Clinical trials (CTs) are important for advancing public health and medical research,
however, CT recruitment is challenging. The high reading level of CT information and the …

Background/Aims: Participant understanding is a key element of informed consent for
enrollment in research. However, participants often do not understand the nature, risks …

Ethically sound clinical research requires that prospective study participants provide
voluntary informed consent before any study procedures begin. The original intent was to …

The development and evaluation of training programs with the potential to improve informed
consent and accrual to clinical trials depend heavily on the ability to measure outcomes of …

OBJECTIVE: To discover whether the provision of clinical trials information via a multi-media
platform could better meet the needs, preferences and practices of potential cancer trial …

Despite increasing need to boost the recruitment of underrepresented populations into
cancer trials and biobanking research, few tools exist for facilitating dialogue between …

This study addresses the national clinical trial recruitment crisis by chronicling the
development of a campaign to move people toward enrollment in an online clinical research …

Objective: Given participants' research literacy is essential for clinical trial participation,
evidence-based strategies are needed that improve literacy and easily accessed online. We …

Background: Research suggests that participants do not always adequately understand
studies. While some consent interventions increase understanding, methodologic …

Background Knowledge about clinical trials affects efficient and equitable clinical trial
recruitment and retention. This study explored correlates of clinical trial knowledge in a …