The Importance of Advocacy Outreach for Patient Recruitment

The Importance of Advocacy Outreach for Patient Recruitment

By Aaron Fleishman on Tue, Aug 25, 2015

Advocacy Outreach Patient RecruitmentPartnering with advocacy groups is a vital component to any clinical trial outreach effort. The approach to working with advocacy groups has changed in recent years. It is not just about the one connection you may have with one organization. These days it’s about working with the condition community as a whole for one common goal. Advocacy groups often have direct connections to people affected by a condition and can be highly beneficial to enrollment throughout the patient recruitment process.

Below is a recap of some common questions BBK gets regarding advocacy outreach for patient recruitment. 

How do you get rid of the negative stereotypes associated with clinical trials and promote a more positive image?

I think it is important to note that more and more advocacy groups are becoming well informed about clinical research, including the process, confidentiality restrictions, protocols, etc. In the discussions I have had with advocacy organizations, many say they are concerned about the promotion of one study over another. If they work with one sponsor to raise awareness of a specific clinical research opportunity, and they do not pay attention to another study that might benefit their members, is that favoritism? Seems as though that would not be the most beneficial process for helping their members find clinical trials that could help. It is important for clinical research sponsors to incorporate a plan for patients so if they do not qualify for their study, they also make available all of the other studies specific to their condition. That way there is an avenue for patients to stay informed about clinical research and eases the advocacy organization’s worry about promoting one study over another. As a sponsor, your task is to put your study in the best position possible to enroll. In addition, there is a corporate responsibility to help patients find the study that is the right fit for them.

How does working with advocacy groups as a patient recruitment tactic differ in the U.S. as compared to outside of the U.S.?

No matter where you are in the world, it all comes down to how educated the advocacy group is about clinical research and what their comfort level is in working with sponsors. Some organizations are going to have restrictions. Some countries are going to have restrictions. Understanding those restrictions and evaluating the options you have to work with will help shape and determine the tactics you use.

Getting time with the advocacy groups can be difficult, as the competition for their attention is increasing. What do you suggest to support our efforts?

This is why building relationships with advocacy is so important. I think there is a common misconception that you only have to work with advocacy groups when you have a specific study in mind. That simply is not the case. Sponsors should never stop working with advocacy groups. At the beginning of this blog, I highlighted how it’s not about one connection at one advocacy organization, but rather about working with the condition community as a whole. This is another reason why that is so important. Advocacy groups are being called upon more and more. We are competing for their time, but maintaining lasting relationships with a variety of groups – even when you’re not promoting a specific study, is what will ultimately enable you to stand out.

We will continue to look at the important role advocacy groups play and how we can best leverage these relationships so be sure to check the blog frequently.

 

Topics: Patient Recruitment, Patient Advocacy