Skip to main content

SYSTEMATIC REVIEW article

Front. Aging Neurosci., 19 July 2022
Sec. Alzheimer's Disease and Related Dementias
This article is part of the Research Topic Activities of Daily Living and Everyday Functioning: From Normal Aging to Neurodegenerative Diseases View all 14 articles

Effects of combined cognitive and physical intervention on enhancing cognition in older adults with and without mild cognitive impairment: A systematic review and meta-analysis

  • 1School of Rehabilitation, Capital Medical University, Beijing, China
  • 2China Rehabilitation Research Center, Beijing Bo'ai Hospital, Beijing, China
  • 3Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, VIC, Australia
  • 4University of Health and Rehabilitation Sciences, Qingdao, China
  • 5Cheeloo College of Medicine, Shandong University, Jinan, China

Background: Combined cognitive and physical intervention is commonly used as a non-pharmacological therapy to improve cognitive function in older adults, but it is uncertain whether combined intervention can produce stronger cognitive gains than either single cognitive or sham intervention. To address this uncertainty, we performed a systematic review and meta-analysis to evaluate the effects of combined intervention on cognition in older adults with and without mild cognitive impairment (MCI).

Methods: We systematically searched eight databases for relevant articles published from inception to November 1, 2021. Randomized controlled trials (RCTs) and non-randomized controlled trials (NRCTs) were used to compare the effects of the combined intervention with a single cognitive or sham intervention on cognition in older adults with and without MCI aged ≥ 50 years. We also searched Google Scholar, references of the included articles, and relevant reviews. Two independent reviewers performed the article screening, data extraction, and bias assessment. GRADEpro was used to rate the strength of evidence, and RevMan software was used to perform the meta-analysis.

Results: Seventeen studies were included in the analysis, comprising eight studies of cognitively healthy older adults and nine studies of older adults with MCI. The meta-analysis showed that the combined intervention significantly improved most cognitive functions and depression (SMD = 0.99, 95% CI 0.54–1.43, p < 0.0001) in older adults compared to the control groups, but the intervention effects varied by cognition domains. However, there was no statistically significant difference in the maintenance between the combined and sham interventions (SMD = 1.34, 95% CI −0.58–3.27, p = 0.17). The subgroup analysis also showed that there was no statistical difference in the combined intervention to improve global cognition, memory, attention, and executive function between cognitive healthy older adults and older adults with MCI.

Conclusions: Combined intervention improves cognitive functions in older adults with and without MCI, especially in global cognition, memory, and executive function. However, there was no statistical difference in the efficacy of the combined intervention to improve cognition between cognitive healthy older adults and older adults with MCI. Moreover, the maintenance of the combined intervention remains unclear due to the limited follow-up data and high heterogeneity. In the future, more stringent study designs with more follow-ups are needed further to explore the effects of combined intervention in older adults.

Systematic review registration: https://www.crd.york.ac.uk/PROSPERO/#recordDetails, identifier: CRD42021292490.

Introduction

As the global population ages, cognitive decline has become an increasingly critical factor affecting the health and quality of life of older adults, ranging from normal cognitive function to mild cognitive impairment (MCI) even dementia (Anderson, 2020). In recent years, the prevalence of MCI has increased in older adults, exacerbating the potential impact on global physical and mental health (Vos et al., 2015; Overton et al., 2019). A study has shown that the proportion of participants with depression among older adults with MCI ranged from 20.1 to 44.3% (Panza et al., 2010), and improvement in this state of MCI plus depression (MCI/D) is an essential factor in improving quality of life. MCI is an early stage of memory loss or other cognitive ability loss in individuals who maintain the ability to independently perform most activities of daily living (ADL) (Jack et al., 2018). Moreover, MCI has a high risk of progressing into Alzheimer's disease (AD) and other dementias, with reported conversion rates of 50% in 2-3 years (Marioni et al., 2015) and even as high as 60–100% in 5–10 years (Albert et al., 2011).

MCI refers to a cognitive and functional decline syndrome with no currently available cure. At present, pharmacological treatments for patients with MCI have not been proven to be completely effective, and adverse effects have been observed (Briggs et al., 2016). Cognitive interventions using non-invasive and non-pharmacological treatments based on the theories of neuroplasticity (Greenwood and Parasuraman, 2010; Rajji, 2019) and rich environments have attracted more attention (Marlats et al., 2020; Liu et al., 2021). A previous study reported that older adults with and without MCI showed signs of cognitive decline to varying degrees, and combined cognitive and physical intervention effectively improves cognition (Wu et al., 2019), which also becomes a research hotspot in recent years. Shatil (2013) conducted a 16-week randomized controlled trial (RCT) of combined cognitive and physical intervention, single cognitive intervention, and sham intervention in 29, 33, and 29 cognitively healthy older adult subjects, respectively, and found that combined intervention was significantly better than single cognitive intervention in improving memory and naming, while sham intervention showed no improvement in cognition. Additionally, Park et al. (2019) conducted a 24-week RCT in 49 older adult subjects with amnesic MCI (aMCI), in which 25 subjects performed aerobic exercise while doing number crunching and found that combined intervention improved working memory and executive function, but the sham intervention did not improve cognition in the other 24 subjects.

Although many meta-analyses have reported the cognitive benefits of the combined intervention for older adults with and without MCI (Stanmore et al., 2017; Gheysen et al., 2018; Gavelin et al., 2021), they were mixed across age groups and included articles that varied considerably in terms of study designs, comparisons, and study qualities. Therefore, the efficacy of the combined intervention to improve cognition is yet to be determined, especially when compared to single cognitive intervention (Law et al., 2014; Wollesen et al., 2015; Zhu et al., 2016). To address the above limitations, this meta-analysis developed a more detailed inclusion criteria and separately reported the effects of the combined intervention compared with a single cognitive or sham intervention on cognition in older adults with and without MCI.

The objectives of this systematic review and meta-analysis are as follows: (1) to compare the effects of combined intervention with a single cognitive or sham intervention on cognition in older adults; (2) to explore the differences in cognitive efficacy of the combined intervention for cognitively healthy older adults and those with MCI; and (3) to summarize and compare the maintenance and safety of combined intervention in order to provide practical strategies and methods for improving cognition in older adults.

Methods

We report the systematic review and meta-analysis following the Preferred Reporting Items for Systematic Reviews and Meta-analysis guidelines (Moher et al., 2009) and register the review in the International Prospective Register of Systematic Reviews (CRD42021292490).

Search strategy

We implemented the search strategy by using a combination of MESH terms, free-text words, and truncation retrieval, and we searched for articles on combined cognitive and physical intervention to enhance cognition in older adults with and without MCI published in PubMed, Embase, Web of Science, Cochrane Library, PsycINFO, Scopus, EBSCO and Ovid from inception to November 1, 2021. Furthermore, we screened all reference lists of the selected articles and related review articles, and we used the same search terms in Google Scholar to perform additional searches. The search was limited to publications in English. The complete search strategy (Supplementary Table S1) is provided in the Supplementary Material.

Selection criteria

The inclusion criteria of this meta-analysis is detailed below.

Participants

Studies were included if the participants: were cognitively healthy older adults or those diagnosed with MCI; had an age of 50 years or older.

Interventions

Combined cognitive and physical training as an intervention that is either a simultaneous or a sequential dual or multi-tasking (Gallou-Guyot et al., 2020), refers to performing two or even more cognitive and physical tasks separately or simultaneously (Tait et al., 2017; MacPherson, 2018). We did not limit the cognitive or physical training type in the combined intervention.

Comparisons

The intervention in the control group included either single cognitive or sham intervention (e.g., placebo control, blank control, and passive control) for older adults with or without MCI.

If the study had two or more control groups (e.g., single physical intervention, single cognitive intervention, or sham intervention), only data from the control group with single cognitive or sham intervention were included.

Outcomes

The primary outcome was cognitive function, including global cognitive function, memory, attention, and executive function; the secondary outcome was depression.

Cognition evaluation

Mini-Mental State Examination (MMSE) and the Montreal Cognitive Assessment (MoCA) to evaluate the global cognition; Logical Memory (LM), Digit Span Test (DST), Trail Making Test Parts A (TMT-A), Rey Auditory Verbal Learning Test (RAVLT), and Complex Figure Test (CFT) to evaluate memory function; Symbol Digit Substitution Test (SDST), Brief Test of Attention (BTA), Test of Everyday Attention (TEA), and attentional Matrices (AM) to evaluate attention; Trail Making Test Parts B (TMT-B) and Executive Function Cognitive Assessment Scale (FUCAS) to assess executive function; Stroop color-word test (SCWT) to evaluate inhibition and executive control function.

Depression evaluation

The included studies used the Geriatric Depression Scale (GDS) or the Cornell Scale for Depression in Dementia (CSDD) to assess depression.

Design

Studies that were randomized controlled trials (RCTs) or non-randomized controlled trials (NRCTs) were included in this review.

Study selection and data extraction

Two reviewers (HKY, TZQ) worked independently to screen the articles, extract information, and cross-check. In case of a disagreement, the articles were reviewed by a third reviewer (SWL). The authors of the original study were contacted via email to clarify or add any missing information. The articles were initially screened by reading the title and abstract before reading of the full text for re-screening. For each eligible study, we used a self-designed standardized form (Supplementary Table S2) to extract the first author's name, year of publication, country, clinical diagnosis of disease, number of participants, male ratio, age, education level, intervention methods, intervention characteristics, outcome measures, and drop-out.

Risk of bias and study quality assessment

Two reviewers (HKY, TZQ) independently assessed the studies according to the Cochrane Handbook for Systematic Reviews of Interventions (Higgins et al., 2011), and disagreements on assessments were resolved by discussion with the third reviewer (SWL). The assessment scale included the following seven items: random sequence generation and allocation concealment (selection bias), blinding of participants and personnel (performance bias), blinding of outcome assessment (detection bias), incomplete outcome data (attrition bias), selective reporting (reporting bias), and other bias. Three degrees of assessment were used to grade each item: “low,” “unclear,” and “high.”

The PEDro scale, comprising 11 items, was used to assess the quality of the included studies, and studies with a score of seven or higher were considered to be of medium and high quality (Maher et al., 2003). Based on the risk of bias, inconsistency, indirectness, imprecision, and publication bias, the online GRADEpro method was used to evaluate the quality of evidence for pooled results in the meta-analysis (Cui et al., 2019).

Data analysis and statistical methods

We used RevMan software 5.4 to perform the meta-analysis. Since all data were continuous information and were pooled by the same outcome using inconsistent scales, we selected the Standardized Mean Difference (SMD) as an effective indicator and provided the 95% confidence interval (CI). We used the Cochrane Q statistic to qualitatively determine whether heterogeneity existed among the included studies (test level α = 0.05), while the I2 statistic was used to quantitatively determine the magnitude of heterogeneity. If the P-value was ≥ 0.1 and I2 ≤ 50%, the heterogeneity was considered to be insignificant and we selected the fixed-effects (FE) model. Conversely, if the heterogeneity was considered to be significant, we selected the random-effects (RE) model and performed a subgroup analysis and sensitivity analysis to identify the factors that contributed to the heterogeneity. Descriptive analysis was performed if the source of heterogeneity could not ultimately be determined.

Results

Study selection

The flowchart of study selection is shown in Figure 1. We initially retrieved 1,353 articles from the nine databases and identified one article through other sources. Eight hundred and forty-four articles remained after removing duplicates using a reference management software. After reading the titles and abstracts for screening, 797 articles were excluded. Subsequently, after screening the full text of the remaining 47 articles, 10 articles were not full data available, nine articles had a non-conforming control group, three articles had no cognitive assessment results, six articles had no conforming neuropsychological tests, and the full text of two articles were not available. Finally, 17 articles were included in this review.

FIGURE 1
www.frontiersin.org

Figure 1. PRISMA flowchart of study selection.

Characteristics of the included studies

As shown in Supplementary Table S2, eight studies of cognitively healthy older adults were eligible (Fabre et al., 2002; Marmeleira et al., 2009; Shatil, 2013; Hars et al., 2014; Nishiguchi et al., 2015; Rahe et al., 2015a,b; Morita et al., 2018), with 181 participants in the combined intervention group, 68 in the single cognitive intervention group, and 142 in the sham intervention group. Regarding the study design, six studies were RCTs (Fabre et al., 2002; Marmeleira et al., 2009; Shatil, 2013; Hars et al., 2014; Nishiguchi et al., 2015; Rahe et al., 2015a) and two studies were NRCTs (Rahe et al., 2015b; Morita et al., 2018). Regarding the modes of combined intervention, four studies performed simultaneous combined cognitive and physical training (Marmeleira et al., 2009; Shatil, 2013; Hars et al., 2014; Nishiguchi et al., 2015; Morita et al., 2018) and four studies performed sequential combined intervention (Fabre et al., 2002; Shatil, 2013; Rahe et al., 2015a,b), all of which reported greater cognitive gains in the combined intervention. Regarding the comparison condition, three studies used single cognitive intervention (Shatil, 2013; Rahe et al., 2015a,b), one study used reading as a placebo control (Shatil, 2013), four studies used a blank control (Fabre et al., 2002; Marmeleira et al., 2009; Hars et al., 2014; Nishiguchi et al., 2015), and one study used non-exercise as a passive control (Morita et al., 2018). Additionally, five studies implemented interventions longer than 12 weeks (Marmeleira et al., 2009; Shatil, 2013; Hars et al., 2014; Nishiguchi et al., 2015; Morita et al., 2018). Only one study had a follow-up - up to 1 year -and reported that combined intervention can produce more significant long-term effects than single cognitive intervention, especially in attention (Rahe et al., 2015b).

Nine studies of older adults with MCI were eligible (Kounti et al., 2011; Lam et al., 2015; Delbroek et al., 2017; Park, 2017; Donnezan et al., 2018; Mrakic-Sposta et al., 2018; Park et al., 2019, 2020; Rojasavastera et al., 2020), with 217 participants in the combined intervention group, 41 in the single cognitive intervention group, and 176 in the sham intervention group. Regarding the study design, eight studies were RCTs (Lam et al., 2015; Delbroek et al., 2017; Park, 2017; Donnezan et al., 2018; Mrakic-Sposta et al., 2018; Park et al., 2019, 2020; Rojasavastera et al., 2020) and one study was NRCT (Kounti et al., 2011). Regarding the modes of combined intervention, seven studies included simultaneous combined cognitive and physical training (Kounti et al., 2011; Delbroek et al., 2017; Park, 2017; Donnezan et al., 2018; Mrakic-Sposta et al., 2018; Park et al., 2019, 2020) and two studies performed sequential combined intervention (Lam et al., 2015; Rojasavastera et al., 2020), all of which reported greater cognitive improvements in the combined intervention. Regarding the comparison condition, three studies used single cognitive intervention (Park, 2017; Donnezan et al., 2018; Park et al., 2020), one study used social activities as a placebo control (Lam et al., 2015), and five studies used a blank control (Kounti et al., 2011; Delbroek et al., 2017; Mrakic-Sposta et al., 2018; Park et al., 2019; Rojasavastera et al., 2020). Additionally, four studies implemented interventions longer than 12 weeks (Kounti et al., 2011; Lam et al., 2015; Donnezan et al., 2018; Park et al., 2019). Only three studies had follow-up—up to 1, 3, and 6 months, respectively—and they also reported greater long-term cognitive improvements in combined intervention group (Donnezan et al., 2018; Park et al., 2019; Rojasavastera et al., 2020).

Risk of bias and quality assessment

The PEDro scale showed that all studies were non-low quality (Supplementary Table S2). The risk of bias of the included studies is shown in Figure 2. Of the 17 studies included, three studies did not use randomization methods (Kounti et al., 2011; Rahe et al., 2015b; Morita et al., 2018) and four did not report allocation concealment (Marmeleira et al., 2009; Kounti et al., 2011; Morita et al., 2018; Park et al., 2019). The participants and personnel of three studies were not blinded to the combined intervention because of the intervention design's characteristics, which were considered to have a high risk of bias (Park, 2017; Donnezan et al., 2018; Park et al., 2019), while the outcome assessments of seven studies were blinded (Kounti et al., 2011; Hars et al., 2014; Lam et al., 2015; Rahe et al., 2015a; Delbroek et al., 2017; Park, 2017; Morita et al., 2018). A total of 13 studies showed a low risk of bias in attrition, reporting, and other biases (Fabre et al., 2002; Marmeleira et al., 2009; Shatil, 2013; Hars et al., 2014; Nishiguchi et al., 2015; Rahe et al., 2015a; Delbroek et al., 2017; Park, 2017; Morita et al., 2018; Mrakic-Sposta et al., 2018; Park et al., 2019, 2020; Rojasavastera et al., 2020).

FIGURE 2
www.frontiersin.org

Figure 2. Results from the Cochrane risk of bias (ROB) tool. (A) ROB graph and (B) ROB summary.

For global cognitive function, the GRADE ratings from the included studies showed the effectiveness of “moderate” and “low” using the MMSE and MoCA to measure outcome (Table 1).

TABLE 1
www.frontiersin.org

Table 1. Summary of the GRADEpro.

Effects of the combined intervention

Effects of combined intervention in cognitively healthy older adults

Global cognition

Three studies used MMSE to assess the efficacy of the combined intervention on global cognition in cognitively healthy older adults (Hars et al., 2014; Nishiguchi et al., 2015; Morita et al., 2018). Application of the RE model to the pooled SMD revealed that the global cognitive level was significantly higher in the combined group than in the control group (SMD = 1.77, 95% CI 0.94–2.59, p < 0.0001, Supplementary Figure S1). Next, due to the high heterogeneity (I2 = 73%, χ2 = 7.53, p = 0.02), we excluded one study at a time to perform sensitivity analysis. The result after excluding one study (Morita et al., 2018) showed the heterogeneity decreased (I2 = 53%, χ2 = 2.11, p = 0.15), as well as a change in the overall pooled effect (SMD = 1.40, 95% CI 0.85–1.96, p < 0.00001, Figure 3).

FIGURE 3
www.frontiersin.org

Figure 3. Forest plot of the efficacy of the combined intervention on global cognition in cognitively healthy older adults compared to the control group (sensitive analysis).

Cognition domains

Based on different cognition domains, we performed a subgroup analysis that compared the efficacy of the combined intervention with single cognitive, sham interventions to improve cognition in cognitively healthy older adults. Compared with single cognitive intervention (Figure 4A), the pooled SMD showed that combined intervention significantly improved working memory (SMD = 0.45, 95% CI 0.06–0.84, p = 0.02), but no significant improvement in figural memory (SMD = 0.57, 95% CI −0.14–1.28, p = 0.11) and inhibition (SMD = 0.78, 95% CI −0.01–1.57, p = 0.05). Compared with the sham intervention (Figure 4B), the combined intervention significantly improved memory recall (SMD = 1.93, 95% CI 1.33–2.54, p < 0.00001), divided attention (SMD = 1.01, 95% CI 0.14–1.87, p = 0.02) and speed processing (SMD = 1.91, 95% CI 0.79–3.03, p = 0.0008). However, this subgroup analysis showed a significant heterogeneity (I2 = 75%, χ2 = 20.40, p = 0.001), and we did not perform sensitivity analysis to identify the heterogeneity sources because of the limited number of studies in each subgroup. Different cognitive rating scales, intervention frequency, and duration may have contributed to the observed heterogeneity.

FIGURE 4
www.frontiersin.org

Figure 4. Forest plot of the efficacy of the combined intervention on cognition domains in cognitively healthy older adults. (A) Combined intervention vs. single cognitive intervention, (B) combined intervention vs. sham intervention.

Effects of combined intervention in older adults with MCI

Global cognition

Eight studies assessed the efficacy of the combined intervention on global cognition using the MMSE and MoCA (Kounti et al., 2011; Lam et al., 2015; Delbroek et al., 2017; Park, 2017; Mrakic-Sposta et al., 2018; Park et al., 2019, 2020; Rojasavastera et al., 2020). In a subgroup analysis based on different cognitive scales, the pooled SMD showed that combined intervention was more beneficial for improving global cognition (SMD = 0.83, 95% CI 0.41–1.25, p = 0.0001, Supplementary Figure S2). We performed a sensitivity analysis due to the high heterogeneity (I2 = 66%, χ2 = 20.39, p = 0.005). After excluding one study (Park et al., 2020), the heterogeneity decreased (I2 = 8%, χ2 = 6.50, p = 0.37), and the pooled result also changed (SMD = 0.73, 95% CI 0.50–0.97, P < 0.00001, Figure 5).

FIGURE 5
www.frontiersin.org

Figure 5. Forest plot of the efficacy of the combined intervention on global cognition in older adults with MCI compared to the control group (sensitive analysis).

Cognition domains

Subgroup analysis compared the efficacy of the combined intervention with single cognitive, sham intervention to improve cognition in older adults with MCI. Compared with the single cognitive intervention (Supplementary Figure S3), the results showed that combined intervention significantly improved working memory (SMD = 2.00, 95% CI 0.40–3.60, p = 0.01) and speed processing (SMD = 3.98, 95% CI 2.78–5.17, p < 0.00001). When we performed a sensitivity analysis due to the high heterogeneity (I2 = 90%, χ2= 29.43, p < 0.00001), the heterogeneity decreased (I2 = 57%, χ2 = 2.34, p = 0.13) after excluding one study (Park et al., 2020), and the overall pooled effect in working memory also changed (SMD = 1.18, 95% CI 0.29–2.07, p = 0.009, Figure 6A). Additionally, compared with the sham intervention (Figure 6B), under acceptable heterogeneity (I2 = 54%, χ2 = 10.90, p = 0.05), the subgroup analysis revealed that combined intervention significantly improved memory recall (SMD = 0.97, 95% CI 0.67–1.26, p < 0.00001) and executive function (SMD = 1.77, 95% CI 1.31–2.23, p < 0.00001), but no significant improvement in attention (SMD = 0.96, 95% CI −0.10–2.02, p = 0.08).

FIGURE 6
www.frontiersin.org

Figure 6. Forest plot of the efficacy of the combined intervention on cognition domains in older adults with MCI. (A) Combined intervention vs. single cognitive intervention (sensitive analysis), (B) combined intervention vs. sham intervention.

Depression

Only three studies assessed the efficacy of the combined intervention to improve depression in older adults with MCI, with one study using CSDD (Lam et al., 2015) and two studies using GDS (Park, 2017; Park et al., 2019). Under acceptable heterogeneity (I2 = 48%, χ2 = 3.84, p = 0.15), the pooled results showed that combined intervention induced a significant improvement in depression (SMD = 0.99, 95% CI 0.54–1.43, p < 0.0001, Figure 7).

FIGURE 7
www.frontiersin.org

Figure 7. Forest plot of the efficacy of the combined intervention on depression in older adults with MCI compared with the control group.

Efficacy differences of combined intervention between cognitively healthy older adults and older adults with MCI

As shown in Table 2, in order to reduce heterogeneity, we used the same comparison and outcome assessment scales to analyze the efficacy differences of the combined intervention in older adults with and without MCI. Therefore, the number of studies included was limited. After sensitivity analysis, the subgroup analysis showed that there were no statistical difference within the combined intervention to improve global cognition (SMD = 1.40, 95% CI 0.85–1.96, p < 0.00001; vs. SMD = 0.81, 95% CI 0.51–1.11, p < 0.00001), memory (SMD = 0.70, 95% CI 0.18–1.23, p = 0.009; vs. SMD = 1.18, 95% CI 0.29–2.07, p = 0.009), attention (SMD = −0.04, 95% CI −0.60–0.51, p = 0.88; vs. SMD = −0.08, 95% CI −0.94–0.78, p = 0.85), and executive function (SMD = 0.39, 95% CI −0.42–1.20, p = 0.35; vs. SMD = 0.62, 95% CI −0.07–1.30, p = 0.08) between cognitive healthy older adults and older adults with MCI.

TABLE 2
www.frontiersin.org

Table 2. Efficacy differences of combined intervention on cognition between cognitively healthy older adults and older adults with MCI after sensitive analysis.

The maintenance and safety of combined intervention

As shown in Figure 8, only two studies were included to assess the maintenance of the combined intervention on global cognition in older adults with MCI compared to the sham intervention (Park et al., 2019; Rojasavastera et al., 2020), and the results showed no statistical difference (SMD = 1.34, 95% CI −0.58–3.27, p = 0.17). Similarly, due to limited follow-up data, we did not perform a subgroup analysis based on the different cognitive scales, which may have been a source of the observed high heterogeneity.

FIGURE 8
www.frontiersin.org

Figure 8. Forest plot of the maintenance on global cognition in older adults with MCI compared with sham intervention.

The minor adverse event was the risk of falls in older adults while performing physical training. The researchers increased safety protection and education for older adults to minimize this risk.

Moderator analysis for combined intervention

As shown in Table 3, because the outcome assessment scales and comparisons were not fully the same among studies, we only assessed the effect of the moderator variables on the efficacy of the combined intervention in order to improve global cognition in older adults with MCI. The results of the subgroup analyses showed that age (SMD = 0.73, 95% CI −0.21–1.66, p = 0.13; vs. SMD = 0.74, 95% CI 0.49–0.99, p < 0.00001), education (SMD = 0.75, 95% CI 0.49–1.01, p < 0.00001; vs. SMD = 0.73, 95% CI −0.21–1.66, p = 0.13), intervention duration (SMD = 0.37, 95% CI −0.1–0.85, p = 0.13; vs. SMD = 0.79, 95% CI 0.08–1.511, p = 0.03) and the mode of combined intervention (SMD = 0.69, 95% CI 0.35–1.03, p < 0.0001; vs. SMD = 0.65, 95% CI 0.03–1.27, p = 0.04) had an effect on the efficacy of the combined intervention in improving cognition. However, we were unable to draw a precise conclusion about whether intervention frequency affected the efficacy of the combined intervention because there was only one study with an intervention frequency more than 3 days per week.

TABLE 3
www.frontiersin.org

Table 3. Effects of moderators on the efficacy of combined intervention to improve cognition in older adults with MCI after sensitive analysis.

Discussion

Summary of findings

Global cognition

The results of our analysis showed that the combined intervention group was superior to the control group in improving global cognition in older adults with and without MCI, which is consistent with the results of other studies (Karssemeijer et al., 2017; Gavelin et al., 2021). Dual or multi-tasking training of combined cognitive and physical intervention is the basis to improve global cognition and ADL, which can reduce neurophysiological changes in cognition by reducing bilateral prefrontal cortical oxygenation, increasing hippocampal volume, and increasing white matter integrity (Tait et al., 2017). However, due to the limited number of studies, we did not perform subgroup analyzes according to different comparison conditions in global cognition. Additionally, seven studies assessed global cognition by MMSE (Kounti et al., 2011; Hars et al., 2014; Lam et al., 2015; Nishiguchi et al., 2015; Delbroek et al., 2017; Park, 2017; Morita et al., 2018), but two of them (Lam et al., 2015; Morita et al., 2018) using modified MMSE, which may limit the credibility of the results, so the results should be interpreted carefully. This also emphasizes the necessity on further evaluate the specific cognition domains to draw accurate conclusions.

Cognition domains

There is growing evidence that even the aging brain displays cognitive plasticity (Park and Bischof, 2013; Pauwels et al., 2018). Yang et al. (2020) reported that combined intervention improved most cognitive function in older adults with and without MCI, but had no effect on attention, and it was uncertain whether these positive effects would persist (Yang et al., 2020), which is consistent with our findings. Based on the theory of dual-task interference, the superior effect of the combined intervention may not be observed in the short term because of the cognitive and physical interaction. Therefore, the follow-up assessments are critical when studying the efficacy of the combined intervention to improve cognition in older adults in the future.

Depression

Based on the pathophysiological mechanisms of cognitive deficits and depression, we found an apparent correlation between them (Geda et al., 2006; Pellegrino et al., 2013), In older adults with MCI, patients with depression ranged from 20.1 to 44.3% (Panza et al., 2010). The statistical results of a study showed a positive correlation between the severity of depression and MCI, with depression significantly affecting delayed recall, verbal fluency, attention, and executive function in older adults (Dillon et al., 2009). Furthermore, depression as a risk factor for MCI has significant public health implications. Our results revealed that combined intervention had a small to moderate positive effect on depression, and other studies have reported that improvements in depression reduce the severity of MCI (Kessing et al., 2011; Pellegrino et al., 2013). A study by Barnes and Yaffe (2011) reported that a 10% reduction in depression prevalence could lead to 326,000 fewer AD cases worldwide.

Efficacy differences of combined intervention between cognitively healthy older adults and older adults with MCI

Our review reported that there was no statistical difference in the efficacy of the combined intervention for improving cognition in older adults with and without MCI, which is inconsistent with the findings of Wu et al. (2019), who suggested that the combined intervention was more effective in improving global cognition in older adults with MCI compared to cognitively healthy older adults (Wu et al., 2019). We used the same comparison and outcome assessment scales to assess efficacy differences, resulting in a limited number of studies included for this outcome; therefore, the results should be interpreted cautiously.

The maintenance and safety of combined intervention

Due to limited follow-up data, this meta-analysis only reported that the efficacy of the combined intervention in improving global cognition in older adults with MCI was not maintained (Park et al., 2019; Rojasavastera et al., 2020); however, another three studies found positive maintenance of the combined intervention (Barnes et al., 2013; Lee et al., 2016; Norouzi et al., 2019). In summary, we found heterogeneity primarily in two areas: the types of physical tasks within the combined intervention and the modes of the combined intervention. Regarding the types of physical task, resistance training (Norouzi et al., 2019), combined aerobic and resistance training (Barnes et al., 2013; Lee et al., 2016) improved the long-term working memory and global cognition within older adults with MCI; however, aerobic training alone was not found to have positive efficacy maintenance (Park et al., 2019; Rojasavastera et al., 2020). Thus far, combined aerobic and resistance training is the most commonly used and effective type of exercise (Kelly et al., 2014). Furthermore, the modes of combined intervention are divided into sequential (Park et al., 2019; Rojasavastera et al., 2020) and simultaneous interventions (Barnes et al., 2013; Norouzi et al., 2019). It was found that simultaneous intervention is superior to sequential intervention during efficacy maintenance, which may be based upon the mechanisms of physical-cognitive interaction. This result validates the intervention mode derived in our review as an influential factor in the efficacy of the combined intervention and is also consistent with the results of other meta-analyses (Zhu et al., 2016). However, it remains controversial whether the time of each sequential intervention is the same as that of simultaneous intervention (Joubert and Chainay, 2018).

Except for a slight risk of falls, none of the included studies reported significant adverse events during the combined intervention. Furthermore, due to the limited sample size, the safety and maintenance of the combined intervention will need to be validated via multicenter studies with larger sample sizes, and more follow-ups.

Moderators analysis for combined intervention

In terms of demographic characteristics, this review found that age and education level were influential factors in the efficacy of the combined intervention. Moreover, the combined intervention was more effective during advanced age as well as less educated older adults, which may be related to this population's lower baseline cognitive performance. Previous studies found a positive association between age and the efficacy of the combined intervention, while no correlation was reported in education (Powers et al., 2013; Toril et al., 2014; Qarni and Salardini, 2019).

Different intervention durations also affected the efficacy of the combined intervention. Law et al. (2014) found that an intervention duration of 3–6 months was more beneficial for improving cognition in older adults with MCI (Law et al., 2014), and is consistent with the results of our study. Suzuki et al. (2012) also reported that a 6-month combined intervention effectively improved cognition in older adults; however, the efficacy did not last until the end of the 12 month treatment regimen. Due to the limited number of included studies, we were unable to draw a precise conclusion about whether intervention frequency affected the efficacy of the combined intervention. However, a previous meta-analysis found that high-frequency combined intervention might be ineffective (Zhu et al., 2016). Two studies on working memory also reported that high-frequency intervention might lead to cognitive fatigue causing participants to drop out of the study (Penner et al., 2012; Wang et al., 2014). In conclusion, selecting the appropriate intervention frequency and duration is likely to be an essential factor in improving the efficacy of a combined intervention.

Limitations

This meta-analysis also has some limitations. First, the number of included studies was limited. Second, the outcome measurements did not use imaging, electroencephalogram (EEG), or other objective evaluation methods. The evidence suggests structural and functional magnetic resonance imaging or electrophysiological measurements of brain activity can more accurately evaluate the changes of specific areas in the brain (Bherer et al., 2013). Third, only English articles were included.

Implications for future studies

Two points need to be improved in the future. First, to maximize the effect of intervention, future studies need to stringently design the mode, frequency, and duration of the combined intervention, and a long-term follow-up. Second, we need to select more appropriate outcome measurement indexes, comprehensive neuropsychological assessments, and objective evaluation tools (e.g., imaging and EEG) to accurately assess the efficacy of the combined intervention.

Conclusion

In summary, this meta-analysis showed that combined cognitive and physical intervention effectively improves cognition in older adults with and without MCI compared with single cognitive or sham intervention, although the intervention effects vary by cognition domains. However, it is challenging to draw an obvious conclusion in the combined intervention maintenance because of the limitations. Additionally, there was no statistical difference in the efficacy of the combined intervention to improve cognition between cognitive healthy older adults and older adults with MCI. The results should be interpreted carefully due to the different intervention designs and the diversity of evaluation methods. In the future, more stringent study designs with more follow-ups are needed to clarify the effects of the combined intervention and provide guidance on the optimum intervention regime for improving cognitive function in older adults.

Data availability statement

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author/s.

Author contributions

KH contributed to study design, literature search, figures, data extraction, data analysis, and writing. ZT contributed to literature search, data extraction, and data analysis. ZB and WS contributed to figures, data extraction, data interpretation, and writing. HZ contributed to study design and data interpretation. All authors contributed to the article and approved the submitted version.

Funding

This work was supported by the National Key Research and Development Program of China (Grant No. 2018YFC2001703), Capital Health Research and Development of Special Fund (Grant No. 2020-1-6011), and China Rehabilitation Research Center Key Project (Grant No. 2021ZX-02).

Acknowledgments

We are grateful to those who offered any help in this article. The authors thank AiMi Academic Services (www.aimieditor.com) for the English language editing and review services.

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.

Publisher's note

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.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fnagi.2022.878025/full#supplementary-material

References

Albert, M. S., DeKosky, S. T., Dickson, D., Dubois, B., Feldman, H. H., Fox, N. C., et al. (2011). The diagnosis of mild cognitive impairment due to Alzheimer's disease: recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease. Alzheimers Dement. J. Alzheimers Assoc. 7, 270–279. doi: 10.1016/j.jalz.2011.03.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Anderson, N. D. (2020). State of the science on mild cognitive impairment. J. Gerontol. B. Psychol. Sci. Soc. Sci. 75, 1359–1360. doi: 10.1093/geronb/gbaa040

PubMed Abstract | CrossRef Full Text | Google Scholar

Barnes, D. E., Santos-Modesitt, W., Poelke, G., Kramer, A. F., Castro, C., Middleton, L. E., et al. (2013). The mental activity and exercise (MAX) trial: a randomized controlled trial to enhance cognitive function in older adults. JAMA Intern. Med. 173, 797–804. doi: 10.1001/jamainternmed.2013.189

PubMed Abstract | CrossRef Full Text | Google Scholar

Barnes, D. E., and Yaffe, K. (2011). The projected effect of risk factor reduction on Alzheimer's disease prevalence. Lancet Neurol. 10, 819–828. doi: 10.1016/S1474-4422(11)70072-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Bherer, L., Erickson, K. I., and Liu-Ambrose, T. (2013). A review of the effects of physical activity and exercise on cognitive and brain functions in older adults. J. Aging Res. 2013, 657508. doi: 10.1155/2013/657508

PubMed Abstract | CrossRef Full Text | Google Scholar

Briggs, R., Kennelly, S. P., and O'Neill, D. (2016). Drug treatments in Alzheimer's disease. Clin. Med. Lond. Engl. 16, 247–253. doi: 10.7861/clinmedicine.16-3-247

PubMed Abstract | CrossRef Full Text | Google Scholar

Cui, S., Chen, N., Yang, M., Guo, J., Zhou, M., Zhu, C., et al. (2019). Cerebrolysin for vascular dementia. Cochrane Database Syst. Rev. 2019, CD008900. doi: 10.1002/14651858.CD008900.pub3

PubMed Abstract | CrossRef Full Text | Google Scholar

Delbroek, T., Vermeylen, W., and Spildooren, J. (2017). The effect of cognitive-motor dual task training with the biorescue force platform on cognition, balance and dual task performance in institutionalized older adults: a randomized controlled trial. J. Phys. Ther. Sci. 29, 1137–1143. doi: 10.1589/jpts.29.1137

PubMed Abstract | CrossRef Full Text | Google Scholar

Dillon, C., Allegri, R. F., Serrano, C. M., Iturry, M., Salgado, P., Glaser, F. B., et al. (2009). Late- versus early-onset geriatric depression in a memory research center. Neuropsychiatr. Dis. Treat. 5, 517–526. doi: 10.2147/NDT.S7320

PubMed Abstract | CrossRef Full Text | Google Scholar

Donnezan, L., Perrot, A., Belleville, S., Bloch, F., and Kemoun, G. (2018). Effects of simultaneous aerobic and cognitive training on executive functions, cardiovascular fitness and functional abilities in older adults with mild cognitive impairment. Ment. Health Phys. Act. 15, 78–87. doi: 10.1016/j.mhpa.2018.06.001

CrossRef Full Text | Google Scholar

Fabre, C., Chamari, K., Mucci, P., Massé-Biron, J., and Préfaut, C. (2002). Improvement of cognitive function by mental and/or individualized aerobic training in healthy elderly subjects. Int. J. Sports Med. 23, 415–421. doi: 10.1055/s-2002-33735

PubMed Abstract | CrossRef Full Text | Google Scholar

Gallou-Guyot, M., Mandigout, S., Bherer, L., and Perrochon, A. (2020). Effects of exergames and cognitive-motor dual-task training on cognitive, physical and dual-task functions in cognitively healthy older adults: an overview. Ageing Res. Rev. 63, 101135. doi: 10.1016/j.arr.2020.101135

PubMed Abstract | CrossRef Full Text | Google Scholar

Gavelin, H. M., Dong, C., Minkov, R., Bahar-Fuchs, A., Ellis, K. A., Lautenschlager, N. T., et al. (2021). Combined physical and cognitive training for older adults with and without cognitive impairment: a systematic review and network meta-analysis of randomized controlled trials. Ageing Res. Rev. 66, 101232. doi: 10.1016/j.arr.2020.101232

PubMed Abstract | CrossRef Full Text | Google Scholar

Geda, Y. E., Knopman, D. S., Mrazek, D. A., Jicha, G. A., Smith, G. E., Negash, S., et al. (2006). Depression, apolipoprotein E genotype, and the incidence of mild cognitive impairment: a prospective cohort study. Arch. Neurol. 63, 435–440. doi: 10.1001/archneur.63.3.435

PubMed Abstract | CrossRef Full Text | Google Scholar

Gheysen, F., Poppe, L., DeSmet, A., Swinnen, S., Cardon, G., De Bourdeaudhuij, I., et al. (2018). Physical activity to improve cognition in older adults: can physical activity programs enriched with cognitive challenges enhance the effects? A systematic review and meta-analysis. Int. J. Behav. Nutr. Phys. Act. 15, 63. doi: 10.1186/s12966-018-0697-x

PubMed Abstract | CrossRef Full Text | Google Scholar

Greenwood, P. M., and Parasuraman, R. (2010). Neuronal and cognitive plasticity: a neurocognitive framework for ameliorating cognitive aging. Front. Aging Neurosci. 2, 150. doi: 10.3389/fnagi.2010.00150

PubMed Abstract | CrossRef Full Text | Google Scholar

Hars, M., Herrmann, F. R., Gold, G., Rizzoli, R., and Trombetti, A. (2014). Effect of music-based multitask training on cognition and mood in older adults. Age Ageing 43, 196–200. doi: 10.1093/ageing/aft163

PubMed Abstract | CrossRef Full Text | Google Scholar

Higgins, J. P. T., Altman, D. G., Gøtzsche, P. C., Jüni, P., Moher, D., Oxman, A. D., et al. (2011). The Cochrane Collaboration's tool for assessing risk of bias in randomised trials. BMJ 343, d5928. doi: 10.1136/bmj.d5928

PubMed Abstract | CrossRef Full Text | Google Scholar

Jack, C. R., Bennett, D. A., Blennow, K., Carrillo, M. C., Dunn, B., Haeberlein, S. B., et al. (2018). NIA-AA research framework: toward a biological definition of Alzheimer's disease. Alzheimers Dement. J. Alzheimers Assoc. 14, 535–562. doi: 10.1016/j.jalz.2018.02.018

PubMed Abstract | CrossRef Full Text | Google Scholar

Joubert, C., and Chainay, H. (2018). Aging brain: the effect of combined cognitive and physical training on cognition as compared to cognitive and physical training alone - a systematic review. Clin. Interv. Aging 13, 1267–1301. doi: 10.2147/CIA.S165399

PubMed Abstract | CrossRef Full Text | Google Scholar

Karssemeijer, E. G. A., Aaronson, J. A., Bossers, W. J., Smits, T., Olde Rikkert, M. G. M., and Kessels, R. P. C. (2017). Positive effects of combined cognitive and physical exercise training on cognitive function in older adults with mild cognitive impairment or dementia: a meta-analysis. Ageing Res. Rev. 40, 75–83. doi: 10.1016/j.arr.2017.09.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Kelly, M. E., Loughrey, D., Lawlor, B. A., Robertson, I. H., Walsh, C., and Brennan, S. (2014). The impact of exercise on the cognitive functioning of healthy older adults: a systematic review and meta-analysis. Ageing Res. Rev. 16, 12–31. doi: 10.1016/j.arr.2014.05.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Kessing, L. V., Forman, J. L., and Andersen, P. K. (2011). Do continued antidepressants protect against dementia in patients with severe depressive disorder? Int. Clin. Psychopharmacol. 26, 316–322. doi: 10.1097/YIC.0b013e32834ace0f

PubMed Abstract | CrossRef Full Text | Google Scholar

Kounti, F., Bakoglidou, E., Agogiatou, C., Lombardo, N. B. E., Serper, L. L., and Tsolaki, M. (2011). RHEA,* a nonpharmacological cognitive training intervention in patients with mild cognitive impairment: a pilot study. Top. Geriatr. Rehabil. 27, 289–300. doi: 10.1097/TGR.0b013e31821e59a9

CrossRef Full Text | Google Scholar

Lam, L. C.-W., Chan, W. C., Leung, T., Fung, A. W.-T., and Leung, E. M.-F. (2015). Would older adults with mild cognitive impairment adhere to and benefit from a structured lifestyle activity intervention to enhance cognition?: a cluster randomized controlled trial. PLoS ONE 10, e0118173. doi: 10.1371/journal.pone.0118173

PubMed Abstract | CrossRef Full Text | Google Scholar

Law, L. L. F., Barnett, F., Yau, M. K., and Gray, M. A. (2014). Effects of combined cognitive and exercise interventions on cognition in older adults with and without cognitive impairment: a systematic review. Ageing Res. Rev. 15, 61–75. doi: 10.1016/j.arr.2014.02.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Lee, Y.-Y., Wu, C.-Y., Teng, C.-H., Hsu, W.-C., Chang, K.-C., and Chen, P. (2016). Evolving methods to combine cognitive and physical training for individuals with mild cognitive impairment: study protocol for a randomized controlled study. Trials 17, 526. doi: 10.1186/s13063-016-1650-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, C. S., Herrmann, N., Song, B. X., Ba, J., Gallagher, D., Oh, P. I., et al. (2021). Exercise priming with transcranial direct current stimulation: a study protocol for a randomized, parallel-design, sham-controlled trial in mild cognitive impairment and Alzheimer's disease. BMC Geriatr. 21, 677. doi: 10.1186/s12877-021-02636-6

PubMed Abstract | CrossRef Full Text | Google Scholar

MacPherson, S. E. (2018). Definition: dual-tasking and multitasking. Cortex J. Devoted Study Nerv. Syst. Behav. 106, 313–314. doi: 10.1016/j.cortex.2018.06.009

PubMed Abstract | CrossRef Full Text | Google Scholar

Maher, C. G., Sherrington, C., Herbert, R. D., Moseley, A. M., and Elkins, M. (2003). Reliability of the PEDro scale for rating quality of randomized controlled trials. Phys. Ther. 83, 713–721. doi: 10.1093/ptj/83.8.713

PubMed Abstract | CrossRef Full Text | Google Scholar

Marioni, R. E., Proust-Lima, C., Amieva, H., Brayne, C., Matthews, F. E., Dartigues, J.-F., et al. (2015). Social activity, cognitive decline and dementia risk: a 20-year prospective cohort study. BMC Public Health 15, 1089. doi: 10.1186/s12889-015-2426-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Marlats, F., Bao, G., Chevallier, S., Boubaya, M., Djabelkhir-Jemmi, L., Wu, Y.-H., et al. (2020). SMR/theta neurofeedback training improves cognitive performance and eeg activity in elderly with mild cognitive impairment: a pilot study. Front. Aging Neurosci. 12, 147. doi: 10.3389/fnagi.2020.00147

PubMed Abstract | CrossRef Full Text | Google Scholar

Marmeleira, J. F., Godinho, M. B., and Fernandes, O. M. (2009). The effects of an exercise program on several abilities associated with driving performance in older adults. Accid. Anal. Prev. 41, 90–97. doi: 10.1016/j.aap.2008.09.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Moher, D., Liberati, A., Tetzlaff, J., and Altman, D. G., and PRISMA Group (2009). Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. BMJ 339, b2535. doi: 10.1136/bmj.b2535

PubMed Abstract | CrossRef Full Text | Google Scholar

Morita, E., Yokoyama, H., Imai, D., Takeda, R., Ota, A., Kawai, E., et al. (2018). Effects of 2-year cognitive-motor dual-task training on cognitive function and motor ability in healthy elderly people: a pilot study. Brain Sci. 8, E86. doi: 10.3390/brainsci8050086

PubMed Abstract | CrossRef Full Text | Google Scholar

Mrakic-Sposta, S., Di Santo, S. G., Franchini, F., Arlati, S., Zangiacomi, A., Greci, L., et al. (2018). Effects of combined physical and cognitive virtual reality-based training on cognitive impairment and oxidative stress in mci patients: a pilot study. Front. Aging Neurosci. 10, 282. doi: 10.3389/fnagi.2018.00282

PubMed Abstract | CrossRef Full Text | Google Scholar

Nishiguchi, S., Yamada, M., Tanigawa, T., Sekiyama, K., Kawagoe, T., Suzuki, M., et al. (2015). A 12-week physical and cognitive exercise program can improve cognitive function and neural efficiency in community-dwelling older adults: a randomized controlled trial. J. Am. Geriatr. Soc. 63, 1355–1363. doi: 10.1111/jgs.13481

PubMed Abstract | CrossRef Full Text | Google Scholar

Norouzi, E., Vaezmosavi, M., Gerber, M., Pühse, U., and Brand, S. (2019). Dual-task training on cognition and resistance training improved both balance and working memory in older people. Phys. Sportsmed. 47, 471–478. doi: 10.1080/00913847.2019.1623996

PubMed Abstract | CrossRef Full Text | Google Scholar

Overton, M., Pihlsgård, M., and Elmståhl, S. (2019). Prevalence and incidence of mild cognitive impairment across subtypes, age, and sex. Dement. Geriatr. Cogn. Disord. 47, 219–232. doi: 10.1159/000499763

PubMed Abstract | CrossRef Full Text | Google Scholar

Panza, F., Frisardi, V., Capurso, C., D'Introno, A., Colacicco, A. M., Imbimbo, B. P., et al. (2010). Late-life depression, mild cognitive impairment, and dementia: possible continuum? Am. J. Geriatr. Psychiatry 18, 98–116. doi: 10.1097/JGP.0b013e3181b0fa13

PubMed Abstract | CrossRef Full Text | Google Scholar

Park, D. C., and Bischof, G. N. (2013). The aging mind: neuroplasticity in response to cognitive training. Dialogues Clin. Neurosci. 15, 109–119. doi: 10.31887/DCNS.2013.15.1/dpark

PubMed Abstract | CrossRef Full Text | Google Scholar

Park, H., Park, J. H., Na, H. R., Hiroyuki, S., Kim, G. M., Jung, M. K., et al. (2019). Combined intervention of physical activity, aerobic exercise, and cognitive exercise intervention to prevent cognitive decline for patients with mild cognitive impairment: a randomized controlled clinical study. J. Clin. Med. 8, E940. doi: 10.3390/jcm8070940

PubMed Abstract | CrossRef Full Text | Google Scholar

Park, J. H. (2017). Does a cognitive-exercise combined dual-task training have better clinical outcomes for the elderly people with mild cognitive impairment than a single-task training? Ther. Sci. Rehabil. 6, 71–83. doi: 10.22683/tsnr.2017.6.2.071

CrossRef Full Text | Google Scholar

Park, J. S., Jung, Y.-J., and Lee, G. (2020). Virtual reality-based cognitive-motor rehabilitation in older adults with mild cognitive impairment: a randomized controlled study on motivation and cognitive function. Healthc. Basel Switz. 8, E335. doi: 10.3390/healthcare8030335

PubMed Abstract | CrossRef Full Text | Google Scholar

Pauwels, L., Chalavi, S., and Swinnen, S. P. (2018). Aging and brain plasticity. Aging 10, 1789–1790. doi: 10.18632/aging.101514

PubMed Abstract | CrossRef Full Text | Google Scholar

Pellegrino, L. D., Peters, M. E., Lyketsos, C. G., and Marano, C. M. (2013). Depression in cognitive impairment. Curr. Psychiatry Rep. 15, 384. doi: 10.1007/s11920-013-0384-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Penner, I.-K., Vogt, A., Stöcklin, M., Gschwind, L., Opwis, K., and Calabrese, P. (2012). Computerised working memory training in healthy adults: a comparison of two different training schedules. Neuropsychol. Rehabil. 22, 716–733. doi: 10.1080/09602011.2012.686883

PubMed Abstract | CrossRef Full Text | Google Scholar

Powers, K. L., Brooks, P. J., Aldrich, N. J., Palladino, M. A., and Alfieri, L. (2013). Effects of video-game play on information processing: a meta-analytic investigation. Psychon. Bull. Rev. 20, 1055–1079. doi: 10.3758/s13423-013-0418-z

PubMed Abstract | CrossRef Full Text | Google Scholar

Qarni, T., and Salardini, A. (2019). A multifactor approach to mild cognitive impairment. Semin. Neurol. 39, 179–187. doi: 10.1055/s-0039-1678585

PubMed Abstract | CrossRef Full Text | Google Scholar

Rahe, J., Becker, J., Fink, G. R., Kessler, J., Kukolja, J., Rahn, A., et al. (2015a). Cognitive training with and without additional physical activity in healthy older adults: cognitive effects, neurobiological mechanisms, and prediction of training success. Front. Aging Neurosci. 7, 187. doi: 10.3389/fnagi.2015.00187

PubMed Abstract | CrossRef Full Text | Google Scholar

Rahe, J., Petrelli, A., Kaesberg, S., Fink, G. R., Kessler, J., and Kalbe, E. (2015b). Effects of cognitive training with additional physical activity compared to pure cognitive training in healthy older adults. Clin. Interv. Aging 10, 297–310. doi: 10.2147/CIA.S74071

PubMed Abstract | CrossRef Full Text | Google Scholar

Rajji, T. K. (2019). Impaired brain plasticity as a potential therapeutic target for treatment and prevention of dementia. Expert Opin. Ther. Targets 23, 21–28. doi: 10.1080/14728222.2019.1550074

PubMed Abstract | CrossRef Full Text | Google Scholar

Rojasavastera, R., Bovonsunthonchai, S., Hiengkaew, V., and Senanarong, V. (2020). Action observation combined with gait training to improve gait and cognition in elderly with mild cognitive impairment A randomized controlled trial. Dement. Neuropsychol. 14, 118–127. doi: 10.1590/1980-57642020dn14-020004

PubMed Abstract | CrossRef Full Text | Google Scholar

Shatil, E. (2013). Does combined cognitive training and physical activity training enhance cognitive abilities more than either alone? A four-condition randomized controlled trial among healthy older adults. Front. Aging Neurosci. 5, 8. doi: 10.3389/fnagi.2013.00008

PubMed Abstract | CrossRef Full Text | Google Scholar

Stanmore, E., Stubbs, B., Vancampfort, D., de Bruin, E. D., and Firth, J. (2017). The effect of active video games on cognitive functioning in clinical and non-clinical populations: a meta-analysis of randomized controlled trials. Neurosci. Biobehav. Rev. 78, 34–43. doi: 10.1016/j.neubiorev.2017.04.011

PubMed Abstract | CrossRef Full Text | Google Scholar

Suzuki, T., Shimada, H., Makizako, H., Doi, T., Yoshida, D., Tsutsumimoto, K., et al. (2012). Effects of multicomponent exercise on cognitive function in older adults with amnestic mild cognitive impairment: a randomized controlled trial. BMC Neurol. 12, 128. doi: 10.1186/1471-2377-12-128

PubMed Abstract | CrossRef Full Text

Tait, J. L., Duckham, R. L., Milte, C. M., Main, L. C., and Daly, R. M. (2017). Influence of sequential vs. simultaneous dual-task exercise training on cognitive function in older adults. Front. Aging Neurosci. 9, 368. doi: 10.3389/fnagi.2017.00368

PubMed Abstract | CrossRef Full Text | Google Scholar

Toril, P., Reales, J. M., and Ballesteros, S. (2014). Video game training enhances cognition of older adults: a meta-analytic study. Psychol. Aging 29, 706–716. doi: 10.1037/a0037507

PubMed Abstract | CrossRef Full Text | Google Scholar

Vos, S. J. B., Verhey, F., Frölich, L., Kornhuber, J., Wiltfang, J., Maier, W., et al. (2015). Prevalence and prognosis of Alzheimer's disease at the mild cognitive impairment stage. Brain J. Neurol. 138, 1327–1338. doi: 10.1093/brain/awv029

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, Z., Zhou, R., and Shah, P. (2014). Spaced cognitive training promotes training transfer. Front. Hum. Neurosci. 8, 217. doi: 10.3389/fnhum.2014.00217

PubMed Abstract | CrossRef Full Text | Google Scholar

Wollesen, B., Voelcker-Rehage, C., Willer, J., Zech, A., and Mattes, K. (2015). Feasibility study of dual-task-managing training to improve gait performance of older adults. Aging Clin. Exp. Res. 27, 447–455. doi: 10.1007/s40520-014-0301-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Wu, C., Yi, Q., Zheng, X., Cui, S., Chen, B., Lu, L., et al. (2019). Effects of mind-body exercises on cognitive function in older adults: a meta-analysis. J. Am. Geriatr. Soc. 67, 749–758. doi: 10.1111/jgs.15714

PubMed Abstract | CrossRef Full Text | Google Scholar

Yang, C., Moore, A., Mpofu, E., Dorstyn, D., Li, Q., and Yin, C. (2020). Effectiveness of combined cognitive and physical interventions to enhance functioning in older adults with mild cognitive impairment: a systematic review of randomized controlled trials. Gerontologist 60, 633–642. doi: 10.1093/geront/gnz149

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhu, X., Yin, S., Lang, M., He, R., and Li, J. (2016). The more the better? A meta-analysis on effects of combined cognitive and physical intervention on cognition in healthy older adults. Ageing Res. Rev. 31, 67–79. doi: 10.1016/j.arr.2016.07.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: combined cognitive and physical intervention, cognition, older adults, mild cognitive impairment, systematic review, meta-analysis

Citation: Han K, Tang Z, Bai Z, Su W and Zhang H (2022) Effects of combined cognitive and physical intervention on enhancing cognition in older adults with and without mild cognitive impairment: A systematic review and meta-analysis. Front. Aging Neurosci. 14:878025. doi: 10.3389/fnagi.2022.878025

Received: 17 February 2022; Accepted: 28 June 2022;
Published: 19 July 2022.

Edited by:

Inga Liepelt-Scarfone, University of Tübingen, Germany

Reviewed by:

Walter Maetzler, University of Kiel, Germany
Carla Tatiana Toro, University of Warwick, United Kingdom
Ondrej Bezdicek, Charles University, Czechia

Copyright © 2022 Han, Tang, Bai, Su and Zhang. 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: Hao Zhang, crrczh2020@163.com

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.