Patient Recruitment and Enrollment in Clinical Trials

Patient Recruitment and Enrollment in Clinical Trials

Blog Article

Attracting participants for clinical trials is frequently tougher than conducting the trials themselves. A delay in recruitment extends the study's timeline, pushing back the treatment's market availability. Check out 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

72% of participants are existing patients, while 28% are new.
Top sources of clinical trial information:
58% from primary care physicians
40% from online registries
Thirty percent from search engines
19% from primary care nurses
19% from pharmaceutical companies
Motivations for Participation

Top perceived benefits:
26% to advance medicine
36% to improve others' lives
Fifteen percent to improve their condition
Eight percent as the best treatment option
5% for monetary compensation
Factors influencing participation:
60% physical location
Sixty-three percent confidentiality
73% types of procedures
75% study purpose
83% 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.
70% of the public haven't considered clinical trials, with nineteen percent unwilling to participate and 7% unsure.
Top perceived risks:
40% side effects
Thirty-three percent overall health risks
7% receiving placebo
Seven percent stopping beneficial treatments
Forty percent 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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