Trial Information
Summary: Sickle Cell Adult Neurological Dysfunction (SCAN) Study
What is the purpose of this study?
The Sickle Cell Adult Neurological Dysfunction (SCAN) research
study examines brain structure and memory and attention function in
adults with sickle cell disease. The study will use magnetic
resonance imaging (MRI) to examine the brain structure and
neuropsychological testing to examine brain function of adults with
sickle cell disease in order to find possible links to memory and
attention problems. The MRI and testing results will be compared
with MRI and testing results of adults with similar backgrounds who
do not have sickle cell disease. Study researchers will also
attempt to find out if certain treatments, such as blood
transfusions, can improve memory and attention problems.
Who will be included in this study?
Participants should be 21 to 55 years old and have been diagnosed
with sickle cell disease. Adults ages 21 to 55 who have not been
diagnosed with sickle cell disease will also participate in the
study. People who have had a stroke, are pregnant, or may become
pregnant should not participate in this research study.
What is involved?
This study lasts about one month and requires four visits to
Cincinnati Children's Hospital Medical Center. During Visit 1,
a research team member will ask the participant several questions
to determine eligibility. Several forms will be completed by the
participant, and a small quantity of blood, about a teaspoonful,
will be drawn. During Visits 2 and 3, the participant will meet
with a specially trained psychologist who will perform
neuropsychological testing. The testing lasts four to six hours. An
MRI will be performed at Cincinnati Children's Hospital Medical
Center. Visit 4 is a follow-up visit. Participants will receive a
summary of the test results and have an opportunity to meet with a
medical professional to go over the results and to ask questions.
If the test results indicate potential problems, participants will
be given specific recommendations about what should be done.
What are the benefits?
There may not be any direct benefit to participants who take part
in this study. This study may add to research team's knowledge
about memory and attention in adults with sickle cell disease and
may lead to better understanding of sickle cell disease and better
treatment for sickle cell disease patients. A potential benefit to
participants in the study is that formerly unknown abnormalities in
brain structure or function may be identified. This information may
be useful to the participant and the participant's doctor in
planning medical care.
Will I get all the facts about the study?
Adults interested in participating will be scheduled with a member
of the research team who will thoroughly explain all of the details
of the study. They will review the consent form with the potential
participant and will be sure that all questions are answered. The
consent form goes over all of the procedures, risks, benefits,
compensation, who to contact with questions or concerns and more.
Study procedures will not begin until the adult has signed this
form.
What are the risks?
Having blood drawn for laboratory tests will cause brief pain and
possibly bruising from the needle stick. There are no known risks
associated with filling out questionnaires or completing the
neuropsychological testing. These activities may be tiring or
stressful. There are no known risks from MRI studies, which use far
less energy than a single x-ray. Although MRI scans are painless,
participants may feel some discomfort from loud noises, the feeling
of being closed in while inside the scanner or from sensations on
the skin that resemble gentle taps. Because the MRI scanner
attracts some metals, it is important for the participant to let
the MRI technician know if any metal objects are in his/her body,
including a pacemaker or hardware from surgery. MRI scans can
affect unborn children, so it is important to inform the research
team of pregnancy during the research study.
What is the compensation?
For participating in the study, you will receive a total of $240
for your time and $60 for transportation. If you do not complete
the study, you will receive pro-rated compensation for the visits
you do complete.
Who should I contact for more information?
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Contact:
Aemita Terry, RN, BSN
Cincinnati Children's Hospital Medical Center/Cincinnati Children's Research Foundation
Division of Hematology / Oncology
3333 Burnet Ave.
Cincinnati, OH 45229-3039
Telephone: 513-636-4174
Email:
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Trial listings updated: June 1, 2008 at 5:45:33 AM