Skip to main content
Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Metacognitive preserved generation strategy benefits for both younger and elderly participants with schizophrenia

  • Marie Izaute ,

    Roles Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Project administration, Supervision, Validation, Writing – original draft, Writing – review & editing

    marie.izaute@uca.fr

    Affiliation Université Clermont Auvergne, CNRS, LAPSCO, Clermont-Ferrand, France

  • Flavien Thuaire,

    Roles Data curation, Investigation, Methodology, Resources, Software, Supervision, Writing – review & editing

    Affiliation Université Clermont Auvergne, CNRS, LAPSCO, Clermont-Ferrand, France

  • Alain Méot,

    Roles Data curation, Formal analysis, Methodology, Validation

    Affiliation Université Clermont Auvergne, CNRS, LAPSCO, Clermont-Ferrand, France

  • Fabien Rondepierre,

    Roles Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Supervision, Writing – review & editing

    Affiliation Service de Psychiatrie de l’Adulte A et Psychologie Médicale, Centre Mémoire de Ressources et de Recherche, CHU Clermont-Ferrand, Clermont-Ferrand, France

  • Isabelle Jalenques

    Roles Conceptualization, Formal analysis, Funding acquisition, Investigation, Project administration, Supervision, Writing – review & editing

    Affiliation Service de Psychiatrie de l’Adulte A et Psychologie Médicale, Centre Mémoire de Ressources et de Recherche, CHU Clermont-Ferrand, Institut de Psychiatrie-GDR 3557, Université Clermont Auvergne, Clermont-Ferrand, France

Abstract

Cognitive memory and introspection disturbances are considered core features of schizophrenia. Moreover, it remains unclear whether or not participants with schizophrenia are more cognitively impaired with ageing than healthy participants. The aims of this study were to use a metacognitive approach to determine whether elderly participants with schizophrenia are able to improve their memory performance using a specific generation strategy and to evaluate the memory benefits for them using this strategy. 20 younger and 20 older participants with schizophrenia and their comparison participants matched for age, gender and education learned paired associates words with either reading or generation, rated judgment of learning (JOL) and performed cued recall. Participants with schizophrenia recalled fewer words than healthy comparison participants, but they benefited more from generation, and this difference was stable with ageing. Their JOL magnitude was lower than that of healthy comparison participants, but JOL accuracy was not affected by either age or the pathology. In spite of their memory deficit, elderly and younger participants with schizophrenia benefited remarkably from the memory generation strategy. This result gives some cause for optimism as to the possibility for participants with schizophrenia to reduce memory impairment if learning conditions lead them to encode deeply.

1. Introduction

Memory is acknowledged to be one of the cognitive functions most affected in schizophrenia [14] and cognitive disturbances are seen as better predictors of low functional outcome in participants with schizophrenia than clinical symptoms [5, 6]. Accordingly, improving their memory abilities should increase their functional outcome, and even small gains in their functioning or productivity could translate into large financial savings [7]. A number of neuroimaging studies support the view that high-level memory functions such as control over working memory [8], or semantic organization, proverb comprehension and inference of non-literal studies behind interlocutors’ use of proverbs are impaired in schizophrenia [9, 10]. In a review of neuroimaging studies conducted while participants with schizophrenia were performing executive tasks, Ranganath et al. [11] found that strategic memory encoding is linked to executive functions, and that both are impaired in schizophrenia. Even if executive functions impairment in participants with schizophrenia does not fully account for their memory impairment [12], it leads them to compensate with cognitive resources [13] and usually generates poor semantic performance [14].

Moreover, in addition to cognitive deficits [1, 11, 1520] schizophrenia is often defined as a pathology of consciousness [21] and associated with a lack of self-awareness [22, 23]. Thus, as suggested by Bacon et al. [24], the concept of metamemory, which refers to monitoring of our awareness of our own memory capacity and control of related behaviour [25, 26], is of interest for gaining a better understanding of the cognitive behaviour of participants with schizophrenia. For example, during a learning memory task, monitoring refers to our own subjective assessment and is expressed as metamemory judgments (i.e., judgment of learning [27]). Control is the capacity to regulate our own cognitive behaviour, for example by allocating a given time to study [28] or by choosing an effective strategy. Thus, metamemory is central for learning strategy selection, cognitive resource allocation, and cognitive assessment of memory performance. The prerequisite for efficient monitoring is to be able to assess accurately whether or not a specific information answer is difficult or easy to learn, a process shown to be relatively intact in schizophrenia. Control of a learning task has been shown to be impaired [29, 30]. The strategic regulation of memory function in participants with schizophrenia is impaired not only at the time of retrieval of semantic knowledge, but also during encoding of episodic information. In a general knowledge task assessing semantic memory, Danion et al., (2001) [31] observed that participants with schizophrenia were able to take account of an incentive to obtain better accuracy. Indeed, they based their decisions to withhold or volunteer answers on previous monitoring and improved their memory performance. In a study on strategic control during information retrieval, Akdogan et al., (2014) [32] showed that participants with schizophrenia benefited from the strategic support. Participants with schizophrenia were less accurate than healthy participants when spontaneously reporting information from semantic memory. Nevertheless, when helped with contextual support, they were asked to respond either very precisely or by giving an interval response, their recall results were comparable to those of their healthy counterparts. Like healthy participants, participants with schizophrenia can strategically regulate their memory reporting when answers are to be provided within an experimentally fixed frame [32]. Another interesting finding from this study is that participants with schizophrenia present a deficit with self-initiation of strategy use [33, 34].

For episodic memory, when participants are instructed to learn pairs of words (cue-target), they are asked to predict the likelihood (Judgment of Learning) of recalling the target word during the memory test. These predictions (monitoring process) rely on a variety on contextual cues such as the difficulty of the word pair (association level), the number of times an item was presented, effortful processing during learning [35]. For participants from the general population, several studies have focused on a classic measure of metamemory control, namely self-paced study time. In the absence of time pressure, participants spend more time studying difficult items than easy ones [28]. For participants with schizophrenia, a significant dissociation was obtained between monitoring (relatively intact with sensitivity to contextual cues) and control (impaired during encoding episodic information) [29]. In this study, memory control was assessed using study-time allocation during learning, and memory monitoring was assessed using Judgments of Learning (JOL). During encoding of new information, participants with schizophrenia were able to adapt their JOL estimates to the frequency of item presentation. However, they did not adapt their study-time to this presentation frequency. There was no difference in the amount of study time allocated for an item presented once, twice, or three times. Nevertheless, according to the monitoring-affects-control hypothesis [36], another study [37] showed that when participants’ memory control follows the monitoring, they were able to adapt adequately their study time behaviour. When monitoring precedes the control of a learning phase schizophrenia participants are able to adapt their study time to the difficulty of pairs and spend more time re-studying the non-recalled answer during a second learning phase [37]. Thus metamemory monitoring remains accurate in schizophrenia, and metamemory control can be more efficient if some support is given to participants with schizophrenia.

A metacognitive intervention approach [38] is also essential for elderly people. Indeed, implementation of memory encoding and recovery strategies must be facilitated with age by means of tasks or instructions that will decrease the share of self-initiated processing. At one and the same time the elderly present both difficulties with implementing strategies suited to the nature of the task [39] and difficulties with adjusting their strategies [40]. Nevertheless, these effects of age may be reduced if older adults are encouraged or trained to use strategies. In a meta-analysis of the memory-improvement literature, Verhaeghen et al. (1992) [41] concluded that training older adults to use mnemonic strategies (e.g., imagery or the method of loci) can improve adults’ learning of new materials. For encoding, it is a matter of providing sufficient environmental support to direct learning towards the use of deep processing and encouraging the development of such processing on the information to be memorized (e.g., [38, 42]).

During encoding, other control metamemory processes can be evaluated like a specific memory strategy such as actively generating the to-be-remembered responses which usually produces a higher degree of learning than reading [4347] and a higher accuracy of metamemory judgments [48]. This phenomenon (see for review, [49]), known as “the generation effect”, indicates the improvement in memory performance when participants generate the target word from a cue (lettuce—rab…) rather than just reading the word pair (lettuce—rabbit). This effect has been explained in terms of the active generation process itself which requires activating the semantic network between the cue presented at study and the target word to be generated. In their study, Froger et al. (2011) compared the perceived difficulty of the learning task by using reading and generation (learning strategy) in young and older adults [50]. Their results confirmed that all participants improved their memory performance in the generation condition. An additional aim of their study was to examine the effect of age on study-time allocation during learning strategies. Both groups perceived generation (estimate with overall prediction) as more difficult than reading as a learning strategy. Young participants allocated more time to the perceived difficulty strategy. Although older participants spent the same amount of time on average in both learning conditions (reading and generation), their memory performance was higher after the generation strategy. These results were interpreted as an impairment between young and older participants on control metacognitive process.

As functional capacity is related to neuropsychological abilities in older participants with schizophrenia [51, 52] a central question in schizophrenia is whether cognitive functioning deficits are due to ordinary ageing or degenerative ageing over the person’s life span [46, 5357]. Since schizophrenia is seen as a variant of dementia [58], there has been considerable interest in ascertaining whether older adults with schizophrenia are particularly vulnerable to the cognitive effects of ageing [59]. Moreover, some studies suggest that cognitive performance is predictive of longevity in individuals with schizophrenia [60]. The growing number of studies involving ageing in participants with schizophrenia is a result of the lengthening of their life expectancy which, however, remains below that of the general population [6164]. Understanding the interactions between aging and schizophrenia could provide an opportunity to better design age-sensitive intervention for remediation [52]. In a first pilot study to explore metamemory in elderly participants with schizophrenia [65] monitoring and control processes were evaluated. Participants had to learn pairs of words before assessing their JOLs taking into account the intrinsic characteristics of the material (strongly associated and non-associated word pairs) and then controlling their allocated re-study time in a second learning phase. Judgment of Learning (JOL) as an evaluation of monitoring was accurate, but memory control, as assessed by measuring study time allocation, was not as efficient for memory performance as in the case of healthy comparison participants.

To the best of our knowledge, there are no data available about how participants with schizophrenia and aging participants with schizophrenia cope with a mnesic strategy such as the generation effect. Several studies of the generation effect [42, 46, 47, 66, 67] found that generated words were recalled better than those that were read, even in older participants. Our aim was to examine the effectiveness of the generation strategy to evaluate the memory benefits for young and older adults with schizophrenia. We aimed to create a situation in which generation and reading strategy were implemented in a metacognition paradigm. The first goal of this study was to use a metacognitive approach to determine whether or not participants with schizophrenia are able to improve their memory performance using the generation strategy. Second, our goal was to estimate how participants were able to evaluate their JOL differently according to the difficulty of learning pairs of words and the two different strategies (generation versus reading). Learning difficulty was manipulated by the level of association between the two words of each pairs (weakly and strongly associated words). For metamemory, the level of association is typically regarded as an indicator of the level of difficulty of the material and therefore as an indicator of the evaluation of this difficulty. The Koriat model [68], for example, calls this characteristic an intrinsic cue, in respect of which other works have shown patients to be sensitive to this variation [29, 37]. We predict a replication of sensitivity to this difficulty in the case of participants with schizophrenia. They are able to estimate a higher JOL for the strongly associated pairs than for those whose association is weaker. Our third goal was to evaluate how participants with schizophrenia adapt the amount of time allocated to the study during learning.

2. Methods

2.1. Participants

This study was conducted in accordance with ethical standards and had the approval of the local ethics committee (Comité de Protection des Personnes Sud-Est 1, CHU Saint-Etienne, reference 2010–34). It was performed in accordance with relevant guidelines and was retrospectively registered in clinical trial the 9th November 2017 (URL: https://clinicaltrials.gov/ct2/show/NCT03338179?term=NCT03338179&cntry1=EU%3AFR&rank=1, NCT03338179). Before the investigation started, all the participants and where appropriate their legal representatives provided written informed consent after receiving a full explanation of the study. As justification for the current sample size, to the best of our knowledge, not enough studies have been carried out to allow for an accurate assessment of the power analysis of the effect for participants with schizophrenia. Nevertheless, we did examine previous studies in the literature that used comparable stimuli [29, 31, 37, 69]. They show a deficit in metamemory judgment evaluation, and memory performance, in 18 to 23 participants with schizophrenia. As the task is very similar in terms of stimuli and the population studied, we think we need the same number of participants as previous experiments because the power of the effect ought to be very similar (similar population, similar procedure). For the comparison of elderly participants, only one previous study has been published with this type of paradigm for patients [65]. The group effect was obtained with groups of 13 participants. For the purposes of our study, 20 older (aged over 59 years and 6 months) and 20 younger (aged between 18 and 45 years) participants with schizophrenia living in the community, all of them clinically stable, were recruited from the Psychiatric Department of the University Hospital of Clermont-Ferrand. All of them met the criteria for schizophrenia as set out in the Diagnostic and Statistical Manual of Mental Disorders -IV-TR as determined by the consensus opinion of their current psychiatrist and a senior psychiatrist on the research team. The age of schizophrenia onset was under 40. Potential participants with any current co-morbid psychiatric disorder, including alcohol or substance abuse or dependence, were excluded from the study. Medicated participants with schizophrenia had been treated with stable doses of psychotropic medication for at least 4 weeks. 6 were taking typical neuroleptics, 23 atypical ones, and 10 a mixture of typical and atypical. One older participant with schizophrenia was neuroleptic-free. Their psychiatric symptoms were assessed according to the Positive and Negative Symptoms Scale (PANSS, [70]). Their IQ was assessed using a short version of the Wechsler Adult Intelligence Scale, revised (WAIS-R; [71]). Information processing speed was assessed with the digit/symbol subtest Wechsler Adult Intelligence Scale—WAIS-R [72] and letter comparison test (XO, [73]). Subjective memory complaint was assessed using participants’ responses to the Cognitive Difficulties Scale (see [74]).

Twenty older and 20 younger healthy participants matched with the participants with schizophrenia in terms of age, gender and level of education were also recruited. None of the 40 participants had a known neurological or psychiatric affection or suffered from current or past alcohol or substance abuse or dependence. Table 1 presents demographical, clinical and some descriptive statistics of group comparison data. There was no interaction effect between group and age.

thumbnail
Table 1. Demographic and clinical data for younger and older healthy comparison participants and participants with schizophrenia (standard deviations shown in brackets).

https://doi.org/10.1371/journal.pone.0241356.t001

2.2. Material

The items consisted of 28 weakly-associated word pairs (e.g. lettuce-rabbit) and 28 strongly-associated word pairs (e.g. watch-hour) from Ferrand and Alario [75]. Weakly-associated word pairs had an association value of less than 5 (M = 3.45; SD = 0.96), and strongly-associated word pairs a value higher than 25 (M = 42.81; SD = 16.03). Half of these weakly and strongly associated word pairs were randomly presented in the "reading" condition and the other half in the "generation" condition. The word pairs were then randomly divided into two lists (A and B). The two lists were counterbalanced across tests to avoid a list effect. There was no difference in association between the two lists for either weakly-associated, t(26) = .175, p = .86, or strongly-associated, t(26) = .721, p = .48, words. The experimental design was computerized, and the data were collected automatically.

2.3. Procedure

A computerized version of the tasks was used. The word pairs appeared on the screen one by one, and participants were instructed to read the pair or produce the target word (generation strategy) from the cue. They were then told that they could study each pair for as long as they liked during a maximum of 20 seconds. Participants controlled their own learning time, making it possible to measure their study-time allocation strategy For half of the word pairs participants had to read the pairs aloud, for the other half only the first three letters of the second word appeared on the screen, and participants had to generate the complete second word. After the learning phase, they had to perform a non-verbal distracting task during a 4-minute retention interval [76]. Then, the first item in each word pair (cue) was displayed on the screen without the second item (target). Using a 5-point scale (0%, 25%, 50%, 75% and 100%) participants were asked to give their JOL ratings, immediately following which there was a recall phase when each cue was presented, and they had to try to recall the target word. This procedure, which is easier for participants with schizophrenia, had been used already [65, 37]. Use of the same scale may allow the results obtained with this population to be compared whith those other strategies or memory indices.

2.4. Data analyses

All statistical analyses were run on SPSS Statistics. The significance level was set at p < .05. The analyses described in detail are those that were significant. All analyses of variance (ANOVAs) were computed with Group (healthy comparison participants or participants with schizophrenia) and Age (younger and older participants) as between-subject factors. The within-subject factors were Strategy (reading and generation) and item Association (weakly-associate and strongly associate). The dependent variables (see Table 2) were the percentage of words correctly generated, the percentage of read and generated words recalled for the memory performance analyses, the magnitude of JOL for the monitoring process, and the mean study time allocated for the control process. For the accuracy of metacognitive JOL monitoring in evaluating performance [77], the Goodmann-Kruskal gamma coefficient was calculated for each participant. This relative measure of correspondence, known as resolution or discrimination accuracy [78], refers to participants’ ability to discriminate between words that were recalled and those that were not. An outlier elimination rule was applied to all the analyses using the Tukey exclusion procedure. To avoid too much loss of power given the relatively low number of participants by groups, the Interquartile Range (IQR), the minimum distance below the first or above the third quartiles necessary to consider a data as outlier, was set at two. Only differences due to this elimination of outliers were reported.

thumbnail
Table 2. Mean percentage of generated items, correct recall, judgment of learning, mean study time (in seconds) and gamma coefficient for read and generated weakly associate and strongly associate items (standard deviations in brackets).

https://doi.org/10.1371/journal.pone.0241356.t002

3. Results

Data used in this article are available at: https://osf.io/agzn7/.

3.1. Generation performance

A 2 (group: participants with schizophrenia, healthy comparison participants) x 2 (age: younger, older) x 2 (association: weakly-associate, strongly-associate) repeated-measures analysis of variance (ANOVA) was conducted on the percentage of words correctly generated. The results revealed a main effect of association, F(1,76) = 34.5, p < .001, η2p = .312. Participants generate a higher percentage of answers with strong associates than with weak associates (respectively 94.7% and 86.9%). There was also an associate x group interaction F(1,76) = 7.9, p < .01, η2p = .094. The difference in respect of generated items between participants with schizophrenia and healthy comparison participants appeared for weakly-associate items (respectively 83.2% and 90.6%) and not for strongly-associate items (respectively 94.8% and 94.7%). There were no effects of group, F(1,76) = 2.6, age, F(1,76) = 1.7, interaction group x age, F(1,76) = .06, age x association F(1,76) = .02, or group x age x association, F(1,76) = .07.

3.2. Memory performance

A 2 (group: participants with schizophrenia, healthy comparison participants) x 2 (age: younger, older) x 2 (strategy: reading, generation) x 2 (association: weakly-associate, strongly-associate) repeated-measures analysis of variance (ANOVA) was conducted on the percentage of read and generated words recalled (hereinafter referred to as “correct answers”). The results revealed a main effect of group, F(1,76) = 43.6, p < .001, η2p = .364. Participants with schizophrenia gave a lower percentage of correct answers than healthy comparison participants (respectively 54.9% and 75.5%). There was also a main effect of strategy, F(1,76) = 50.3, p < .001, η2p = .398. Participants gave a higher percentage of correct answers with the generation strategy than with the reading strategy (respectively 70.0% and 60.4%), suggesting that all participants benefited from the generation condition to enhance their memory performance. A main effect of association was obtained, F(1,76) = 243.9, p < .001, η2p = .762. Participants gave a higher percentage of correct answers with strongly-associated words than with weakly-associated words (respectively 77.0% and 53.4%). Then, a strategy x group interaction F(1,76) = 16.3, p < .001, η2p = .176 was obtained. Fig 1 shows the mean percentages of correct answers obtained for participants with schizophrenia and healthy comparison participants as a function of strategy. Scrutiny of this figure reveals that there was a memory advantage for generated items for both participants with schizophrenia and controls, but this advantage was bigger for participants with schizophrenia (47.4% for reading and 62.3% for generation) than for healthy controls (73.5% for reading and 77.6% for generation). This result suggests participants with schizophrenia benefit more from generation than healthy controls. This is true for both young and older adults. There were no effects of age, F(1,76) = 2.1, interaction group x age, F(1,76) = .5, age x strategy F(1,76) = 2.5, group x age x strategy F(1,76) = 1.0, group x associate F(1,76) = 2.2, age x associate F(1,76) = .4, associate x strategy F(1,76) = 1.5, group x association x strategy, F(1,76) = .01, or group x age x association x strategy, F(1,76) = .06.

thumbnail
Fig 1. Mean percentages of correct answers obtained for participants with schizophrenia and healthy comparison participants as a function of strategy (reading and generation).

https://doi.org/10.1371/journal.pone.0241356.g001

To assess whether the difference obtained in terms of the percentage of correctly generated words altered the mnesic performance effects, an ANCOVA was performed. This analysis yielded the same results, namely that the percentage of words recalled did not depend on the percentage of words generated. Thus, the strategy x group interaction and next strategy x association x age interaction cannot be attributed to the percentage of generated words.

Finally, a strategy x association x age interaction, F(1,76) = 5.0, p < .05, η2p = .061, was also obtained. Fig 2 shows the mean percentages of correct answers obtained for younger and older participants as a function of strategy and association.

thumbnail
Fig 2. Mean percentages of correct answers obtained for younger and older participants as a function of strategy (reading and generation) and association (weakly associate and strongly associate).

https://doi.org/10.1371/journal.pone.0241356.g002

Scrutiny of this figure reveals that there was no difference between younger and older participants as regards the increase from reading to generation with strongly associated items (respectively +7.5% for younger participants and +8.6% for older participants). For weakly associated items, however, the difference between reading and generation was greater for younger participants (+15.8%) than for older participants (+6.1%).

3.3. Metamemory monitoring

The same ANOVA was conducted on JOL ratings for all the answers. The results revealed a main effect of group, F(1,76) = 29.7, p < .001, η2p = .281. Participants with schizophrenia estimated lower JOL ratings than healthy comparison participants (respectively 64.6% and 81.1%). There was also a main effect of strategy, F(1,76) = 41.8, p < .001, η2p = .355. Participants estimated higher JOL ratings with generation strategy than with reading strategy (respectively 77.3% and 67.4%). Finally, there was a main effect of association, F(1,76) = 89.0, p < .001, η2p = .539. Participants estimated higher JOL ratings with strongly-associated items than with weakly-associated items (respectively 78.3% and 67.4%). There were no effects of age, F(1,76) = .4, interaction group x age, F(1,76) = .1, group x strategy F(1,76) = 1.6, age x strategy F(1,76) = .8, group x age x strategy F(1,76) = .6, group x associate F(1,76) = 2.2, age x associate F(1,76) = .3, group x age x associate F(1,76) = .5, associate x strategy F(1,76) = 1.1, group x association x strategy, F(1,76) = 2.2, age x association x strategy, F(1,76) = .9, or group x age x association x strategy, F(1,76) = .002.

3.4. Relative correspondence between memory performance and judgment of learning: Gamma coefficient

In metamemory two measures were usually used: calibration (measure of absolute accuracy) and gamma (measure of relative accuracy, [79]). The value of the relative measurement shows that the relative precision (gamma) of participants with schizophrenia is very high, signalling that they are able to discriminate between items they recall and those they do not recall. The gamma coefficient (see Table 2) has to be calculated individually for each participant. The values of the gamma coefficient can range from 1.0 (full agreement between confidence level and answer provided) to -1.0 (complete disagreement between the confidence level rating and answer provided).

A 2 (group: participants with schizophrenia, healthy comparison participants) x 2 (age: younger, older) x 2 (strategy: reading, generation) ANOVA was performed on this gamma coefficient. Excluding outliers resulted in a significant main effect of the strategy F(1,68) = 10.61, p < .01, η2p = .135, with gamma values higher for the generation (.86) task than the reading task (.78), and no interaction effect, indicating that there was no difference in accuracy between younger and older participants or between participants with schizophrenia and healthy comparison participants in this respect. High gamma coefficients indicated that metamemory judgments closely matched true memory performance both for participants with schizophrenia and healthy comparison participants and both for both younger and older participants. There were no effects of group, F(1,76) = .3, age, F(1,75) = 2.9, interaction group x age, F(1,75) = .2, strategy F(1,73) = .3, group x strategy F(1,73) = 1.0, age x strategy F(1,76) = .3, or group x age x strategy F(1,76) = .0002.

3.5. Allocation of study time

A 2 (group: participants with schizophrenia, healthy comparison participants) x 2 (age: younger, older) x 2 (strategy: reading, generation) x 2 (association: weakly-associate, strongly-associate) ANOVA was conducted on time allocation in respect of all the answers. The results revealed a main effect of group, F(1,76) = 8.4, p < .01, η2p = .100. Participants with schizophrenia allocated more time to study than healthy comparison participants (respectively 8.8s and 5.5s). There was a main effect of strategy, F(1,76) = 173.2, p < .001, η2p = .695. Participants allocated a longer study time to the generation strategy than the reading strategy (respectively 8.2s and 6.2s). There was also a main effect of association, F(1,76) = 83.8, p < .001, η2p = .524. Participants allocated a longer study time to weakly associated items than strongly-associated items (respectively 7.6s and 6.7s). A strategy x group interaction, F(1,76) = 6.8, p < .05, η2p = .083, was significant, suggesting that the difference between the two strategies (more time for generation than for reading) was greater for participants with schizophrenia (respectively 10.0s and 7.6s) than for healthy comparison participants (respectively 6.4s and 4.7s). Finally, a strategy x association interaction F(1,76) = 24.9, p < .001, η2p = .247 was obtained. More time was allocated for weakly associate items than for strongly-associate items in generation strategy (respectively for weakly-associate items 8.8s and for strongly-associate 7.5s). There was no difference between these two types of items for reading (respectively, 6.4s and 6s). The same results were obtained with outliers excluded (see the elimination rule in the data analysis) except that the group x age interaction became significant, F(1, 71) = 5.28, p < .05, η2p = .069, indicating a greater difference between participants with schizophrenia and healthy participants for the elderly (respectively, 9.8s and 4.6s for the older and 6.2s and 5.1s for the younger participants). There were no effects of age, F(1,76) = .2, interaction group x age, F(1,76) = 3.1, age x strategy F(1,76) = .1, group x age x strategy F(1,76) = .02, group x associate F(1,76) = .4, age x associate F(1,76) = .6, p>.1, group x age x associate F(1,76) = 1.2, group x association x strategy, F(1,76) = .3, age x association x strategy, F(1,76) = 3.7, or group x age x association x strategy, F(1,76) = 1.1.

4. Discussion

The aims of this study were to examine a specific generation strategy to assess its memory benefits for young and older adults with schizophrenia, and to use a metacognitive approach to determine whether or not participants with schizophrenia are able to improve their memory performance with the help of this generation strategy. The results show that memory performance was lower for both groups with schizophrenia than for both healthy groups. This finding is consistent with evidence which has repeatedly indicated that episodic memory is defective in schizophrenia [1, 37, 8083]. Nevertheless, our results replicated earlier findings that generation improves the memory performance of both young and older adults [50, 84]. To the best of our knowledge, this is the first time a study has shown that participants with schizophrenia benefited more from the generation strategy than healthy comparison participants. Even if memory performance of participants with schizophrenia is still lower than that of healthy comparison participants, the improvement in memory performance with the generation strategy is greater in the case of participants with schizophrenia than healthy comparison participants. This is in contradiction with Iddon et al. (1998) [85], according to whom participants with schizophrenia failed to benefit from strategy selection. In their paradigm, participants had to discover the category exemplar strategy and then apply it. This procedure required self-initiation of the strategy, which is known to be impaired in schizophrenia [33, 34]. Our results indicate that providing cognitive support with generation at encoding helped participants with schizophrenia reduce the gap with comparison participants with respect to memory performance; this result is consistent with the findings of Thuaire et al. 2012 [37]. When the paradigm allows for it and accompanies participants with schizophrenia in the implementation of adapted control, they adapt their study time more precisely and improve memory performance. Indeed, based on their experience, participants benefited from a first attempt at recall, showing that they were able to adapt their study time to the difficulty of pairs and spend more time re-studying the non-recalled answer during a second learning phase. In the same vein, regarding the retrieval process, Akdogan et al. (2014) [32] showed that participants with schizophrenia benefited remarkably from the framing of responding. The same result was obtained with older participants, whose memory performance improved when ‘appropriate environmental support’ was provided [86]. Our study is original in that it examined the generation strategy as a possible remediation tool for participants with schizophrenia as well as elderly participants. The results we obtained with use of a generation strategy indicate that younger and older participants with schizophrenia reap the same benefits as their healthy counterparts. This is consistent with Taconnat and Isingrini (2004) [66], who showed that young, older, and very old participants benefited equally from this strategy. Thus, the present experiment extends the latter result to young and older participants with schizophrenia.

A closer look at our results reveals that mnesic performance is better for stronger associates than weaker associates. However, the improvement with weak associates is greater for generation strategy than reading strategy only in the case of younger participants (healthy and with schizophrenia alike). The same effect was obtained by Taconnat et al. 2008 [42], but only with healthy participants. Our results extend this effect to schizophrenia participants. When the generation strategy is structured with the first letters of the search word, participants use and benefit from using this strategy. Guerrero et al. (2019) [86] suggest it is the implementation of effective encoding processes that accounts for the generation effect. Such efficiency would depend on metamemory accuracy and the capacity to self-initiate internal strategies. Older adults were also less spontaneously aware that generation led to better memory performance [86]. We evaluated this awareness by monitoring judgment of learning. With our results, according to the difficulty of the material to be learned, we observed the classic adaptation in metamemory monitoring results observed with other metamemory paradigms [28]. As with younger participants with schizophrenia, the JOL ratings of elderly participants with schizophrenia were lower overall than those of the healthy participants, corresponding to their lower memory performance. Nevertheless, both groups of participants with schizophrenia were equally as able as their healthy counterparts to assign lower JOLs adequately to weakly-associate word pairs as opposed to strongly-associate word pairs. This finding confirms previous observations [29, 31, 37] which had shown, first, that monitoring by participants with schizophrenia accurately reflects their memory performance. Secondly, participants with schizophrenia were equally as able as their healthy counterparts to attribute JOLs as a function of item difficulty. Third, both schizophrenia groups estimated higher and more accurate JOLs for generation strategy [48] than for reading. Previous studies have shown that their monitoring is also sensitive to cues like item repetition when they make their JOL [29], as well as to partial information about the memory target [69]. Monitoring by participants with schizophrenia therefore seems to be sensitive to the cues provided by the conditions of the memory task, with the basis for monitoring [68] appearing to be relatively intact in participants with schizophrenia. Finally, both schizophrenia groups gave more accurate JOLs in the generation condition, thus extending previous results with healthy participants [48] to participants with schizophrenia. Most studies about metamemory monitoring in ageing have focused on feeling of knowing (FOK) judgments and have found that such judgments are impaired in older participants [87]. However, this impairment seems to be linked to a difficulty among with elderly with retrieving contextual information [88]. Thus, JOLs, which are not based on such contextual information, are not impaired with ageing [89], and older participants show a delayed-JOL effect equivalent to that observed with younger participants [90]. In accordance with these studies and with the preservation of monitoring in schizophrenia [29, 69], older participants with schizophrenia were able to adapt their JOLs to the difficulty of the materials and to the encoding strategy in order to produce accurate judgments [65]. Procedures based on metamemory monitoring and control have been shown to be efficient in older adults [38], who have been observed to improve the effectiveness of learning by accurately monitoring their progress towards a learning goal and by using the monitoring output to allocate study time appropriately. In our procedure, study time is allocated before JOL monitoring. Both participants with schizophrenia and healthy controls were able to adapt their study time during generation strategy: more time was allocated for weakly-associated items than for strongly associated items. However, there was no difference between these two types of items for reading. For all participants, more time was allocated for generated items than for reading. Our results corroborate those of Matvey et al. (2001) [91] who found that participants considered memory was enhanced more by generating than by reading words pairs. In our results, the mnesic improvement with generation is greater for participants with schizophrenia than for healthy comparison participants. Nevertheless, their JOL were not sensitive to this bigger improvement, which reflects the corresponding mnesic results we obtained. Participants with schizophrenia benefit more from the generation strategy than their healthy counterparts. In terms of the strategic control of learning, our results contradict those of Bacon et al., (2007) [29], who found that participants with schizophrenia memory control was impaired because they did not adapt their study time to the frequency of item presentation. In our results, as in typical results [28] and those obtained with participants with schizophrenia [37], all participants allocated more study time to difficult items than easy items. As regards generation, our results contradict those of Froger et al. (2011) who found that older adults took the same time to study the generated and read target words whereas younger adults spent longer on the generation task [50]. In our results, all participants allocated more time to the generation strategy compared to the reading strategy. However, like in our study, despite the differences in study time, there was a similar generation effect on memory performance.

A number of limitations need to be considered when interpreting these results. A first limitation of our study is that most of the participants with schizophrenia were integrated in the community which is known to be an important component of welfare. Another limitation is the nature of the task that had the advantage of examining the amount of generation effect on word pairs in a experimentally controlled study but it was not very ecological memory. More research, with more comprehensive testing, therefore seems necessary. A third limitation is the relatively small samples. Nevertheless, the effect size of the group difference in the generation condition was robust. Moreover, it is important to stress that each patient was matched with one healthy comparison participant in terms of age, gender and level of education. All of our participants with schizophrenia were chronic, medicated treated according to the guidelines for biological treatment of schizophrenia of the World Federation of Societies of Biological Psychiatry (WFSBP, [92]). Therefore, the potential effects of antipsychotic medication cannot be ruled out. It is very unlikely, however, that antipsychotic drugs were responsible for the enhanced memory manipulation observed in schizophrenia [93, 94]. Second, we found there to be no difference between older and younger participants with schizophrenia in respect of memory and metacognitive monitoring and control aspects. This result was confirmed by neuropsychological measurements in which only the two subtests served to assess processing speed (Digit/symbol subtest, Letter comparison test), with older participants performing worse than younger participants. The way the participants were treated, in line with the guidelines, meant it was possible to limit negative side-effects and cognitive decline in the case of elderly participants with schizophrenia.

In conclusion, this study puts forward some original findings. In spite of their memory deficit, older and younger participants with schizophrenia benefited remarkably from the memory generation strategy. Use of efficient memory strategies could contribute to memory rehabilitation. This result gives some cause for optimism as to the possibility for participants with schizophrenia to reduce their memory impairment if learning conditions cause them to encode deeply.

Acknowledgments

This work had technical support from the CNRS, the UCA and the CHU of Clermont-Ferrand. The authors would like thank Gillian Wakenhut for her accuracy and patience with correcting our English.

References

  1. 1. Aleman A, Hijman R, de Haan EHF, Kahn RS (1999) Memory impairment in schizophrenia: A meta-analysis. Am J Psychiatry 156:1358–1366. pmid:10484945
  2. 2. Heinrichs RW, Zakzanis KK (1998) Neurocognitive deficit in schizophrenia: a quantitative review of the evidence. Neuropsychology, 12(3), 426–445. Neuropsychology 12:426–445. https://doi.org/10.1037/0894-4105.12.3.426 pmid:9673998
  3. 3. Moritz S, Woodward TS, Jelinek L, Klinge R (2008) Memory and metamemory in schizophrenia: A liberal acceptance account of psychosis. Psychol Med 38:825–832. pmid:18205963
  4. 4. Mesholam-Gately RI, Giuliano AJ, Goff KP, et al (2009) Neurocognition in First-Episode Schizophrenia: A Meta-Analytic Review. 23:315–336. pmid:19413446
  5. 5. Green MF (1996) What are the functional consequences of neurocognitive deficits in schizophrenia? [see comments]. Am J Psychiatry 153:321–330. pmid:8610818
  6. 6. Green MF, Kern RS, Braff DL, Mintz J (2000) Neurocognitive Deficits and Functional Outcome in Schizophrenia: Are We Measuring the “Right Stuff”? Schizophr Bull 26:119–136. pmid:10755673
  7. 7. Walker AE, Spring JD, Travis MJ (2017) Addressing Cognitive Deficits in Schizophrenia: Toward a Neurobiologically Informed Approach. Biol Psychiatry 81:e1–e3. pmid:27876157
  8. 8. Eich TS, Nee DE, Insel C, et al (2014) Neural correlates of impaired cognitive control over working memory in schizophrenia. Biol Psychiatry 76:146–153. pmid:24239131
  9. 9. Brébion G, David AS, Jones H, Pilowsky LS (2004) Semantic Organization and Verbal Memory Efficiency in Patients with Schizophrenia. Neuropsychology 18:378–383. pmid:15099160
  10. 10. Thoma RJ, Monnig MA, Hanlon FM, et al (2009) Hippocampus volume and episodic memory in schizophrenia. J Int Neuropsychol Soc 15:182–95. pmid:19203430
  11. 11. Ranganath C, Minzenberg MJ, Ragland JD (2008) The Cognitive Neuroscience of Memory Function and Dysfunction in Schizophrenia. Biol Psychiatry 64:18–25. pmid:18495087
  12. 12. Kopald BE, Mirra KM, Egan MF, et al (2012) Magnitude of impact of executive functioning and IQ on episodic memory in schizophrenia. Biol Psychiatry 71:545–551. pmid:22265665
  13. 13. Knowles EEM, Weiser M, David AS, et al (2015) The Puzzle of Processing Speed, Memory, and Executive Function Impairments in Schizophrenia: Fitting the Pieces Together. Biol Psychiatry 78:786–793. pmid:25863361
  14. 14. Doughty OJ, Done DJ (2009) Is semantic memory impaired in schizophrenia? A systematic review and meta-analysis of 91 studies. Cogn Neuropsychiatry 14:473–509. pmid:19894144
  15. 15. Green MF (2016) Impact of cognitive and social cognitive impairment on functional outcomes in patients with schizophrenia. J Clin Psychiatry 77 Suppl 2:8–11. pmid:26919052
  16. 16. Bilder RM, Goldman RS, Robinson D, et al (2000) Neuropsychology of first-episode schizophrenia: initial characterization and clinical correlates. Am J Psychiatry 157:549–559. pmid:10739413
  17. 17. Bryson G, Whelahan HA, Bell M (2001) Memory and executive function impairments in deficit syndrome schizophrenia. Psychiatry Res 102:29–37. pmid:11368837
  18. 18. Burglen F, Marczewski P, Mitchell KJ, et al (2004) Impaired performance in a working memory binding task in patients with schizophrenia. Psychiatry Res 125:247–255. pmid:15051185
  19. 19. Fioravanti M, Carlone O, Vitale B, et al (2005) A meta-analysis of cognitive deficits in adults with a diagnosis of schizophrenia. Neuropsychol Rev 15:73–95. pmid:16211467
  20. 20. Moritz S, Woodward TS (2006) The contribution of metamemory deficits to schizophrenia. J Abnorm Psychol 115:15–25. pmid:16492092
  21. 21. Jardri R, Pins D, Bubrovszky M, et al (2009) Neural functional organization of hallucinations in schizophrenia: Multisensory dissolution of pathological emergence in consciousness. Conscious Cogn 18:449–457. pmid:19201210
  22. 22. Osatuke K, Ciesla J, Kasckow JW, et al (2008) Insight in schizophrenia: a review of etiological models and supporting research. Compr Psychiatry 49:70–77. pmid:18063044
  23. 23. Lysaker PH, Carcione A, Dimaggio G, et al (2005) Metacognition amidst narratives of self and illness in schizophrenia: Associations with neurocognition, symptoms, insight and quality of life. Acta Psychiatr Scand 112:64–71. pmid:15952947
  24. 24. Bacon E, Danion JM, Kauffmann-Muller F, Bruant A (2001) Consciousness in schizophrenia: A metacognitive approach to semantic memory. Conscious Cogn 10:473–484. pmid:11790037
  25. 25. Nelson TO, Narens L (1990) Metamemory: A Theoretical Framework and New Findings. In: Bower GH (ed) The Psychology of Learning and Motivation, Academic P. New York, pp 125–141
  26. 26. Nelson TO, Narens L (1994) Why investigate metacognition? In: Metcalfe J, Shimamura AP (eds) Metacognition: Knowing about knowing. MIT Press, Cambridge, MA, pp 1–25
  27. 27. Nelson T, Dunlosky J (1991) When people’s judgments of learning (JOLs) are extremely accurate at predicting subsequent recall: the “Displaced-JOL effect.” Psychol Sci 2:267–270. https://doi.org/10.1080/09658211.2017.1406523
  28. 28. Son LK, Metcalfe J (2000) Metacognitive and control strategies in study-time allocation. J Exp Psychol Learn Mem Cogn 26:204–221. pmid:10682298
  29. 29. Bacon E, Izaute M, Danion JM (2007) Preserved memory monitoring but impaired memory control during episodic encoding in patients with schizophrenia. J Int Neuropsychol Soc 13:219–227. pmid:17286879
  30. 30. Izaute M, Bacon E (2010) Metamemory in schizophrenia: Monitoring or control deficit? In: Trends and Prospects in Metacognition Research
  31. 31. Danion J-M, Gokalsing E, Robert P, et al (2001) Defective Relationship Between Subjective Experience and Behavior in Schizophrenia. Am J Psychiatry 158:2064–2066 pmid:11729027
  32. 32. Akdogan E, Izaute M, Bacon E (2014) Preserved strategic grain-size regulation in memory reporting in patients with schizophrenia. Biol Psychiatry 76:154–159. pmid:24138925
  33. 33. Bonner-Jackson A, Haut K, Csernansky JG, Barch DM (2005) The influence of encoding strategy on episodic memory and cortical activity in schizophrenia. Biol Psychiatry 58:47–55. pmid:15992522
  34. 34. Christensen BK, Girard TA, Benjamin AS, Vidailhet P (2006) Evidence for impaired mnemonic strategy use among patients with schizophrenia using the part-list cuing paradigm. Schizophr Res 85:1–11. pmid:16632330
  35. 35. Sungkhasettee VW, Friedman MC, Castel AD (2011) Memory and metamemory for inverted words: Illusions of competency and desirable difficulties. Psychon Bull Rev 18:973–978. pmid:21626231
  36. 36. Nelson TO, Leonesio RJ (1988) Allocation of self-paced study time and the “labor-in-vain effect”. J Exp Psychol Learn Mem Cogn 14:676–686. pmid:2972804
  37. 37. Thuaire F, Izaute M, Bacon E (2012) Evidence of some strategic preservation of episodic learning in patients with schizophrenia. Psychiatry Res 195:27–31. pmid:21851990
  38. 38. Dunlosky J, Kubat-Silman AK, Hertzog C (2003) Training monitoring skills improves older adults’ self-paced associative learning. Psychol Aging 18:340–345. pmid:12825781
  39. 39. Souchay C, Isingrini M (2004) Age related differences in metacognitive control: Role of executive functioning. Brain Cogn 56:89–99. pmid:15380879
  40. 40. Dunlosky J, Connor LT (1997) Age differences in the allocation of study time account for age differences in memory performance. Mem Cognit 25:691–700. pmid:9337587
  41. 41. Verhaeghen P, Marcoen A, Goossens L (1992) Improving memory performance in the aged through mnemonic training: a meta-analytic study. Psychol Aging 7:242–251. pmid:1535198
  42. 42. Taconnat L, Froger C, Sacher M, Isingrini M (2008) Generation and associative encoding in young and old adults: The effect of the strength of association between cues and targets on a cued recall task. Exp Psychol 55:23–30. pmid:18271350
  43. 43. Slamecka NJ, Graf P (1978) The generation effect: Delineastion of a phenomenon. J Exp Psychol Hum Learn Mem 4:592–604
  44. 44. McElroy LA, Slamecka NJ (1982) Memorial consequences of generating nonwords: Implications for semantic-memory interpretations of the generation effect. J Verbal Learning Verbal Behav 21:249–259. https://doi.org/10.1016/S0022-5371(82)90593-X
  45. 45. Gardiner JM, Hampton JA. (1985) Semantic Memory and the Generation Effect: Some Testsof the Lexical Activation Hypothesis. J Exp Psychol Learn Mem Cogn 11:732–741. https://doi.org/10.1037/0278-7393.11.1-4.732
  46. 46. Kirkpatrick B, Kennedy BK (2018) Accelerated aging in schizophrenia and related disorders: Future research. Schizophr Res 196:4–8. pmid:28689755
  47. 47. McCurdy MP, Leach RC, Leshikar ED (2017) The generation effect revisited: Fewer generation constraints enhances item and context memory. J Mem Lang 92:202–216. https://doi.org/10.1016/j.jml.2016.06.007
  48. 48. Mazzoni G, Nelson TO (1995) Judgments of learning are affected by the kind of encoding in ways that cannot be attributed to the level of recall. J Exp Psychol Learn Mem Cogn 21:1263–1274. pmid:8744965
  49. 49. Bertsch S, Pesta BJ, Wiscott R, McDaniel MA (2007) The generation effect: A meta-analytic review. Mem Cognit 35:201–210. pmid:17645161
  50. 50. Froger C, Sacher M, Gaudouen MS, et al (2011) Metamemory judgments and study time allocation in young and older adults: Dissociative effects of a generation task. Can J Exp Psychol 65:269–276. pmid:22141753
  51. 51. Evans JD, Heaton RK, Paulsen JS, et al (2003) The relationship of neuropsychological abilities to specific domains of functional capacity in older schizophrenia patients. Biol Psychiatry 53:422–430. pmid:12614995
  52. 52. Kalache SM, Mulsant BH, Davies SJC, et al (2015) The Impact of Aging, Cognition, and Symptoms on Functional Competence in Individuals with Schizophrenia Across the Lifespan. Schizophr Bull 41:374–381. pmid:25103208
  53. 53. Fucetola R, Seidman LJ, Kremen WS, et al (2000) Age and neuropsychologic function in schizophrenia: A decline in executive abilities beyond that observed in healthy volunteers. Biol Psychiatry 48:137–146. pmid:10903410
  54. 54. Harvey PD, Reichenberg A, Bowie CR, et al (2010) The Course of Neuropsychological Performance and Functional Capacity in Older Patients with Schizophrenia: Influences of Previous History of Long-Term Institutional Stay. Biol Psychiatry 67:933–939. pmid:20202624
  55. 55. Shmukler AB, Gurovich IY, Agius M, Zaytseva Y (2015) Long-term trajectories of cognitive deficits in schizophrenia: A critical overview. Eur Psychiatry 30:1002–1010. pmid:26516984
  56. 56. Harvey PD, Rosenthal JB (2018) Cognitive and functional deficits in people with schizophrenia: Evidence for accelerated or exaggerated aging? Schizophr Res 196:14–21. pmid:28506706
  57. 57. Thuaire F, Rondepierre F, Bacon E, et al (2020) Executive functions in schizophrenia aging: Differential effects of age within specific executive functions. Cortex 125:109–121. pmid:31981891
  58. 58. Loewenstein DA, Czaja SJ, Bowie CR, Harvey PD (2012) Age-Associated Differences in Cognitive Performance in Older Patients With Schizophrenia: A Comparison With Healthy Older Adults. Am J Geriatr Psychiatry 20:29–40 pmid:22130385
  59. 59. McGurk SR, Moriarty PJ, Harvey PD, et al (2000) The longitudinal relationship of clinical symptoms, cognitive functioning, and adaptive life in geriatric schizophrenia. Schizophr Res 42:47–55. pmid:10706985
  60. 60. Helldin L, Hjärthag F, Olsson AK, Harvey PD (2015) Cognitive performance, symptom severity, and survival among patients with schizophrenia spectrum disorder: A prospective 15-year study. Schizophr Res 169:141–146. pmid:26391285
  61. 61. Cohen C, Vahia I, Reyes P, et al (2008) Schizophrenia in Later Life: Clinical Symptoms and Social Well-being. Psychiatr Serv 59:232–234. pmid:18308900
  62. 62. Allott K, Liu P, Proffitt TM, Killackey E (2011) Cognition at illness onset as a predictor of later functional outcome in early psychosis: Systematic review and methodological critique. Schizophr Res 125:221–235. pmid:21111577
  63. 63. Vahia I V., Cohen CI (2007) Psychosocial interventions and successful aging: New paradigms for improving outcome for older schizophrenia patients? Am J Geriatr Psychiatry 15:987–990. pmid:18056816
  64. 64. Muralidharan A, Finch A, Bowie CR, Harvey PD (2018) Thought, language, and communication deficits and association with everyday functional outcomes among community-dwelling middle-aged and older adults with schizophrenia. Schizophr Res 196:29–34. pmid:28778553
  65. 65. Izaute M, Jalenques I (2014) Metamemory with ageing in schizophrenia: A first study. Psychiatry Res 219:703–706. pmid:25023367
  66. 66. Taconnat L, Isingrini M (2004) Cognitive operations in the generation effect on a recall test: role of aging and divided attention. J Exp Psychol Learn Mem Cogn 30:827–37. pmid:15238027
  67. 67. Taconnat L, Baudouin A, Fay S, et al (2006) Aging and implementation of encoding strategies in the generation of rhymes: The role of executive functions. Neuropsychology 20:658–665. pmid:17100510
  68. 68. Koriat A (1997) Monitoring one’s own knowledge during study: A cue-utilization approach to judgments of learning. J Exp Psychol Gen 126:349–370. https://doi.org/10.1037/0096-3445.126.4.349
  69. 69. Bacon E, Izaute M (2009) Metacognition in Schizophrenia: Processes Underlying Patients’ Reflections on Their Own Episodic Memory. Biol Psychiatry 66:1031–1037. pmid:19726032
  70. 70. Kay SR, Fiszbein A, Opler LA (1987) The Positive and Negative Syndrome Scale (PANSS) for Schizophrenia. Schizophr Bull 13:261–276. pmid:3616518
  71. 71. Silverstein AB (1982) Two-and Four-Subtest Short Forms of the Wechsler Adult Intelligence Scale-Revised. J Consult Clin Psychol 50:415–418. https://doi.org/10.1037/0022-006x.50.3.415
  72. 72. Wechsler D (1989) Echelle d’intelligence de Wechsler pour adultes forme révisée WAIS-R, ECPA. Paris
  73. 73. Salthouse TA, Babcock RL (1991) Decomposing Adult Age Differences in Working Memory. Dev Psychol 27:763–776. https://doi.org/10.1037/0012-1649.27.5.763
  74. 74. Derouesné C, Dealberto MJ, Boyer P, et al (1993) Empirical evaluation of the ‘Cognitive Difficulties Scale’ for assessment of memory complaints in general practice: A study of 1628 cognitively normal subjects aged 45–75 years. Int J Geriatr Psychiatry 8:599–607. https://doi.org/10.1002/gps.930080712
  75. 75. Ferrand L, Alario FX (1998) Normes d ‘ associations verbales pour 366 noms d ‘ objets concrets. Annee Psychol 98:659–709. https://doi.org/10.3406/psy.1998.28564
  76. 76. Kelemen WL, Weaver CAIII (1997) Enhanced memory at delays: Why do judgments of learning improve over time? J Exp Psychol Learn Mem Cogn 23:1394–1409. pmid:9372607
  77. 77. Nelson TO (1984) A comparison of current measures of the accuracy of feeling-of-knowing predictions. Psychol Bull 95:109–133. https://doi.org/10.1037/0033-2909.95.1.109 pmid:6544431
  78. 78. Yaniv I, Yates JF, Smith JEK (1991) Measures of discrimination skill in probabilistic judgment. Psychol Bull 110:611–617. https://doi.org/10.1037/0033-2909.110.3.611
  79. 79. Nelson TO (1996) Gamma is a measure of the accuracy of predicting performance on one item relative to another item, not of the absolute performance on an individual item: Comments on schraw (1995). Appl Cogn Psychol 10:257–260. https://doi.org/10.1002/(SICI)1099-0720(199606)10:3<257::AID-ACP400>3.0.CO;2-9
  80. 80. Lewis R (2004) Should cognitive deficit be a diagnostic criterion for schizophrenia? J Psychiatry Neurosci 29:102–113 pmid:15069464
  81. 81. Danion JM, Huron C, Vidailhet P, Berna F (2007) Functional mechanisms of episodic memory impairment in schizophrenia. Can J Psychiatry 52:693–701 pmid:18399036
  82. 82. Leavitt VM, Goldberg TE (2009) Episodic memory in schizophrenia. Neuropsychol Rev 19:312–323. pmid:19639413
  83. 83. Bora E, Yücel M, Pantelis C (2010) Cognitive impairment in schizophrenia and affective psychoses: Implications for dsm-v criteria and beyond. Schizophr Bull 36:36–42. pmid:19776206
  84. 84. Vannest J, Maloney T, Kay B, et al (2015) Age related-changes in the neural basis of self-generation in verbal paired associate learning. NeuroImage Clin 7:537–546. pmid:25844310
  85. 85. Iddon JL, Mckenna PJ, Sahakian BJ, Robbins TW (1998) Impaired generation and use of strategy in schizophrenia: Evidence from visuospatial and verbal tasks. Psychol Med 28:1049–1062. pmid:9794012
  86. 86. Guerrero Sastoque L, Bouazzaoui B, Burger L, et al (2019) Optimizing memory strategy use in young and older adults: The role of metamemory and internal strategy use. Acta Psychol (Amst) 192:73–86. pmid:30453098
  87. 87. Perrotin A, Isingrini M, Souchay C, et al (2006) Episodic feeling-of-knowing accuracy and cued recall in the elderly: Evidence for double dissociation involving executive functioning and processing speed. Acta Psychol (Amst) 122:58–73. pmid:16309619
  88. 88. Souchay C, Moulin CJA, Clarys D, et al (2007) Diminished episodic memory awareness in older adults: Evidence from feeling-of-knowing and recollection. Conscious Cogn 16:769–784. pmid:17187992
  89. 89. Hertzog C, Kidder DP, Powell-Moman A, Dunlosky J (2002) Aging and monitoring associative learning: Is monitoring accuracy spared or impaired? Psychol Aging 17:209–225. https://doi.org/10.1037/0882-7974.17.2.209 pmid:12061407
  90. 90. Connor LT, Dunlosky J, Hertzog C (1997) Age-related differences in absolute but not relative metameory accuracy. Psychol Aging 12:50–71. pmid:9100268
  91. 91. Matvey G, Dunlosky J, Guttentag R (2001) Fluency of retrieval at study affects judgements of learning. Mem Cognit 29:222–233 pmid:11352205
  92. 92. Hasan A, Falkai P, Wobrock T, et al (2012) World Federation of Societies of Biological Psychiatry (WFSBP) Guidelines for Biological Treatment of Schizophrenia, Part 1: Update 2012 on the acute treatment of schizophrenia and the management of treatment resistance. World J Biol Psychiatry 13:318–378. pmid:22834451
  93. 93. Arnsten AFT, Girgis RR, Gray DL, Mailman RB (2017) Novel Dopamine Therapeutics for Cognitive Deficits in Schizophrenia. Biol Psychiatry 81:67–77. pmid:26946382
  94. 94. Goldberg TE, Goldman RS, Burdick KE, et al (2007) Cognitive Improvement After Treatment With Second-Generation Antipsychotic Medications in First-Episode Schizophrenia. Arch Gen Psychiatry 64:1115. pmid:17909123