Main objective: Contributing to the debate on the necessity of PPC in episodic memory by support of patient data. Secondary objective: Exploring the episodic memory theorem and developing a more sensitive (neuropsychological) research tool usable in…
ID
Source
Brief title
Condition
- Central nervous system vascular disorders
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
Contributing to the debate on the necessity of PPC in episodic memory by
support of patient data.
Secondary outcome
Exploring episodic memory and developing a more sensitive (neuropsychological)
episodic memory research tool such as a questionnaire or non-invasive memory
test that is also usable in the clinical setting.
Background summary
The influence or necessity of the posterior parietal cortex (PPC) in episodic
memory is currently under debate. Several studies on healthy subjects have
addressed the question whether PPC activity is related to mechanisms central to
episodic memory per se, or rather associated with subsidiary processes such as
attention, motor preparation demands, effort and self-related information
processing. Hence important insights might follow from studying the
consequences of PPC lesions on episodic memory tasks. Its influence on the
other closely related cognitive skills such as perception, mental imagery,
attention, and effort, all indirectly influencing episodic memory, need further
investigation as well. It is also necessary to check for necessary involvement
of other brain areas on episodic memory before the conclusion can be drawn that
PPC and episodic memory are necessarily related. The necessity of involvement
of PPC or other brain areas can only be supported by reporting on patients with
and without lesions in PPC.
Study objective
Main objective: Contributing to the debate on the necessity of PPC in episodic
memory by support of patient data.
Secondary objective: Exploring the episodic memory theorem and developing a
more sensitive (neuropsychological) research tool usable in the clinical
setting.
Study design
A battery of non-invasive tasks aimed at inventorying memory problems and to
profile cognitive skills will be administered. Most neuropsychological tests
used will be standardised tests with normative references. Two experimental
neuropsychological tests will be designed of which normative data needs to be
collected using a control population.
In the early phase, all neuropsychological measurements will take place within
14 days of the admittance of the patients to the University Medical Centre
Utrecht. This assessment is care as usual of the Department of Neurology of the
UMCU.
A follow-up at about six months will take place to measure lasting cognitive
effects of the infarction. This follow-up will take place either at the
University Medical Centre Utrecht, Utrecht University, or at the patient*s
home, depending on the needs and limitations of the patients. This follow-up is
part of a scientific study and is strictly voluntary.
Study burden and risks
The patients have to sit through a neuropsychological evaluation of at
approximately 2 hours (with breaks), depending on the capabilities of the
patient. The duration of the assessment is proven feasible in previous
documented studies. The tests all exist of non-invasive pen and paper tests, or
oral tests. The assessment can be terminated without consequences at any given
time when the participants feel they can take no more, or when the tests
administrator thinks continuation is unwise. The neuropsychological follow-up
assessment of a maximum of 3 hours (with breaks), again consisting of only pen
and paper and oral tests, is also voluntary and can be terminated without
consequences.
Heidelberglaan 100
3508 GA Utrecht
Nederland
Heidelberglaan 100
3508 GA Utrecht
Nederland
Listed location countries
Age
Inclusion criteria
* Patients must be 18 years or older;
* Patients with (sub-)cortical lesions;
* Lesions must be the consequence of an cerebral ischemic stroke
* Lesions must be visible on a CT- or MRI scan;
* Or ischemic stroke patients with expected episodic memory impairments referred by either the Department of Neurology or Neuropsychology of the UMCU.
Exclusion criteria
* No capability to communicate in Dutch or severe global aphasia
* History of alcohol or drug abuse;
* Neurological disorders other than (sub)cortical lesions or psychiatric disorders which could affect / have affected cognitive function;
* Any other non-neurological disorder influencing cognitive functioning.
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL29389.041.09 |