Patient Recruitment and Enrollment in Clinical Trials

Attracting participants for clinical trials is often tougher than conducting the trials themselves. A delay in recruitment extends the study's timeline, delaying the treatment's market availability. Explore the infographic below to grasp 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:
Fifty-eight percent from primary care physicians
Forty percent from online registries
30% 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
5% for monetary compensation
Factors influencing participation:
Sixty percent physical location
63% confidentiality
73% types of procedures
75% study purpose
Eighty-three percent potential risks and benefits
Enrollment Challenges

37% of sites under-enroll, with 11% failing to enroll any patients.
Doubling original timelines helps 90% of trials meet enrollment goals.
Seventy percent of the public haven't considered clinical trials, with 19% unwilling to participate and seven percent unsure.
Top perceived risks:
40% side effects
Thirty-three percent overall health risks
Seven percent receiving placebo
7% stopping beneficial treatments
Forty percent lack confidence in finding a suitable study, and seventy percent seldom consider clinical trials when discussing treatment options.
However, there's optimism for improvement: 74% 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

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