The Research Loop is not meant to be complicated or to require an advanced degree. You do not have to be an expert in the field or well versed in research techniques to provide feedback. All levels of feedback from any background are welcome.

The Research Loop encourages feedback of all kinds whether simple or detailed, positive or critical. The aim of all feedback should be to further the discourse in the subject area so that researchers can gain insight and apply it to their future endeavors.

Tips for better feedback

While feedback need not be in depth, certainly researchers will find it more useful if you can be specific and include details.  Here are a few tips on giving more robust feedback:

  • Posing feedback in the form of questions can be helpful. For instance, asking “Why did you choose to only use patients who were in the hospital?” or “Did you consider that a history of posttraumatic stress disorder might affect this finding?”
  • Commenting on all sections of the research to the extent possible can help the research know both that you read the content and perhaps where the research was not clear.
  • And of course checking spelling and grammar always helps. This includes making sure to spell out acronyms (e.g. posttraumatic stress disorder instead of PTSD).

Prohibited Feedback

Certain feedback will not be permitted by The Research Loop.  This includes feedback that contains:

  • Language that is insulting, inflammatory, or obscene
  • Offensive material
  • Advertisements
  • Self promotion
  • Job requests


Below is an example of feedback a patient or caregiver may offer and how it will be presented to the researcher.  You do not need to be this detailed.

The article for this example is open access and can be found here. You might take a moment to read it so you can understand the following feedback.

Graphics help patients distinguish between urgent and non-urgent deviations in laboratory test results.

Feedback for Dr. Brian Zikmund-Fisher

Article Citation
Zikmund-Fisher, B.J., Scherer, A.M., Witteman, H.O., Solomon, J.B., Exe, N.L., Tarini, B.A., and Fagerlin, A. (2016). Graphics help patients distinguish between urgent and non-urgent deviations in laboratory test results. Journal of the American Medical Informatics Association, 24(3), 520-528.

Date the person read this article (may be best estimate)

This person identifies as a:
Patient, Patient Advocate

This person is from:
United States

The reason person was interested in this study:

  • They were interested in the design and/or findings of this study
  • They were interested in the implications this research had for their care or the care of others they know

Overall impression of the study:
I really like this study.  As a patient, I know how hard it is to interpret test results from my doctor.  Having a colored line I think would be the most helpful to me.

Feedback on the study’s design:
I was glad to see that you had many people to sample from in this project so that you could get diverse views. I was wondering however if you would consider in future projects working with specific patient populations?  For instance, I would assume that cancer patients or patients with type 1 diabetes might have more experience with these areas and thus be able to provide feedback from their experience.

I did not like that you did not have a way for people to select that they might check online  or ask a friend about results before reaching out to their doctor.  I think many people will check online or ask a friend as an action that falls between doing nothing (and perhaps a lower urgency) and doing something (seeking out care). Since these patients are already online, one could assume that they might use online resources to put their findings in context.

Feedback on the study’s findings or conclusions:
I thought these findings were exactly what I would expect from the general public – that a colored line would be more helpful than a table.  In the discussion you talked about how hard it may be to determine the range and might select default display ranges. I think though that the tables already do this by indicating if a result is “Within Normal Limits” (WNL).  Perhaps you do not need to set endpoints as much as make sure there are clear markers for what is WNL.

Ideas for future research:
As I said above, I think it would be important to do a version of this study for patients who more frequently go to appointments – patients with chronic illness or with specific diseases like cancer.

How the person thinks the findings might impact patients or patient care:
I have seen this issue talked about with doctors and patients before – that the numbers and tables are hard to read and interpret. I think this will really help patients. However, it may be overwhelming if there are graphs like this for each result. Often I get maybe 20 results at a time and if I had to look at 20 graphs I might get confused or visually overwhelmed.

How the person thinks the findings might impact healthcare policy:
I think doctors and patients should push for this kind of information to be standard in all patient portals.  I also think in general there should be better patient education of what lab results may mean – perhaps better resources for finding information online.

General questions or feedback:
I was struck at the beginning of this article when you said that patients may “overreact to slightly elevated or reduced values.”  I think this is a very stigmatizing statement. Patients and caregivers do not “overreact” they simply react.  There has been a narrative in medicine for a long time that patients are incapable of determining what results mean.  In fact, I have found myself having to interpret the results on my own many times and pointing out problems to my doctors that they miss.  An article by Francesca Pillemer in PLoS ONE in 2016 talks about the potential releasing these results has to improve patient safety.  In my own experience, I know that my doctors may miss test results that may seem WNL but for me are abnormally high or low.  To say that I am “overreacting” is to dismiss my level of engagement and knowledge about my own care.

To that end, because I track my own results, I often compare my current results to past results.  As EHRs are used more, they may keep track of these differences and make comparisons as well.  How would a graph work that both shows where I am in comparison to WNL and in comparison to my own results?  It seems like a simple line graph may not work for that. 

I have seen a lot of tracking apps and I think the site Patients Like Me has experimented with graphing results. Have you worked with them or others to develop these ideas further?  I worry, just like EHRs, the type of graphs produced if different organizations create their own will mean patients have to learn new graphs each time we get results from a different doctor. We need a way to make this standard.