Patient Recruitment and Enrollment in Clinical Trials

Recruiting participants for clinical trials is frequently tougher than conducting the trials themselves. A delay in recruitment stretches the study's timeline, delaying the treatment's market availability. Check out 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

72% of participants are existing patients, while twenty-eight percent are new.
Top sources of clinical trial information:
Fifty-eight percent from primary care physicians
40% 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
Eight percent as the best treatment option
Five percent for monetary compensation
Factors influencing participation:
60% physical location
63% confidentiality
Seventy-three percent types of procedures
Seventy-five percent study purpose
83% potential risks and benefits
Enrollment Challenges

37% of sites under-enroll, with eleven percent failing to enroll any patients.
Doubling original timelines helps ninety percent 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
7% receiving placebo
Seven percent stopping beneficial treatments
40% 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 ninety-four percent of volunteers would participate again.

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Patient Recruitment and Enrollment in Clinical Trials

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