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The COMPlaints After Stroke (COMPAS) study: protocol for a Dutch cohort study on poststroke subjective cognitive complaints
  1. Marielle W A van Rijsbergen1,
  2. Ruth E Mark1,
  3. Paul L M de Kort2,
  4. Margriet M Sitskoorn1
  1. 1Department of Cognitive Neuropsychology, Centre of Research on Psychology in Somatic diseases (CoRPS), Tilburg University, Tilburg, The Netherlands
  2. 2Department of Neurology, St Elisabeth Hospital, Tilburg, The Netherlands
  1. Correspondence to Dr Ruth E Mark; r.e.mark{at}tilburguniversity.edu

Abstract

Background Although many studies have assessed poststroke objective cognitive impairment, only a few have evaluated patients’ subjective cognitive complaints (SCC). Although these SCC are found to be common in the early and chronic phases after stroke, knowledge about their risk factors, course over time, differences with healthy controls and their diagnostic relevance is limited. The aim of the COMPlaints After Stroke (COMPAS) study is therefore to determine the possible risk factors, prognosis, time course and predictive value of SCC in the first 2 years after stroke.

Methods and design A prospective cohort study is conducted in which patients are compared to non-stroke controls at 3, 6, 12 and 24 months after stroke. Approximately 300 patients are recruited from the stroke units of three hospitals in the Netherlands, while 300 controls are sought among the relatives (spouses excluded) and social networks of participants. A wide range of subjective and objective variables is assessed in both groups using interviews, questionnaires and neuropsychological assessment. The primary outcomes include SCC and objective cognitive impairment, whereas secondary outcomes are quality of life, subjective recovery and daily life functioning.

Ethics and dissemination The study is being carried out in agreement with the Declaration of Helsinki and the Medical Research Involving Human Subjects Act. The protocol has been approved by the medical ethics committees of the participating centres and all participants give written informed consent. The results will be published in peer-reviewed journals and disseminated to the medical society and general public.

Discussion The COMPAS study is the first to systematically evaluate poststroke SCC in a prospective longitudinal design, taking a wide range of subjective and objective variables into account. The results obtained can be used to accurately inform patients and their families, as well as to develop patient-tailored intervention programmes to ultimately improve stroke patient care.

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Article summary

Strengths and limitations of this study

  • Strengths of this study are that it is the first prospective cohort study on subjective cognitive complaints in patients with stroke in which patients and controls are evaluated at multiple assessments, while at the same time a wide range of subjectively and objectively measured variables are taken into account.

  • A limitation is that the most seriously affected patients are unable to participate in the study. This may reduce the generalisability of the results to the stroke population as a whole.

Background

Poststroke cognitive impairment is common after stroke and can be evaluated either objectively, using neuropsychological tests (ie, objective cognitive performances (OCP)), or subjectively, using interviews or self-report questionnaires (ie, subjective cognitive complaints (SCC)). Until now, the majority of studies on poststroke cognitive sequelae have focused on OCP without also evaluating patients’ SCC. However, individuals’ performances in test situations do not always correspond to those in daily life and vice versa.1 ,2 Evaluating one can therefore not be used to draw conclusions about the other.

In a recent systematic review, we found that SCC are common in the early and chronic phases after stroke and that they tend to increase over time.3 The prevalence rates vary between 28.6% and 92.0% and complaints about memory, mental speed and concentration were found to be those most commonly reported.3 Furthermore, patients and their proxies showed moderate agreement on the prevalence and severity of patients' SCC.3 However, one of the main problems in most of these studies is that there is no ‘gold standard’ to define and measure SCC, resulting in heterogenic findings. In our review, we suggested that it is important to differentiate between content of SCC (SCCc) and worrying about SCC (SCCw), as these are two different concepts.3 The first focuses on the specific cognitive difficulties respondents say they experience, while the second indicates whether participants find them worrisome, irritating and whether they say they hinder daily life. A few studies have made this distinction so far.2 ,4 ,5 However, the majority of research on poststroke SCC has evaluated SSCc and not SSCw, probably without being aware of the difference between these aspects of SCC.3

Furthermore, we found in our review that poststroke SCC are inconsistently associated with demographic and clinical characteristics, current depressive symptoms and OCP,3 but they may predict future emotional and cognitive decline.5 ,6 However, most of the research on SCC after stroke carried out so far is limited in that: unvalidated methods for assessing SCC were used, there was no non-stroke control group included, and the focus was on a specific subsample of stroke patients (eg, home-living patients only), thereby impairing the generalisability of the results. While SCC are common among stroke patients, knowledge about the following aspects is only limited or practically non-existent: the risk profile for developing SCC; their course over time; their impact on quality of life (QOL), subjective recovery and activities in daily life (ADL) functioning; and their prognostic implications.

In the general non-stroke population, however, SCC have been more frequently evaluated, in particular memory-related SCC reported by the elderly.7 ,8 Factors found to be associated with these complaints include: demographic characteristics (higher age, women, lower education), psychological distress, somatic symptoms, personality traits (neuroticism in particular) and vascular risk factors.7–11 Furthermore, they are thought to be clinically relevant in this group because of their association with increased healthcare consumption, reduced QoL, current OCP (this link is not always found) and their predictive value for future cognitive decline.7 ,8 ,12 Whether this also applies to poststroke SCC is unknown. More systematic research is therefore needed to gain further knowledge about SCC among stroke survivors, to be able to accurately inform patients and their relatives, to develop adequate treatment programmes and to ultimately improve poststroke care.

We therefore designed the COMPlaints After Stroke (COMPAS) study in which we have four main aims:

  • Determine the prevalence, profile and course over time of SCCc and SCCw.

  • Identify the risk profile for reporting SCC.

  • Evaluate their predictive value for future cognitive functioning.

  • Determine the effect of SCC on QoL, subjective recovery and ADL functioning.

Here we describe the design and protocol of the COMPAS study, which is the first prospective cohort study of SCC in patients with stroke, evaluating both patients and controls, while at the same time a wide range of variables is taken into account.

Methods and analysis

Design

A multicentre, prospective cohort study of patients with stroke and controls is performed. We started in 2009 and the final measurements will be made in 2014. Patients are evaluated five times, starting at the clinical phase (T0), followed by an assessment at 3 months (T1), 6 months (T2), 1 year (T3) and 2 years (T4) after stroke. Controls are seen at the same time intervals, starting at T1.

Study population

Patients with stroke are recruited consecutively from the stroke units of three hospitals in the Netherlands, including the St Elisabeth and TweeSteden Hospitals in Tilburg and the Maxima Medical Centre in Veldhoven. The control group consists of a sample from the non-stroke general population and is recruited among the relatives and the social networks of participants in the COMPAS study. Spouses of patients with stroke are excluded from the control group since they are at a higher risk of having physical, cognitive and psychosocial problems themselves due to the fact that their partner has suffered a stroke.13 ,14

Inclusion criteria

  • Clinical diagnosis of a first or recurrent ischaemic or haemorrhagic stroke (for patients only).

  • At least 18 years old (no upper age limit).

Exclusion criteria

  • Pre-existent health problems interfering with cognitive functioning, including for example:

    • Cognitive decline (as defined by a score >3.6 on the short version of the Informant Questionnaire on Cognitive Decline in the Elderly; IQCODE).15

    • A recent history of severe psychopathology (eg, suicide attempts, alcohol- or drug misuser, diagnosed personality or mood disorders).

    • Severe physical comorbidity (eg, malignant diseases, progressive neurological conditions).

  • Severe communication difficulties (eg, insufficient understanding of the Dutch language, severe aphasia, blindness or deafness).

Procedure

Eligible patients receive oral and written information about the study from their treating physician during the clinical phase (T0). Demographic and clinical characteristics are documented and patients are scheduled for the first assessment 3 months after stroke (T1), during which written informed consent is obtained for inclusion to be definite. Participants acknowledge that they have the intention to complete all four assessments, and that they are allowed to end their participation at any time. For the follow-up assessments (T2–T4), patients are informed by letter and telephone and invited to participate after which an appointment is scheduled.

Potential controls receive oral and written information about the study from the researcher after which they are asked to participate in the study. The rest of the procedure is the same as that for the patient group.

The assessments are administered in a standardised way by trained neuropsychologists and take place at the participating hospitals or, when this is not possible, at the participant’s home or residence (eg, rehabilitation centre).

Measures

Tables 1 and 2 give an overview of the variables assessed and instruments used at each time point.

Table 1

Primary and secondary outcomes in the COMPAS study

Table 2

Possible determinants in the COMPAS study

Outcomes

Primary outcomes of the COMPAS study are SCC and OCP. To measure SCC, two instruments are used, namely: the Dutch version of the Cognitive Failures Questionnaire (CFQ)16 ,17 and the Checklist for Cognitive and Emotional consequences following stroke (CLCE-24).5 The CFQ focuses on SCCc and asks subjects to rate 25 items on the frequency of cognitive slips and errors in daily life on a 5-point Likert scale ranging from 0 (never) to 4 (very often). SCCw is evaluated by four additional general questions regarding the subjective increase of complaints over time, the degree to which these hinder daily life, are annoying and are a source of concern. Each of these extra items is rated on a scale ranging from 1 (not at all) to 5 (extremely).

The CLCE-24 is a structured clinical interview developed to evaluate SCCc and SCCw among stroke survivors.5 It consists of 13 items concerning cognitive complaints and 9 items addressing emotional and behavioural complaints. Each item is scored as 0 (not present), 1 (doubtful), 2 (present, but not affecting daily life) or 3 (present and negatively affecting daily life).

OCP are evaluated using an extensive neuropsychological assessment covering multiple cognitive domains and containing traditional (eg, Rey Complex Figure Test18) and more ecologically valid tests (eg, Rivermead Behavioural Memory Test19). See table 1 for an overview of all OCP tests used. In Spreen and Straus20 and Lezak et al,21 a detailed description of each of the instruments we use is given.

Secondary outcomes include QoL, ADL functioning and subjective stroke recovery. Generic QoL is evaluated using the short version of the self-report WHO Quality of Life Questionnaire (WHOQOL-Bref)22 (26 items) and, because we expect the majority of our population to be elderly (>60 years), the additional OLD module (WHOQOL-OLD)23 comprising 24 items. While the first covers overall well-being on the domains ‘physical’, ‘psychological’, social relationships’ and ‘environment’, the OLD module evaluates aspects of life which are specific to the elderly, including: ‘intimacy’, ‘sensory abilities’, ‘autonomy’, ‘activities in the past, present and future’, ‘social participation’ and ‘dying’.

Subjective recovery after stroke is determined by a single item from the Stroke Impact Scale,24 in which patients are asked to indicate on a scale ranging from 0 (‘no recovery’) to 100 (‘full recovery’) how much they feel they have recovered from their stroke.

ADL functioning is assessed in basic activities, including self-care and mobility, using the Barthel Index25 (10 items) and more complex activities like housekeeping, hobbies and employment, using the Frenchay Activities Index26 (15 items).

All instruments chosen are frequently used (inter)nationally in research and daily clinical practice dealing with stroke patients.

Possible determinants

Depending on the specific outcome considered, SCC, OCP, QoL, subjective recovery and ADL functioning are either dependent or independent variables. A wide range of possible determinants are additionally taken into account, based on what is currently known from the literature on SCC in the general and the stroke population. These include: demographic variables, clinical characteristics (those related to stroke included) and health status; premorbid status (ie, cognitive decline, IQ, cognitive and emotional complaints); comorbid complaints about mood (ie, anxiety and depression), fatigue and stress; personal factors (ie, coping style, personality traits and SCC awareness), and the occurrence and impact of positive and/or negative live events. See table 2 for the specific variables assessed and instruments used.

Planned statistical analyses

Cross-sectional analyses will be used to evaluate group differences at each of the individual time points (T1–T4) and include: χ2 test for categorical variables, the Mann-Whitney U test for ordinal data, and the Student t test or (multivariate) analysis of variances ((M)ANOVA) for continuous dependent variables. Furthermore, differences across the time points will be analysed using multilevel analysis, which allows inclusion of all available data (ie, also those from participants with partly missing values).

The course of SCC over time (T1–T4) will subsequently be evaluated using latent class growth analysis. We will explore whether groups with different trajectories of SCC over time can be distinguished and, if so, what their characteristics are.

The predictive value of the determinants for the primary and secondary outcome measures (ie, SCC, OCP, QoL, subjective recovery and ADL functioning) at T3 and T4 will be determined using multivariate regression analysis. Potential predictors are defined as variables with at least a marginally significant association (p<0.10) with the outcome. Only these variables will be included in the subsequent regression analyses to determine the most important predictors. In general, effects with a two-tailed p<0.05 are considered statistically significant.

Sample size and power calculation

The sample size needed in the COMPAS study is calculated using the method for multilevel analysis according to Twisk.38 Based on a high intraindividual correlation across the different time points (r=0.70), an α level of 0.05 and power of 0.80, there are 180 participants per group needed to be able to detect a small difference (at least 0.2 SD) between the groups. We expect about 40% drop-outs during the 2-year follow-up period due to mortality, comorbidity or refusal to continue participation. Therefore, we aim to include 300 participants at baseline in each group in order to end up with the 180/group needed.

Ethics and dissemination

Ethical considerations

The COMPAS study is conducted in accordance with the ‘Helsinki Declaration’ (Seoul revision, 2008) and the ‘medical Research Involving Human Subjects Act’ (WMO). The study is non-invasive, imposes no risk on participants, and its protocol has been approved by the medical ethical committees of all participating hospitals (ie, St. Elisabeth and TweeSteden Hospitals in Tilburg, and the Maxima Medical Centre in Veldhoven), and has been registered by the Central committee on Research Involving Human Subjects (number NL31208.008.10). Furthermore, written informed consent is obtained from all participants.

Dissemination

The results obtained will be disseminated to the scientific, medical and general public by publication in national and international peer-reviewed journals, as well as by presentations in conferences and meetings with clinicians dealing with patients with stroke.

Discussion

The COMPAS study is the first in which poststroke SCC are systematically evaluated over time, while a wide range of subjective and objective variables in patients and controls is taken into account. While numerous studies have measured poststroke OCP, only a few have also evaluated the patients’ SCC. Also, while these symptoms are found to be common among patients with stroke, knowledge about their risk factors, their course over time, differences with the non-stroke population and their predictive value for future functioning is practically non-existent.

Strong elements of the COMPAS study are its prospective design with multiple assessments during the first two years after stroke, and the extensive evaluations of subjective and objective variables, which, based on the current literature, are potentially relevant to SCC after stroke. This gives us the opportunity to determine a detailed risk profile for experiencing poststroke SCC. Furthermore, the instruments chosen are widely accepted and frequently used in daily clinical practice dealing with patients with stroke. Traditional neuropsychological and more ecologically valid tests (eg, the Rivermead Behavioural Memory Test) are used to evaluate OCP, making it possible to determine whether the ecological validity of tests affects the association between SCC and OCP. Also, a healthy control group is assessed at the same time points as the patients and will be used as a reference group. This enables us to distinguish poststroke SCC in their prevalence, profile and time course from, for example, factors which are associated with ageing. A potential limitation of the study is that the most seriously affected patients with stroke are unable to participate, thereby reducing the possibility to generalise the results to the stroke population as a whole. However, our study differs from those carried out until now in this field in that we include a broad selection of patients with stroke, not only first-ever strokes or patients discharged home.

In conclusion, we feel that the COMPAS study has the potential to contribute to knowledge on poststroke SCC. Owing to the ageing population and healthcare improvements, the number of stroke survivors who will have to deal with poststroke impairment will increase in the future, and the social and economic burdens will rise accordingly.39 ,40 Clinicians are frequently confronted with patients having SCC after their stroke, but the meaning and relevance of these SCC have yet to be determined. We aim to elucidate the possible risk factors, prognosis and the predictive value of poststroke SCC. This information can subsequently be applied by clinicians in daily practice in order to more accurately inform patients and their proxies and to treat SCC. Our data may also prove useful in the future development of patient-tailored intervention programmes to ultimately improve individual stroke patient-centred care, which is the ultimate aim of the COMPAS study.

References

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Footnotes

  • Contributors RM, PK and MR conceptualised the study. MS and RM contributed to the procurement of funding. MR, RM and PK developed procedures for implementing the protocol. All authors contributed to and have checked the final manuscript.

  • Funding This study is financially supported by the Centre of Research on Psychology in Somatic diseases (CoRPS) from Tilburg University, The Netherlands.

  • Competing interests None.

  • Ethics approval Medical Ethics Committee St Elisabeth Hospital, TweeSteden Hospital in Tilburg, and Maxima Medical Centre in Veldhoven.

  • Provenance and peer review Not commissioned; internally peer reviewed.

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