| Literature DB >> 17680369 |
Ilse A D A van Halteren-van Tilborg1, Erik J A Scherder, Wouter Hulstijn.
Abstract
Since elderly people suffering from dementia want to go on living independently for as long as possible, they need to be able to maintain familiar and learn new practical skills. Although explicit or declarative learning methods are mostly used to train new skills, it is hypothesized that implicit or procedural techniques may be more effective in this population. The present review discusses 23 experimental studies on implicit motor-skill learning in patients with Alzheimer's disease (AD). All studies found intact implicit motor-learning capacities. Subsequently, it is elaborated how these intact learning abilities can be exploited in the patients' rehabilitation with respect to the variables 'practice' and 'feedback.' Recommendations for future research are provided, and it is concluded that if training programs are adjusted to specific needs and abilities, older people with AD are well able to (re)learn practical motor skills, which may enhance their autonomy.Entities:
Mesh:
Year: 2007 PMID: 17680369 PMCID: PMC2039835 DOI: 10.1007/s11065-007-9030-1
Source DB: PubMed Journal: Neuropsychol Rev ISSN: 1040-7308 Impact factor: 7.444
Summary of results of experimental studies on motor-skill learning in Alzheimer’s disease
| Author | Year | Sample size and types | Task(s) | Amount of learninga | Results on learning capacity |
|---|---|---|---|---|---|
| Sabe, L., et al. | 1995 | 20 AD with co-morbid depression, 35 AD without co-morbid depression, 14 depressive, non-demented patients, 16 healthy controls | Maze test | AD: 19%Co: 22% | The AD patients showed significant deficits in declarative learning but only a minor (although statistically significantly) drop in procedural learning. The AD group with comorbid depression showed a similar learning pattern as the non-depressed AD group. |
| GroupxTrial: | |||||
| Starkstein, S.E., et al. | 1997 | 55 AD (13 with mild, 12 with severe and 30 without anosognosia) | Maze test | AD no: 48% | There was no group difference in declarative learning. As to procedural learning, the patients with severe anosognosia showed a significantly poorer performance whereas the patients with mild or no anosognosia showed no deficits. |
| AD mild: 39% | |||||
| AD severe: −16% | |||||
| – | |||||
| Taylor, R. | 1998 | 58 AD, 58 multi-infarct dementia | Maze test | – | When age and overall neuropsychological functioning were taken into account, Maze performance was better in the AD patients than in the patients with multi-infarct dementia |
| – | |||||
| Kuzis, G., et al. | 1999 | 15 AD, 15 PD, 10 PD and dementia, 24 healthy controls | Maze test | AD: 10% | The AD group showed deficits on all measures of explicit memory. There were no significant between-group differences in the measures of implicit memory between the AD, control, and PD groups. |
| Co: 39% | |||||
| – | |||||
| Heidel, W.C., et al. | 1988 | 10 AD, 10 HD, 4 amnestic 20 healthy controls | Rotor Pursui | AD: 147% | The AD patients showed preserved motor-skill learning while the patients with HD showed no motor learning. |
| Co: 115% | |||||
| GroupxTrial: n.s. | |||||
| Heindel, W.C. et al. | 1989 | 16 AD, 13 HD, 17 PD, 22 healthy controls | Rotor Pursuit | AD: 101% | The AD patients showed preserved motor-skill learning while the patients with HD showed impaired motor learning. |
| Co: 118% | |||||
| GroupxTrial: n.s. | |||||
| Beatty, W.W., et al. | 1995 | 4 AD, 1 corticbasal degeneration | Rotor Pursuit | – | The AD patients showed preserved motor skill learning |
| – | |||||
| Deweer, B., et al. | 1994 | 13 AD institutionalized, 10 healthy controls, 17 AD out patients, 9 healthy controls | Rotor Pursuit | AD in.:86% | Explicit memory was severely impaired in the AD patients but they showed normal procedural learning. |
| Co: 48% | |||||
| GroupxTrial: n.s. | |||||
| AD out: 161% | |||||
| Co: 139% | |||||
| GroupxTrial: n.s. | |||||
| Dick, M.B., et al. | 1995 | 12 AD, 12 healthy controls | Rotor Pursuit | AD: 47% | Performance significantly improved during the first 40 trials but additional practice provided no further beneficial effects. The AD patients showed minimal retention problems across four retention tests. |
| Co: 81% | |||||
| GroupxTrial: n.s. | |||||
| Libon, D.J., et al. | 1998 | 16 AD, 14 vascular dementia | Rotor Pursuit | AD: 60% | The AD patients obtained a lower score on a verbal-learning task-recognition index and high scores on the Rotor Pursuit. |
| – | |||||
| Jacobs, D.H., et al. | 1999 | 12 AD, 12 healthy controls | Rotor Pursuit | AD: 124% | The AD patients and the controls were able to learn the motor task. |
| Co: 106% | |||||
| GroupxTrial: | |||||
| Dick, M.B., et al. | 2001 | 18 AD, 18 healthy controls | Rotor Pursuit | AD: 27% | In normal-vision trials no differences in learning between the AD patients and the controls were found. |
| Co: 36% | |||||
| GroupxTrial: n.s. | |||||
| Dick, M.B., et al. | 2003 | 99 AD, 100 healthy controls | Rotor Pursuit | The AD patients and controls receiving constant practice outperformed those in the blocked and random conditions. The AD patients only benefited from constant practice. | |
| Poe, M.K. et al. | 1997 | 9 AD, 14 healthy controls | Puzzle Assembly | – | Even when the subjects had no explicit memory of practicing the task, they all demonstrated savings upon relearning. |
| GroupxTrial: n.s. | |||||
| Rouleau, I., et al. | 2002 | 12 AD, 12 healthy controls | Mirror Tracing | AD: 44% | Those AD patients that were able to perform the basic mirror-tracing task did not differ from the controls in level of performance, learning over trails, retention over a delay interval and generalization to other tasks |
| Co: 49% | |||||
| GroupxTrial: n.s. | |||||
| Knopman, D.S., et al. | 1987 | 35 AD, 13 healthy controls | SRTT | AD: 22% | The AD patients showed learning of the repeated sequence, although they responded more slowly. |
| Co: 38% | |||||
| GroupxTrial: n.s. | |||||
| Graftman, J., et al. | 1990 | 42 AD, 7 PSP, 44 healthy controls | SRTT | AD: 36% | The AD patients and controls showed motor-skill learning while the PSP patients did not. |
| – | |||||
| Knopman, D. | 1991 | 16 AD, 17 healthy controls | SRTT | AD: 37% | The AD patients showed learning of the sequence but they showed an inferior level of learning when the data were log-transformed. |
| Co: 33% | |||||
| Ferraro, F.R., et al. | 1993 | 27 very mild AD, 15 mild AD, 17 PD, 26 healthy controls | SRTT | AD mild: 11% | The very mildly AD patients showed preserved learning comparable with the controls. The mildly AD patients and PD patients showed less implicit learning. |
| AD very mild: | |||||
| 22% | |||||
| Co: 20% | |||||
| Willingham, D.B., et al. | 1997 | 20 AD, 20 healthy controls | SRTT, Incompatible SRTT, Pursuit Tracking (randomized and repetitive pattern) | SRTT: | The dementia ratings predicted the ability to perform tasks but not the ability to learn them. AD patients can have a performance deficit but they have no general deficit in motor-skill learning. |
| AD: 52% | |||||
| Co: 60% | |||||
| GroupXTrial: p > 0.2 | |||||
| Pursuit: | |||||
| AD: 12% | |||||
| Co: 17% | |||||
| GroupxTrial: p > 0.2 | |||||
| Hirono, N., et al. | 1997 | 36 AD, 19 healthy controls | Bi-manual coordinated Tracing task | AD: 37% | Skill learning in those AD patients that completed the tasks was as good as in the controls. |
| Co: 39% | |||||
| GroupxTrial: | |||||
| Dick, M.B., et al. | 1996 | 23 AD, 22 healthy controls | Tossing | The AD patients given constant practice were able to learn and retain the tossing task similarly well as the controls. The AD patients showed less improvement when practicing at various distances. | |
| Dick, M.B., et al. | 2006 | 58 AD, 58 healthy controls | Tossing | The AD patients showed significant improvements under constant practice only. None of the practice conditions facilitated intermediate transfer in the AD patients whereas constant practice did benefit them on tests assessing near transfer. |
AD= Alzheimer’s disease; HD= Huntington’s disease; PD= Parkinson’s disease; PSP= Progressive supranuclear palsy.
aexpressed as a percentage of the difference score between the last and first trial with respect to the score on the first trial. The GroupxTrial interaction for the AD and Co group is also reported when available.