| Literature DB >> 35280288 |
Rachana Gangwani1,2, Amelia Cain1, Amy Collins1, Jessica M Cassidy1.
Abstract
The International Classification of Functioning, Disability and Health framework recognizes that an individual's functioning post-stroke reflects an interaction between their health condition and contextual factors encompassing personal and environmental factors. Personal factors significantly impact rehabilitation outcomes as they determine how an individual evaluates their situation and copes with their condition in daily life. A key personal factor is self-efficacy-an individual's belief in their capacity to achieve certain outcomes. Self-efficacy influences an individual's motivational state to execute behaviors necessary for achieving desired rehabilitation outcomes. Stroke rehabilitation practice and research now acknowledge self-efficacy and motivation as critical elements in post-stroke recovery, and increasing evidence highlights their contributions to motor (re)learning. Given the informative value of neuroimaging-based biomarkers in stroke, elucidating the neurological underpinnings of self-efficacy and motivation may optimize post-stroke recovery. In this review, we examine the role of self-efficacy and motivation in stroke rehabilitation and recovery, identify potential neural substrates underlying these factors from current neuroimaging literature, and discuss how leveraging these factors and their associated neural substrates has the potential to advance the field of stroke rehabilitation.Entities:
Keywords: biomarker; motivation; neuroimaging; neurorehabilitation; self-efficacy; stroke
Year: 2022 PMID: 35280288 PMCID: PMC8907401 DOI: 10.3389/fneur.2022.823202
Source DB: PubMed Journal: Front Neurol ISSN: 1664-2295 Impact factor: 4.003
Neural correlates of self-efficacy identified in healthy individuals.
|
|
|
|
|
|
|---|---|---|---|---|
| Farrer and Frith ( | 12 | 29 | fMRI | AIC, R IPL |
| Yomogida et al. ( | 28 | 18–24 | fMRI | SMA, L CB, R PPC, R EBA |
| Nahab et al. ( | 20 | 18–33 | fMRI | PPC, STS, DLPFC, pre-SMA, precuneus, insula, CB |
| Davis et al. ( | 79 | 65–75 | MRI | Total brain and gray matter volumes |
| Kang et al. ( | 19 | 22–35 | EEG | Alpha (8–12 Hz) band oscillations, anterior frontal area |
| Nakagawa et al. ( | 1,204 | 20.7 ± 1.8 | MRI | Lenticular nucleus |
| Hirao ( | 89 | 19.7 ± 0.6 | fNIRS | L PFC |
Age presented as range or mean ± standard deviation. N, Number of study participants; AIC, anterior insular cortex; CB, cerebellum; DLPFC, dorsolateral prefrontal cortex; EBA, extrastriate body area; EEG, electroencephalography; fMRI, functional magnetic resonance imaging; IPL, inferior parietal lobule; L, left; MRI, magnetic resonance imaging; fNIRS, functional near-infrared spectroscopy; PFC, prefrontal cortex; PPC, posterior parietal cortex; R, right; SMA, supplementary motor area; STS, superior temporal sulcus.
Neural correlates of motivation identified in healthy individuals.
|
|
|
|
|
|
|---|---|---|---|---|
| Schmidt et al. ( | 20 | 19–27 | fMRI | BG |
| Lee and Reeve ( | 161 | 19–24 | fMRI | AIC |
| Quirin et al. ( | 17 | 23.6 ± 3.2 | fMRI | L PFC |
| Radke et al. ( | 36 | 19–48 | fMRI | NA, MCC, precuneus |
| Myers et al. ( | 20 | 11.2 ± 2.1 | fMRI | Connectivity between striatum and medial PFC and dorsal/rostral ACC |
| Lee and Reeve ( | 22 | 22.9 ± 2.8 | fMRI | Connectivity between AIC and striatum |
| Kohli et al. ( | 100 | 20–46 | fMRI | Striatum, midbrain, sensorimotor and occipital cortices |
Age presented as range or mean ± standard deviation. N, Number of study participants; AIC, anterior insular cortex; ACC, anterior cingulate cortex; BG, basal ganglia; fMRI, functional magnetic resonance imaging; L, left; MCC, middle cingulate cortex; NA, nucleus accumbens; PFC, prefrontal cortex.