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OUR MAIN DONORS

Department
for International Development

Handicap
International
European Commission
European Initiative for Democracy and Human Rights
*This website has been produced with the assistance of
the European Union. The contents of this website is the
sole responsibility of Handicap International South East
Europe and can in no way be taken to reflect the views
of the European Union.
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| INTERVIEW |
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| CONDUCTING
RESEARCH
interview with Marija Dragovic,
Project Assistant, Association of Students with Disabilities
(ADS) Belgrade
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The
Association of Students with Disabilities (ADS) of Serbia
network has a good amount of experience in conducting research
as they have either given or worked as a partner in three
surveys1 on disability. The first one was in 2001 on the promotion
of inclusive higher education in Southeast Europe. The second
was conducted in December 2003 to January 2004, dubbed the
“Promotion of Inclusive High School Education” in Serbia and
Montenegro. The last “survey” was named “Disability is a Matter
of Human Rights”, looking at individual experiences related
to the discrimination of people with disabilities, conducted
from November 2005 to February 2006. In their “surveys“, ADS
used a wide definition of disability, which also includes
people with chronic medical problems.
This last “survey“ was conduced amongst the population with
disabilities and had a sample of 545 people covering 15 municipalities
in Serbia and 12 in Montenegro. The questionnaire contained
both multiple-choice questions and those that people could
answer themselves and it consisted of 5 different parts, each
covering a different area of interest.
What
was the need behind the research on discrimination?
This research
was conducted before the anti-discrimination law on disability
was passed. ADS was part of the team drafting the law, so
we were aware of it, but the general population was definitely
not and our research reflected this. Yet, at that time our
specific reason for carrying out this kind of “survey“ was
to see if and how we should offer legal aid services to people
with disabilities, to see if they were ready to use it. So,
one of the aims of the survey was to see how to design legal
aid services. We are still working with the results we collected,
analyzing them, in order to develop this kind of service.
How
did the implementation go?
There were 14
people who administered the “survey“ throughout the municipalities
in Serbia and Montenegro. We wanted to include all the actors
involved in problem of discrimination; line ministries,
institutions and city services, but we ended up conducting
it in cooperation with centers for social welfare, the Ministry
of Human and Minority Rights and the People’s Office. The
common reply from the other stakeholders was that people
with disabilities were not under their jurisdiction.
In terms of timing, it took us a long time to formulate
the questionnaire, more than a month in total. The time
it took to get answers from the participants varied but
the topic of discrimination can be very personal and people
have lots of bottled up emotions so they often have a need
to speak at some length.
Once we had the responses from all survey takers, we had
to begin the data analysis process. A psychology student
assisted us in the analysis of the data as he had experience
in conducting surveys. He also helped to teach us how to
use SPSS, a statistics computer program for analyzing data.
Which
results would you stress?
The understanding
of discrimination varies widely amongst people. Some people
with disabilities even thought
that discrimination meant not receiving the benefits they
were entitled to; others understood it as being insulted
on the grounds of their disability by a person without one.
It is also striking how a personal experience of discrimination
can differ even if the situation and the personal background
are practically the same; some people just do not recognize
it as such. However, it took us by surprise that the feeling
of discrimination was the highest in the most unexpected
of places: in hospitals and at physical rehabilitation facilities.
At the same time, we expected to find a much higher level
of respondents who felt discrimination. Instead we have
some 60 percent who answered affirmatively that they have
not ever experienced discrimination.
Another important finding: the readiness to go to court
with an individual discrimination case was significantly
higher among those who felt that they had not been discriminated
against. That says a lot.
What are you going to do with the findings of the survey?
Will you present it to the general public through the media?
Or do you submit the results directly to state institutions
and bodies?
For this “survey“ we will publish a brochure in which we
present the results. We are also planning round tables across
the country, gathering several municipalities together;
putting the local NGO’s together with representatives of
local authorities.
What
were the specific problems?
The length of
the questionnaire is definitely something to seriously consider.
Looking at it now I see that in some places we have repeated
things or have asked the questions in such a way that the
responses are unusable. This is where the role of an expert
is crucial: they act as a guide, putting boundaries on the
questionnaire. In addition, they can make sure that the
questionnaire matches the general purpose you are trying
to achieve with your research.
Yet, the more resounding problem is how to get a sample
from a wider population. There is no database you can use,
with names and contacts of people with disabilities of all
ages and educational and geographic backgrounds. So, a wider
sample was not really possible even though we tried our
best to achieve it, even using the snowball method2.
Not having a large source of data, we were forced to get
our sample from the members of other organizations of people
with disabilities that were willing to cooperate. Anyway,
having mainly DPO members as the sample also produced biased
results. Members of the disability movement are far more
aware of human rights issues and discrimination than other
people with disabilities and the results show that. For
example, 26% of the respondents had higher education, whereas
according to data shown in the Poverty Reduction Strategy
Paper for Serbia (PRSP), only 7 percent of people with disabilities
completed university - a striking discrepancy. The results
of the “survey“ also showed that in answering questions
pertaining to household income, 42% of the respondents were
below the official poverty line, whereas according to the
PRSP, it is over 70%.
What
would be your specific recommendations, by different stages
in conducting a survey: the concept design, the implementation,
results analysis, and the dissemination and use of the findings?
Only people
with specific experience and training can administer surveys,
there is no question about it. Also, in “surveys“ like this,
next time we will include the definition of the key concept;
in this case, discrimination. If the participants had heard
the definition of discrimination, their position might have
been more clear and therefore of more use to us.
Also, the team of people administering the survey needs
to be very well informed on the philosophy and the ideas
behind disability issues. For example, they should be able
to explain the social model, plainly and with ease. Also,
whoever is planning to do a survey should definitely work
with an expert to design the questionnaire. By expert, I
mean psychologists and sociologists who have had experience
carrying out this kind of research.
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1 The research conducted is
more of a census of DPO members than a survey as the sample
was not determined randomly.
2 The snowball sampling method is a special non-probability
method used when the desired sample characteristic is rare.
It may be extremely difficult or cost prohibitive to locate
respondents in these situations. Snowball sampling relies
on referrals from initial subjects to generate additional
subjects. While this technique can dramatically lower search
costs, it comes at the expense of introducing bias because
the technique itself reduces the likelihood that the sample
will represent a good cross section from the population.
More information available at:
http://www.statpac.com/surveys/sampling.htm
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