Social Communication
Social Communication
Social Communication
(from the June 2004 newsletter, Thinking Ahead) Department at Craig Hospital. It is a project of
the Rocky Mountain Regional Brain Injury System,
which is funded by the US Department of Education’s
Do you talk better than you communicate? National Institute on Disability & Rehabilitation
Research. If you would like more information
call: 303-789-8308
There is much more to communicating than just or email us at: [email protected]
talking. To actually “communicate,” we must also
share information with another person. We The views expressed here are those of Craig Hospital and
need to be able to listen to and remember what are not necessarily those of the US Department of Education.
we hear. We need to take turns speaking, and
not interrupt the other person.
We need to be accurate and not ramble when we talk. What we say needs to be
organized and make sense. And, we must always be aware of how our words, our tone
and our emotions are affecting the other person.
Communicating takes skill! It’s something that is difficult for everyone. Often, it is made
even more difficult by a traumatic brain injury (TBI).
A while ago, in our June 2004 issue of Thinking Ahead, we told you about a research
project that we are doing. That project studied Social Communication.
Social Communication has to do with things other than talking. People who have trouble
with Social Communication may speak or talk very well, but they may not listen to others
when they are speaking. They may interrupt and not take turns when talking. Some
ramble on and on. Other people may not make sense when they speak, or they may get
their facts wrong. All of these problems have one thing in common: they leave the
listener confused, disappointed, or maybe even uncomfortable.
Many people with TBI have problems with Social Communication. Their problems with
Social Communication can affect their social life. They can make it harder to make
friends. Social Communication problems can make it hard to find someone to date.
They can make it hard to have a successful job interview. Over time, Social
Communication problems can make someone isolated.
Many people who read our June 2004 newsletter about Social Communication told us
then that they wanted to learn more about this project. So this is the second of what will
be three newsletters about Social Communication. In this one we will tell you about the
60 people with TBI who participated in the project. In a future newsletter we’ll tell you
about how successful the groups and classes were. We hope all of these newsletters
will give you information you can use.
First, here is some information about the 60 people in the study. We’ll call them
“survivors” here.
• 83% of the survivors were men, 17% were women.
• Their average age was 39 years. (The youngest was 20 years old; the oldest: 63
years old).
• The survivors were injured an average of seven years (The shortest amount of time
anyone had been injured was 1 year; the longest was 21 years).
• 65% of the survivors had severe injuries. The rest were milder or moderate.
• Their average length of inpatient rehab was 74 days (The shortest was 15; the
longest was 244 days).
• 80% of the survivors had completed at least some college.
• Only 20% were working for pay when the study started. Another 5% were students
or homemakers.
• All of the survivors had pretty good memories. Their comprehension and speaking
skills were also pretty good at the time they signed up for the research.
These 60 people took several different tests. (These are listed at the end of this
newsletter.) They rated their communications skills. They told us how active they were
socially and in their communities. They also rated their life satisfaction. Family
members, spouses, boyfriends, girlfriends, or partners also rated the 60 survivors. We’ll
call these people “significant others” or “SOs.” In addition, we videotaped each survivor
as he or she had a conversation with another person. The researchers then watched this
video and rated the survivors’ communication skills and problems.
Here is a summary of what we found. It is a description of what the people were like
before they even started their group discussion course to try to improve their Social
Communication skills. It gives you some idea of how they saw themselves, and how
thier SOs saw them.
1. The survivors were able to identify some of their own communication problems. The
problems they saw had to do with:
• keeping the conversation going, thinking of new things to talk about or coming up
with new questions to ask
• knowing when and how to end a conversation
• changing subjects smoothly
• interrupting the other person smoothly
• keeping their thoughts organized.
2. SOs reported even more problems. Families and SOs thought the problems were
more severe than the survivors did. And, they often did not agree with what the
survivors saw as problems.
What does this mean? You probably already know if Social Communication is a
problem for you. Your own rating of your problems may be pretty correct. But, the
opinions of others around you are also helpful. They may go a step further and give
you even more information. They might help you identify other areas to work on to
improve your communication skills. Talk with your friends and family members.
Listen to their suggestions. Work on the areas where they tell you improvement is
needed.
3. Families, SOs, and rehab people often see two types of problems that the survivor is
not aware of. One problem has to do with the survivor’s nonverbal cues. These
include facial expression, tone of voice, and emotions. Sometimes any or all of these
are not appropriate for the situation. The other problem has to do with how well the
survivor pays attention to the other person when having a conversation. The
survivor may not take turns. She may not ask the other person about him or herself.
He may not give the other person a chance to answer. She may not pay attention
when the other person talks. He may talk about himself too much.
What does this mean? – First, non verbal cues
are very important. What you are saying with your body can be just as important as
the words that come out of your mouth. If the two don’t “match,” the listener can be
confused or uncomfortable. Ask someone you trust to tell you about your body
language, your gestures, and your facial expression when you talk. Second, try to
be very aware of the other person when you are having a conversation. Yes, it is
very hard to worry about the other person when you are already working very hard
just to communicate what you need to. But, this is a very important area. Try to
work on it. Get help. Practice. A person who talks less – or even one who talks
poorly – will probably still be more successful if he pays close attention to the cues
from, and the needs of, the person he is communicating with. People like very much
to know that you are listening and paying attention to them. They also like it when
you are not just talking about yourself. They want you ask them about themselves
also. They like it best when conversations are 50-50.
4. The longer survivors are hurt, the more they seem to notice communication
problems.
What does this mean? This probably does not mean that your communication only
gets worse over time. Instead it means that people’s insight increases, at least for
the first several years after the injury. As a result, their ablity to see their own
problems and concerns may improve. This is a no lose situation for you: it means
that, for a few years after your injury, you will probably become more and more
aware of how other people see you. So, there is good reason to be hopeful. But, we
also said above that SOs and rehab staff can identify more communication problems
right now. This means that you don’t need to wait to get help until a problem
becomes obvious to you. You can begin now to work on problems that other people
help you identify. The bottom line: ask people you trust for advice. Ask them what
would make them enjoy conversations with you more. Practice improving the things
they identify.
5. We also found that survivors who thought they had problems with Social
Communication also reported lower satisfaction with their lives. They also tended to
be less active in their communities. They were less likely to be working or going to
school.
What does this mean? This is a very important finding. Your communication skills
can affect all areas of your life. Many, many things can affect your social life. A lot
of them can be related to your TBI. Could your social life be better? Could you be
happier with your life? Could you be more active in your community? Think about
this: Regardless of how good you think your communication skills are now, maybe
improving them could improve other areas of your life as well. It doesn’t really matter
if you have a problem with communication. What really matters is this: Better
communication skills could make you more confident, more social, and more
involved in life. Look for ways to get help and practice. Use your friends and
families. In our next newsletter, we’ll also tell you about how effective special
communication groups might be.
These are the surveys the participants completed: The Social Communication
Questionnaire (McGann W, Werven G, Douglas M. Social competence and head injury:
a practical approach. Brain Injury 1997; 11:621-628); The Profile of Functional
Impairment in Communication (Linscott R, Knight R, Godfrey H. The profile of functional
impairment in communication (PFIC): a measure of communication impairment for
clinical use. Brain Injury 1996; 10:397-412); The Craig Handicap Assessment and
Reporting Technique – Short Form ; (Whiteneck GG, Charlifue SW, Gerhart KA,
Overholser JD, Richardson GN. Quantifying handicap: a new measure of long-term
rehabilitation outcomes. Arch Phys Med
Rehabil 1992; 73:519-26); Thinking Ahead is published by the Research
The Community Integration Questionnaire Department at Craig Hospital. It is a project of
(Willer B, Rosenthal M, Kreutzer J, Gordon the Rocky Mountain Regional Brain Injury System,
W, Remple R. Assessment of community which is funded by the US Department of Education’s
integration following rehabilitation. Journal of National Institute on Disability & Rehabilitation
Research. If you would like more information
Head Trauma Rehabilitation 1993; 3:75-79.); call: 303-789-8308
The Satisfaction with Life Scale (Diener E, or email us at: [email protected]
Emmons R, Larsen J, Griffin S. The
satisfaction with life scale. J Personality The views expressed here are those of Craig Hospital and
are not necessarily those of the US Department of Education.
Assessment 1985; 49:71-75.)
Social Communication Classes: Do They Work?
(from the January 2007 newsletter, Thinking Ahead)
As part of our TBI Model System project, we ran special communication groups or
classes. We wanted to see if they could help improve Social Communication for people
with TBI. This is our third newsletter about Social Communication research. The first
one explained the problem (June 2004). The second newsletter described the people
who were in our study (January 2006). This one will tell you what we learned. It will tell
you if and how the classes helped. But, before we go on, let’s review a little bit.