This forum is dedicated to personal health in all its many facets: decision-making,
goal setting, celebration, discovery, reflection, coordination—even entertainment.
We’ll look at innovations in interactive technologies and how they help address
current critical healthcare challenges.
Elizabeth D. Mynatt, Editor
What Are Our Responsibilities
When Designing Sociotechnical
Health Interventions?
Katie A. Siek
University of colorado, boulder | ksiek@cs.colorado.edu
ceases. Based on these experiences,
I started thinking more deeply
about what our responsibilities
are when we design sociotechnical
health interventions. Here, I briefly
outline some of the responsibilities and questions the community
should think about before thrusting
technology on the next population
that could benefit from it.
September + October 2011
interactions
Maybe you heard a horrible statistic
about a health-related issue and
thought, “Technology could help
with this.” Or perhaps an event
in your own life prompted you to
think about how technology could
improve the health and wellness of
others. Whenever I have an experience that highlights a potential new
avenue of research, I begin by learning more about the health matter,
reviewing current health informat-ics applications, and then investigating methods for learning about
the needs of the target population.
Then I collaborate with a multidisciplinary team to create a health
intervention prototype that people
use for a short period of time to
validate its feasibility and effectiveness. It is this latter part that gives
me pause about what I do.
I occasionally receive email
messages from people at risk of
an illness or already battling a
chronic illness asking if they could
use some part of our prototype.
People are free to use what we create, but its utility for the general
population—straight from our
open source repository—is often
questionable since it is a research
project that does not come with
much support after the funding
Whose Values Should
Be Considered?
When we design sociotechnical
health interventions, there must be
some consideration of the accepted
or correct way to achieve good
health. Indeed, there are many
guidelines from various federal
agencies to help us understand
everything from what a balanced
diet is to what movements our child
should make at three months old.
But as soon as we decide on which
guideline to use in our intervention,
we are implicitly applying a set of
values to the population who will
use that intervention. Is this what
we should be doing through our
design work?
One argument is that this is
exactly what we should be doing—if
it is a health intervention, it must
be backed by evidenced-based
research illustrating if people
do these steps, they should live
a healthier life. Indeed, health-
care providers traditionally treat
patients in this manner; they pro-
vide a list of dos and don’ts based
on well-established research. One
of the projects I worked on followed
this argument because we were
designing a nutrition-monitoring
application for people with chronic
kidney disease. These patients
must follow a restrictive diet; if
they don’t, serious health problems
can result. We worked with nurses,
dietitians, and a nephrologist to
identify the ideal diet for this popu-
lation [ 1]. But one of our design con-
siderations was to include foods the
population was encouraged not to
eat (for example, potassium-loaded
strawberries). We wanted to respect
the person as an individual and
provide them with the ability to
consider non-recommended foods
to test how these foods affected
their restricted dietary limits for
certain nutrients. This prompted
discussions with the research team
about how we should talk to users
who routinely record foods that
put them over their dietary limits.
There is a fine line between lectur-
ing/admonishing and having an