View all newsletters
Receive our newsletter – data, insights and analysis delivered to you

Decentralised Clinical Trials Raise Concerns About Informed Consent

Under pressure of the COVID-19 pandemic, multitudes of clinical trials of new medications and treatments have moved to a decentralized model, bringing them to the patients rather than having patients come to a central trial site such as an urban medical center. At the same time, recent research shows a worrying lack of patients’ informed consent to the treatment they are undergoing. “This,” says Dr. Harsha Rajasimha, founder and CEO of Jeeva Informatics, “is not an acceptable situation. The extent to which patients comprehend the consent they grant is essential to the ethical conduct of medical research.”

Informed consent as defined by the U.S. Food and Drug Administration does not, Rajasimha points out, mean simply getting a research participant’s signature on a consent form. It includes:

  • Providing enough information to allow for an informed decision about participating in the clinical investigation
  • Verifiably ensuring the potential participant understands the information
  • Enough time for the potential participant to ask questions and discuss the trial with friends and family
  • Obtaining the potential participant’s voluntary consent to participate
  • Continuing to provide clarifications as the study progresses.

Objections to clinical trial management

Both regulators and participants, says Rajasimha, have raised objections to decentralized clinical trials. Regulators including institutional review boards (IRBs) view informed consent as a divine contract between researchers and patients that is foundational for trust building. Their objections include a lack of ability to:

  • Verify the patient’s comprehension via a quiz or questionnaire;
  • Provide convenient means for the patient to ask questions;
  • Document—presumably through a signed letter of agreement—that the patient has understood to what he or she is consenting.

Participants, says Rajasimha, raise their own objections to the informed consenting process. They tend to include:

  • A sense of compulsion—that this may be the only chance they have to see the doctor before making a decision;
  • A sense of being hurried to make a decision within a 15-min consultation;
  • Cultural humility and aspects such as language or religion—having a faith, for example, which precludes their doing something on a seven-day-a-week schedule.

The best way to deal with these issues, suggests Rajasimha, is to use human-centric technology to resolve these objections. For both trial regulators and participants, the basic concerns are free information exchange and verification—both parties understanding what has been told—and a way to resolve side issues.

With digital communication, he notes, prospective clinical trial participants can ask questions, discuss the trial with investigator team, to complete a proper informed consent remotely. Trial sponsors can translate background material, including educational videos, into as many languages as needed. Enabling participants to join a trial from any browser enabled device that they are already comfortable with—smartphone, tablet, or laptop—can also create better ties with the community.

“Both sides need options,” says Rajasimha. “Clinical trial participants need to be able to get information from the comfort and safety of their own homes. Trial sponsors need to make the field of participants as diverse as possible, and at the same time they need to make sure they’re getting informed consent. Digital technology—particularly bring your own device (BYOD)—is the way to satisfy all stakeholder requirements.”

In Other News…

Dr. Rajasimha will be at the 40th Annual J.P. Morgan Health Care Conference, which is currently under way until this Thursday, Jan. 13. The conference, which is taking place in a virtual format, gathers global industry leaders, up-and-coming companies, innovators, and investors at the largest and most informative health care investment symposium in the healthcare and life sciences industry.

The conference gives hundreds of companies the opportunity to connect with thousands of investors from around the world. Present at the event are companies representing the entire health care community, including pharmaceutical firms, health care service providers, medical device manufacturers, profit and non-profit health care companies, and others.

Our Jeeva Clinical cloud-based software provides a seamless solution that improves the experience of investigators and patients by decentralizing clinical trials.
When clinical investigators and study coordinators start planning a new study design in the new normal, speed and efficiency are paramount.
Clinical trials are the regulatory mechanisms agencies like the Food and Drug Administration (FDA) use to evaluate and review evidence of safety and efficacy of...
NEWSLETTER Sign up Tick the boxes of the newsletters you would like to receive. Key drug pipeline and competitive landscape changes based on the latest clinical activity, sent every Tuesday. Curated analysis and data-driven insights on clinical trials strategy and operations, sent every Thursday. The pharmaceutical industry's most comprehensive news and information delivered every month.
I consent to GlobalData UK Limited collecting my details provided via this form in accordance with the Privacy Policy
SUBSCRIBED

THANK YOU