Science topic

Neuropsychological Tests - Science topic

Tests designed to assess neurological function associated with certain behaviors. They are used in diagnosing brain dysfunction or damage and central nervous system disorders or injury.
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Would like to see the tamil version of MMSE.(mini mental state examination). clarify is it recently got copyrighted; requires purchase for using?
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Sir can you share the tamil version of mmse? Email: shan.mukh025@gmail.com
Thankyou in advance.
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I am working on a regression based approach to provide norms for a neuropsychological test battery. However, i do not know how to easily and accurately use the cumulative frequency distribution to convert raw-scores into scaled standard scores (mean on 10, SD of 3). Anyone who can help me?
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Donald,
Thank you very much for your valuable answer.
Nicolò
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We are two third year bachelor of psychology students looking into using PsychoPy for a continuous performance task. (CPT)
Our project is about the interactions between boredom proneness and sustained attention in the context of mindfulness meditation.
If you have any references or tips for us, we would gratefully take in account your advices.
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I'm sorry I do not know
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Dear All,
Anyone of you have an idea about specifications and version for CANTAB software. I intend to order one for my psychology laboratory but there are different versions and categories. What should be best to order for a new psychology lab ?
Any leads would be appreciated.
Regards,
Afreen
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I think it depends on your goal in project,there are many option.
Actually it depends on variables you want to study on.
For example in our field of research mostly use Task are:
MT:multitasking
OTC:one touch stocking
SST:stop signal task
RVP:rapid visual information processing
So we can just provide these Tasks.
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I need to device an experiment with the n-Back Pointing task without any hardware complement; e.g., no tablet to execute the reaching movements or computer touch screen to select the presumed correct items. The paradigm should be consistent with an ambulatory setting, as a traditional neuropsychological test.
Thanks in advance.
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I need to device an experiment with the n-Back Pointing task without any hardware complement; e.g., no tablet to execute the reaching movements or ...
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Pearson's Q-Global is expensive, and does not have Indian versions of tests or norms!
a. Are there cheaper, culture-fair online tests that are psychometrically sound, for research?
b. What are people's experiences of adapting existing neuropsych tests to videoconferencing for research purposes?
Thanks in advance!
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Teleneuropsychology: A model for clinical practice.
One more relevant publication for your reference:
Thibodaux, L. K., Breiger, D., Bledsoe, J., Sato, J., Hilsman, R., & Paolozzi, A. (2021). Teleneuropsychology: A model for clinical practice. Practice Innovations, 6(3), 189-198.
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Dear Colleagues,
Has anyone used a composite score based on the LEAP-Q?
I work with bilingual data and I would like to apply a LEAP-Q composite score. However, I have not found any studies that would apply an aggregate score for LEAP-Q results.
Thank you,
Monika
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LEAP-Q is great for assessment of each of the multilingual’s languages, but w/out composite score.
Potential alternative instrument to consider for dominance score:
Bilingual Language Profile, BLP (Birdsong, Gertken, & Amengual, 2012)
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it can be either a neuropsychological assessmentfrom age 8 years old or a wel research paradigm
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YES NEPSY and WISC
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Hello,
I am currently busy with my masterthesis and I have a question regarding the bootstrap of the paired samples t test. My data contains a small sample size (n =18). My supervisor advised to do a bootstrap paired samples t test. When I run the test (n = 18), because of missing data.
However, now I have a question regarding the interpretation. In total, I have examined 9 neuropsychological tests (on two time points). Two results seem very contradictory.
One pair has a BCa 95% CI of (-.21, -.07) and a p value of .113
Another pair has a BCa 95% CI of (-.07, -.21) and a p value of .111
Now I was wondering where to check for the significance. The 0 is not in the CI (so it is significant)? However the p value is > 0.05. Does anyone know how to solve this?
Thankyou in advance!
Best,
Anouk
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Hi,
The p values from either of the sets are not significant at or below 0.05. The C.Is is not wide. The null hypothesis is accepted.
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I have come across various neuropsychological studies and found that most of the studies have used different neuropsychological tests (TMT, WCST, Stroop...etc) to measure executive function. So can we combine the results of different neuropsychological tests of executive function for a meta-analysis?
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Two thoughts:
1. In order to combine results across tests that use different scales, one must place the results on the same metric. The easiest thing to do here would be to convert all standard scores to z scores. (You could probably do this starting with percentiles as well, but if possible, start with standard scores.)
2. I would not automatically lump all of these tests together as "executive function tests," because executive functions are complex, multifactorial in nature, and the tests are imperfect anyhow in that they also tap into other abilities (processing speed, memory, and so forth). So begin by analyzing each test separately. Then maybe do a meta-analysis of their correlations with one another (e.g., how closely related are Trails B and the Stroop?). Only if two measures are strongly related to each other should they then be combined into a higher-order meta-analysis.
You have your work cut out for you!
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In reviewing an article from 2010 for a test of learning and memory, the author presents a table of normative data. Within the same trial, a score is equated with different percentiles. For example on the second learning trial, a raw score of 6 is equated with two different percentiles, 10 and 5. While the qualitative interpretation of the score is not significantly different in my opinion, as both represent impairment in comparison to the normative group, but it becomes confusing as to which percentile to report.
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I am planning to conduct a study where the verbal responses of the participants will be recorded while sitting and also while standing. I want to use software that can precisely record the responses (i.e. converting speech to text) along with the reaction time of the responses or it can at least give accurate timestamps of the responses. Please suggest any reliable software or platform that can be used for this purpose.
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If you intend to use a paid software, then E-Prime would be helpful when used with Chronos and microphone.
E-Prime can record voice after each stimuli and keep it as separate recordings and it can get response times from the start of vocal responses.
You can use AudioInRecord Task Event, but have a look at their webinar on this topic for more information.
I don't think it can automatically convert the recording to text though.
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I am beginning an experiment assessing timing-related behavior in adults with ADHD and the perceptual measures I plan to use are adaptive, and determine perceptual thresholds using standard adaptive algorithm procedures (e.g. staircase method). However, I'm concerned about the inevitable impact of attentional lapses on thresholds. I am interested in suggestions for how best to tune the staircase parameters and/or suggestions for other adaptive algorithms that may be more resilient to lapses of attention. Any thoughts?
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2-the adaptive procedure: I think, indeed the most suitable are the staircase
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I want to use CABTAB for my master’s thesis about pilots ?
which tests would be more related to assess pilot cognitive functions?
Does any body have its report interpretation(CANTAB report interpretation)?
thsnks,
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I don't have a direct answer to your question, however the following may be of help:
Sci Rep. 2019 May 22;9(1):7688. doi: 10.1038/s41598-019-44082-w.
Influences of age, mental workload, and flight experience on cognitive performance and prefrontal activity in private pilots: a fNIRS study.
Causse M1, Chua ZK2, Rémy F3,4.
Author information
1ISAE-SUPAERO, Université de Toulouse, Toulouse, France. mickael.causse@isae.fr.2ISAE-SUPAERO, Université de Toulouse, Toulouse, France.3Université de Toulouse, UPS, Centre de Recherche Cerveau et Cognition, Toulouse, France.4CNRS, Cerco, Toulouse, France.
Abstract
The effects of aging on cognitive performance must be better understood, especially to protect older individuals who are engaged in risky activities (e.g. aviation). Current literature on executive functions suggests that brain compensatory mechanisms may counter cognitive deterioration due to aging, at least up to certain task load levels. The present study assesses this hypothesis in private pilots engaged in two executive tasks from the standardized CANTAB battery, namely Spatial Working Memory (SWM) and  One Touch Stockings of Cambridge (OTS). Sixty-one pilots from three age groups (young, middle-aged, older) performed these two tasks from low to very high difficulty levels, beyond those reported in previous aging studies. A fNIRS headband measured changes in oxyhemoglobin (HbO2) in the prefrontal cortex. Results confirmed an overall effect of the difficulty level in the three age groups, with a decline in task performance and an increase in prefrontal HbO2 signal. Performance of older relative to younger pilots was impaired in both tasks, with the greatest impairment observed for the highest-load Spatial Working Memory task. Consistent with this behavioral deficit in older pilots, a plateau of prefrontal activity was observed at this highest-load level, suggesting that a ceiling in neural resources was reached. When behavioral performance was either equivalent between age groups or only slightly impaired in the older group, there were not any age-related differences in prefrontal activity. Finally, older pilots with extensive flying experience tend to show better preserved spatial working memory performance when compared to mildly-experienced of the same age group. The present findings are discussed in the frames of HAROLD and CRUNCH theoretical models of cognitive and neural aging, evoking the possibility that piloting expertise may contribute to preserve executive functions throughout adulthood.
PMID: 31118436 PMCID: PMC6531547 DOI: 10.1038/s41598-019-44082-wFree PMC Article
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For MMSE (Mini Mental State Exam), illiterate people are unable to answer questions requiring them to read and follow instructions, such as the question asking them to follow instructions to close their eyes. Individuals who are paralysed are also unable to complete the tasks of taking the paper in their right hand, folding it in half and putting it on the floor. For such cases, how should we interpret their results? Should those items be excluded entirely (i.e their score is upon 29 instead of 30) and be scaled to be upon 30?
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I had the same question years ago. I searched then and found an Apa article with adjustment of MMSE with age and level of education. I translated it in romanian for my supervised and attached it that way (“varsta“ = age). I’ll look for the paper and come back.
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Dear all,
I am trying to develop an Neuropsychological scale which would measure the levels of engagement, performance and satisfaction of people. Are there any experimental tests available which I could build or adapt upon?
Thanks in advance,
Shardul
Edit: A small addition, I am NOT looking for survey questionnaires, I am trying to build a scale that could be used to measure these variables in a more interactive way.
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For testing satisfaction with life we used the following scale:
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Hello.
My research involves analyzing the change between five test intervals on four different composites of a neuropsychological test. I was planning on running four separate repeated-measures ANOVA's. I know that the repeated-measures ANOVA and pairwise comparisons automatically correct for multiple comparisons in one test during analysis, however I was planning on adjusting for Bonferroni's post-hoc to control for Type 1 error from conducting four separate ANOVA's (i.e. the dependent variable used in each ANOVA is part of an 'overall' family of tests).
Unfortunately, my data is not normally distributed and I now plan on running four separate Friedman's ANOVA's and four Wilcoxon Signed Ranks Tests (one Friendman's ANOVA and one Wilcoxon Signed Ranks Test for each composite).
However I'n not sure what to do about Bonferroni's. Do I apply the Bonferroni's correction to control for Type 1 error from running four separate Friedman's ANOVA's post-hoc (i.e. 0.05 / 4)? I know I have to apply Bonferroni's to the Wilcoxon Signed Ranks Tests (the non-parametric equivalent of a paired t-test), for the 10 comparisons from having five test intervals (i.e. Time 1-2; 1-3; 1-4; 1-5; 2-3; 3-4; 4-5; 2-5; 3-5; 2-4). Do I also have to apply Bonferroni's correction to the Wilcoxon Signed Ranks test to control for Type 1 error from running four Wilcoxon Signed Ranks tests, in addition to the Bonferroni's correction for the 10 comparisons within each composite?
Any help would be greatly appreciated!
Thanks in advance!
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As Bonferroni correction relates only to the p-values per se, it does not matter if it is parametric or non-parametric clusters of p-values that are corrected. For Kruskal-Wallis can Dunn-Bonferroni be applied.
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e.g. default mode to performance on attention tasks, salience network to emotional salience tasks, and executive motor component to executive tasks.
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Thanks but that is exactly the problem. The ICA components are being ascribed functions on indirect evidence and no direct evidence exists.
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With advances in emergency medicine, and worldwide training programs for advanced cardiorespiratory life support, more and more patients survive with little or no neurologic sequela. With standardized post-reanimation treatment and diagnostic algorithms, neuroimaging studies are performed in many patients, sometimes regardless of their neurologic short-term outcome. However, abnormal signs (not restricted to ischemic/hypoxic changes) may impact the patients' social and economic lives significantly. As pathologic results from neurocognitive and neuropsychologic tests are well accepted by insurances, the benefit from early neuroimaging studies in cardiorespiratory arrest survivors with good short-term neurologic and functional recovery can be questioned.
Should routine neuroimaging studies be performed in such survivors with good short-term outcome?
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Dear Dr. Jan,
Thank you for your informatio. I completly agree that formal studies in this context are needed. However, such a study would be very difficult to perform from an ethical standpoin. The only way would perhaps be an interinstitutional comparison of medical care centers performing neuroimaging following different local strategies or standard operating procedures.
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Hello😊
I have a question regarding Intraclass Correlation Coefficients (ICCs). My research is investigating the test-retest reliability of a neuropsychological test over five different test administrations one year apart. The test consists of five composites. In addition to using a repeated-measures ANOVA to investigate the significance of score change over the five years on all five composites, I wanted to use ICCs as a statistic for test-retest reliability as other test-retest reliability studies in this area use them. However, all other studies are over three test administrations and produce ICCs for times 1-2, 2-3, and 1-3 on all five composites. I have five test sessions and wanted to produce ICCs for 1-2, 1-3, 1-4, 1-5, 2-3, 3-4, 4-5 on all five composites. That’s 7 different comparisons/correlations (I’m not sure which it is). Would this be possible? I read that the ICC model is based on an ANOVA model, so I am concerned about Bonferroni’s correction. Does the error Bonferroni’s corrects applies when using ICCs?
Any guidance would be greatly appreciated.
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ICCs are like Pearson Correlations (when two variable are considered). Generally, using ICC for ordinal measurements are not correct. However, for ordinal measurement with more than 10-15 levels, ICCs are used.
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Can anyone recommend a neuropsychological test to assess problem solving, preferably with easy application for dementia? It can be a sub-test of a large battery. Thanks very much in advance.
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Hi,
Maybe this article will interest you:
Article The Mindstreams MCI score: a practical clinical tool for ear...
Best regards,
Ya'akov
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I am working on a regression based approach to provide new norms for a neuropsychological test battery.
I am trying to use a similar apporach to Heaton et al, or
However, i do not know how to easily and accurately use the cumulative frequency distribution to convert raw-scores into scaled standard scores (mean on 10, SD of 3):
Anyone who can help me?
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Assuming that your data are more or less normally distributed, you can convert to z scores as follows:
For each case, subtract the mean score for the sample from the score obtained by that individual. Then divide by the standard deviation for the sample. You can probably use the calculator at http://vassarstats.net/standard.html to make this happen quickly & easily.
The z score, of course, has a mean of 0 and a standard deviation of 1. To transform these into Wechsler-type scaled scores (mean of 10, SD of 3), I think you'd simply multiple by 3 and then add 10.
If the distribution is badly skewed or bimodal, you can still use this approach but you will not have the "expected" number of cases with each possible score. I haven't seen this issue discussed with regard to the Wechsler scaled scores, but it crops up in the literature on T Scores (more common in personality tests). The standard scores you get using the basic formula above preserve the original distribution of the data. If you want to force your scores to fall along a normal curve, there are extra steps to take. (The first approach yields a linear T Score; the second, a uniform or normalized T Score.) Erik Mortensen of the U. of Copenhagen (who is on ResearchGate) wrote a paper on normalized T scores, and Auke Tellegen (U. of Minnesota, now retired) wrote one on uniform T Scores, both in the 1990s.
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Hi,
I would be thankful for any piece of literature introducing short, accessible and uncomputerised psychological tests for executive functioning and visual-motor processing. I am most interested in assessment of spatial and hierarchical planning.
Thank you
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Stephen, thank you for the reply. I didn't correctly express myself and have now corrected the question. I am not interested in one test which would merge all the functions but in all the tests available which cover the mentioned (not all in one test).
I am familiar with the Tower of Hanoi and I saw that the set can be bought online for a reasonable price, but was still hoping that other planning assessment tasks would be available.
Thank you for suggesting the Porteus Maze test, I will look into it.
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Hi!
When measuring context memory, I found that there are big interindividual differences regarding the accuracy in spatial and temporal memory tasks, such that one person might perform very well on spatial memory but badly on temporal memory, but another person might perform well on temporal memory and badly on spatial memory.
I would be interested in finding out where this difference comes from and include some tests regarding these differences in a future study.
For spatial memory, there are many tests to choose from (spatial abilities etc.), but for temporal memory, I have no clue what could contribute to their performance (executive functions,time perception,..?)
Do you know any literature, neuropsychological tests or questionnaires that assess this?
Thank you very much!
Melanie
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I'll look into that, thanks :)
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I'm usually using Bonferroni for ANOVA post hoc testing, but I was also told this test is too "demanding" and I might lose some interesting data with it.
I usually need this analysis to compare sociodemographic characeristics in neuropsychological tests performance.
Thanks!
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Without claiming to be a great statistician (I'm not), I've always suspected that the Bonferroni correction is mainly a way of discouraging researchers who might otherwise be inclined to "shotgun" data sets with lots of variables. But it accomplishes this by being excessively stringent. Take the case of a correlational study with 80 cases and 10 variables (this could be something as simple as the subtests of an ability measure or the scales on an omnibus personality test). The correlation matrix will have 50 entries. Using the conventional p<.05 standard, correlations of .217 or greater will be deemed "significant" and therefore interpretable. But if you apply the Bonferroni correction (.05 divided by 50) and demand a .001 level, then you would need r = .362 to proceed. Given how many actual correlations in personality, social, and clinical research hover in the low thirties, this would indeed mean skipping over lots of potentially important information - or even claiming that relationships did not exist when in fact they did (good old Type II error).
My recollection is that the Scheffe test is the most conservative of the post-hoc significance tests in that it controls for Type I error across all possible comparisons. So if, in an ANOVA, you had four groups (say, mild cognitive impairment, Alzheimer's, frontotemporal, and subcortical dementias), it would control not only for pairwise comparisons but also for combinations such as (MCI + FTD) vs. (ALZ + PAR). Sometimes this is an important set of comparisons, sometimes not.
The Tukey (not Turkey) HSD controls for all possible pairwise comparisons. So in the above example, your risk of Type I error could be set at five percent (.05) for MCI vs. ALZ, MCI vs. FTD, MCI vs. PAR, ALZ vs. FTD, ALZ vs. PAR, and FTD vs. PAR combined. Which, in that example, would probably be more than sufficient.
On the whole, I like to just use the Tukey test. And even if you do perform the occasional analysis combining groups, you're still being pretty conservative - and I've never had a reviewer or editor take me to task for it.
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Do we expect the cognitive level of functioning to be stable 1 year post surgery or is further and significant remission possible 2 years post surgery ? One study , Grammaldo et al (2009) reports further remission 1-2 years post surgery. Do you know of other studies addressing this question ?
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Please let me know if the following references/sites are useful to you:
1.  Neuropsychology in Epilepsy-Surgery - ta-service
Basic principle: comprehensive neuropsychological test inventory examining ... issues in surgical treatment of temporal lobe epilepsy. Neuropsychology in Epilepsy-Surgery ..... Verbal memory deficits in patients after dominant hemisphere.
2.  Neuropsychological outcomes after epilepsy surgery: Systematic ...
by E Sherman - ‎2011 - ‎Cited by 182 - ‎Related articles
Jan 20, 2011 - gains and losses after epilepsy surgery, and this varies across neuropsychological tests and cognitive domains. For these reasons, empirically ...
3.  Psychological and Neuropsychological Assessment Before and After ...
by GA Baker - ‎2001 - ‎Cited by 11 - ‎Related articles
Psychological and Neuropsychological Assessment Before and. After Surgery for Epilepsy: Implications for the Management of. Learning-Disabled People.
Dennis
Dennis Mazur
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temporal lobe, wernicke area, neuropsychological assessment 
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What about subtests from Wechsler battery?
Verbal fluency should be very informative. 
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Dear All,
I am preparing my Master's thesis, where I would like to use a standardised Neuropsychological Test battery (computerised one), that will estimate general cognitive performance.
I have found many positive opinions regards the Cambridge Neuropsychological Test Automated Battery (CANTAB).  I would like to ask if anyone has an experience with this test battery? If yes, is the CANTAB a recommended tool?
Kind regards,
Adriana
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We used CANTAB for several years. We saw pros and cons. The pros were a wide range of tasks and when they worked, the system was pretty slick. I really like the reporting function although it took a few minutes to figure it out; it wasnt logical unless you were thinking like a programmer. The downside: some tasks would freeze in mid task and that was a recurring problem. The freeze would sometimes trash that participants file. THe help desk was...not helpful. Let me say that w e bought a turn key system from them; a laptop and the software and we installed no other apps on this system. After a lot of back and forth, they admitted to us that their system would never be failsafe on the hardware they sold us and so they suggested that the solution was to buy an all new system. Our response was to punt. I would say that they were very pleasant and tried to be helpful but for the licensing cost (not small) we felt we were 60%? 7-% satisfied. 
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I am currently writin a literature review on several tools for assessing prospective memory. Would you have the normative data (sample characteristics, reliability, validity, sensitivity, specificity, etc.) of the RBMT-III and the CAMPROMPT (Wilson et al., 2008;2005) ? 
Thanks in advance for your help.
Regards,
Geoffrey.
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Your question contains links to the best sources. The tests will come with detailed Manuals. If you don't have a budget to purchase, then try contacting a Pearson Clinical representative; I know they want to facilitate research/publications regarding their products.
Another good source would be the Mental Measurements Yearbook, published by the Buros Institute. Your library may have a subscription; otherwise, you have to pay about $15 US per article. These are commissioned reviews by assessment experts. I know they published one about the Cambridge Prospective Memory Test in 2005, and I think the most recent review of the Rivermead was in 2008.
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We would like to use the FCSRT in our clinical routine but we don't find any standardized norms for the German version. Could maybe someone, who is using the FCSRT not only for Research, tell me where I could find reliable norms or which cut-offs they use?
Thank you!
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Hi Lara,
thank you very much for all the Information! It is very helpful!
Regards,
Sarah
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Usually assessments are based on gait and balance, bladder control, and neuropsychological testings. Many neurosurgeons expressed their confusion regarding worsening after initial improvement or frequent unexplained changes ups and downs during post-shunt follow ups.
In a guideline article by Prof. Marmou with others; “Outcome of shunting in NPH and the value of assessment in shunted patients”. Prof. Marmou guideline was there is no validated, universally accepted scale for assessment of treated or untreated NPH. So there is a universal neurosurgical non-agreement regarding measuring outcome post-shunt.
Added to what mentioned above, it is well known that shunt function is notoriously unpredictable.
What are your personal observations with your patients?
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@ jetty: Thank you too much for the important links mentioned above. The most NPH detailed was the third one which is giving precious comprehensive knowledge.
The problem is that the different testings available at the time being are crude and not sensitive enough to achieve optimal CSF pressure adjustment without possibility of serious risks. So most neurosurgeons would rationally prefer some under drainage which is safer. This compromise is not the optimal treatment as patients might suffer significant symptoms when adjusted above optimal. The dynamic changing nature of CSF is another problem they are facing. It looks as if the optimal point is escaping easily from them in some patients. Optimal adjustment would also logically help to prolong shunt life.
I am not denying the great researches which are going on to improve hydrocephalus understanding and management. Hydrocephalus researchers and experts have used to declare these problems and controversies very frankly and honestly. I am trying to share.
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Dear Researchers, 
I am working with an animal model to test the Benefit of an antibody on cognitive function in a mice model  but the problem that I have several cognitive testing and I think i need to give mice a break between the tests! How long should I wait to do that? a week or several days? what do you think? 
Regards, 
Mohammed 
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Dear Beatrice, 
Thank you very much for your answer. I want to test Y Maze, and Morris Maze ? 
How much time needed to separate between the two tests in aged mice ?
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I am a clinical psychologist who happens to use an immense number of psychological (and sometimes neuropsychological) tests regularly, looking for strengths as well as pathology. I have been looking without much success for a test of Emotional/Social Maturity, and so have constructed one using various sources including Goleman (Emotional Intelligence). If interested is experimenting with my draft, email me. (email removed by admin). presently, I am working with the possibility of subcategories of feelings awareness, relationship ability, awareness of others, self development, character development, and problems.
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I'll join if it's possible, thank you
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I am assessing specific cognitive abilities (using reaction time tests) within my project and would like to control for processing speed performance. 
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Trail Making Test B
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If a concussed athlete after 5 days of rehabilitation have a normal (equal to baseline) SCAT3 (i.e. no symptoms; no balance errors; normal SAC etc) is there a need for a neuropsychological test?
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the components of executives functions well as long-term episodic memory are not sufficiently contemplated no CAT3 . The instrument 's sensitivity to these cognitive functions is low and the atlhete can easily return to the cognitive base level. The evaluation through reaction time tests as well as larger list of words and Stroop test could provide more information.
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I'm looking for examples of the use of MANOVA in research on the influence of polomorfisms on cognitive functions. In our research we have 11 polimorfisms and 9 results from 3 neuropsychological tests (dependent variables). The sample comprised 460 persons. I would like to avoid alpha inflation due to multiple comparisons. But, according to my knowledge, we have too many independent variables to put them in a single MANOVA (?)
I'm sorry for the level of generality of my question, but I'm not an expert in genetic research. I'm doing analysis for my colleague.
Thank you in advance for any tips!
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thank you to everybody: the discussion has been pleasant; I could take advantage of many contributions, Mauro
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We are currently conducting a systematic review focusing on cognition in elderly aged 90 years and older without dementia. So far, we have included a number of studies that meet our inclusion criteria, but we are still interested in including more scientific papers. The potential papers will have to meet the following criteria:
Inclusion criteria:
- The study contains neuropsychological test results that are specifically reported for individuals aged 90 years and older.
Exclusion criteria:
- Studies that only contain a population with a specific disease or condition (for example, patients with a stroke or patients undergoing surgery) will be excluded.
- Studies that only contain subjects admitted to the hospital (inpatients) will be excluded.
- Articles that only include subjects living at nursing homes, will be excluded.
- Language: any article that is not written in English, Dutch, German or French will be excluded.
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Hi, maybe this can help:
Article: Neuropsychological Test Performance in Cognitively Normal Spanish-speaking Nonagenarians with Little Education
Elizabeth Guerrero-Berroa · James Schmeidler · Henriette Raventos · Daniel Valerio · Michal Schnaider Beeri · José R. Carrión-Baralt · Lara Mora-Villalobos · Patricia Bolaños · Mary Sano · Jeremy M. Silverman
Article: Heritability of cognitive functions in families of successful cognitive aging probands from the Central Valley of Costa Rica
Tiffany A Greenwood · Michal S Beeri · James Schmeidler · Daniel Valerio · Henriette Raventós · Lara Mora-Villalobos · Karla Camacho · José R Carrión-Baralt · Gary Angelo · Laura Almasy · Mary Sano · Jeremy M Silverman
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Hello,
I want to do study on patients with  anxiety and depression. Could anyone suggest me good Neuropsychological test and stimuli tasks for EEG?
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To the best of my knowledge as a former EEG researcher, the EEG does not produce a reliable way to measure anxiety. As you may know, the EEG reflects only that part of the brain's electrical functioning that can cross the rather nonconductive skullbone. In addition, it reflects only a weak vector summation of millions of synapses. Finally, the signal is masked by the blood vessels of the head, large and small, which conduct various electrical signals (including Alpha waveforms) much better than bone due to their being filled with blood, which is electrically conductive due to its salt content.
While there is much controversial or fringe research that shows various EEG effects as a result of meditation, anxiety, and even thinking and task-solving, none of this research, to the best of my knowledge, is part of accepted medical knowledge. It cannot as yet be considered fact.
If you want a reliable measure of anxiety, you cannot do better than the State-Trait Anxiety Inventory for Adults (STAI Form Y), available at http://www4.parinc.com/Products/Product.aspx?ProductID=STAI . This is an accepted psychological instrument, having itself been validated in various human populations.
Research involving a measurement of anxiety that is based only on EEG readings may have only limited acceptance due to its dependence on the unreliability and lack of validation of the EEG as a measure of anxiety, to the best of my knowledge.
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In clinical settings?
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Olá Almir,
Look these papers which I sent to you. I think that you should find your response.
I hope this helps.
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Does anyone know of an episodic memory task or test in which we can study the strategic contribution to episodic memory functions? We prefer an experimental task that can be programmed or used in E-Prime over neuropsychological tests.
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Dear Dr. Cheke and Dear Dr. Goettems-Bastos, 
Many thanks for your recommendations. I think that these papers will bew very useful to our purposes.
Best wishes, Esteve
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To obtain z-scores, raw scores from the CANTAB can be compared with the norm group according to age, gender, and IQ.
...But, what about race and SES? If these other variables are not considered for comparisons, does anyone know if the CANTAB describes the race distribution and SES features of the norm groups?
Thank youuuu
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thank youuuuuuuuuu
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Dear colleagues,
I'm working on a small set of data (N = 36) of patients with mild cognitive impairment (N = 18) and dementia (N = 18), assessed at two time points (baseline and follow-up). My dependent variable is the decline in functional measures. For this, I used a psychometric scale of functional performance (scores ranging from 0 to 8 and normally distributed) both at baseline and in the follow-up.
The objective of the research is to assess the role of cognitive measures at baseline (neuropsychological tests) as predictors of change in the functional variable between baseline and follow-up.
I have no experience with longitudinal analysis and do not know what would be the best method to assess this question. Can someone help me? Preferably with methods that can be performed in SPSS.
I appreciate your collaboration!
Jonas
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You may want to consider regressing  T1-T2 and T1+T2  for the two groups and test whether the slopes are significantly different.  Regressing T1-T2 with T1 has some inherent bias. See the article by Bland and Altman (1995) in Lancet: "Comparing methods of measurement: why plotting difference against standard method is misleading"
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and what about 10/36 visoespatial memory test?
These two tests belongs to Rao´s neuropsychological battery used to evaluate cognition in multiple sclerosis.
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excellent Beatrice!! thanks!!
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In Classical Conditioning one perform a CS1->UCS acquisition, then separately a CS2->UCS acquisition (the UCS must be the same). Let's suppose to neglect the context cue, or let's assume the CS1 consists of both a cue1 and a context1 and the same for CS2 which consists of a different cue2 and a different context2 respect CS1.
Finally follows the extinction of only one of the two, let's say CS2. Does CS1 change respect the CS2-pre-extinction and CS2-post-extinction? There exists literature which details experimentally about this paradigm?
Luca P.
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It seems unlikely, from a common sense point of view, from an evolutionary perspective, and from learning theoretical considerations, that the attenuation of the CS1 - UCS bond should affect the association between CS2 and UCS. If the first loses its predictive value, why should the second lose it as well? That would impair the organism's adaptation. Only if CS2 (plus context) resembles CS1 (plus context), or is otherwise related to CS1, it may lose somewhat of its predictive value.
Fernando, thanks for the references.
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I am searching for a neuropsychological task on mental rotation that directly compares abilities in rotating abstract shapes and/or letters with rotating body-parts (e.g., hands or whole-bodies). Ideally the task is applicable in clinical practice.
On a sidenote, can anyone provide me with a version of the hand-laterality judgment task?
Thanks in advance,
Andreas
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I have used a task of right-left orientation clinically for many years that I developed based on a British test using schematic human figures in four different orientations, half inverted, half upright, facing either forward or backward and holding a "large blue ball" in one hand only.  This task requires mental rotation and is described in my article in Developmental Neuropsychology, which I've attached in case it may prove of interest to you and your work.  Tom Snyder. 
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Which of the following neuropsychological test tools would you recommend for the assessment  of Mild Cognitive Impairment (MCI) and to delineate from the healthy ageing controls:
a) RBANS
b) CNS Vital Signs
Or would it be better if I go for domain-specific subtests such as CVLT II, TMT Part A & B, WMS, and etc?
Kind regards,
Vic
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Don't forget about a detailed clinical interview (i.e. assessing pre-morbid functioning and ADL decilne), interview of significant other, and a review of existing medical records. These are essential in the assessment process.
Ruling out emotional factors is also important in these types of evaluations.
We use a four hour battery that includes many of the above mentioned measures as well as an IQ measure, motor testing, and more detailed domain specific measures similar to those found in the RBANS that vary in complexity.
When time is a factor, such as on inpatient settings we often use the MOCA, RBANS, TMT, BNT, FAS+Animals, and a short emotional screener.
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In the software system requirements they specify only a CPU faster than 1 GHz, and it is not officially tested on these popular cheaper Windows tablets. Maybe it runs reliably on a weaker CPU, maybe not.
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Well, I do not think it is possible, the full suite requires an usb key. Some simplier mental test runs in iPad.
Anyway, I purchased a Toshiba wt310 tablet (Core i5), it is all OK, except the occasional muted sound, which must be a docking problem.
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I think you should not apply the test so early. Students don´t have to rebember nothing about it. I worked in a neuropsychology center and we applied the corresponding test once a year or more. Or when the patient had reach his goals. We never had any problem.
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I need the neuropsychological tests which measure executive function, particularly ability to anticipation.
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Dear Alexabdre,
You can ask it from E-mail: e.vandenberg-6@umcutrecht.nl
who wrote the paper:
The Brixton Spatial Anticipation Test as a test for executive function: Validity in patient groups and norms for older adults
ESTHER VAN DEN BERG et al. 2009
Correspondence and reprint requests: Esther van den Berg, University Medical Center Utrecht, Department of Neurology G03.228, P.O. Box 85500, 3508 GA Utrecht, The Netherlands. E-mail: e.vandenberg-6@umcutrecht.nl
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I´m especially asking about psychological tests, which can be done with patients, not with their caregivers.
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You can try CANTAB - the tests are language-independent. An evaluation version of the tests is available on the web page. I suggest Spatial Working Memory test.
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I need the norms for age 16-20.
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I believe Richard Frederick PhD in Missouri has that data.
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I was wondering if there was a Persian (Farsi) version of the Montreal mini mental status exam with trial data.  I have seen other non-western versions (Korean).  Thank you
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There is also a Persian version of the NUCOG, our cognitive screening tool - I'd be happy to forward our validation paper or put you in touch with the author. 
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I know about the link between the cerebral cortex (which plays an important role in  memory, attention, perceptual awareness, thought, language) and I would like to find out how a person which suffers from epilepsy can improve their memory.
I think there has to be some neuropsychological tests (to have a clear vision about the affected areas/skills).
Any information about the link between epilepsy and memory could be useful.
Thanks.
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Dear Roxana
As you know, during the memory procedure, some changes will occur in synaptic transmission in some brain areas which lead to increasing (or sometime decreasing) the activity of synapses, a process named synaptic plasticity. Occurance of synaptic plasticity, especiallt in the form of long-term potentiation (LTP)  is a necessary phenomenon in learning and memory.
When epileptic seizures happen, the hyperactivity of neural circuits will lead to a kind of synaptic plasticity in glutamatergic synapses which increases the synaptic strength. This kind of plasticity (which leads to increase in synaptic strength) is a kind of synaptic potentiation. Thus, in epileptic patients, the synapes are very potentiated, so that it is very difficult to induce a new LTP during learning and memory. Therefore, in these patients, the occurance of LTP is very difficult and this will result to impairement of LTP induction. Impairement of LTP induction will results to memory impairement per se. On the other hand, in epileptic patients, the synapses are so saturated that cannot undergo new potentiation. This is why memory function in epileptic patients is not similar to normal persons.
Of course, we have notice that some antiepileptic drugs can also affect learning and memory.
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Neuropsychological testing in ADHD adults becomes more relevant for adults with ADHD. As some research indicates its corroborating role for the diagnostic process, its role for treatment planning and therapy is not often addressed.
Any specific literature recommendations or experiences made in clinical practice?
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"For example, the symptom of impulsivity can be independently observed as an increase in commission errors."
Is there validation that the increase in commission errors in a neuropsych test is linked to the observed impulsive behaviors of the ADHD patient? If the behavior is observed to occur, what added value do you get from the test? If the patient is able to perform the test, does that negate the observation of behavior? And if someone is willing to be deceptive in reporting behavior, would they also be able to deceive on the test?
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As i will participate at a study on Epilepsy in Tanzanian children with epilepsy (3-18 years) and intend to perform neuropsychological assessment using standard test batteries. As i do not speak the native language (Kiswahili) i thought about using nonverbal IQ test that cover a wide age-range, wide cognitive range, are nonverbal, measure and discriminate different parameters of intelligence are short and well established.
Does anyone have an experience with cToni, UNIT, Raven, nonverbal Wechsler WNV or others in rural african children?
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MANY TESTS THAT PRESUMABLY MEASURE "NON-VERBAL" INTELLIGENCE HAVE POOR REFERENCE POINTS, AND DO NOT CORRELATE WELL WITH RECOGNIZED "GENERAL ABILITY" MEASURES SUCH AS THE WECHSLER SCALES. THEREFORE, IT IS VERY DIFFICULT TO BE CONFIDENT ABOUT WHAT YOU ARE MEASURING. THAT SAID, THE RAVEN'S PROGRESSIVE MATRICES ARE ARGUABLY THE BEST MEASURE OF "g." THEY ARE AVAILABLE IN CHILD, ADULT, AND ADVANCED VERSIONS, SOLD BY A PUBLISHER IN THE UK. IMHO, THIS IS YOUR BEST BET; IT IS ALSO PRESUMABLY "CULTURE FREE," BUT I'M NOT SURE HOW THAT IS ESTABLISHED IF "TEST TAKING" IN GENERAL IS NOT PART OF ONE'S CULTURE.
AGAIN IMHO, I'M NOT SURE THAT "IQ" IS "THE" VARIABLE OF INTEREST IN EPILEPSY. I'M ASSUMING THAT YOU ARE EQUATING "NON-VERBAL" WITH NOT ORALLY EXPRESSIVE - A TEST THAT DOES NOT REQUIRE AN ACTIVE VERBAL REPLY. HOWEVER, THIS CAN BE MISLEADING, SINCE PEOPLE OFTEN USE VERBAL THINKING TO SOLVE PROBLEMS, EVEN WHEN NOT VERBALIZING A REPLY; STUDIES HAVE SHOWN THAT IN THE ABSENCE OF AN ACTIVE VERBAL REPLY, LANGUAGE NETWORKS ARE ACTIVATED ANYWAY; SIMILARLY, IT HAS BEEN DEMONSTRATED THAT ON WORD LIST LEARNING TASKS, THE BEST LEARNERS ACTIVATE ANTERIOR RIGHT HEMISPHERE BRAIN REGIONS. . MOST IQ TESTS HAVE SEVERAL/MANY SUBTESTS, AND THESE SUBTESTS ALMOST ALWAYS REQUIRE MULTIPLE COMPONENT COGNITIVE PROCESSES AND ACTIVATE WHATEVER BRAIN NETWORKS ARE REQUIRED, DEPENDENT UPON TASK DEMANDS. I AM TEMPTED TO THINK THAT IN SEIZURE DISORDERS, WITH A SPECIFIC FOCUS OF IMPAIRMENT, SELECTIVE BRAIN NETWORKS WOULD BE AFFECTED, SO INTELLIGENCE TEST SUBTESTS WILL NOT NECESSARILY SOLVE THE PROBLEM OF IDENTIFYING SPECIFIC REGIONAL NETWORK INVOLVEMENT.  YOUR BEST MEASURES MIGHT BE THOSE TESTS THAT ARE RELATIVELY "PURE," THOSE MEASURES THAT ARE INTERPRETED AS PATHOGNOMONIC SIGNS, OR PERHAPS THOSE TESTS WITH A SKEWED DISTRIBUTION, THOSE THAT DO NOT FOLLOW THE PERFORMANCE DISTRIBUTION OF A "BELL-SHAPED CURVE."  SEE LEZAK, ALMOST ANY EDITION, FOR FURTHER EXPLANATION. THIS WILL BE FOUND IN THE "BASIC CONCEPTS" CHAPTERS OF THE BOOK. - LK
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Referring to the score of the Go–No Go (inhibitory control) task, Dubois et al. (2000)’s original article stated as follows:
No error: 3
One or two errors: 2
More than two errors: 1
Patient taps like the examiner at least four consecutive times: 0.
However, it’s not correct to say that if patient imitates the examiner at least four consecutive times is an error, since the presented series (1-1-2-1-2-2-2-1-1-2) and the instructions: when the patient responds with one tap at the examiner’s single tap, it is of course an imitation but he/she is following the given instruction, that it can't be considered as an error.
In the clinical practice, 0 is given for 4 consecutive errors, but to my knowledge no article reported this statement.
Does anyone have any suggestions?
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Why did the patient start failing? did he forget the instructions? (then maybe memory is involved) Is he uncapable of inhibiting behaviour when he is not directly focused on doing so? How many time is allowed for him to respond? It's not the same when you have to act immediatly after the instruction than when you have some time to prepare. The meaning of behaviour is not the same, as other variables affect (e.g. speed of processing and psychomotor speed)
As far as I understand from your text is that the paper by Dubois states that 4 consecutive imitations = 0 score, so there you have your report.
What I wonder is why 3 errors are considered more impaired than 2 errors. I suppose that scaling scores is intended for grading severity, but I think that this kind of tests are usually performed close to ceiling, so any one or two errors indicate impairment. Does three errors reflect more inhibition impairments than two errors? Is it not reflected on daily behavior?
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We have collected pre and post cognitive function data using the ADAS-COG, but are struggling to find in-depth guidelines for analysis of data.
For example, how is the number cancellation section scored? Surely it needs to be transferred in to some kind of scaled score, as this item is positively scored and the rest negatively. Do all subscales need transforming to a scaled score so that, for example, word recall (scored out of 10) does not contribute more overall than naming (scored out of 5)?
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Dear Natasha,
Have you ever thought of performing a linear regression to find out how much each of the tasks load on the total score? It would be interesting to get those data and provide a simple algorithm for other researchers. Best.
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The MMSE is commonly used as an outcome measure for cognitive ability in non-pathological (and pathological populations). Should the MMSE only be limited to be a screening tool in healthy aging studies?
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There are many issues with using the MMSE as an outcome measure. First and foremost, if you are collecting multiple time points (e.g., pre, post, etc.), the MMSE has horrific practice effects. Scores will increase, particularly with relatively healthy older adults, simply by remembering the 30 items on the test. For example, it would not be uncommon to have an older adult in clinic tell you they went home and practiced WORLD backwards or serial 7s. They'll also practice all of the orientation questions with a caregiver/spouse on the way in. Finally, there are so many issues with with loading towards verbal strengths and not enough executive functioning assessment. I would stay away from it unless you are interested in a quick and dirty global functioning assessment. If you cannot construct a quick 30-40 minute neuropsych screening/assessment battery, I would recommend something a bit more comprehensive than the MMSE, such as the MOCA or Kokmen. Just my 2...
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We are trying to determine if this is a viable option in countries other than U.S.
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In Germany, testing on a computer is reimbursable.
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I know about using just the verbal tests from WAIS-1V and WMS-!V, but other suggestions would be helpful.
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Another test would be the TOMAL-R (Test of memory and learning) which has various verbal memory tasks. Also, some substest of the Woodckock Johnson Psychoeducational Battery. Finally, verbal reasoning from the FAVRES could be of use for some fucntional verbal problem solving... plus the BRIEF. The total loss of vision is not so frequent after a TBI. Is this due to bilateral damage to the primary visual cortex?
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Mild cognitive impairment (MCI) diagnosis is generally accepted as an intermediate condition between cognitive non-normality and dementia. Nevertheless, the exact role of cognitive and daily living autonomy assessment remains quite indefinite. For example, ADL and IADL and MMSE must be normal? The concept of 1.5 standard deviation different from the cognitive performance of a standardized sample, is not very clear neither completely reliable. The use of equivalent points is not diffuse in all countries. Standardized neuropsychological tests are not always available as well as standardized translation of tests. A minimal but sufficient battery of neuropsychological tests has not yet been defined nor widely accepted. For these reasons, MCI diagnosis criteria can be quite different in the some studies, determining differences in findings of epidemiology and in conversion rate from MCI to dementia. What are the proposals to overcome these issues?
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It is a great how hard question. For instance, we are working to developing a basic test for the evaluation of the memory / cognition of the space (Caffò et al. 2012 AJAAD, DOI: 10.1177/1533317512452035). We considered Petersen's criteria too strict at least for the people we work with, often with a very low level of education. For the definition of aMCI we established that at least two memory tests should be impaired. For the diagnosis of naMCI was necessary that at least two neuropsychological, not memory, tests showed to be impaired (usually those pertaining the area of ​​executive functions). For the diagnosis of multiple domains we set a criterion of four tests impaired. Obviously, any strategy seems to be too little or too severe. We had the feeling that even when patients failed to neuropsychological tests, their performance in daily activities wasn't so compromised. We also became convinced that major markers are those that indicate a change in habits: "I ​​do not drive anymore because I get lost in the streets", "I do not play more cards because I forget my previous hands." In other words, I believe that a well-motivated group of researchers could build a test/interview able to capture the change in daily life, before the deterioration is blown.