Patient Recruitment and Enrollment in Clinical Trials

Finding participants for clinical trials is often 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 twenty-eight percent are new.
Top sources of clinical trial information:
58% from primary care physicians
40% from online registries
Thirty percent from search engines
Nineteen percent from primary care nurses
19% from pharmaceutical companies
Motivations for Participation

Top perceived benefits:
26% to advance medicine
Thirty-six percent to improve others' lives
Fifteen percent 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
Seventy-five percent study purpose
Eighty-three percent potential risks and benefits
Enrollment Challenges

37% of sites under-enroll, with eleven percent 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 nineteen percent unwilling to participate and 7% unsure.
Top perceived risks:
Forty percent side effects
33% overall health risks
Seven percent receiving placebo
7% stopping beneficial treatments
40% lack confidence in finding a suitable study, and seventy percent seldom consider clinical read more trials when discussing treatment options.
However, there's optimism for improvement: 74% are open to discussing trial participation in online peer communities, and ninety-four percent of volunteers would participate again.

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Patient Recruitment and Enrollment in Clinical Trials

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