Abstract
Objective:
Self-appraisal of cognitive performance, a potentially useful marker of brain functioning, is typically assessed at a single time point where testees are naïve to what constitutes “good” or “bad” performance. Here, we determine whether familiarizing individuals with self-appraisal with daily memory testing for 7 days provides a more accurate estimate of cognitive functioning and mood.
Method:
225 participants (mean age ± standard deviation: 74.1±8.3 years; 66% female; median education 16.0 years) completed the online Boston Remote Assessment for NeuroCognitive Health (BRANCH), which includes two associative memory tasks, for seven consecutive days. Each day, participants self-appraised their performance. At baseline, they completed various cognitive and mood measures. We computed Pearson’s correlations between task performance and self-appraisal on days 1 and 7 and used linear models to examine the relationship between self-appraisal scores and clinical measures.
Results:
Accuracy (day 1: 0.44±0.12; day 7: 0.81±0.16) and self-appraisal (day 1: 0.36±0.15; day 7: 0.70±0.21) increased, as did the association between accuracy and self-appraisal (day 1: correlation coefficient (r)=0.22, 95% confidence interval (95%CI)=[0.09, 0.34], p=.001; day 7: r=0.69, 95%CI=[0.62, 0.76], p<.001). Self-appraisal scores on day 7, but not day 1, showed significant relationships with in-clinic measures.
Conclusions:
Repeated remote cognitive assessments may help elucidate individuals’ capacities to refine their self-perception of cognitive performance during multi-day learning. The weak association between accuracy and test-naïve self-appraisal warrants caution about using this metric cross-sectionally. Experienced self-appraisal could be especially relevant at the early stages of neurodegenerative diseases when subtle learning difficulties emerge and could improve our capacity to detect early meta-cognitive changes.
Keywords: subjective cognitive decline, awareness, cognitive test, self-appraisal, cognition, Alzheimer’s disease
Introduction
Self-perceived cognitive functioning represents a person’s general perception of their cognitive abilities. It is common for older adults to self-perceive changes in their cognitive functioning (Rabin et al., 2023), and these changes may or may not be an early sign of underlying neurodegenerative disease (Jessen et al., 2020). Self-perceived cognitive functioning is commonly assessed using questionnaires that probe various aspects of everyday functioning, including a person’s experience of their memory, language, organizational, and everyday functioning abilities (Clare et al., 2011; Rickenbach et al., 2015).
Self-appraisal encompasses a person’s rating of their performance on a test they just completed. Various studies have focused on metacognitive monitoring, which can be prospective or retrospective in nature and may represent an individual’s judgment of how well they learned information they have just learned or their confidence that they may later recall it (Hertzog & Dunlosky, 2011; Siegel & Castel, 2019). On the other hand, retrospective confidence ratings, which ask individuals to judge how well they recalled information, have also been shown to predict future performance (Putnam et al., 2022). Comparing retrospective self-appraisal to objective performance on a test allows for making inferences about a person’s self-awareness of their cognitive performance on a given test. If someone performs well on a test but reports doing poorly, this may reflect a hyperawareness of cognitive issues (Cacciamani et al., 2021). At the same time, a poor performance perceived as good could indicate a lowered awareness of one’s cognitive impairment. While the individual’s cognitive status contributes to their ability to judge their performance, many other factors may also come into play. For example, depressive symptoms have been linked to lower self-rated memory performance (O’Shea et al., 2016).
While it has been documented that older adults can gauge their performance on memory tasks with a certain precision (Zakrzewski et al., 2021), it may be challenging to gauge a good or a poor performance on a test they have never taken. With repeated exposure to the same task and stimuli, a person’s self-appraisal of their performance might change as their understanding of what is expected of them in the task improves. It is well-established that objective performance increases with repeated exposure (Hausknecht et al., 2007). A study by Koriat et al. (2002) demonstrated that repeated learning of a word list not only improved the objective learning curve but also enhanced the subjective learning curve, gradually increasing participants’ accuracy in assessing their memory performance. This suggests that repeated learning plays a crucial role in fine-tuning self-perception of cognitive performance.
In the multiday Boston Remote Assessment for Neurocognitive Health (BRANCH), older adults complete the exact same remote cognitive tasks every day for a week. Diminished practice effects (i.e., reduced performance improvements on repeated testing), particularly when retesting the same stimuli, represent a decrement in memory consolidation that may be a hallmark of Alzheimer’s disease (Papp et al., 2024; Samaroo et al., 2020). Previous studies have shown that performance on BRANCH improves over time (Jutten et al., 2023; Papp et al., 2024; Weizenbaum et al., 2024) and that differences in learning curves are associated with cognitive performance as measured using in-clinic pencil-and-paper neuropsychological tests (Weizenbaum et al., 2024). BRANCH also includes measures of self-appraisal of performance. With multiday BRANCH, we can investigate whether we can observe changes in test performance and self-appraisal over repeated exposure.
We asked participants to rate their performance on BRANCH following each daily assessment. We aimed to investigate how self-appraisal of cognitive performance changes after repeated exposure to the same stimuli within the multiday BRANCH. We hypothesized that self-appraisal after the first exposure would be less strongly associated with actual performance than self-appraisal after a week of daily repeated exposure because individuals learn to understand what a good performance is from taking the same tests multiple times. Further, we hypothesized that higher self-appraisal would be associated with better cognitive functioning, better self-perceived cognitive functioning, and fewer depressive symptoms. We also expected self-appraisal after repeated exposure to be more strongly related to the other measures than on the first day, as participants had the benefit of multiple opportunities to assess their performance, allowing them to refine their self-perception based on their multiple past performances.
Methods
Participants
Participants were recruited through the Harvard Aging Brain Study (P01AG036694), the Instrumental Activities of Daily Living Study (R01AG053184 and R01AG067021), and the Subjective Cognitive Decline Study (R01AG058825), all of which focused on aging and preclinical Alzheimer’s disease. In addition to the three parent studies’ inclusion criteria, participants were selected for the present study if they were cognitively normal (Clinical Dementia Rating [CDR] global score = 0, Mini-Mental State Examination [MMSE] score >25, and Logical Memory Delayed Recall [LMDR] score above education-adjusted cutoffs). Participants who had a recent history of alcohol or drug abuse, severe head trauma, or a current unstable medical condition or primary psychiatric diagnosis were excluded. A few participants (n = 11, 5%) received a CDR global score of 0.5 but were considered cognitively normal in a multidisciplinary consensus meeting based on their overall clinical presentation and performance on neuropsychological testing. These participants were also included in the study. All participants gave written informed consent before any study procedures. The institutional review board of Massachusetts General Brigham approved this study.
Materials
Boston Remote Assessment of Cognitive Health (BRANCH)
The Boston Remote Assessment of Cognitive Health (BRANCH) comprises two associative memory tasks and a digit–symbol substitution task. The two associative memory tasks are (1) the ‘Face–Name’ (FNAME) test, an adaptation of the Face–Name Associative Memory Exam (Rentz et al., 2011), in which twenty face-name pairs are shown with participants asked to identify the learned faces following a delay; and (2) the ‘Groceries Prices’ test, where participants needed to associate visually represented grocery items with prices ranging from $1.09 to $12.99 (Castel, 2005). BRANCH is described in more detail elsewhere (Papp et al., 2024; Weizenbaum et al., 2024). As described in Weizenbaum et al. (2024), participants attested to completing tasks independently without recording stimuli or responses at the beginning of each session. If participants failed to respond in the allotted time, a pop-up message would appear asking participants to confirm that they were ready to proceed with the test. Study coordinators were available to support participants via phone and email as needed.
In the present study, we focus exclusively on the composite performance accuracy of the two associative memory tasks, as they assess the same cognitive process. Performance accuracy was captured by dividing the number of correct responses by the total number of responses. The resulting score fell on a scale from 0 to 1, with higher scores representing better performance. After completion of each task, participants were prompted, but not required, to “please rate [their] performance on the test today,” using a visual analog scale ranging from 0 to 100 (with higher scores indicating better self-perceived performance). We will refer to this as their ‘self-appraisal.’ The self-appraisal ratings were rescaled to the same scale as performance accuracy, ranging from 0 to 1, with higher scores indicating better performance and self-appraisal.
Standard clinical and cognitive measures
At baseline, participants completed the Preclinical Alzheimer’s Cognitive Composite–5 (PACC5; Donohue et al., 2014; Papp et al., 2017). PACC5 performance is rated as a Z-score, calculated as the mean score of five measures (the Mini-Mental State Examination (Folstein et al., 1975), Wechsler Memory Scale–Revised Logical Memory Delayed Recall (Wechsler & Stone, 1987), Digit-Symbol Coding Test (Wechsler, 1981), the free plus total recall of the Free and Cued Selective Reminding Test (Grober et al., 2009), and category fluency). The PACC5 Z-score has a mean of 0 and a standard deviation of 1 in a cognitively unimpaired sample. Higher scores represent better global cognitive performance. The PACC5 and its components have shown favorable reliability and validity (Donohue et al., 2014; Papp et al., 2017).
The Clinical Dementia Rating (CDR), a semi-structured interview to determine cognitive and functional impairment (Hughes et al., 1982), was administered to participants and their study partners. Study partners were the participants’ spouses, children, friends, or family members. Based on information from both sources, scores between 0 (no impairment) and 3 (severe impairment) are given in various areas (“boxes,” including memory, judgment and problem-solving, home and hobbies, and personal care). Scores from the separate boxes are summed to a “sum of boxes” score ranging from 0–18). Further, a global CDR score ranging from 0 to 3 is calculated using a previously established scoring logic (Morris, 1993); the global score scale corresponds to the individual box scores.
Participants and their study partners also completed the Cognitive Function Index (CFI), a 15-item questionnaire about self-perceived cognitive functioning (Amariglio et al., 2015). Items are scored between 0, 0.5, or 1 and are summed for a total score (range 0–15). Higher scores indicate greater subjective cognitive complaints. The CFI has been shown to have a strong internal reliability, sensitivity to change over time, and discriminative abilities (Amariglio et al., 2015).
Finally, as a measure of depressive symptoms, we administered the 30-item Geriatric Depression Scale (GDS; Yesavage et al., 1982). Each item is rated 0 if the response does not indicate depressive symptoms and 1 if it does. Total scores thus potentially range from 0–30, with higher scores representing more depressive symptoms. The GDS has high internal consistency, strong test-retest reliability, and good criterion and construct validity (Yesavage et al., 1982).
Procedures
Participants completed the clinical measures at an initial in-clinic baseline visit and subsequently completed the BRANCH remotely and unsupervised on their own device (personal computer or mobile device) once daily for seven consecutive days. Each BRANCH session included the same stimuli and required approximately 10 to 15 minutes to complete.
Statistical analysis
All analyses were run in R version 4.3.2. We created composites of the objective performance (i.e., accuracy) and the self-appraisal metrics for the FNAME and the Groceries Prices tasks by averaging both tasks’ metrics. These composites serve as the primary outcomes of this study.
Pearson’s correlations were calculated for the composite accuracy and self-appraisal on day 1 and compared to the correlations on day 7. Linear models were used to examine further the relationship between the day 1 (“test-naïve”) and day 7 (“experienced”) composite self-appraisal scores and the PACC5, CDR, CFI, and GDS. To account for the potentially modifying effects of baseline demographic characteristics, these models were adjusted for age, sex, education, as well as objective performance on the task. We repeated these analyses for the FNAME and Groceries Prices tasks separately; these results are shown in Supplemental Table 1. As self-appraisal ratings were not a forced response, we excluded day 7 self-appraisals of precisely 50 (the default on the visual analog scale; occurred in n = 9 participants [4%]) in sensitivity analyses, reported in Supplemental Table 2. There were no outliers. Analyses were run with the available data.
Last, we calculated the difference between task accuracy and self-appraisal on days 1 and 7 by subtracting accuracy from self-appraisal and subsequently classified participants’ relative estimations over the seven-day testing period into the following groups: (a) consistent underestimation (i.e., participants self-appraised their performance as worse than their actual accuracy on day 1 and on day 7); (b) consistent overestimation (i.e., participants self-appraised their performance as better than their actual accuracy on day 1 and on day 7); (c) variable estimation (i.e., participants either self-appraised their performance as better or as worse than their actual accuracy on day 1 and vice-versa on day 7). We report descriptive statistics for these groups. Group differences were computed using t-tests or chi-square tests, as appropriate.
Transparency and Openness
The data and analyses used for this publication can be made available upon reasonable request from the corresponding author. This study was not preregistered.
Results
We included 225 cognitively unimpaired participants (74.1 ± 8.3 years old; 66% female). Baseline characteristics are displayed in Table 1.
Table 1.
Participant Characteristics.
| Variable | Whole sample |
|---|---|
| N | 225 |
| Age in years | 74.1 ± 8.3 |
| Female sex, N (%) | 148 (65.8) |
| Education in years, M (IQR) | 16.0 (15–18) |
| Race, N (%) | |
| Black | 23 (10) |
| Asian | 7 (3) |
| Native American/Alaskan Native | 1 (1) |
| White | 194 (86) |
| Ethnicity, N (%) | |
| Hispanic | 3 (1) |
| Non-Hispanic | 222 (99) |
| PACC5 | 0.14 ± 0.72 |
| CDR | |
| Global, M (IQR) | 0 (0–0) |
| Sum of Boxes | 0.14 ± 0.33 |
| CFI | |
| Participant | 2.46 ± 2.45 |
| Study partner | 1.49 ± 2.32 |
| GDS | 4.56 ± 4.13 |
| BRANCH objective performance | |
| Day 1 |
0.44 ± 0.12 |
| Day 7 | 0.81 ± 0.16 |
| BRANCH self-appraisal | |
| Day 1 | 0.36 ± 0.15 |
| Day 7 | 0.70 ± 0.21 |
Note: All data displayed as mean ± standard deviation, except otherwise noted.
Abbreviations: BRANCH, Boston Remote Assessment for NeuroCognitive Health; CDR, Clinical Dementia Rating; CFI, Cognitive Function Index; GDS, Geriatric Depression Scale; IQR, interquartile range; M, median; PACC5, Preclinical Alzheimer’s Cognitive Composite–5.
Day 1: Test-naïve self-appraisal
On the first day of testing, the performance accuracy of the FNAME and Groceries Prices tests’ composite was (mean =) 0.44 ± (standard deviation =) 0.12, while the participants’ self-appraisal was 0.36 ± 0.15. Performance accuracy and self-appraisal had a weak association (correlation coefficient (r) = 0.22, 95% confidence interval (95%CI) = [0.09, 0.34], p = .001). Linear models that were adjusted for baseline demographics and initial task accuracy revealed that the self-appraisal scores on day 1 were associated only with the GDS (estimate (B) = −0.005, 95%CI = [−0.010, −0.0003], p = .039) so that a lower GDS was associated with higher self-appraisal. None of the other clinical measures were associated with test-naïve self-appraisal. All associations are displayed in Table 2.
Table 2.
Linear Models Showing the Relationship Between Self-Appraisal and Various Clinical Measures.
| Measure | Day 1 |
Day 7 |
||
|---|---|---|---|---|
| B [95%CI] | P-value | B [95%CI] | P-value | |
| PACC5 | −0.022 [−0.053, 0.010] | .175 | 0.058 [0.020, 0.096] | .003 |
| CDR-SB | −0.011 [−0.071, 0.048] | .703 | −0.079 [−0.151, −0.007] | .032 |
|
CFI Participant Study partner1 |
−0.003 [−0.011, 0.005] −0.002 [−0.012, 0.006] |
.478 .492 |
−0.012 [−0.021, −0.002] −0.007 [−0.018, 0.004] |
.017 .195 |
| GDS | −0.005 [−0.010, −0.0003] | .039 | −0.008 [−0.014, −0.002] | .008 |
Note: All models are adjusted for baseline age, sex, years of education, and objective performance on day 1. Effects with p < .05 are displayed in bold.
Data missing for n = 5 (2%).
Abbreviations: B, estimate; CDR-SB, Clinical Dementia Rating Sum of Boxes; CFI, Cognitive Fit Index; GDS, Geriatric Depression Scale; PACC, Preclinical Alzheimer’s Cognitive Composite; 95%CI, 95% confidence interval.
Day 7: Experienced self-appraisal after repeated exposure
Accuracy scores improved quickly over the first three days of testing, after which the improvement tapered off until reaching 0.81 ± 0.16 on day 7. Self-appraisal also increased over repeated exposures up to 0.70 ± 0.21 on day 7. Figure 1 displays the change in objective performance and self-appraisal over the seven days of BRANCH. By day 7, objective performance and self-appraisal showed a substantially stronger association (r = 0.69, 95%CI = [0.62, 0.76], p < .001) than on day 1, as seen in Figure 2.
Figure 1.
Change in objective performance and self-appraisal over seven days of testing. Objective performance is shown in orange, and participant self-appraisal is shown in purple. For both metrics, we averaged the scores across FNAME and Groceries.
Figure 2.
Relationship between objective performance and self-appraisal on the first (left) and last day of testing (right).
Self-appraisal scores on day 7 showed significant relationships with all in-clinic measures except for the study partner-reported CFI (Table 2). Of note, the direction of the relationship between self-appraisal and PACC5 flipped from a (non-significant) negative association on day 1 to a positive association on day 7. When separating the two associative learning tasks, we noted that the results for test-naïve self-appraisal were identical, while the association between GDS and experienced Groceries self-appraisal was marginally stronger than between GDS and experienced FNAME self-appraisal (see Supplemental Table 1). The overall results remained the same when removing participants who may not have rated their performance on the last day of testing (see Supplementary Table 2).
Self-appraisal relative to objective performance
Out of 217 participants who completed all days of testing, most consistently underestimated their performance (i.e., self-rated their performance as lower relative to their objective performance) on day 1 and day 7 (n = 129, 59.4%; Figure 3). A smaller proportion consistently overestimated their performance (n = 22, 10.1%). Others varied in their estimation (n = 66, 30.4%), most initially overestimating their performance and underestimating it by the end of testing (n = 47, 21.7%).
Figure 3.
Discrepancy between participants’ objective performance and self-appraisal on days 1 (Y-axis) and 7 (X-axis). The top right quadrant (in green) shows consistent overestimation (n = 22, triangles), while the bottom left quadrant (in purple) shows consistent underestimation (n = 128, circles). The other quadrants (in yellow) show variable estimation (n = 67, squares).
Objective performance was lower on day 1 and day 7 among participants who consistently overestimated their performance compared to participants in the other two groups. Conversely, those who consistently underestimated their performance had the highest accuracies of all participants on both day 1 and day 7. Participants who consistently overestimated their performance had lower baseline PACC5 scores than participants who consistently underestimated their performance (Table 3). The groups did not differ in any other demographic aspect. All baseline descriptive statistics by group are displayed in Table 3.
Table 3.
Descriptive Statistics of the Three Under and Overestimation Groups.
| Variable | Consistently underestimated a | Consistently overestimated b | Variably under/overestimated c | Group differences |
|---|---|---|---|---|
| N (%) 1 | 129 (59.0) | 22 (10.1) | 67 (30.9) | — |
| Age in years | 74.1 ± 8.6 | 74.5 ± 8.3 | 73.9 ± 7.8 | n.d. |
| Female sex, N (%) | 83 (64.8) | 16 (72.7) | 45 (67.2) | n.d. |
| Education in years, M (IQR) | 18 (15–18) | 17 (14–18) | 16 (14–18) | n.d. |
| PACC5 | 0.24 ± 0.71 | −0.22 ± 0.76 | 0.14 ± 0.69 | a > b |
| CDR sum of boxes | 0.16 ± 0.34 | 0.05 ± 0.15 | 0.14 ± 0.36 | n.d. |
|
CFI Participant Study Partner |
2.70 ± 2.73 1.67 ± 2.49 |
2.55 ± 2.09 1.34 ± 1.83 |
2.01 ± 1.97 1.28 ± 2.23 |
n.d. n.d. |
| GDS | 5.11 ± 4.37 | 4.36 ± 4.66 | 3.63 ± 3.36 | n.d. |
|
BRANCH objective performance Day 1 Day 7 |
0.47 ± 0.13 0.84 ± 0.15 |
0.39 ± 0.10 0.72 ± 0.20 |
0.41 ± 0.09 0.81 ± 0.14 |
a > b, c a, c > b |
|
BRANCH self-appraisal Day 1 Day 7 |
0.30 ± 0.13 0.66 ± 0.21 |
0.53 ± 0.09 0.81 ± 0.19 |
0.43 ± 0.13 0.73 ± 0.18 |
b > c > a b > a |
Note: All data displayed as mean ± standard deviation, except as noted otherwise.
data missing for n = 8 (3.6%).
Abbreviations: BRANCH, Boston Remote Assessment for NeuroCognitive Health; CDR, Clinical Dementia Rating; CFI, Cognitive Function Index; GDS, Geriatric Depression Scale; IQR, interquartile range; M, median; n.d., no difference; PACC5, Preclinical Alzheimer’s Cognitive Composite–5.
Discussion
In this study, we investigated participants’ self-appraisal of memory performance on a remote cognitive battery over seven consecutive days of testing. Specifically, we were interested in how self-appraisal relates to objective performance before and after repeated assessments with the same test material. We noted that the participants’ objective performance and subjective experience improved with repeated exposures over seven days. Initial, test-naïve self-appraisal was only weakly related to actual performance, but repeated exposure to the same stimuli fortified this relationship by the last day. Experienced but not test-naïve self-appraisal related to several clinical measures, including self-reported cognitive complaints and mood.
Practice effects are a well-described phenomenon in cognitive testing (Duff et al., 2024; Goldberg et al., 2015; Jutten et al., 2020; Young et al., 2023) and have even been demonstrated over relatively extended follow-up durations (e.g., six months). With multiday BRANCH, participants were exposed to the same memory test with the same stimuli every day for a week. In line with the practice effects literature, participants performed exponentially better over the first two or three days of testing, with the increase in performance subsequently slowing down somewhat at the group level over the remaining three to four days. Previous studies with BRANCH have shown how these brief, daily assessments may provide further insight into learning in the context of healthy aging, as well as in Alzheimer’s disease (Jutten et al., 2023; Papp et al., 2021; Samaroo et al., 2020; Weizenbaum et al., 2024). Still, it is not as well-understood how self-appraisal changes over the course of such a repeated testing paradigm.
Several studies have asked people about their perceived performance on specific cognitive and functional tests (Eslinger et al., 2005; Huber & Fulton, 2024; Massimo et al., 2013; Mora & Suchy, 2023; Scherling et al., 2016). For example, poorer self-appraisal of performance on an executive functioning task was predictive of future decline in individuals with mild cognitive impairment (Scherling et al., 2016). These studies were cross-sectional and performed in individuals with a degree of cognitive impairment. It is known that self-awareness of cognitive ability is diminished in the presence of impairment, a state termed anosognosia. However, the findings reported in those studies likely do not translate to the general population of cognitively unimpaired older adults.
Unfamiliarity with the task might cause a person to be unaware of what constitutes a good or a poor performance on that test, making it harder for them to estimate their ability. Even though someone may have a general idea of how they did (e.g., “I remembered about half the faces”), it is the opportunity to compare the self-perceived success on one assessment with that of a previous assessment that helps contextualize one’s performance (e.g., “Today I was able to remember three more faces than yesterday”). With repeated exposure to the same test, one can learn better what is expected of them and revise their self-perceived performance. In our study, test-naïve self-appraisal was somewhat lower than objective performance, but over time, participants rated their performance as increasingly better. The increase in self-appraisal appeared to follow a linear trajectory, i.e., self-appraisal went up gradually with approximately the same amount each day. Thus, an individual’s ability to update their perception of their performance appears to lag behind the increase in their actual performance: the distance between self-appraisal and accuracy grew over the first few days of the week and gradually shrunk by the end of the seven days of testing. Consequently, we postulate that self-appraisal provides essential additional information, mainly when probed after familiarization with the task. The question remains: What does experienced self-appraisal of cognitive performance reflect, and how does it differ from test-naïve self-appraisal?
Test-naïve self-appraisal appeared random: it was not associated with objective performance or most clinical measures taken at baseline, such as study partner- and self-perceived cognitive functioning. We only observed a subtle relationship between test-naïve self-appraisal and self-reported mood, where those who reported more depressive symptoms self-appraised their performance as being worse. This is in line with the well-established finding that individuals with more depressive symptoms will report lower self-perceived cognitive functioning (O’Shea et al., 2016). At the same time, depressive symptoms may also impact objective performance, although participants included in this study did not endorse high levels of depressive symptoms. The impact of mood complaints on objective performance is thus likely minimal.
By the end of the week, participants had completed the same test seven times, giving them an experienced self-appraisal of their performance. We observed that on the last day of testing, self-appraisal was more strongly associated with objective performance and that it was also related to cognitive and functional status, as well as self-reported cognitive functioning and mood. The relationships with cognitive and functional measures corroborate that the self-appraisal reflects cognition. Those who performed better on the in-clinic cognitive composite thought they performed better on the BRANCH tasks by the seventh day. Similarly, those who consider their global self-perceived cognitive functioning to be worse self-rated their performance on the test as worse after seven days. Interestingly, these associations were not apparent on the first day of testing. Perhaps the test-naïve self-appraisal that individuals made after the first exposure to the test without a frame of reference for a good performance is more strongly related to factors we did not investigate here, such as personality or neuropsychiatric symptoms (Martyr et al., 2019). Put together; these findings suggest that self-appraisal, particularly after repeated exposure to the same test, is more than simply a proxy for objective cognitive functioning; it represents a person’s ability to update their understanding of their cognitive functioning with repeated exposure, as well as their mood and potentially other factors not investigated here, such as implicit theories the participant may have (e.g., “I am getting better because I have done this test before”), familiarity with being tested, or the expectation of being asked to self-reflect on their performance.
When we compared self-appraisal and objective performance, we noted that most participants consistently reported their performance to be worse than it was. Others have previously shown that older individuals with or without cognitive impairment often underestimate their cognitive performance, as compared with their study partners (Amariglio et al., 2021; Cacciamani et al., 2017) or with objective performance (Scherling et al., 2016; Vannini et al., 2017). In line with this previous work, we found that those who consistently underestimated their performance had better cognitive functioning as measured using an in-clinic cognitive composite, as well as better BRANCH performance, than those who overestimated their performance or those who estimated their performance variably. Underestimators did not differ from the other participants in other aspects, such as age, sex, education, mood, or functional status. According to the cue-utilization theory, individuals judge their performance by relying on intrinsic, extrinsic, and mnemonic cues rather than objective accuracy (Koriat, 1997). Factors such as the perceived difficulty of the task (intrinsic), repetition frequency (extrinsic), and ease of retrieval of the material (mnemonic) may have contributed to the self-appraisals found here. Future work will have to elucidate further the value of informed self-appraisal in biomarker-confirmed neurodegenerative diseases such as Alzheimer’s disease, including in individuals with cognitive impairments, to determine whether it may be used to identify individuals at risk for cognitive decline. Future studies might also include a control group assessing repeated self-appraisal without repeated testing to investigate how self-appraisal changes on its own.
Constraints on generality
Most participants were highly educated and predominantly White and female, thus limiting the generalizability of these findings to other populations. As multiday BRANCH is rolled out in other cohorts, we aim to include minoritized individuals to verify whether these findings hold in the broader population. Using a slider scale to capture self-appraisal somewhat limited our qualitative interpretation of the self-appraisal data, as a given number on the sliding scale can represent different things to different people. We also could not determine with total confidence that participants responded to the self-appraisal question, as the slider’s default was set to 50 (the middle of the scale), and a response was not forced. We tried to mitigate these limitations by avoiding the interpretation of given self-appraisals as “bad,” “average,” or “good” and by running sensitivity analyses excluding participants who rated their performance as exactly 50/100 on the last day. Our reasoning was that on the first day, a rating of 50 might indicate uncertainty about the objective performance, whereas a rating of 50 on the last day more likely reflects non-response. The results presented here did not change when excluding participants who likely did not respond to the self-appraisal questions on the last day of testing. We investigated relative estimations of cognitive performance by considering any difference greater than zero between objective performance and self-appraisal to indicate over or underestimation, but it should be noted that there are other ways to investigate the accuracy of self-appraisals of cognitive performance. Further, BRANCH is administered digitally, precluding those without Internet access from participating in this research or benefiting from this study’s findings. As the digital divide continues to narrow, this point may become somewhat less concerning. Future work will need to further elucidate the value of repeated self-appraisal as a diagnostic or prognostic tool in neurodegenerative disease, for instance by uncovering the factors that moderate the relationship between objective cognitive performance and the self-appraisal of such performance.
Conclusion
In conclusion, repeated assessments of individuals’ self-perceived performance on a cognitive test may help elucidate their capacity to update their self-perception during multiday learning. Our finding that test-naïve self-appraisal and accuracy were only weakly correlated warrants caution about using self-appraisal as a proxy for metamemory accuracy cross-sectionally. Repeated objective and self-perceived performance may be especially helpful in distinguishing healthy aging from the earliest stages of neurodegenerative diseases such as Alzheimer’s disease.
Supplementary Material
Key points.
Question:
How does self-appraisal of cognitive test performance change among cognitively normal older adults after short-term repeated exposure?
Findings:
Self-appraisal on the first day of testing was only weakly correlated with objective performance and other clinical measures, yet after seven days of taking the same test, self-appraisal was related more strongly to objective performance and associated with various measures of cognition and mood.
Importance:
Asking someone about their self-perceived performance on a test after repeated exposure provides an improved estimation of their objective cognitive performance than after a single assessment.
Next steps:
To further distinguish the worried well from those who harbor underlying disease, repeated self-appraisal may be combined with daily momentary assessments of an individual’s mood, activities, health, and state of mind.
References
- Amariglio RE., Donohue MC., Marshall GA., Rentz DM., Salmon DP., Ferris SH., Karantzoulis S., Aisen PS., Sperling RA., & Study ADC. (2015). Tracking early decline in cognitive function in older individuals at risk for Alzheimer disease dementia: the Alzheimer’s Disease Cooperative Study Cognitive Function Instrument. JAMA Neurology, 72(4), 446–454. 10.1001/jamaneurol.2014.3375 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Amariglio RE, Sikkes SAM, Marshall GA, Buckley RF, Gatchel JR, Johnson KA, Rentz DM, Donohue MC, Raman R, Sun C-K, Yaari R, Holdridge KC, Sims JR, Grill JD, Aisen PS, & Sperling RA (2021). Item-Level Investigation of Participant and Study Partner Report on the Cognitive Function Index from the A4 Study Screening Data. The Journal of Prevention of Alzheimer’s Disease, 8(3), 257–262. 10.14283/jpad.2021.8 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cacciamani F, Houot M, Gagliardi G, Dubois B, Sikkes S, Sánchez-Benavides G, Denicolò E, Molinuevo JL, Vannini P, & Epelbaum S (2021). Awareness of Cognitive Decline in Patients With Alzheimer’s Disease: A Systematic Review and Meta-Analysis. Frontiers in Aging Neuroscience, 13. 10.3389/fnagi.2021.697234 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cacciamani F, Tandetnik C, Gagliardi G, Bertin H, Habert MO, Hampel H, Boukadida L, Révillon M, Epelbaum S, & Dubois B (2017). Low Cognitive Awareness, but Not Complaint, is a Good Marker of Preclinical Alzheimer’s Disease. Journal of Alzheimer’s Disease, 59(2). 10.3233/JAD-170399 [DOI] [PubMed] [Google Scholar]
- Castel AD (2005). Memory for grocery prices in younger and older adults: the role of schematic support. Psychology and Aging, 20(4), 718–721. 10.1037/0882-7974.20.4.718 [DOI] [PubMed] [Google Scholar]
- Clare L, Marková IS, Roth I, & Morris RG (2011). Awareness in Alzheimer’s disease and associated dementias: Theoretical framework and clinical implications. Aging & Mental Health, 15(8), 936–944. 10.1080/13607863.2011.583630 [DOI] [PubMed] [Google Scholar]
- Donohue MC, Sperling RA, Salmon DP, Rentz DM, Raman R, Thomas RG, Weiner M, Aisen PS, Australian Imaging Biomarkers, of Ageing, L. F. S., Initiative, A. D. N., & Study, A. D. C. (2014). The preclinical Alzheimer cognitive composite: measuring amyloid-related decline. JAMA Neurology, 71(8), 961–970. 10.1001/jamaneurol.2014.803 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Duff K, Dixon A, & Embree L. (2024). A Closer Look at Practice Effects in Mild Cognitive Impairment and Alzheimer’s Disease. Archives of Clinical Neuropsychology, 39(1), 1–10. 10.1093/arclin/acad046 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Eslinger PJ, Dennis K, Moore P, Antani S, Hauck R, & Grossman M. (2005). Metacognitive deficits in frontotemporal dementia. Journal of Neurology, Neurosurgery, and Psychiatry, 76(12), 1630–1635. 10.1136/jnnp.2004.053157 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Folstein MF, Folstein SE, & McHugh PR (1975). “Mini-mental state”. A practical method for grading the cognitive state of patients for the clinician. Journal of Psychiatric Research, 12(3), 189–198. 10.1016/0022-3956(75)90026-6 [DOI] [PubMed] [Google Scholar]
- Goldberg TE, Harvey PD, Wesnes KA, Snyder PJ, & Schneider LS (2015). Practice effects due to serial cognitive assessment: Implications for preclinical Alzheimer’s disease randomized controlled trials. Alzheimer’s & Dementia : Diagnosis, Assessment & Disease Monitoring, 1(1), 103–111. 10.1016/j.dadm.2014.11.003 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Grober E, Ocepek-Welikson K, & Teresi JA (2009). The free and cued selective reminding test: evidence of psychometric adequacy. Psychol Sci Q, 51, 266–282. [Google Scholar]
- Hausknecht JP, Halpert JA, Di Paolo NT, & Moriarty Gerrard MO (2007). Retesting in selection: a meta-analysis of coaching and practice effects for tests of cognitive ability. The Journal of Applied Psychology, 92(2), 373–385. 10.1037/0021-9010.92.2.373 [DOI] [PubMed] [Google Scholar]
- Hertzog C, & Dunlosky J. (2011). Metacognition in Later Adulthood. Current Directions in Psychological Science, 20(3), 167–173. 10.1177/0963721411409026 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Huber BN, & Fulton EK (2024). Meta-prospective memory accuracy in older adults with and without suspected Mild Cognitive Impairment (sMCI). Applied Neuropsychology: Adult, 1–16. 10.1080/23279095.2024.2334892 [DOI] [PubMed] [Google Scholar]
- Hughes CP, Berg L, Danziger WL, Coben LA, & Martin RL (1982). A new clinical scale for the staging of dementia. British Journal of Psychiatry, 140(6). 10.1192/bjp.140.6.566 [DOI] [PubMed] [Google Scholar]
- Jessen F, Amariglio RE, Buckley RF, van der Flier WM, Han Y, Molinuevo JL, Rabin L, Rentz DM, Rodriguez-Gomez O, Saykin AJ, Sikkes SAM, Smart CM, Wolfsgruber S, & Wagner M. (2020). The characterisation of subjective cognitive decline. Lancet Neurology, 19(3), 271–278. 10.1016/S1474-4422(19)30368-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jutten RJ, Grandoit E, Foldi NS, Sikkes SAM, Jones RN, Choi S-E, Lamar ML, Louden DKN, Rich J, Tommet D, Crane PK, & Rabin LA (2020). Lower practice effects as a marker of cognitive performance and dementia risk: A literature review. Alzheimer’s & Dementia : Diagnosis, Assessment & Disease Monitoring, 12(1), e12055. 10.1002/dad2.12055 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jutten RJ, Soberanes D, Weizenbaum EL, Hsieh S, Molinare C, Johnson KA, Rentz DM, Sperling RA, Amariglio RE, & Papp KV (2023). Longitudinal multi-day learning curves (MDLCs) to capture subtle cognitive changes in preclinical Alzheimer disease. Alzheimer’s & Dementia, 19(S18). 10.1002/alz.078818 [DOI] [Google Scholar]
- Koriat A. (1997). Monitoring one’s own knowledge during study: A cue-utilization approach to judgments of learning. Journal of Experimental Psychology: General, 126(4), 349–370. 10.1037/0096-3445.126.4.349 [DOI] [Google Scholar]
- Koriat A, Sheffer L, & Ma’ayan H. (2002). Comparing objective and subjective learning curves: Judgments of learning exhibit increased underconfidence with practice. Journal of Experimental Psychology: General, 131(2), 147–162. 10.1037/0096-3445.131.2.147 [DOI] [PubMed] [Google Scholar]
- Martyr A, Nelis SM, Quinn C, Rusted JM, Morris RG, Clare L, & programme team I. (2019). The relationship between perceived functional difficulties and the ability to live well with mild-to-moderate dementia: Findings from the IDEAL programme. International Journal of Geriatric Psychiatry, 34(8), 1251–1261. 10.1002/gps.5128 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Massimo L, Libon DJ, Chandrasekaran K, Dreyfuss M, McMillan CT, Rascovsky K, Boller A, & Grossman M. (2013). Self-appraisal in behavioural variant frontotemporal degeneration. Journal of Neurology, Neurosurgery, and Psychiatry, 84(2), 148–153. 10.1136/jnnp-2012-303153 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mora MG, & Suchy Y. (2023). Know thyself: Executive functioning and sex predict self-appraisal of functional abilities in community-dwelling older adults. The Clinical Neuropsychologist, 37(8), 1686–1709. 10.1080/13854046.2023.2167738 [DOI] [PubMed] [Google Scholar]
- Morris JC (1993). The Clinical Dementia Rating (CDR): Current version and scoring rules. Neurology, 43(11), 2412. 10.1212/WNL.43.11.2412-a [DOI] [PubMed] [Google Scholar]
- O’Shea DM, Dotson VM, Fieo RA, Tsapanou A, Zahodne L, & Stern Y. (2016). Older adults with poor self-rated memory have less depressive symptoms and better memory performance when perceived self-efficacy is high. International Journal of Geriatric Psychiatry, 31(7), 783–790. 10.1002/gps.4392 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Papp KV, Jutten RJ, Soberanes D, Weizenbaum E, Hsieh S, Molinare C, Buckley R, Betensky RA, Marshall GA, Johnson KA, Rentz DM, Sperling R, & Amariglio RE (2024). Early Detection of Amyloid-Related Changes in Memory among Cognitively Unimpaired Older Adults with Daily Digital Testing. Annals of Neurology, 95(3), 507–517. 10.1002/ana.26833 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Papp KV, Rentz DM, Orlovsky I, Sperling RA, & Mormino EC (2017). Optimizing the preclinical Alzheimer’s cognitive composite with semantic processing: The PACC5. Alzheimer’s & Dementia : Translational Research & Clinical Interventions, 3(4), 668–677. 10.1016/j.trci.2017.10.004 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Papp KV, Samaroo A, Chou H-C, Buckley R, Schneider OR, Hsieh S, Soberanes D, Quiroz Y, Properzi M, Schultz A, García-Magariño I, Marshall GA, Burke JG, Kumar R, Snyder N, Johnson K, Rentz DM, Sperling RA, & Amariglio RE (2021). Unsupervised mobile cognitive testing for use in preclinical Alzheimer’s disease. Alzheimer’s & Dementia : Diagnosis, Assessment & Disease Monitoring, 13(1), e12243. 10.1002/dad2.12243 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Putnam AL, Deng W, & DeSoto KA (2022). Confidence ratings are better predictors of future performance than delayed judgments of learning. Memory, 30(5), 537–553. 10.1080/09658211.2022.2026973 [DOI] [PubMed] [Google Scholar]
- Rabin LA, Sikkes SA, Tommet DC, Jones RN, Crane PK, Elbulok-Charcape MM, Dubbelman MA, Koscik RL, Amariglio RE, Buckley RF, Boada M, Chetélat G, Dubois B, Ellis KA, Gifford KA, Jefferson AL, Jessen F, Johnson SC, Katz MJ, … Wolfsgruber S. (2023). Linking Self-Perceived Cognitive Functioning Questionnaires Using Item Response Theory: The Subjective Cognitive Decline Initiative. Neuropsychology, 37(4). 10.1037/neu0000888 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rentz DM, Amariglio RE, Becker JA, Frey M, Olson LE, Frishe K, Carmasin J, Maye JE, Johnson KA, & Sperling RA (2011). Face-name associative memory performance is related to amyloid burden in normal elderly. Neuropsychologia, 49(9), 2776–2783. 10.1016/j.neuropsychologia.2011.06.006 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rickenbach EH, Agrigoroaei S, & Lachman ME (2015). Awareness of Memory Ability and Change: (In)Accuracy of Memory Self-Assessments in Relation to Performance. Journal of Population Ageing, 8(1–2), 71–99. 10.1007/s12062-014-9108-5 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Samaroo A, Amariglio RE, Burnham S, Sparks P, Properzi M, Schultz AP, Buckley R, Johnson KA, Sperling RA, Rentz DM, & Papp KV (2020). Diminished Learning Over Repeated Exposures (LORE) in preclinical Alzheimer’s disease. Alzheimer’s & Dementia : Diagnosis, Assessment & Disease Monitoring, 12(1), e12132. 10.1002/dad2.12132 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Scherling CS, Wilkins SE, Zakrezewski J, Kramer JH, Miller BL, Weiner MW, & Rosen HJ (2016). Decreased self-appraisal accuracy on cognitive tests of executive functioning is a predictor of decline in mild cognitive impairment. Frontiers in Aging Neuroscience, 8(JUN). 10.3389/fnagi.2016.00120 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Siegel ALM, & Castel AD (2019). Age-related differences in metacognition for memory capacity and selectivity. Memory, 27(9), 1236–1249. 10.1080/09658211.2019.1645859 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vannini P, Amariglio R, Hanseeuw B, Johnson KA, McLaren DG, Chhatwal J, Pascual-Leone A, Rentz D, & Sperling RA (2017). Memory self-awareness in the preclinical and prodromal stages of Alzheimer’s disease. Neuropsychologia, 99, 343–349. 10.1016/j.neuropsychologia.2017.04.002 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wechsler D. (1981). WAIS-R: manual : Wechsler adult intelligence scale–revised. Harcourt Brace Jovanovich [for] Psychological Corp. [Google Scholar]
- Wechsler D, & Stone CP (1987). Wechsler Memory Scale-revised. Psychological Corporation. [Google Scholar]
- Weizenbaum EL, Soberanes D, Hsieh S, Molinare CP, Buckley RF, Betensky RA, Properzi MJ, Marshall GA, Rentz DM, Johnson KA, Sperling RA, Amariglio RE, & Papp KV (2024). Capturing learning curves with the multiday Boston Remote Assessment of Neurocognitive Health (BRANCH): Feasibility, reliability, and validity. Neuropsychology, 38(2), 198–210. 10.1037/neu0000933 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yesavage JA, Brink TL, Rose TL, Lum O, Huang V, Adey M, & Leirer VO (1982). Development and validation of a geriatric depression screening scale: A preliminary report. Journal of Psychiatric Research, 17(1), 37–49. 10.1016/0022-3956(82)90033-4 [DOI] [PubMed] [Google Scholar]
- Young CB, Mormino EC, Poston KL, Johnson KA, Rentz DM, Sperling RA, & Papp KV (2023). Computerized cognitive practice effects in relation to amyloid and tau in preclinical Alzheimer’s disease: Results from a multi-site cohort. Alzheimer’s & Dementia : Diagnosis, Assessment & Disease Monitoring, 15(1), e12414. 10.1002/dad2.12414 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zakrzewski AC, Sanders EC, & Berry JM (2021). Evidence for Age-Equivalent and Task-Dissociative Metacognition in the Memory Domain. Frontiers in Psychology, 12. 10.3389/fpsyg.2021.630143 [DOI] [PMC free article] [PubMed] [Google Scholar]
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