Abstract
Objective:
Cognitive remediation (CR) techniques (interventions to enhance cognitive functioning) have proven moderately effective in improving cognition and daily functioning in major depressive disorder (MDD). However, baseline predictors of treatment response are lacking. The present study aimed to identify factors influencing long-term CR outcomes in a sample with current or previous, mild or moderate MDD and with self-reported cognitive deficits.
Methods:
Forty-two completers of group-based CR (strategy learning or drill-and-practice), were pooled into one sample. Based on change scores from baseline to 6-month follow-up, participants were categorized as “improvers” or “non-improvers” using reliable change index calculations. Measures included a questionnaire of everyday executive functioning and a neuropsychological test of attention. Finally, improvers and non-improvers were compared in terms of various sociodemographic, psychological, illness-related, and neuropsychological baseline variables.
Results:
Seventeen participants improved reliably in everyday executive functioning, and fourteen demonstrated a reliable improvement in attention. No statistically significant differences emerged between improvers and non-improvers.
Conclusion:
No major predictors of CR were identified. Importantly, the current findings are insufficient to guide clinical decision-making. Large-scale studies with a priori hypotheses are needed to make advances in the future.
Introduction
Major depressive disorder (MDD) is characterized by deficits in cognitive functions, including attention, memory, and executive functions (EF) (; ). However, the heterogeneity of the cognitive profile in MDD appears to be large, with distinct neurocognitive subgroups (). For those experiencing cognitive difficulties, deficits often persist into remission () and have a deleterious effect on everyday functioning (). Cognitive deficits, particularly in EF, are additionally associated with unfavorable depression outcomes, such as impaired long-term recovery () and reduced antidepressant medication effectiveness (). Hence, cognitive functioning represents a potential treatment target in MDD ().
Nonetheless, both antidepressant medication and cognitive–behavioral therapy (CBT) show limited effectiveness in alleviating cognitive deficits (; ). Cognitive remediation (CR) interventions – specifically targeting cognitive dysfunction – intended to produce lasting improvements in everyday functioning are thus emerging. Although the heterogeneity of treatment approaches labeled “CR” is large (), these interventions can be divided into either bottom-up drill-and-practice approaches or top-down approaches focusing on strategy learning. Bottom-up approaches typically consist of computerized cognitive training (CCT) tasks intended to improve basic cognitive processes through the process of neuroplasticity (). In contrast, top-down approaches consist of learning compensatory strategies for wide appliance in daily living, to compensate for the cognitive difficulties. Findings indicate moderate effectiveness in improving cognition and everyday functioning following CR, but there is a paucity of evidence for improved EF or on its long-term effects (for a meta-analysis, see ). In this context, it has been argued that the substantial heterogeneity in the cognitive profile of MDD may influence the effectiveness of CR ().
The lack of factors associated with successful treatment outcomes may be a barrier to improving CR effectiveness (; ). The identification of pretreatment predictors could improve efficacy by facilitating individualized clinical decision-making. Moreover, it may be helpful for the development of future treatments by providing insight into the mechanisms of CR interventions (). The investigation of CR predictors and moderators in MDD is scarce, but a meta-analysis covering a range of CCT interventions found decreased treatment effectiveness with increased age (). Additional variables, such as gender and receiving concurrent treatment (antidepressant medication or psychotherapy), did not significantly influence outcomes. In a recent study dedicated to identifying the predictors in a CR intervention consisting of both CCT and strategy learning, observed a shorter duration of illness to be the only factor associated with improvement on a neuropsychological measure of attention in a partially remitted MDD sample. Several sociodemographic, neurocognitive, psychopathological, and training-specific factors thus failed to predict outcomes. However, the study was limited by its exploratory approach, modest sample size, and exclusive focus on the attention domain (). Interestingly, CR findings diverge from psychotherapy research in MDD, where illness characteristics such as greater depression symptom severity, younger age at onset, and more previous episodes have all been associated with poorer responses in relation to depressive symptom alleviation (). Moreover, in schizophrenia research, where predictors and moderators of CR effectiveness have been more frequently studied, most of the factors reviewed fail to significantly influence CR treatment response (; ). However, in a selection of studies, better baseline performance in several cognitive domains predicted both cognitive and functional improvement, while increased chronicity and severity of schizophrenia has been associated with worse CR outcomes (; ; ; ).
The main aim of the present study was to explore whether a selection of sociodemographic, neuropsychological, illness-related, and psychological variables could predict long-term CR outcomes in a sample with current or previous mild or moderate MDD. Data were collected as part of a single-blind randomized controlled trial (RCT) comparing the effectiveness of a strategy-based CR approach, Goal Management Training (GMT), with drill-and-practice CCT, in improving EF (). Both groups improved on measures of EF in daily life, neuropsychological tests of EF and attention, and depression symptom severity following CR. That is, no significant differences emerged between groups in the original study, although within-group changes in everyday EF and depression symptom severity were only significant following GMT. Owing to the limited number of previous studies examining predictors of CR in MDD, the present study applied an exploratory approach with no a priori hypothesis.
Materials and Methods
The original RCT was preregistered at clinicaltrials.gov with the identifier NCT03338413, and the study protocol was approved by the Regional Committee for Medical and Health Research Ethics, South-Eastern Norway (2017/666). The study was conducted following the World Medical Association’s Declaration of Helsinki, and all participants gave their written informed consent. For more detailed information on the methodological approach of the original RCT study, see .
Participants
The sample (n = 63) included participants diagnosed with mild or moderate MDD according to International Classification of Diseases – 10th Revision (ICD-10) criteria (), either as a primary or as a secondary diagnosis. All participants had undergone a diagnostic evaluation and completed treatment at the Return-to-Work clinic at Lovisenberg Diaconal Hospital within 2 years before inclusion. The Return-to-Work clinic offers short-term outpatient psychotherapeutic treatment to patients with mental health issues of mild to moderate severity, at risk of receiving sick leave because of mental illness. In addition, to be included, participants had to be between 18 and 60 years of age and to have self-reported everyday EF deficits (e.g., difficulties with memory, organizing/planning, emotional regulation, and/or concentration) in a custom-made telephone interview. All participants were additionally asked to confirm that depression symptoms represent a major mental health complaint. Exclusion criteria included comorbid neurological conditions, ongoing alcohol or substance abuse, and severe cognitive problems or mental disorders (psychotic disorders and severe personality disorders). No cutoff scores were specified for current depressive symptom severity. There were no restrictions on participants concerning additional concurrent psychotherapeutic or antidepressant treatment.
Study Design and Blinding
All participants completed a baseline assessment (T1) before being randomly assigned to nine sessions of either GMT or CCT, using computer-generated simple randomization. Participants were reassessed immediately following treatment completion (T2) and at a 6-month follow-up (T3). The assessments consisted of neuropsychological tests and self-report rating scales. Assessments were not blind, because the person responsible for data collection also acted as a therapist in both interventions. To compensate, an external assessor performed a limited set of blind T3 assessments (n = 5) for comparison. However, the study was single-blind because participants were not informed whether they had been allocated to the condition considered to be the active treatment.
Cognitive Remediation Interventions
Goal Management Training
GMT is a manual-based CR intervention to improve everyday EF (). A central element of GMT is to learn and internalize strategies for wide application in daily living, promoting goal-directed behavior through increased executive control and improved problem-solving capacities. Strategies consist of a self-instruction to stop ongoing behavior, check the current content of working memory, state and define goals, apply a systematic approach to problem-solving, and monitor performance.
In the present study, the Norwegian translation of the standard GMT protocol was employed (; ). A clinical psychologist and a neuropsychologist delivered GMT in groups of five to seven participants in 9 weekly 2 h sessions. In-class exercises included practicing the use of the compensatory strategies (e.g., practice a systematic approach to problem-solving by arranging a fictitious wedding party). Mindfulness exercises (), intended to enhance attentional control, were also practiced in class. Sessions emphasized group discussions addressing personal examples of dysexecutive behavior. Between-session assignments included monitoring EF-related errors, mindfulness exercises, and the application of learned strategies in daily life (Table 1).
TABLE 1
| GMT session | Objective | CCT task | Objective |
| The present and the absent mind | Tracking absentmindedness/Practice mindfulness techniques | Double decision | Attention |
| Inattentive Errors | Condition for, and consequences of, absentmindedness | Divided attention | Attention/Inhibition |
| The Automatic Pilot | How automatic behavior leads to inappropriate responding | Target tracker | Attention |
| Stop the automatic pilot | Make a habit of stopping/Bring attention to the present | Syllable stacks | Working memory |
| The mental blackboard | Check the content of working memory | Scene crasher | Working memory |
| State your goal | State goals to facilitate goal maintenance | Face-to-Face | Processing Speed/Social Cognition |
| Making decisions | Goal conflict in decision-making/Making to-do lists | Sound sweeps | Processing speed |
| Splitting tasks into subtasks | Split overwhelming tasks into subtasks/Step-by-step approach | ||
| Checking (STOP!) | Adapting behavior to situational change/Summary of training |
GMT sessions, CCT tasks, and objectives.
GMT, Goal Management Training; CCT, computerized cognitive training.
Computerized Cognitive Training
The CCT consisted of seven exercises from the BrainHQ platform. Repetition is the hallmark feature of CCT, and neuroplasticity is its theoretical foundation (). Cognitive improvements, including EF, have been identified using BrainHQ or similar exercises (; ), and these studies established the empirical basis for the selection of exercises. In addition, exercise selection was based on the provider’s description1.
The CCT consisted of nine twice-weekly 1 h sessions by groups of three participants. Exercises targeted attention, memory, processing speed, and EF. To ensure appropriate levels of mastery and frustration, the platform adapted difficulty levels to the individual participants’ performance, keeping the success rate at 80% throughout. A clinical psychologist acted as a therapist and gave participants positive feedback on their efforts. The first session included psychoeducation, with the therapist introducing the concept of neuroplasticity, typical cognitive deficits in depression, and the importance of cognitive processes in different everyday situations. Participants had online access to the training platform and were encouraged to practice for at least 30 min between each session (Table 1).
Completer Sample
Participants had to attend a minimum of six training sessions and complete the 6-month follow-up assessment (T3) to be included in the completer sample. Forty-two completers from both groups were pooled into one sample. The pooling of participants receiving different treatments was done to increase the sample size (Figure 1).
FIGURE 1
Outcome Measures
The Global Executive Composite (GEC) from the Behavior Rating Inventory of Executive Function – Adult version (BRIEF-A) (
The Conners Continuous Performance Test – Third edition (CPT-3) (
Predictors of Treatment Effect
Sociodemographic Factors
Sociodemographic factors included age, gender, years of education, and employment status, all self-reported in a custom-made interview. Employment status was transformed into a dichotomous variable with the categories “full-time employment/full-time student” and “other” (including “part-time employment/part-time student,” “sick leave,” and “looking for a job”).
Illness-Related Factors
Illness-related factors included current depressive symptom severity in addition to the self-reported number of previous depressive episodes, age of onset, duration of illness, and current antidepressant medication use. Depressive symptom severity was assessed with the Beck Depression Inventory (BDI) (
Psychological Factors
Psychological factors included overall psychological distress and a tendency to ruminate. The Clinical Outcomes in Routine Evaluation – Outcome Measure (CORE-OM) (
Neuropsychological Factors
Neuropsychological factors included estimated IQ, assessed with the two-subtest form (Matrix reasoning; Vocabulary) of the Wechsler Abbreviated Scale of Intelligence (WASI) (
Other Factors
Received intervention (GMT or CCT) was included as a training-specific factor. In addition, baseline performance scores on the outcome variables were included as predictors.
Statistical Analysis
Calculation of Reliable Change Index
The reliable change index (RCI) (
SEdiff was derived from the standard error of measurement (SE), calculated using the test–retest reliability (rxx) of the instrument, and the standard deviation (SD) using the following formulas:
An RCI smaller than –1.96 (because of measurement direction) was required to be considered as a reliable improvement. A change surpassing the ±1.96 threshold occurs by chance in only 5% of cases. Information on test–retest reliability and standard deviation was collected from the test manuals (
Comparison of Improvers and Non-improvers
For each of the two outcome measures, participants were categorized as either “improvers” or “non-improvers” based on their RCI score. Improvers were compared with non-improvers in the pooled completer samples using the non-parametric Mann–Whitney U test and chi-square test, for pairs of continuous and dichotomous variables, respectively. In addition, the T3 results on the outcome measures were compared between assessors (blind/non-blind), and T1 results between completers and non-completers, using the Mann–Whitney U test. All tests were two-tailed, and to partially account for multiple testing, the significance level was set to 0.01. Values between 0.01 and 0.05 were interpreted as trends. SPSS version 24.0 for Windows was applied for all analyses.
Results
The completers (n = 42) had a median age of 41 years (range = 28–59) and a median of 15 years of education (range = 9–18). The majority were female (79.1%), and 76.7% did not currently use antidepressant medication. Furthermore, their average depression symptom severity was in the mild range (BDI: median = 17.0, range = 4.0–34.0) (
TABLE 2
| Disorder | Frequency |
| Generalized anxiety disorder (F 41.1) | 6 |
| Panic disorder (F 41.0) | 3 |
| Post-traumatic stress disorder (F 43.1) | 1 |
| Agoraphobia (F 40.0) | 1 |
| Social phobia (F 40.1) | 1 |
| Anxiety disorder, unspecified (F 41.9) | 1 |
| Nonorganic insomnia (F 51.0) | 2 |
| Mental and behavioral disorders due to psychoactive substance use (F 10–F 19) | 2 |
Comorbid ICD-10 diagnoses in the completer sample.
Number of participants with comorbidities, n = 14. Multiple comorbid diagnoses are possible for each participant. ICD-10 = International Classification of Diseases – 10th Revision.
The sample reported substantial executive dysfunction in daily living (BRIEF-A GEC T-score: median = 64, range = 44–80) but performed in the normal range for the included CPT-3 subscales at baseline (Commissions T-score: median = 48, range = 35–73; HRT SD T-score: median = 44, range = 33–75). At follow-up, completers reported overall fewer EF deficits in daily life (BRIEF-A GEC T-score: median = 59.5, range = 36–78) and performed better on the measure of attention (CPT-3: Commissions T-score, median = 44, range = 25–71; HRT SD T-score, median = 41, range = 31–56). No statistically significant differences emerged for any of the outcome measures at follow-up between the blinded and non-blinded assessors. Finally, the completers were not significantly different from the non-completers (n = 21) on any of the included variables.
Comparison of Everyday Executive Functioning of Improvers and Non-improvers
Seventeen participants (40.5%) were identified to improve reliably on the BRIEF-A GEC between T1 and T3. For participants to surpass the critical value for improvement, a 13-point reduction in BRIEF-A GEC raw score was required. The mean BRIEF-A GEC raw score of improvers at follow-up was 107.9 (SD = 17.9). No statistically significant differences emerged between improvers and non-improvers for any of the predictors. However, improvers had a higher estimated IQ than non-improvers at trend level (p = 0.044) (Table 3).
TABLE 3
| Variable | Improvers | Non-improvers | p-value |
| (n = 17) | (n = 25) | ||
| Categorical variables | |||
| Gender (female) | 14 | 19 | 0.622 |
| Work status (full-time) | 11 | 18 | 0.616 |
| Antidepressant use (yes) | 2 | 8 | 0.131 |
| Dep. ep. (1 ep.) | 5 | 9 | 0.754 |
| Received intervention (GMT) | 10 | 13 | 0.663 |
| Continuous variables | Mean (SD) | Mean (SD) | |
| Age (years) | 44.9 (8.7) | 40.8 (8.5) | 0.098 |
| Years of education | 15.5 (2.0) | 14.4 (2.1) | 0.071 |
| Age of onset (years) | 32.7 (12.9) | 26.0 (10.3) | 0.087 |
| Illness duration (years) | 12.2 (10.4) | 14.8 (9.7) | 0.317 |
| WASI (IQ estimate) | 115.3 (6.7) | 108.8 (12.1) | 0.044 |
| TMT 2 (seconds) | 30.8 (10.2) | 31.4 (9.7) | 0.488 |
| TMT 4 (seconds) | 71.2 (21.6) | 84.1 (34.6) | 0.109 |
| CVLT-II SF Long delay | 8.4 (1.2) | 8.3 (0.8) | 0.299 |
| WAIS-IV DS Forward | 9.7 (2.4) | 9.1 (1.5) | 0.539 |
| WAIS-IV DS Backward | 10.0 (2.3) | 9.8 (1.8) | 0.815 |
| BDI | 19.0 (6.7) | 15.2 (7.1) | 0.063 |
| RRS | 56.3 (10.5) | 55.0 (12.2) | 0.710 |
| CORE-OM | 14.7 (5.5) | 13.4 (6.0) | 0.522 |
| CPT-3 Commissions (T-score) | 50.2 (11.3) | 51.5 (8.4) | 0.336 |
| CPT-3 HRT SD (T-score) | 46.6 (9.8) | 44.8 (9.8) | 0.293 |
| BRIEF-A GEC | 137.3 (17.9) | 128.6 (15.2) | 0.124 |
Characteristics of improvers and non-improvers in everyday EF.
SD, standard deviation, Dep., depression; ep., episode; GMT, Goal Management Training; WASI, Wechsler Abbreviated Scale of Intelligence; TMT, Trail-Making Test; CVLT-II SF, California Verbal Learning Test–Second edition – Short form; WAIS-IV, Wechsler Adult Intelligence Scale – Fourth edition; DS, digit span; BDI, Beck Depression Inventory; RRS, Ruminative Response Scale; CORE-OM, Clinical Outcomes in Routine Evaluation – Outcome Measure; CPT, Conners Continuous Performance Test; HRT, hit reaction time; BRIEF-A GEC, Behavior Rating Inventory of Executive Function – Adult version Global Executive Composite; EF, executive functions. All scores reported are raw scores, except when otherwise specified. Higher scores indicate greater impairment, except for WASI, CVLT-II, and WAIS-IV.
Comparison of Attention by Improvers and Non-improvers
Fourteen participants (33.3%) were identified as improvers on the measure of attention. Twelve participants improved on the Commissions subscale and four on the HRT SD subscale, while two participants improved on both subscales. For participants to surpass the critical value for improvement, a change in T-score of 10 (Commissions) or 13 (HRT SD) was required. At follow-up, the mean T-score for the improver group (n = 14) was 42.2 (SD = 6.5) on the Commission subscale and 39.9 (SD = 7.5) on the HRT SD subscale. No statistically significant differences emerged between improvers and non-improvers. However, at trend level, fewer of the improvers compared with the non-improvers (p = 0.011) had experienced only one previous depressive episode (Table 4). The mean number of self-reported previous depressive episodes was 4.8 (SD = 3.3) for improvers and 3.4 (SD = 3.2) for non-improvers (values > 10 were recoded > 10 = 10).
TABLE 4
| Variable | Improvers | Non-improvers | p-value |
| (n = 14) | (n = 28) | ||
| Categorical variables | |||
| Gender (female) | 11 | 22 | 0.999 |
| Work status (full-time) | 10 | 19 | 0.813 |
| Antidepressant use (yes) | 1 | 9 | 0.073 |
| Dep. ep. (1 ep.) | 1 | 14 | 0.011 |
| Received intervention (GMT) | 7 | 16 | 0.661 |
| Continuous variables | Mean (SD) | Mean (SD) | |
| Age (years) | 42.9 (9.4) | 42.3 (8.5) | 0.915 |
| Years of education | 15.1 (2.1) | 14.8 (2.1) | 0.539 |
| Age of onset (years) | 29.3 (13.6) | 28.4 (11.0) | 0.957 |
| Illness duration (years) | 13.6 (9.3) | 13.9 (10.4) | 0.947 |
| WASI (IQ-estimate) | 114.9 (6.4) | 109.6 (12.0) | 0.194 |
| TMT 2 (seconds) | 30.3 (7.6) | 31.5 (10.8) | 0.904 |
| TMT 4 (seconds) | 79.1 (21.4) | 79.2 (34.3) | 0.566 |
| CVLT-II SF Long delay | 8.3 (0.9) | 8.3 (1.0) | 0.801 |
| WAIS-IV DS Forward | 10.1 (2.1) | 9.0 (1.7) | 0.092 |
| WAIS-IV DS Backward | 10.5 (1.8) | 9.6 (2.0) | 0.151 |
| BDI | 18.8 (6.5) | 15.7 (7.3) | 0.169 |
| RRS | 58.4 (10.7) | 54.1 (11.7) | 0.279 |
| CORE-OM | 16.5 (4.9) | 12.6 (5.9) | 0.056 |
| CPT-3 Commissions (T-score) | 54.8 (9.3) | 49.0 (9.3) | 0.050 |
| CPT-3 HRT SD (T-score) | 49.5 (13.3) | 43.5 (6.7) | 0.224 |
| BRIEF-A GEC | 137.6 (14.5) | 129.4 (17.3) | 0.157 |
Characteristics of improvers and non-improvers in attention.
SD, standard deviation; Dep., depression; ep., episode; GMT, Goal Management Training; WASI, Wechsler Abbreviated Scale of Intelligence; TMT, Trail-Making Test; CVLT-II SF, California Verbal Learning Test–Second edition – Short form; WAIS-IV, Wechsler Adult Intelligence Scale – Fourth edition; DS, digit span; BDI, Beck Depression Inventory; RRS, Ruminative Response Scale; CORE-OM, Clinical Outcomes in Routine Evaluation – Outcome Measure; CPT, Conners’ Continuous Performance Test; HRT, hit reaction time; BRIEF-A GEC, Behavior Rating Inventory of Executive Function – Adult version Global Executive Composite. All scores reported are raw scores, except when otherwise specified. Higher scores indicate greater impairment, except for WASI, CVLT-II, and WAIS-IV.
Overlap Between Improvers Across Outcomes
Fifteen participants (35.7%) improved on neither measure, and four participants (9.5%) improved reliably on both the BRIEF-A GEC and the CPT-3.
Discussion
The present study aimed to identify factors predicting long-term treatment outcomes following CR in an MDD sample. None of the variables emerged as major predictors of change in either everyday EF or attention. The lack of factors associated with CR improvement is generally consistent with previous research on MDD (
Even though none of the illness-related factors emerged as major predictors, surprisingly, a reliable improvement in attention was associated at trend level with having experienced more than one previous depressive episode. Recurrence of episodes arguably indicates greater illness severity and chronicity, previously associated with reduced CR effectiveness for both MDD (
The present study failed to replicate the single significant finding from a previous meta-analysis investigating moderators of CR outcomes in MDD, namely, that treatment effectiveness decreases with increasing age (
Cognitive performance at baseline did not predict outcomes for attention or EF in our sample. This finding is contrary to a selection of findings regarding schizophrenia (
Delivering CR therapies to patients with MDD hinges on the theoretical assumption that cognitive deficits impair everyday functioning and act as risk factors for depressive symptoms. Thus, it is striking that cognitive performance at baseline (i.e., the degree of the cognitive deficits) lacks support as a moderator of CR outcome (
Rumination is proposed to have a bidirectional relationship with EF (
Pooling participants who received CR interventions that differed in content and theoretical foundation was necessary to obtain an acceptable sample size. This may have obscured the effect of predictors on each treatment. Nevertheless, the number of improvers was similar across interventions for both outcome measures in the present study; moreover, a previous meta-analysis of schizophrenia has indicated that different approaches produce similar overall effects on measures of cognition (
Clinical Implications and Future Directions
The percentage of improvers in the present study (33.3–40.5%) and previous studies (34.2%) (
The present study focused on identifying baseline predictors that could be easily disseminated into clinical practice. Hence, it did not include several factors identified as potential mediators or moderators of CR in MDD or schizophrenia, such as the number of training sessions (
Strengths and Limitations
The study was based on data from a single-blind RCT, applied a multimodal selection of outcome measures, and used a stringent approach to define improvement. In addition, the study attempted to extend on previous research by applying a long follow-up period as an endpoint, aiming to identify predictors of durable change following CR. However, the following limitations should be considered when interpreting the above findings. No a priori hypotheses were generated, and the analyses were exploratory, calling for caution in the interpretation of results. Another notable limitation was the modest sample size, reducing statistical power and increasing the risk of type II errors. Furthermore, multiple testing inflated the risk of type I errors, even if partially accounted for by lowering the significance level.
The neuropsychological measure of attention was not corrected for practice effects (
A selection of variables was transformed into dichotomous categories, which may result in a loss of information and power (
Conclusion
In the present study, no major predictors of long-term improvement in attention or executive functioning following CR emerged. The results are consistent with previous research, which mostly failed to identify predictors of CR treatment. Importantly, the current findings are insufficient to guide clinical decision-making, and there is a need for large-scale and fine-grained investigations to extend current knowledge.
Statements
Data availability statement
The datasets for this article are not publicly available because of restrictions specified in the study consent-form, and conditions for approval from the local ethics committee, concerning patient confidentiality and participant privacy. Requests to access the datasets should be directed to Jan Stubberud, jan.stubberud@psykologi.uio.no.
Ethics statement
The studies involving human participants were reviewed and approved by the Regional Committee for Medical and Health Research Ethics, South-Eastern Norway (2017/666). The patients/participants provided their written informed consent to participate in this study.
Author contributions
BH completed the data collection and data curation, analyzed the data, and wrote the manuscript draft. The study was part of a doctoral thesis by BH. JS provided supervision, conceptualized the original trial, acted as principal investigator, and contributed with revisions of the manuscript draft. BL and NL contributed to the conceptualization of the original trial and revision of the manuscript draft. EK contributed with revisions of the manuscript draft. All authors contributed to the article and approved the submitted version.
Funding
This study was funded by the South-Eastern Norway Regional Health Authority (Grant No. 2019120) and the research fund at the Lovisenberg Diaconal Hospital. The funding sources were not otherwise involved in the research.
Acknowledgments
We would like to thank all participants for their contributions. Also, we thank Milada Cvancarova Småstuen (Lovisenberg Diaconal Hospital, Oslo Metropolitan University) for contributions to the statistical analysis and the results section of the manuscript.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Footnotes
References
1
AhernE.SemkovskaM. (2017). Cognitive functioning in the first-episode of major depressive disorder: a systematic review and meta-analysis.Neuropsychology3152–72. 10.1037/neu0000319
2
BarkhamM.MargisonF.LeachC.LucockM.Mellor-ClarkJ.EvansC.et al (2001). Service profiling and outcomes benchmarking using the CORE-OM: toward practice-based evidence in the psychological therapies.J. Consult. Clin. Psychol.69184–196. 10.1037/0022-006x.69.2.184
3
BauneB. T.MillerR.McAfooseJ.JohnsonM.QuirkF.MitchellD. (2010). The role of cognitive impairment in general functioning in major depression.Psychiatry Res.176183–189. 10.1016/j.psychres.2008.12.001
4
BeckA. T.SteerR. A.CarbinM. G. (1988). Psychometric properties of the Beck Depression Inventory: twenty-five years of evaluation.Clin. Psychol. Rev.877–100. 10.1016/0272-7358(88)90050-5
5
BeckA. T.WardC. H.MendelsonM.MockJ.ErbaughJ. (1961). An Inventory for Measuring Depression.Arch. Gen. Psychiatry4561–571. 10.1001/archpsyc.1961.01710120031004
6
BuonocoreM.BosiaM.BechiM.SpangaroM.CavedoniS.CocchiF.et al (2017). Is longer treatment better? A comparison study of 3 versus 6 months cognitive remediation in schizophrenia.Neuropsychology31467–473. 10.1037/neu0000347
7
CheluneG. J.NaugleR. I.LüdersH.SedlakJ.AwadI. A. (1993). Individual change after epilepsy surgery: practice effects and base-rate information.Neuropsychology741–52. 10.1037/0894-4105.7.1.41
8
ConnersC. K. (2015). Conners’ Continuous Performance Test 3rd editionTM(Conners’ CPT 3TM), Conners’ Continuous Auditory Test of Attention (Conners’ CATATM) Manual.Canada: Multi-Health Systems Incorporated.
9
DavisR. N.Nolen-HoeksemaS. (2000). Cognitive inflexibility among ruminators and nonruminators.Cogn. Ther. Res.24699–711.
10
DelisD. C.KaplanE.KramerJ. H. (2001). Delis-Kaplan Executive Function System (D-KEFS).San Antonio, TX: Psychological Corporation.
11
DelisD. C.KramerJ. H.KaplanE.OberB. A. (2000). CVLT-II: California Verbal Learning Test: Adult Version.San Antonio, TX: Psychological Corporation.
12
DuffK. (2012). Evidence-based indicators of neuropsychological change in the individual patient: relevant concepts and methods.Arch. Clin. Neuropsychol.27248–261. 10.1093/arclin/acr120
13
ElgamalS.DenburgS.MarriottM.MacQueenG. (2010). Clinical factors that predict cognitive function in patients with major depression.Canad. J. Psychiatry55653–661. 10.1177/070674371005501004
14
GrovesS. J.DouglasK. M.PorterR. J. (2018). A systematic review of cognitive predictors of treatment outcome in major depression.Front. in Psychiatry9:382. 10.3389/fpsyt.2018.00382
15
HagenB. I.LauB.JoormannJ.SmåstuenM. C.LandrøN. I.StubberudJ. (2020). Goal Management Training as a cognitive remediation intervention in depression: a randomized controlled trial.J. Affect. Disord.275267–277. 10.1016/j.jad.2020.07.015
16
HamiltonK. E.DobsonK. S. (2002). Cognitive therapy of depression: pretreatment patient predictors of outcome.Clin. Psychol. Rev.22875–893. 10.1016/S0272-7358(02)00106-X
17
HasselbalchB. J.KnorrU.KessingL. V. (2011). Cognitive impairment in the remitted state of unipolar depressive disorder: a systematic review.J. Affect. Disord.13420–31. 10.1016/j.jad.2010.11.011
18
HuddyV.ReederC.KontisD.WykesT.StahlD. (2012). The effect of working alliance on adherence and outcome in cognitive remediation therapy.J. Nerv. Ment. Dis.200614–619. 10.1097/nmd.0b013e31825bfc31
19
JacobsonN. S.TruaxP. (1991). Clinical significance: a statistical approach to defining meaningful change in psychotherapy research.J. Consult. Clin. Psychol.5912–19. 10.1037/0022-006x.59.1.12
20
Kabat-ZinnJ. (1990). Full Catastrophe Living: The Program of the Stress Reduction Clinic at the University of Massachusetts Medical Center.New York, NY: Delacorte Press.
21
KaserM.ZamanR.SahakianB. J. (2017). Cognition as a treatment target in depression.Psychol. Med.47987–989. 10.1017/s0033291716003123
22
KosterE. H. W.HoorelbekeK.OnraedtT.OwensM.DerakshanN. (2017). Cognitive control interventions for depression: a systematic review of findings from training studies.Clin. Psychol. Rev.5379–92. 10.1016/j.cpr.2017.02.002
23
KurtzM. M.SeltzerJ. C.FujimotoM.ShaganD. S.WexlerB. E. (2009). Predictors of change in life skills in schizophrenia after cognitive remediation.Schizophr. Res.107267–274. 10.1016/j.schres.2008.10.014
24
LevineB.SchweizerT. A.O’ConnorC.TurnerG.GillinghamS.StussD. T.et al (2011). Rehabilitation of executive functioning in patients with frontal lobe brain damage with goal management training.Front. Hum. Neurosci.5:9. 10.3389/fnhum.2011.00009
25
LewandowskiK. E.SperryS. H.CohenB. M.NorrisL. A.FitzmauriceG. M.OngurD.et al (2017). Treatment to enhance cognition in bipolar disorder (TREC-BD): efficacy of a randomized controlled trial of cognitive remediation versus active control.J. Clin. Psychiatry78e1242–e1249.
26
LindenmayerJ. P.FregentiS.KangG.OzogV.LjuriI.KhanA.et al (2017). The relationship of cognitive improvement after cognitive remediation with social functioning in patients with schizophrenia and severe cognitive deficits.Schizophr. Res.185154–160. 10.1016/j.schres.2017.01.007
27
ListunovaL.BartolovicM.KienzleJ.JaehnA.GrütznerT. M.WolfR. C.et al (2020). Predictors of cognitive remediation therapy improvement in (partially) remitted unipolar depression.J. Affect. Disord.26440–49. 10.1016/j.jad.2019.12.006
28
MacCallumR. C.ZhangS.PreacherK. J.RuckerD. D. (2002). On the practice of dichotomization of quantitative variables.Psychol. Methods719–40. 10.1037/1082-989X.7.1.19
29
MarazzitiD.ConsoliG.PicchettiM.CarliniM.FaravelliL. (2010). Cognitive impairment in major depression.Eur. J. Pharmacol.62683–86.
30
MedaliaA.RichardsonR. (2005). What predicts a good response to cognitive remediation interventions?Schizophr. Bull.31942–953. 10.1093/schbul/sbi045
31
MorimotoS. S.WexlerB. E.LiuJ.HuW.SeirupJ.AlexopoulosG. S. (2014). Neuroplasticity-based computerized cognitive remediation for treatment-resistant geriatric depression.Nat. Commun.51–7. 10.1038/ncomms5579
32
MotterJ. N.PimontelM. A.RindskopfD.DevanandD. P.DoraiswamyP. M.SneedJ. R. (2016). Computerized cognitive training and functional recovery in major depressive disorder: a meta-analysis.J. Affect. Disord.189184–191. 10.1016/j.jad.2015.09.022
33
PetersenJ. Z.PorterR. J.MiskowiakK. W. (2019). Clinical characteristics associated with the discrepancy between subjective and objective cognitive impairment in depression.J. Affect. Disord.246763–774. 10.1016/j.jad.2018.12.105
34
PhilippotP.BrutouxF. (2008). Induced rumination dampens executive processes in dysphoric young adults.J. Behav. Ther. Exp. Psychiatry39219–227. 10.1016/j.jbtep.2007.07.001
35
PorterR. J.BourkeC.CarterJ. D.DouglasK. M.McIntoshV. V. W.JordanJ.et al (2016). No change in neuropsychological dysfunction or emotional processing during treatment of major depression with cognitive–behaviour therapy or schema therapy.Psychol. Med.46393–404. 10.1017/s0033291715001907
36
PuS.NodaT.SetoyamaS.NakagomeK. (2018). Empirical evidence for discrete neurocognitive subgroups in patients with non-psychotic major depressive disorder: clinical implications.Psychol. Med.482717–2729. 10.1017/s003329171800034x
37
QuinnM. E.KeilD. C.UtkeS.JoormannJ. (2014). Trait rumination moderates the effect of executive control training.J. Exp. Psychopathol.5289–301. 10.5127/jep.038713
38
ReserM. P.SlikboerR.RossellS. L. (2019). A systematic review of factors that influence the efficacy of cognitive remediation therapy in schizophrenia.Austral. N. Z. J. Psychiatry53624–641. 10.1177/0004867419853348
39
RockP. L.RoiserJ. P.RiedelW. J.BlackwellA. D. (2014). Cognitive impairment in depression: a systematic review and meta-analysis.Psychol. Med.442029–2040. 10.1017/s0033291713002535
40
RothR. M.IsquithP. K.GioiaG. (2005). Behavioral Rating Inventory of Executive Function–Adult Version.Lutz, FL: Psychological Assessment Resources.
41
SchulzK. F.AltmanD. G.MoherD. (2010). CONSORT 2010 statement: updated guidelines for reporting parallel group randomised trials.BMC Med.8:18. 10.1186/1741-7015-8-18
42
SeccomandiB.TsapekosD.NewberyK.WykesT.CellaM. (2020). A systematic review of moderators of cognitive remediation response for people with schizophrenia.Schizophr. Res.19:100160. 10.1016/j.scog.2019.100160
43
ShilyanskyC.WilliamsL. M.GyurakA.HarrisA.UsherwoodT.EtkinA. (2016). Effect of antidepressant treatment on cognitive impairments associated with depression: a randomised longitudinal study.Lancet Psychiatry3425–435. 10.1016/s2215-0366(16)00012-2
44
SiegleG. J.GhinassiF.ThaseM. E. (2007). Neurobehavioral therapies in the 21st century: summary of an emerging field and an extended example of cognitive control training for depression.Cogn. Ther. Res.31235–262. 10.1007/s10608-006-9118-6
45
SiegleG. J.PriceR. B.JonesN. P.GhinassiF.PainterT.ThaseM. E. (2014). You gotta work at it: pupillary indices of task focus are prognostic for response to a neurocognitive intervention for rumination in depression.Clin. Psychol. Sci.2455–471. 10.1177/2167702614536160
46
SnyderH. R. (2012). Major depressive disorder is associated with broad impairments on neuropsychological measures of executive function: a meta-analysis and review.Psychol. Bull.13981–132. 10.1037/a0028727
47
StubberudJ.LangenbahnD.LevineB.StanghelleJ.SchankeA.-K. (2013). Goal management training of executive functions in patients with spina bifida: a randomized controlled trial.J. Int. Neuropsychol. Soc.19672–685. 10.1017/s1355617713000209
48
TornåsS.LøvstadM.SolbakkA.-K.EvansJ.EndestadT.HolP. K.et al (2016). Rehabilitation of executive functions in patients with chronic acquired brain injury with goal management training, external cuing, and emotional regulation: a randomized controlled trial.J. Int. Neuropsychol. Soc.22436–452. 10.1017/s1355617715001344
49
TreynorW.GonzalezR.Nolen-HoeksemaS. (2003). Rumination reconsidered: a psychometric analysis.Cogn. Ther. Res.27247–259.
50
TwamleyE. W.BurtonC. Z.VellaL. (2011). Compensatory cognitive training for psychosis: who benefits? Who stays in treatment?Schizophr. Bull.37(Suppl._2), 55–62. 10.1093/schbul/sbr059
51
VelliganD. I.KernR. S.GoldJ. M. (2006). Cognitive rehabilitation for schizophrenia and the putative role of motivation and expectancies.Schizophr. Bull.32474–485. 10.1093/schbul/sbj071
52
VeneziaR. G.GorlynM.BurkeA. K.OquendoM. A.MannJ. J.KeilpJ. G. (2018). The impact of cognitive reserve on neurocognitive performance in major depressive disorder.Psychiatry Res.270211–218. 10.1016/j.psychres.2018.09.031
53
Vicent-GilM.Keymer-GaussetA.Serra-BlascoM.Carceller-SindreuM.de Diego-AdeliñoJ.TrujolsJ.et al (2018). Cognitive predictors of illness course at 12 months after first-episode of depression.Eur. Neuropsychopharmacol.28529–537. 10.1016/j.euroneuro.2018.02.001
54
VictorM.LauB.RuudT. (2016). Patient characteristics in a return to work programme for common mental disorders: a cross-sectional study.BMC Public Health16:745. 10.1186/s12889-016-3431-0
55
VitaA.DesteG.De PeriL.BarlatiS.PoliR.CesanaB. M.et al (2013). Predictors of cognitive and functional improvement and normalization after cognitive remediation in patients with schizophrenia.Schizophr. Res.15051–57. 10.1016/j.schres.2013.08.011
56
WechslerD. (1999). Manual for the Wechsler abbreviated intelligence scale (WASI).San Antonio, TX: The Psychological Corporation.
57
WechslerD. (2014). Wechsler adult intelligence scale–Fourth Edition (WAIS–IV).San Antonio, TX: Psychological Corporation.
58
World Health Organization (2004). ICD-10: International Statistical Classification of Diseases and Related Health Problems: Tenth Revision, 2nd Edn. Geneva: World Health Organization.
59
WykesT.HuddyV.CellardC.McGurkS. R.CzoborP. (2011). A meta-analysis of cognitive remediation for schizophrenia: methodology and effect sizes.Am. J. Psychiatry168472–485. 10.1176/appi.ajp.2010.10060855
Summary
Keywords
depression, cognitive remediation, treatment predictors, executive functions, attention
Citation
Hagen BI, Landrø NI, Lau B, Koster EHW and Stubberud J (2020) Predictors of Long-Term Improvement Following Cognitive Remediation in a Sample With Elevated Depressive Symptoms. Front. Psychol. 11:2232. doi: 10.3389/fpsyg.2020.02232
Received
28 April 2020
Accepted
10 August 2020
Published
11 September 2020
Volume
11 - 2020
Edited by
Peter L. Fisher, University of Liverpool, United Kingdom
Reviewed by
Tobias Kube, Harvard Medical School, United States; Brooke Schneider, University Medical Center Hamburg-Eppendorf, Germany
Updates

Check for updates
Copyright
© 2020 Hagen, Landrø, Lau, Koster and Stubberud.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Bjørn Ingulfsvann Hagen, boha@lds.no
This article was submitted to Psychology for Clinical Settings, a section of the journal Frontiers in Psychology
Disclaimer
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.