Ways to Boost Patient Experience in Clinical Trials
A decade ago, the life sciences sector was junctured to improve patient trust and clinical trial results. Companies have realized that patients and advocates need to sit at the table and center on enterprise models, commercialization, and research and development. It’s a lofty goal to collect as many data points as possible in the shortest amount of time feasible. And how can we recognize the impact that taking part in a clinical study has on the patients we are attempting to help in this way?
Patients Should Be Walked Through The Clinical Process Frequently And Early
In most clinical trials, participants don’t think about the additional treatments they’ll be subjected to while selecting whether or not to take part. Is it worth missing several weeks of your life to have therapy that is only available in a few select places?
During Study Design, Consider the Patient’s Perspective
It is very accurate when it comes to creating a positive patient experience. It’s essential to consider the study’s overall goal while deciding what procedures should be included in the protocol, even if many minor details are involved. Even if a surgery isn’t too taxing on its own, the cumulative toll on the patient can be staggering.
Solicit Patient Input On Your Study Protocol
Some patients consider clinical trials to help themselves and, more importantly, to help others in the future. As healthcare community members, we can’t take advantage of that desperation. Sponsors must consider the patient a partner in research and the end of their product. In the absence of this step, sponsors risk having a trial that can’t be conducted correctly and, unfortunately, won’t gather the data needed for the proposed study. Our focus must always be on the patients, the driving force behind continuous improvement in the healthcare industry.
Using technology to reduce the patient burden
Life sciences companies have to examine their current practices in light of the year 2020’s events and determine how to meet patients’ needs better while also prioritizing patient safety while planning clinical trials. To save their studies, several sponsors have scoured their networks and relationships for methods to collect clinical trial data from problems that are still in progress. It was when technology stepped in.
When conducting clinical trials remotely or with minimal in-person visits, a clinical trial becomes more patient-centered by design. Clinical investigators and site staff can communicate by teleconference, reducing travel stress on the patient and allowing for a more flexible visit schedule.
Both researchers and patients benefit from clinical studies. Because these studies are critical, it’s natural to focus on how effective the therapies are when considering their significance. Patients’ experiences in clinical studies are just as meaningful; however, As a patient, what are clinical trials like, and how can healthcare practitioners enhance their experience? Enroll in our certificate program for Clinical Trial Management today. This program is designed to meet the needs of the industrial market.
