Background: Poststroke dementia and cognitive impairment are associated with poor long-term outcomes after stroke. The contribution of genetic factors such as the presence of apolipoprotein (ApoE) ɛ4 allele and its association with cognitive impairment poststroke remains inconclusive, particularly in Middle Eastern regions.
Objective: The aim of this study is to examine all correlates and potential predictors of cognitive impairment including self-awareness and regulation deficits in stroke patients and compare these functions with healthy older adults from a Middle Eastern population.
Methods: A prospective stroke sample of 200 patients (case group) and 100 healthy aging individuals (control group) will be recruited from the largest medical complex in Bahrain. A neuropsychological battery of cognitive assessments (global, executive, and metacognition) will be conducted on all participants. Participants will be categorized into 4 subgroups (nonvascular cognitive impairment, vascular cognitive impairment with no dementia, vascular dementia, and mixed dementia) using standardized cognitive assessment scores and the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, dementia criteria. Biomarkers will include ApoE genotype, soluble form of receptor for advanced glycation end products, neprilysin, beta-secretase 1, biochemistry, and hematology measurements.
Results: The primary study outcome is to determine early risk factors for cognitive impairment after stroke in a Bahraini cohort. The study has received full ethical approval from the Bahrain Ministry of Health and from the affiliated university.
Conclusions: With increasing stroke incidence rates in the Middle East, this research study will provide useful biological and epidemiological data for future development and planning of health policies and guidelines for stroke care within the Gulf region.
Crowdfunding campaign to support this specific research
We help JMIR researchers to raise funds to pursue their research and development aimed at tackling important health and technology challenges. If you would like to show your support for this author, please donate using the button below. The funds raised will directly benefit the corresponding author of this article (minus 8% admin fees). Your donations will help this author to continue publishing open access papers in JMIR journals. Donations of over $100 may also be acknowledged in future publications.
Suggested contribution levels: $20/$50/$100
Stroke is becoming a major health problem in the Middle East as incidence rates are increasing comparably with western countries [- ]. In tandem with this increasing number of new cases of stroke per annum are the growing demands and pressures impacting health systems in the region. Advances in stroke research internationally have aimed to improve patient care and quality of life while reducing the perceived burden and health care system demands. However, empirical evidence regarding the presentation of the most common consequences poststroke is currently not available in the Middle East.
Cognitive impairment is one of the most common sequelae following stroke with 40% to 75% of stroke survivors experiencing some sort of cognitive deficit [, ]. For the majority of patients, some degree of cognitive impairment will be evident in the acute phase poststroke [ ]. Predictors of cognitive impairment include type of stroke, recurrent episodes, the site and laterality of the lesion(s), volume of cerebral infarction, medial temporal lobe atrophy, and coexistent neurodegenerative pathology. Other biological factors known to exacerbate cognitive impairment further are aphasia, diabetes mellitus, atrial fibrillation, and depression [ ]. Many of the cognitive problems resolve over time, but approximately 35% of individuals will be left with some residual cognitive impairment [ , ]. Poststroke dementia and cognitive impairment are associated with poor long-term outcomes, including survival and disability, up to 4 years after stroke [ , ]. There has been some investigation regarding the contribution of apolipoprotein (ApoE) ɛ4 allele [ ] and its association with cognitive impairment poststroke and overall disease outcome [ - ]. However, results remain inconclusive, and further research is required in order to determine and clarify the role of ApoE ɛ4 allele in stroke incidence and outcome particularly in Middle Eastern regions.
Many studies have been performed concerning the effect of stroke on global and executive cognitive function [- ]; however, fewer studies have been conducted on other higher-order cognitive functions such as metacognition [ , ]. The concept of metacognition consists of self-awareness, which includes knowledge about cognitive abilities and strategies, and self-regulation, which includes cognitive monitoring and cognitive control [ ]. Therefore, metacognition involves conscious knowledge of cognitive processes as well as the ability to consciously monitor and regulate one’s ongoing activities while engaging in a task [ ]. These higher-order cognitive functions are required in order for individuals to recognize or be aware of their deficits post–brain injury so that they are capable of selecting activities within their capability for safe and independent functioning [ ]. Deficits in relation to these cognitive functions can present significant problems in terms of motivation and goal attainment as part of rehabilitative programs. Assessment and test procedures for self-regulatory functions and metacognitive processes remain limited and are currently being considered to be included as part of cognitive function tests in future protocols [ ]. The aim of this study is to examine all correlates and potential predictors of cognitive impairment including self-awareness and regulation deficits in stroke patients and compare these functions with healthy older adults from a Middle Eastern population.
This is a case-control study. A longitudinal quantitative approach will be conducted to examine the research objectives.
Participants: Inclusion and Exclusion Criteria
The study will involve recruiting 2 separate sample groups. The first group, known as the case group, will include recruiting individuals within 4 weeks poststroke (see). The second group, known as the control group, will include recruiting healthy older adults who will be age- and gender-matched with the individuals in the case group (see ). The case group will be recruited from the largest urban teaching hospital in Bahrain and the control group from 2 large primary health care centers within close geographical proximity to the recruiting hospital.
All consecutive admissions with a confirmed diagnosis of stroke (defined as symptoms of rapid onset lasting more than 24 hours and of presumed vascular origin reflecting a focal disturbance of cerebral function, excluding isolated impairment of higher function)  and in accordance with International Statistical Classification of Diseases and Related Health Problems, Tenth Revision, diagnostic criteria will be tracked for eligibility to participate in the study.
Procedure and Measures
All stroke participants will be recruited to the study within 1 to 4 weeks poststroke and will be followed up 12 months later. Initial information collected from participants will include date of birth, gender, number of years spent in formal education, marital status, and living arrangements. Information regarding the participant’s medical history will be retrieved from the healthy participants directly through interview and for stroke participants via their medical charts. This information will include past medical history of any conditions, history of medications, date of stroke, stroke type, localization of stroke, side affected, and computer tomography (brain) and/or magnetic resonance imaging (brain) results. Case and control groups will be administered the same questionnaires with the exception of the FAST, the National Institutes of Health Stroke Scale (NIHSS), and the Checklist for Cognitive and Emotional Consequences Following Stroke (CLCE-24), which will be assessed in the stroke participants only (see).
Selection criteria for case group.
- ≥18 years of age
- Written informed consent to participate
- First-ever or recurrent stroke within 1 month of assessment
- Ability to participate in interview assessment with sufficient language (aphasia will be assessed using the shortened version of the Frenchay Aphasia Screening Test [FAST] with a cut-off score of ≥14)
- Transient ischemic attacks (TIAs) and related syndromes
- Nonverbal communication as a result of aphasia or as determined by a score of ≤13/20 on the shortened version of the FAST score
- Too medically unstable to participate in the study
- Formal diagnosis of prestroke vascular dementia or prestroke cognitive impairment
- Traumatic brain injury or traumatic intracranial or subarachnoid hemorrhage
- Visual or hearing impairment that would hinder participation in assessments
- Neurodegenerative disease (eg, Parkinson disease) or previously documented diagnosis of dementia
Selection criteria for control group.
- Healthy adults both male and female
- Age and gender matched with case group participants
- English or Arabic speaking
- Previous use of psychotropic medication
- Neurodegenerative disease (eg, Parkinson disease, dementia, or stroke)
- Previous stroke or transient ischemic attack (TIA)
- Meets cognitive impairment criteria
The expected time for each stroke participant interview, including all assessments, should take 45 to 60 minutes, and for each healthy participant, the interview should take 20 to 40 minutes. The control group will include healthy individuals with no history of psychological or mental illness (including ever having been prescribed psychotropic medication) or any neurodegenerative diseases. Therefore, this group will create a baseline to identify the normal level of cognitive function that is age- and gender-matched to the case group individuals. In order for measurement to be relevant to the Bahrain region population, questionnaires have been translated into Arabic and either the English or Arabic battery of tests will be used depending on the participant’s native tongue. All assessment tools have been translated from English to Arabic in accordance with international translation guidelines [, ], and reliability tests (internal consistency) will be reported on all translated versions.
The case group will be categorized into 4 subgroups [, , ] based on the Mini-Mental State Examination (MMSE), Montreal Cognitive Assessment (MoCA), and Trail-Making Test (TMT) scores alongside Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, (DSM-IV) dementia criteria (see ).
|Generic variable name||Instrument/measure name||Case group||Control group|
|4 weeks PSa||12 months PS|
|Participant demographics||Age, gender, nationality, marital status, living situation, education and occupation, hand preference||x||x|
|Clinical details||Past medical history |
Oxfordshire Community Stroke Project classification
|TOASTb classification of stroke||x|
|Length of hospital stay||x|
|Stroke severity||National Institute of Health Stroke Severity Scale||x|
|Aphasia screening||Frenchay Aphasia Screening Test||x||x|
|Global cognition||Mini-Mental State Examination||x||x||x|
|Montreal Cognitive Assessment||x||x||x|
|Executive function||Trail-Making Test (A+B)||x||x||x|
|Checklist for Cognitive and Emotional Consequences Following Stroke to be completed by participant and by proxy||x||x||x|
|Premorbid cognitive functioning||Informant Questionnaire on Cognitive Decline in Elderly||x||x||x|
|Mood||Hospital Anxiety and Depression Scale||x||x||x|
|Activities of daily living||Barthel Index||x||x||x|
|Biomarkers||Lipid profile, HbA1cc, homocysteine levels, coagulation profile||x||x||x|
sRAGEe, BACE1f and NEPg
bTOAST: Trial of Org 10172 in Acute Stroke Treatment.
cHbA1c: hemoglobin A1c.
dApoE: apolipoprotein E.
esRAGE: soluble form of receptor for advanced glycation end products.
fBACE1: beta-secretase 1.
Clinical Laboratory Analysis
Blood will be drawn within 1 week of admission for the case group and after interview assessment for the control group. Blood specimens for the measurement of ApoE genotypes will be collected in edetic acid tubes. DNA will be purified from white blood cells using the MagNA Pure Compact Nucleic Acid Isolation Kit and stored at –20°C. ApoE genotype analysis will be performed by polymerase chain reaction–restriction fragment length polymorphism according to the method of Zivelin et al . For the serum biomarkers (sRAGE, BACE-1 and NEP), blood will be collected in serum separator tubes, and the serum will be separated and stored at –80°C. The serum biomarkers will be measured using commercially available double sandwich enzyme-linked immunosorbent assay (ELISA) kits in conjunction with an ELISA plate reader. ApoE and serum biomarker analysis will be conducted at Princess Al-Jawhara Center for Genetics and Inherited Diseases. Routine biochemical analysis, including lipid profile, complete blood count, electrolytes, serum proteins, creatinine, homocysteine, and coagulation profile will be conducted at Salmaniya Medical Complex.
The number of participants required to produce a statistically meaningful change in cognition between the stroke patients and healthy controls was calculated using the following formula by Bland  for the comparison of 2 independent samples. A sample of 75 or more in each group will detect a minimum effect size in cognition and biomarkers with a power of 0.8 at a significance level of .05. Therefore, the study will aim to recruit a minimum sample size of 100 for both the case and control groups. For conducting multiple regressions models, the study will adhere to the Green proposal where the minimum sample size should be greater than 50+8k, where k is equal to the number of independent variables [ ]. Nonparametric statistical analysis will be conducted for the cognitive impairment groups’ comparisons as classified in .
Classification of cognitive impairment.
- Stroke with no vascular cognitive impairment:
- MMSE score≥24 (with no education add 2 points, >80 years of age add 1 point)
- MoCA score≥26 (add 1 point if≤12 years education)
- TMT score: Trail A<78 seconds, Trail B<273 seconds
- Vascular cognitive impairment with no dementia:
- MMSE score 21-24
- MoCA score 18-25
- TMT score: Trail A>78 seconds, Trail B>273 seconds
- MMSE score 10-20
- MoCA score 10-17
- TMT score: Trail A>78 seconds, Trail B>273
- Vascular dementia: classified according to the DSM-IV dementia criteria
- Mixed dementia: classified according to the DSM-IV dementia criteria
All independent and dependent study variables will be reported using descriptive statistics. Comparisons between variables for control and case groups will be determined using independent t tests, analysis of variance, and multivariate analysis of variance where multiple variables will be analyzed together. Other statistical tests will include correlational analysis including uni- and multivariate analysis using Pearson’s correlation and multiple regression. All variables will be checked for normal distribution in order to justify use of parametric statistics. Psychometric analysis will be conducted on all measures including and specifically those that are translated from English to Arabic (Metacognitive Questionnaire-30 and Hospital Anxiety and Depression Score). Nonparametric tests will be conducted for subgroup analysis where group sizes may be small using Spearman’s correlation and Wilcoxon tests.
Estimated Study Outcomes
The effects of stroke will be determined by assessing all cognitive functions. The relationship between stroke severity and metacognitive functioning will be determined as will the association between cognitive impairment in the acute phase poststroke and the presence of ApoE and other biomarkers in a Middle Eastern cohort. Arabic versions of cognitive assessment tools will be validated.
Study Organization and Funding
The study protocol has been approved by the Ministry of Health, Kingdom of Bahrain, and the Royal College of Surgeons in Ireland–Bahrain (RCSI-Bahrain) research ethics committees. Research funding was awarded for this study from the RCSI-Bahrain (grant number BR00021). Written informed consent will be obtained from all participants willing to take part; they will be informed of the right to withdraw from the study at any time.
Seefor the baseline characteristics of the case and control group samples to date.
|Baseline characteristics||Stroke||Healthy controls|
|Age in years, mean (SD)||59.33 (13.93)||57.51 (8.14)|
|Gender, n (%)|
|Male||40 (78)||26 (53)|
|Nationality, n (%)|
|Bahraini||31 (61)||46 (94)|
|Non-Bahraini||20 (39)||3 (6)|
|Living arrangement, n (%)|
|Living alone||11 (22)||0 (0)|
|Living with others—family/friends||32 (63)||46 (94)|
|Other||8 (15)||3 (6)|
|Education, n (%)|
|Primary||12 (23)||6 (12)|
|Secondary||20 (39)||22 (45)|
|Third level||10 (19)||14 (29)|
|Illiterate||9 (19)||7 (14)|
|Occupation, n (%)|
|Manual||16 (31)||5 (10)|
|Nonmanual/self-employed||16 (31)||10 (20)|
|Unemployed/retired||19 (38)||34 (69)|
|History, n (%)|
|TIAa||6 (12)||0 (0)|
|Stroke||9 (17)||0 (0)|
|Cardiovascular disease||9 (17)||6 (12)|
|Atrial fibrillation||5 (10)||4 (8)|
|Hypertension||32 (63)||27 (55)|
|Diabetes||20 (39)||22 (45)|
|Hyperlipidemia||19 (38)||24 (49)|
|Psychiatric conditions||1 (2)||0 (0)|
|Lesion location, n (%)|
|Right hemispheric||26 (51)||—|
|Left hemispheric||20 (39)||—|
|Stroke subtype, n (%)|
|Hemorrhagic, intracerebral||8 (16)||—|
|Hemorhhagic, subarachnoid||0 (0)||—|
|OCSPb classification, n (%)|
|Total anterior circulation||4 (8)||—|
|Partial anterior circulation||18 (35)||—|
|Posterior circulation||8 (16)||—|
|TOASTc classification, n (%)|
|Large artery atherosclerosis||14 (28)||—|
|Small artery occlusion||24 (48)||—|
|Determined or undetermined etiology||11 (20)||—|
|NIHSSd, mean (SD)||5.77 (5.01)||—|
|0-4, n (%)||20 (39)||—|
|5-15, n (%)||30 (59)||—|
|≥16, n (%)||1 (2)||—|
|Cognitive status at baseline|
|MMSEe, mean (SD)||24.09 (4.81)||27.86 (2.42)|
|MoCAf, mean (SD)||19.78 (6.64)||25.49 (3.60)|
|MCQ-30g, mean (SD)||62.42 (14.29)||63.2 (15.60)|
|Barthel Index, mean (SD)||69.00 (31.07)||99.49 (2.10)|
|Independent, n (%)||13 (25)||49 (100)|
|Dependent, n (%)||38 (75)||—|
aTIA: transient ischemic attack.
bOCSP: Oxfordshire Community Stroke Project.
cTOAST: Trial of Org 10172 in Acute Stroke Treatment.
dNIHSS: National Institute of Health Stroke Severity Scale.
eMMSE: Mini-Mental State Examination.
fMoCA: Montreal Cognitive Assessment.
gMCQ-30: Metacognitive Questionnaire-30.
Advances in stroke research internationally have aimed to improve patient care and quality of life and reduce perceived burden and demands on health care systems. In terms of advancing the research agenda for the management of stroke in the Middle East, some strategic approaches may be considered from previous research reviews and studies conducted. Previous research studies and reviews have highlighted core aspects relevant for stroke management in terms of the adaptation process [, ], clinical assessment, and adherence to evidence-based practice [ , ]. Therefore, moving the stroke research agenda forward in a region such as Bahrain requires stroke studies based on potential frameworks [ , ] that can address stroke management in the context of specific regional preferences. The aim of this research study is to investigate a very current topic in the field of stroke research regarding identifying the main correlates and predictors, including biological markers, for detecting those patients most at risk for developing cognitive impairment poststroke. This research study, in addition to addressing a relatively novel research area such as metacognition, will also record the clinical and demographical profile of stroke patients. Identifying core risk factors [ ] in Bahrain will provide useful epidemiological data for future development and planning of health policies and guidelines for the overall prevention [ - ], management, and delivery of stroke care. These outcomes will aid in developing stroke management and rehabilitation within a contextual framework by tailoring the population’s health needs based on specific cultural variations. Findings from these type of cognition studies will also inform future developments required for cognitive training interventions [ ] specific for stroke patients and other populations with cognitive deficits as a result of neurological pathologies living in Middle Eastern countries. Finally this study will aim to ascertain recruitment considerations [ ] for both healthy older adults and stroke patients who are at risk of developing dementia in this particular region.
Conflicts of Interest
- Al-Jishi AA, Mohan PK. Profile of stroke in Bahrain. Neurosciences (Riyadh) 2000 Jan;5(1):30-34. [Medline]
- Azarpazhooh MR, Etemadi MM, Donnan GA, Mokhber N, Majdi MR, Ghayour-Mobarhan M, et al. Excessive incidence of stroke in Iran: evidence from the Mashhad Stroke Incidence Study (MSIS), a population-based study of stroke in the Middle East. Stroke 2010 Jan;41(1):e3-e10 [FREE Full text] [CrossRef] [Medline]
- Benamer HT, Grosset D. Stroke in Arab countries: a systematic literature review. J Neurol Sci 2009 Sep 15;284(1-2):18-23. [CrossRef] [Medline]
- Chung CS, Pollock A, Campbell T, Durward BR, Hagen S. Cognitive rehabilitation for executive dysfunction in adults with stroke or other adult non-progressive acquired brain damage. Cochrane Database Syst Rev 2013;CD008391. [CrossRef] [Medline]
- Vakhnina NV, Nikitina LY, Parfenov VA, Yakhno NN. Post-stroke cognitive impairments. Neurosci Behav Physiol 2009 Oct;39(8):719-724. [CrossRef] [Medline]
- Brainin M, Dachenhausen A. Psychosocial distress, an underinvestigated risk factor for stroke. Stroke 2013 Feb;44(2):305-306 [FREE Full text] [CrossRef] [Medline]
- Kalaria RN, Ballard C. Stroke and cognition. Curr Atheroscler Rep 2001 Jul;3(4):334-339. [Medline]
- Tatemichi TK, Desmond DW, Stern Y, Paik M, Sano M, Bagiella E. Cognitive impairment after stroke: frequency, patterns, and relationship to functional abilities. J Neurol Neurosurg Psychiatry 1994 Feb;57(2):202-207 [FREE Full text] [Medline]
- Patel M, Coshall C, Rudd AG, Wolfe CD. Natural history of cognitive impairment after stroke and factors associated with its recovery. Clin Rehabil 2003 Mar;17(2):158-166. [Medline]
- Patel MD, Coshall C, Rudd AG, Wolfe CD. Cognitive impairment after stroke: clinical determinants and its associations with long-term stroke outcomes. J Am Geriatr Soc 2002 Apr;50(4):700-706. [Medline]
- Sudlow C, Martínez González NA, Kim J, Clark C. Does apolipoprotein E genotype influence the risk of ischemic stroke, intracerebral hemorrhage, or subarachnoid hemorrhage? Systematic review and meta-analyses of 31 studies among 5961 cases and 17,965 controls. Stroke 2006 Feb;37(2):364-370 [FREE Full text] [CrossRef] [Medline]
- Allan LM, Rowan EN, Firbank MJ, Thomas AJ, Parry SW, Polvikoski TM, et al. Long term incidence of dementia, predictors of mortality and pathological diagnosis in older stroke survivors. Brain 2011 Dec;134(Pt 12):3716-3727 [FREE Full text] [CrossRef] [Medline]
- Ballard CG, Morris CM, Rao H, O'Brien JT, Barber R, Stephens S, et al. APOE epsilon4 and cognitive decline in older stroke patients with early cognitive impairment. Neurology 2004 Oct 26;63(8):1399-1402. [Medline]
- Dik MG, Deeg DJ, Bouter LM, Corder EH, Kok A, Jonker C. Stroke and apolipoprotein E epsilon4 are independent risk factors for cognitive decline: A population-based study. Stroke 2000 Oct;31(10):2431-2436 [FREE Full text] [Medline]
- Rowan E, Morris CM, Stephens S, Ballard C, Dickinson H, Rao H, et al. Impact of hypertension and apolipoprotein E4 on poststroke cognition in subjects >75 years of age. Stroke 2005 Sep;36(9):1864-1868 [FREE Full text] [CrossRef] [Medline]
- Wagle J, Farner L, Flekkøy K, Wyller TB, Sandvik L, Eiklid KL, et al. Association between ApoE epsilon4 and cognitive impairment after stroke. Dement Geriatr Cogn Disord 2009;27(6):525-533. [CrossRef] [Medline]
- Wagle J, Farner L, Flekkøy K, Wyller TB, Sandvik L, Eiklid KL, et al. Cognitive impairment and the role of the ApoE epsilon4-allele after stroke: a 13 months follow-up study. Int J Geriatr Psychiatry 2010 Aug;25(8):833-842. [CrossRef] [Medline]
- Gottesman RF, Hillis AE. Predictors and assessment of cognitive dysfunction resulting from ischaemic stroke. Lancet Neurol 2010 Sep;9(9):895-905 [FREE Full text] [CrossRef] [Medline]
- Hayes S, Donnellan C, Stokes E. The measurement and impairment of executive function after stroke and concepts for physiotherapy. Phys Ther Rev 2011;16:178-190.
- Hayes S, Donnellan C, Stokes E. Associations between executive function and physical function poststroke: a pilot study. Physiotherapy 2013 Jun;99(2):165-171. [CrossRef] [Medline]
- Skidmore ER, Whyte EM, Holm MB, Becker JT, Butters MA, Dew MA, et al. Cognitive and affective predictors of rehabilitation participation after stroke. Arch Phys Med Rehabil 2010 Feb;91(2):203-207 [FREE Full text] [CrossRef] [Medline]
- Leung DP, Liu KP. Review of self-awareness and its clinical application in stroke rehabilitation. Int J Rehabil Res 2011 Sep;34(3):187-195. [CrossRef] [Medline]
- Ownsworth TL, Turpin M, Andrew B, Fleming J. Participant perspectives on an individualised self-awareness intervention following stroke: a qualitative case study. Neuropsychol Rehabil 2008;18(5-6):692-712. [CrossRef] [Medline]
- Fernandez-Duque D, Baird JA, Posner MI. Executive attention and metacognitive regulation. Conscious Cogn 2000 Jun;9(2 Pt 1):288-307. [CrossRef] [Medline]
- Hacker D. Definitions and empirical foundations. In: Dunlosky J, Graesser A, editors. Metacognition in Educational Theory and Practice. Mahwah, NJ: Lawrence Erlbaum Associates; 1998.
- Barrett AM. Rose-colored answers: neuropsychological deficits and patient-reported outcomes after stroke. Behav Neurol 2010;22(1-2):17-23 [FREE Full text] [CrossRef] [Medline]
- Hachinski V, Iadecola C, Petersen RC, Breteler MM, Nyenhuis DL, Black SE, et al. National Institute of Neurological Disorders and Stroke-Canadian Stroke Network vascular cognitive impairment harmonization standards. Stroke 2006 Sep;37(9):2220-2241 [FREE Full text] [CrossRef] [Medline]
- Aho K, Harmsen P, Hatano S, Marquardsen J, Smirnov VE, Strasser T. Cerebrovascular disease in the community: results of a WHO collaborative study. Bull World Health Organ 1980;58(1):113-130 [FREE Full text] [Medline]
- Lenderking WR. Comments on the ISPOR Task Force Report on Translation and Adaptation of Outcomes Measures: guidelines and the need for more research. Value Health 2005;8(2):92-93 [FREE Full text] [CrossRef] [Medline]
- McKenna SP, Doward LC. The translation and cultural adaptation of patient-reported outcome measures. Value Health 2005;8(2):89-91 [FREE Full text] [CrossRef] [Medline]
- Jaillard A, Grand S, Le Bas JF, Hommel M. Predicting cognitive dysfunctioning in nondemented patients early after stroke. Cerebrovasc Dis 2010;29(5):415-423. [CrossRef] [Medline]
- Qian L, Ding L, Cheng L, Zhu X, Zhao H, Jin J, et al. Early biomarkers for post-stroke cognitive impairment. J Neurol 2012 Oct;259(10):2111-2118. [CrossRef] [Medline]
- Zivelin A, Rosenberg N, Peretz H, Amit Y, Kornbrot N, Seligsohn U. Improved method for genotyping apolipoprotein E polymorphisms by a PCR-based assay simultaneously utilizing two distinct restriction enzymes. Clin Chem 1997 Sep;43(9):1657-1659 [FREE Full text] [Medline]
- Bland M. An Introduction to Medical Statistics. 3rd edition. New York, NY: Oxford University Press; 2000.
- Green SB. How many subjects does it take to do a regression analysis. Multivariate Behav Res 1991 Jul 1;26(3):499-510. [CrossRef] [Medline]
- Donnellan C, Hevey D, Hickey A, O'Neill D. Defining and quantifying coping strategies after stroke: a review. J Neurol Neurosurg Psychiatry 2006 Nov;77(11):1208-1218 [FREE Full text] [CrossRef] [Medline]
- Donnellan C, Hevey D, Hickey A, O'Neill D. Adaptation to stroke using a model of successful aging. Neuropsychol Dev Cogn B Aging Neuropsychol Cogn 2012;19(4):530-547. [CrossRef] [Medline]
- Donnellan C, Sweetman S, Shelley E. Health professionals' adherence to stroke clinical guidelines: a review of the literature. Health Policy 2013 Aug;111(3):245-263. [CrossRef] [Medline]
- Donnellan C, Sweetman S, Shelley E. Implementing clinical guidelines in stroke: a qualitative study of perceived facilitators and barriers. Health Policy 2013 Aug;111(3):234-244. [CrossRef] [Medline]
- Donnellan C, Martins A, Conlon A, Coughlan T, O'Neill D, Collins DR. Mapping patients' experiences after stroke onto a patient-focused intervention framework. Disabil Rehabil 2013 Mar;35(6):483-491. [CrossRef] [Medline]
- Donnellan C, O'Neill D. Baltes' SOC model of successful ageing as a potential framework for stroke rehabilitation. Disabil Rehabil 2014;36(5):424-429. [CrossRef] [Medline]
- Auais MA, Alzyoud JM, Sbieh Z, Abdulla FA. The risk factors of CVA in Jordan. Physiother Theory Pract 2012 Nov;28(8):588-594. [CrossRef] [Medline]
- Kamran S, Bener AB, Deleu D, Khoja W, Jumma M, Inshashi J, et al. The level of awareness of stroke risk factors and symptoms in the Gulf Cooperation Council countries: Gulf Cooperation Council stroke awareness study. Neuroepidemiology 2007;29(3-4):235-242. [CrossRef] [Medline]
- Alaqeel A, AlAmmari A, AlSyefi N, Al-Hussain F, Mohammad Y. Stroke awareness in the Saudi community living in Riyadh: prompt public health measures must be implemented. J Stroke Cerebrovasc Dis 2014 Mar;23(3):500-504. [CrossRef] [Medline]
- Hickey A, O'Hanlon A, McGee H, Donnellan C, Shelley E, Horgan F, et al. Stroke awareness in the general population: knowledge of stroke risk factors and warning signs in older adults. BMC Geriatr 2009;9:35 [FREE Full text] [CrossRef] [Medline]
- Cruz VT, Pais J, Bento V, Mateus C, Colunas M, Alves I, et al. A rehabilitation tool designed for intensive web-based cognitive training: description and usability study. JMIR Res Protoc 2013;2(2):e59 [FREE Full text] [CrossRef] [Medline]
- Pendlebury ST, Chen P, Bull L, Silver L, Mehta Z, Rothwell PM, et al. Methodological factors in determining rates of dementia in transient ischemic attack and stroke: (I) impact of baseline selection bias. Stroke 2015 Mar;46(3):641-646 [FREE Full text] [CrossRef] [Medline]
|BACE-1: beta-secretase 1|
|CLCE-24: Checklist for Cognitive and Emotional Consequences Following Stroke|
|DSM-IV: Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition|
|ELISA: enzyme-linked immunosorbent assay|
|FAST: Frenchay Aphasia Screening Test|
|MCQ-30: Metacognitive Questionnaire-30|
|MMSE: Mini-Mental State Examination|
|MoCA: Montreal Cognitive Assessment|
|NIHSS: National Institutes of Health Stroke Scale|
|OCSP: Oxfordshire Community Stroke Project|
|RCSI-Bahrain: Royal College of Surgeons in Ireland–Bahrain|
|sRAGE: soluble form of receptor for advanced glycation end products|
|TIA: transient ischemic attack|
|TMT: Trail-Making Test|
|TOAST: Trial of Org 10172 in Acute Stroke Treatment|
Edited by G Eysenbach; submitted 25.04.16; peer-reviewed by K Jellinger, M Ursin, M Danovska; comments to author 14.07.16; revised version received 19.08.16; accepted 03.09.16; published 28.11.16Copyright
©Claire Donnellan, Mona Al Banna, Noor Redha, Adel Al Jishi, Isa Al Sharoqi, Safa Taha, Moiz Bakhiet, Fatema Abdulla, Patrick Walsh. Originally published in JMIR Research Protocols (http://www.researchprotocols.org), 28.11.2016.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in JMIR Research Protocols, is properly cited. The complete bibliographic information, a link to the original publication on http://www.researchprotocols.org, as well as this copyright and license information must be included.