidence: 88%
“…However, ICU research is challenging for many reasons, including high patient acuity, the time-sensitive nature of certain interventions, protocol complexity, the lack of decisional capacity of most critically ill patients, and limited research funding. With these points in mind, the successful conduct of ICU research is dependent on collaborative contributions of clinicians and researchers in consultation with substitute decision makers and, when possible, patients (3,4).…”
mentioning
confidence: 99%
“…Centers participating in the pilot phase were those self-referred by committed local investigators or selected for participation based upon prior preparatory work or prior trial successes and existing research infrastructure, including the presence of experienced research coordinators [34]. Between years 1 and 4 of the full trial, consent rates increased each year, in keeping with growing familiarity of the research and clinical staff with trial communication.…”
Section: Discussionmentioning
confidence: 99%