Patient Recruitment and Enrollment in Clinical Trials
Patient Recruitment and Enrollment in Clinical Trials
Blog Article
Finding participants for clinical trials is frequently tougher than conducting the trials themselves. A delay in recruitment stretches the study's timeline, pushing back the treatment's market availability. Explore the infographic below to comprehend how the public discovers clinical trials, motivations for participation, and the hurdles faced in enrollment.
Patient Recruitment and Enrollment Infographic
Discovering Clinical Trials
Seventy-two percent of participants are existing patients, while 28% are new.
Top sources of clinical trial information:
58% from primary care physicians
Forty percent from online registries
Thirty percent from search engines
Nineteen percent from primary care nurses
Nineteen percent from pharmaceutical companies
Motivations for Participation
Top perceived benefits:
26% to advance medicine
36% to improve others' lives
15% to improve their condition
8% as the best treatment option
Five percent for monetary compensation
Factors influencing participation:
Sixty percent physical location
63% confidentiality
73% types of procedures
75% study purpose
83% potential risks and benefits
Enrollment Challenges
Thirty-seven percent of sites under-enroll, with eleven percent failing to enroll any patients.
Doubling original timelines helps ninety percent of trials meet enrollment goals.
70% of the public haven't considered clinical trials, with 19% unwilling to participate website and 7% unsure.
Top perceived risks:
40% side effects
33% overall health risks
7% receiving placebo
7% stopping beneficial treatments
40% lack confidence in finding a suitable study, and 70% seldom consider clinical trials when discussing treatment options.
However, there's optimism for improvement: Seventy-four percent are open to discussing trial participation in online peer communities, and 94% of volunteers would participate again.
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Patient Recruitment and Enrollment in Clinical Trials