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Can cognitive enhancers reduce the risk of falls in older people with Mild Cognitive Impairment? A protocol for a randomised controlled double blind trial

BMC Neurology volume 9, Article number: 42 (2009) Cite this article

Abstract

Background

Older adults with cognitive problems have a higher risk of falls, at least twice that of cognitively normal older adults. The consequences of falls in this population are very serious: fallers with cognitive problems suffer more injuries due to falls and are approximately five times more likely to be admitted to institutional care. Although the mechanisms of increased fall risk in cognitively impaired people are not completely understood, it is known that impaired cognitive abilities can reduce attentional resource allocation while walking. Since cognitive enhancers, such as cholinesterase inhibitors, improve attention and executive function, we hypothesise that cognitive enhancers may reduce fall risk in elderly people in the early stages of cognitive decline by improving their gait and balance performance due to an enhancement in attention and executive function.

Method/Design

Double blinded randomized controlled trial with 6 months follow-up in 140 older individuals with Mild Cognitive Impairment (MCI). Participants will be randomized to the intervention group, receiving donepezil, and to the control group, receiving placebo. A block randomization by four and stratification based on fall history will be performed. Primary outcomes are improvements in gait velocity and reduction in gait variability. Secondary outcomes are changes in the balance confidence, balance sway, attention, executive function, and number of falls.

Discussion

By characterizing and understanding the effects of cognitive enhancers on fall risk in older adults with cognitive impairments, we will be able to pave the way for a new approach to fall prevention in this population. This RCT study will provide, for the first time, information regarding the effect of a medication designed to augment cognitive functioning have on the risk of falls in older adults with Mild Cognitive Impairment. We expect a significant reduction in the risk of falls in this vulnerable population as a function of the reduced gait variability achieved by treatment with cognitive enhancers. This study may contribute to a new approach to prevent and treat fall risk in seniors in early stages of dementia.

Trial Registration

The protocol for this study is registered with the Clinical Trials Registry, identifier number: NCT00934531 http://www.clinicaltrials.gov

Peer Review reports

Background

Cognitive Decline and Falls: A well-known couple

An important goal of geriatric medicine is to reduce the gap between life expectancy and disability-free life expectancy. A substantial portion of this gap is caused by two major geriatric syndromes: cognitive impairment and mobility limitation, which ultimately manifest as dementia and falls, respectively. Interestingly, these manifestations often coexist in elderly people: falling is a common geriatric syndrome affecting about a third of older adults each year, and dementia has a prevalence of 8% of Canadians aged 65 and 35% in people over age 85 [1–3]. This interrelationship has been attributed to specific brain networks selectively affected by diseases that accompany, but are not necessarily caused by, ageing [4].

Older adults with cognitive problems have a higher risk of falls, with annual incidence of around 60–80%; at least twice that of cognitively normal older adults [5]. The consequences of falls in this population are very serious; fallers with cognitive problems are approximately five times more likely to be admitted to institutional care than people with cognitive issues who do not fall [6]. They are also at high risk of major fall-related injuries such as fractures and head injuries leading to increased mortality. Falls are a major cause of disability and dependence in older people, and more so for those with cognitive problems. In addition to indirect costs and caregiver burden, the direct costs of emergency, acute, rehabilitation and long-term care are substantial and increasingly unsustainable for the health care system. Although the mechanisms of increased fall risk in cognitively impaired people are not completely understood, it is known that impaired cognitive abilities can reduce attentional resource allocation while walking [7]. As well, since executive function is an important cognitive resource for normal walking, impairments in this domain are also associated with both dementia and risk of falls [8].

One approach to mitigating fall risk in people with memory problems is to target them in the early stages of cognitive decline. Mild Cognitive Impairment (MCI) is a recognized clinical entity that is a transitional state between benign age-related cognitive change and early dementia. Specific diagnostic criteria have been developed and validated [9–13] to diagnose MCI, with the prevalence of the diagnosis being estimated at 19% among older adults, increasing to 29% in those over age 85 [14]. People with MCI have been found to have a 10 to 15 times higher risk of developing Alzheimer's disease (AD), as well as a higher risk of falling compared with age-matched controls [15, 16].

The role of cognition on gait: The dual-task paradigm and gait variability

Although walking has long been considered primarily as an automatic motor task, emerging evidence suggests that this view is overly simplistic [17]. Cognitive function may play a key role even in the regulation of routine walking, particularly in older adults. Attention is a necessary cognitive resource for maintaining normal walking and there is evidence that cognitive and attentional deficits are independently associated with postural instability, impairment in performing daily living activities, and future falls [8]. The role of cognition in walking is even more marked in people with cognitive dysfunction, whose gait performance is affected by any extra cognitive load. Since Lundin-Olsson and colleagues' seminal "stops walking while talking" study [18] demonstrated that the inability to maintain a conversation while walking is a marker for future falls in older adults, observing people walking while they perform a secondary task ("dual-task paradigm") has become the accepted way to assess the interaction between cognition, gait, and risk of falling. Previous research on the effect of dual-tasking on gait performance showed specific associations between slowing gait and executive dysfunction and attention deficits [15, 17, 19–25]. In a previous study, we assessed 60 elderly individuals with MCI and found that impairments in several cognitive domains (attention, executive function, and working memory) are associated with both a slow usual gait velocity and slower gait velocity under dual-task conditions, demonstrating that these specific cognitive domains are crucial for maintaining normal gait performance [26].

A sensitive measure of gait performance is gait variability, defined as the stride-to-stride variation in time [27]. This measure quantifies the automaticity of gait, with greater variability indicating less rhythmicity and a more unstable gait pattern. Evaluating gait variability is an accurate methodology to identify subtle changes in walking due to pathological conditions or disease. For instance, cognitively normal older adults have low gait variability; however, high gait variability has been described in Parkinson's disease, Alzheimer disease, and has been associated with high risk of future falls and mobility decline [28]. Additionally, previous studies have demonstrated that gait variability may serve as a clinically relevant parameter in the evaluation of mobility, and may be a responsive measure for different interventions in fall prevention [29].

There is a lack of effective strategies for preventing falls in older people with memory problems

Previous trials in cognitively normal older adults have demonstrated that both multifactorial (e.g. review of medications, strength and balance training, visual and hearing corrections, and environmental modifications) and some single interventions (resistance and balance exercises) are effective in preventing falls [30]. By contrast, most of the studies targeting falls in people with cognitive problems have been unable to prevent falls [31–33].

A recent systematic review and meta-analysis [31] concluded that the benefit of these single and multifactorial interventions does not translate from cognitively normal older adults to those with dementia. It is possible that different underlying mechanisms are at work in those with dementia; thus, a different approach may be necessary to target fall risk in this population. Although much is known about the multifactorial nature of falls in cognitively normal individuals, knowledge about the nature of falls in those with cognitive problems is limited and as a consequence, the number of falls and fall related injuries in this population continues to increase [33].

Pharmacological Treatment for Cognitive Problems

Cholinesterase inhibitors (ChEI), although modest in effect, are the most useful pharmacological treatment available for Alzheimer's Disease and vascular dementia [2, 34]. Although not curative, their effects include memory stabilization and delays in functional decline and nursing home placement [2].

The molecular mechanism of action of ChEI is through increased cortical and hippocampal acetylcholine, an important neurotransmitter for memory regulation and neural plasticity. However, the mechanism of the clinical improvements in delaying functional decline is not well understood. One possible explanation may relate to not only the cognitive action of the drug, but also to subtle improvements in the motor function of these patients. Whether by direct effect or mediated through cognition, motor function improvement would consequently serve to stabilize mobility and delay functional decline. In Figure 1, we propose possible levels of action of ChEI on motor function and gait.

Figure 1
figure 1

Regulation and Neural Control of Gait.

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Cholinesterase inhibitors have also been tried in individuals with MCI, with the goal of delaying the progression to dementia. A recent RCT demonstrated that cognitive enhancers might improve cognition in this population; however, the effect was weak and had questionable clinical significance [12]. Currently, there is no indication to use cognitive enhancers to treat people with MCI with the goal of delaying or preventing further functional or mobility decline.

Recently, it has been suggested that ChEI may improve gait performance [35] through an improvement in attentional resource allocation due to the fact that ChEI are known to improve attention and executive function [34]. Besides this effect on mobility through cognition, cholinergic neurotransmission has a potential effect on mobility and gait regulation not mediated through cognitive improvement since cholinergic neurons in the striatum are involved in movement and motor functions. For instance, dysfunction of cholinergic neurons in the striatum is known to occur in movement disorders (such as Huntington's chorea), and an imbalance between dopaminergic and cholinergic transmission is found in Parkinson's disease and related drug-induced dyskinesias [36]. These related findings lend both clinical and mechanistic plausibility to the hypothesis that cognitive enhancers may also have a potential effect on motor function and gait.

Effect of cognitive enhancers on motor function

Despite the well-recognized effect of cognitive enhancers on cognitive status, there is a shortage of studies investigating their effect on motor functioning, especially on walking, which will most likely have an impact on fall risk in this population. A recent pilot study has shown that fine motor skills as evaluated by hand movements improved with cognitive enhancer treatment [37]. This was an open label study in 12 patients with Alzheimer's Disease (AD) using the ChEI, donepezil, at 5 mg/day for 4 weeks then increased to 10 mg/day for 8 weeks. The investigators noted a trend toward improved (i.e. faster) finger tapping scores following donepezil treatment. Similarly, a case series showed that individuals with dementia taking galantamine (a cholinesterase inhibitor similar to donepezil) for 24 weeks had less decline in gait performance compared with age matched controls [35]. Nevertheless, there have been no studies to date evaluating the effect of ChEI on fall risk, balance confidence, and gait variability in elderly people with Mild Cognitive Impairment.

Pilot data and Rationale

As a proof of principle for this proposed RCT, we assessed the effect of donepezil, over four months of treatment, on gait using an electronic walkway (GAITRite System) in six individuals with AD [38]. An increase in gait velocity and a reduction in gait variability were seen following cognitive enhancer treatment. In brief, participants with AD taking donepezil increased their mean gait velocity (G-vel) after one month (from 89.7 ± 11 to 106.9 ± 22, p = .045) under a single-tasking condition. These increases were sustained and improved after four months, suggesting a dose-response pattern as shown in Figure 2. Gait variability (G-var), assessed as coefficient of variation of stride time, decreased during follow-up (single-task from 22.3 to 11.30, p = .04). Since it is known that gait performance declines over time in older people, we compared these results with observational data from eight comparison individuals with MCI and found that the MCI group experienced a reduction of gait velocity over time. (Figure 2)

Figure 2
figure 2

Changes in Gait Velocity in people with early Alzheimer's disease (AD) taking donepezil (intervention group) and Mild Cognitive Impairment (MCI; control group).

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Although the small sample size and the lack of randomization are limitations of this open label study, these preliminary findings provide preliminary data and rationale for pursuing the current clinical trial. We will assess whether donepezil treatment will improve gait performance under single and dual-task conditions in older individuals with MCI by comparing them with MCI controls receiving placebo. Additionally, we will test the effect of the intervention on two well-established clinical markers of fall risk such as balance sway and the balance confidence scale (ABC) [39], and also on the actual number of falls. All assessments will be completed over a 6-month follow-up period.

Currently, there is no clinical indication for prescribing cognitive enhancers in people with MCI, so there is genuine equipoise about the effect of cognitive enhancers on gait, balance, and risk of falls in this population.

Methods/Design

Design

Double blinded randomized controlled trial with 6 months follow-up in 140 older individuals with MCI. Participants will be randomized, in blocks of four, to the control and the intervention groups (Figure 3).

Figure 3
figure 3

Trial Design. Adapted from the CONSORT diagram [61, 62].

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Participant Selection

Our pilot study referenced above has given us preliminary research experience with this patient population. Participants will be recruited from the Aging Brain and Memory Clinic at Parkwood Hospital. The clinical investigators will enrol an average of five (5) participants per week, thereby recruiting the 140 participants over a period of 7 months. In order to maximize enrolment possibilities, the recruitment period will be extended to 10 months if the 140 participants are not reached at month 7.

Inclusion criteria

  • patients who have MCI (diagnosed using criteria suggested by Winblad et al [13])

  • Aged 65 years and older

  • Able to walk independently 10 meters without any gait aid (for example: walker, cane)

  • Able to travel to the clinic for the assessments

Exclusion criteria

  • Unable to understand English

  • History of psychiatric illness within the last two years, including depression

  • Parkinsonism or any neurological disorder with residual motor deficit (e.g. stroke, epilepsy)

  • Musculoskeletal disorder detected by clinical examination which affects gait performance

  • Active osteoarthritis affecting the lower limbs (America College of Rheumatology criteria [40–42])

  • Chronic Bradycardia (baseline heart rate below 60 beats/minute)

  • Use of psychotropic medication, which can affect motor performance (e.g. neuroleptics and benzodiazepines)

  • Depression (score above 8/15 on the Geriatric Depression Scale – GDS [43, 44]) since depression has been shown to reduce gait performance.

In order to increase generalizability of the results, the inclusion/exclusion criteria have been restricted to factors that can compromise study adherence and gait evaluation. The exclusions are to reduce the statistical noise introduced by specific diseases or disabilities that have strong known effects on gait. Exclusions will be based on a formal medical examination. The diagnosis of MCI is based on clinical criteria [15, 45], which includes the presence of subjective memory complaints from the patient and family, objective memory impairment, preserved general intellectual function assessed clinically, absence of significant functional impairment, and absence of clinical dementia as assessed by a skilled geriatrician with extensive experience in a memory clinic setting. Objective memory impairment is operationalized, following the criteria set out by Petersen and colleagues [11]; demonstrated by memory impairment judged as beyond the normal range for age and education by a skilled geriatrician. Additionally, global cognition will be assessed using the Mini Mental State Examination (MMSE; scored 0–30), and the Montreal Cognitive Assessment (MoCA; scored 0–30, with higher scores indicating better performance). The MoCA test is a validated tool used to assess global cognition and was originally created to assist in the diagnosis of MCI [46]. In brief, when considering MMSE and MoCA performance in the same individual, a pattern of low MoCA score (<26) with normal MMSE score (>26) is associated with the diagnosis of MCI [46].

The Health Sciences Research Ethics Board at The University of Western Ontario approved the research protocol – Research Protocol Number 16086. This RCT has been registered in clinical trials.gov (identifier number: NCT00934531)

Measurements and Procedures

All participants will undergo a baseline, one month, and a final six-month assessment. Baseline gait assessment will occur within one week prior to starting donepezil (T0), with a second assessment occurring after 4 weeks of treatment at 5 mg of medication (T1). The third and final assessment will occur after participants have been on the full dose of donepezil, 10 mg, for a period of 5 months (T2), yielding a total period of follow-up of 6 months from baseline. Assessments at each of these time-points will include gait analysis, balance sway, and balance confidence as well as cognitive measurement of attention and executive function. Falls will be retrieved by phone interview as has been done in previous studies [47, 48]. A timeline for the proposed study can be found in Figure 4.

Figure 4
figure 4

Schematic timeline of the proposed RCT.

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Hypothesis and Objectives

  • Hypothesis 1: Cognitive enhancers reduce fall risk in elderly people with MCI by improving their gait performance.

  • Hypothesis 2: Cognitive enhancers improve balance and balance confidence in elderly people with MCI.

  • Mechanistic Hypothesis: The improvement on gait and balance measures is due to an enhancement in attention and executive function.

  • Objective 1: To assess the effect of donepezil on gait velocity and gait variability in elderly people with MCI using an electronic walkway (Gait Rite System, CIR Systems Inc.).

  • Objective 2: To evaluate the effect of donepezil on balance and in balance confidence in elderly people with MCI using a balance platform (Bertec Inc.) and the Activities-Specific Balance Confidence Scale (ABC).

  • Objective 3: To test if these potential improvements on gait and balance are mediated through an enhancement in attention and executive function.

Outcomes measures

Primary outcomes

  1. 1.

    Improvements in gait velocity (cm/second) at month six

  2. 2.

    Reduction in gait variability assessed as standard deviation (SD) and coefficient of variation (CoV) at month 6.

Secondary outcomes

Between-group improvement in:

  1. 1.

    Balance confidence as evaluated by the Activities-Specific Balance Confidence Scale (ABC)

  2. 2.

    Balance sway, maximum saggital displacement, using a force platform (Bertec Inc.)

  3. 3.

    Attention measured with the Digit Span Test

  4. 4.

    Executive function using the Trail Making Test, parts A and B

  5. 5.

    Reduction of number of falls: The total number of falls by month 6 (T2) and proportion of participants who fall are also secondary outcome measures to be evaluated.

Randomisation

Once informed consent has been obtained and the baseline assessment has been completed, participants will be allocated to one of the two arms at a ratio of 1:1. Stratified randomization within strata based on fall history (0 falls, 1+ fall in past 12 months) will be performed. A block randomization by four will be applied to ensure a cumulative balance of participants between arms. The randomization sequence of the participants will be generated by a computer program and allocation to groups will be done with sequentially numbered opaque sealed envelopes. A professional bio-statistician not involved in recruitment and assessment will perform the randomization

Follow-up

As shown in the timeline (Figure 4), participants will be followed for 6 months after their baseline measurements. Improvements in the primary outcomes of interest are expected after 4 months of treatment based on our pilot study and on a previous report of the potential effect of cognitive enhancers on gait and mobility. However, a six-month follow-up will increase the probability of finding a significant reduction of the number of falls and the adverse events because of the intervention. The three assessments will be conducted by trained research assistants and all the questionnaires will be checked for missing data and completed with the participants under their supervision.

Evaluations

Inclusion/exclusion criteria will be verified through a standardized neurological and musculoskeletal examination by the principal investigator.

Instrumentation

Gait performance will be assessed using an electronic walkway system (GAITRite®) under single and dual-task conditions. The GAITRite® system includes a portable electronic walkway mat (600 cm in length and 64 cm in width) for the automated measurement of spatiotemporal gait parameters. As participants walk along the mat, imbedded sensors are activated by the pressure of their feet and deactivated when the pressure is released. A computer processes the footsteps, providing data for both spatial and temporal parameters. Gait parameters are recorded using only the footprint of the participants, thereby eliminating the need for external sensors attached to the body or lower limbs that may interfere with gait performance or may confuse an older individual with a cognitive impairment. The mat is located in a well-lit, 10-meter long hallway at the Division of Geriatric Medicine at Parkwood Hospital. Start and end points will be marked on the floor with tape one meter from either end of the mat to avoid recording acceleration and deceleration phases.

Gait Assessments

Participants will be given standardized instructions and a visual demonstration of the different gait task. Participants will then be asked to perform three single-task trials and three dual-task trials. The single task trials consist of walking the length of the mat at a self-selected pace. For the dual-task trials, participants will be asked to walk while counting aloud backward from one hundred by ones. This dual-task condition is selected based on previous research which demonstrated that counting backwards requires both working memory and attention [49]. Participants will be instructed to pay attention to both gait and the cognitive task; if a participant stops either task during the trial they will be prompted to continue. Allowing both gait and cognitive task to vary has previously been shown to provide a better representation of what happens naturally [8, 50].

Balance Confidence Scale

Balance confidence will be evaluated using the Activities-Specific Balance Confidence Scale (ABC) [39]. Respondents self-rate their confidence about their balance while performing a series of daily tasks on this 16-item questionnaire. The described tasks range in difficulty from those of basic daily living (e.g. walking around the house, going up and down stairs), to more difficult tasks generally performed in the community (e.g. walking in crowded areas like shopping centres, using escalators). Respondents are asked to rate their confidence on a scale from 0% (no confidence) to 100% (complete confidence) based on the following cue question: "How confident are you that you will not lose your balance or become unsteady when you [list of items follows]." The scale's wide range of item difficulty makes it well suited to assessing balance as a construct in populations with varying levels of functioning, including high-functioning community living seniors. This scale has been validated in previous studies as a marker of risk of falling [39, 51].

Balance Sway Test

Balance will be quantified as body sway using a Digital Balance Platform available in our service (Bertec Inc.). Displacements of the body in frontal and saggital direction will be recorded in millimetres. Peak-to-peak amplitude (maximum displacement of center of pressure, CoP) in the saggital and frontal direction will be calculated. Sway area will be calculated by multiplying the maximal frontal diameter with maximal saggital diameter following the method validated by Lord and colleagues [52]. Testing will be performed with subjects standing directly on the balance plate and standing on a foam rubber mat placed on the balance plate, with both measures being repeated with the participants having their eyes open and closed.

Falls

A fall is defined as 'an unintentionally coming to rest on the ground, floor, or other lower level and not due to a seizure or an acute stroke [63]. Recurrent falls are defined as two or more events in a six-month period during the trial. An absolute reduction of 10 points in the rate of falls is expected in intervention group after six months of follow-up (20% in the control to 10% in the intervention). Because falls tend to be forgotten if no injuries are involved, a fall calendar enabling prospective assessment will be implemented [64]. At the baseline session, participants will receive a fall calendar and instructed in its use (i.e. they will be asked to record every day whether they have had a fall). Each monthly calendar page detaches along a perforation and becomes a postage-paid postcard addressed to the study office. Calendar pages each have a unique study ID number and no identifying information. If a calendar is not received by two weeks into the following month, or is missing or incomplete the research assistant will contact the participant by phone and together they will complete the page. Participants who indicate one or more fall will be contacted by study staff and interviewed about the circumstances and outcomes of the falls. These methods have been used locally in previous research [47, 48].

Data acquisition of the quantitative gait variables

GAITRite software Version 3.8 will be used to process the footstep data using an algorithm for light and short footsteps as older individuals with cognitive problems may be more likely to slow down or hesitate while dual-tasking. Participants will be instructed to wear comfortable clothes and shoes. Gait variability will be analyzed in terms of stride time variability, and reported as coefficient of variation [27]. Validity and reliability of the GAITRite system has been established in older adults with memory problems by ourselves [53] and other research groups [54–56].

Sample size determination

Sample size determination is based on our primary outcomes and using the values from the pilot data described above. We expect a 10% improvement in gait velocity (G-vel), measured in cm/s (effect size of 0.10 m/s, from 1.0 m/s to 1.10 m/s), and a reduction in gait variability (G-var) (stride time variability) of 10% as assessed by decreases in standard deviation and coefficient of variation. These expected changes are based on our preliminary data which showed that mean G-vel increased by 15% after one month of treatment and these changes were sustained and improved in the 4 months follow up [38]. In this study, we found that the mean stride time at usual gait was 1190 ± 266 milliseconds (ms), after one month of treatment was 1053 ± 178 ms, and after 4 month was 999 ± 112 ms. The absolute reduction of the mean group CoV was 11 points (from 22.4% to 11.3%). Therefore, it is reasonable to expect similar improvements in our proposed study with a larger sample. Thus, in order to detect a group reduction of variability of 10% with a type II error of 0.20, 69 participants in each arm will be needed for the final analysis; assuming a 5 percent drop-out rate (which was seen after 6 months in two previous studies testing medications on MCI), 75 per arm participants will need to be recruited. This sample will also allow the detection of a 10% difference in the mean scores of the ABC, which is considered clinically significant. While we will not have sufficient power for a definitive analysis of changes in fall rate or risk, we will be able to compare changes in the mean values of the primary outcomes with between-group differences in fall rate. This will add mechanistic evidence that changes in fall rate are due to changes in gait parameters, and will provide a point estimate needed for the sample size calculations for a future trial powered to detect a reduction in falls as a primary endpoint.

Statistical Analysis

Analyses will be performed according to an intention-to-treat principle. Baseline characteristics and gait parameters will be descriptively summarized using either means and standard deviations or frequencies and percentages, as appropriate. Comparisons of the changes in the mean balance confidence score will be assessed using t-test. The coefficient of variation [CoV = (SD/mean)*100] will be used to quantify gait variability. We will use linear regression to perform between-group comparisons using three data points (baseline, one month, six months) with baseline – 1 mo. corresponding to before treatment and 1 mo. – 6 mo. corresponding to treatment with donepezil. Linear regression models, both unadjusted and adjusted for age, sex, and history of falls, will be used for comparison of individual variables. Using the baseline value of an endpoint as a covariate is more powerful statistically than comparing the differences from baseline. The statistical significance of the results will be determined by Hochberg's variation of the Bonferroni procedure for multiple testing [65]. Two-sided p < 0.05 will be considered statistically significant. All calculations will be made using SPSS software package version 16.0 (SPSS Inc., Chicago, IL).

Anticipated problems and contingency plans

Recording falls

Since falls tend to be forgotten or underreported, a strict definition of falls and a fall calendar will be implemented as "unintentionally coming to rest on the ground or other lower level." Participants will be asked to record any falls on the calendar every day and mail the completed calendar to the study office at the end of each month. Research assistants will verify the accuracy of all positive responses by phone interview, and will contact participants if calendars are more than two weeks late being mailed in. This strategy has been proven to be very effective for fall recording by others and us [47, 57, 58].

Tolerance to the medication

Donepezil is judged to be fairly well tolerated in older people at the 10 mg/day standard dose regimen. We selected Donepezil for our study since, according to the last Cochrane Review on cholinesterase inhibitors [59], fewer patients suffer adverse events on Donepezil when compared with other cognitive enhancers such as Rivastigmine. The most common reported intolerance is due to gastrointestinal problems such as abdominal pain, anorexia, nausea, vomiting, diarrhoea, and rarely dizziness, headache, and insomnia, which were significantly more frequent in the ChEI than in placebo groups in the referenced meta-analysis. Participants who would develop gastrointestinal intolerance with Donepezil at 10 mg/day will have the dose reduced to 5 mg/day and switched to a bedtime regimen as per current clinical practice. Participants who have persistent intolerance, and anyone who experiences a major adverse reaction, will be withdrawn from the study and the events reported to the Research Ethics Board and to Health Canada.

Effect of Donepezil on balance

The last Cochrane review and meta-analysis [59, 60] on adverse events associated with cholinesterase inhibitors showed that adverse events such as gait disturbances, falls or balance problems are not significantly more frequent in the ChEI groups than in placebo. These findings were pooled evidence from six or more studies in the referenced meta-analysis. In our ongoing pilot project involving 16 participants with early dementia we have not found any participants who experienced adverse events related to balance, bradycardia, or hemodynamic changes. As per clinical practice, participants having bradycardia before randomization (baseline heart rate below 60 beats/minute) will be excluded of the study. Therefore, based on published evidence and our accumulating direct experience, we do not expect a significant negative effect of ChEI in balance and/or hemodynamic changes in our population.

Discussion

Elderly adults with cognitive problems are one of the most vulnerable sectors of our society with clear mental, social, and physical disadvantages. They are more likely to experience falls, and experience further mobility decline due to having fallen; therefore is an urgent need to identify evidence based interventions for reducing the risk of falls and related injuries in people with cognitive impairment. To date, no adequately- powered studies have investigated the effect of cognitive enhancers to reduce falls in people with MCI. As falls are one of the most common reasons for both hospital admissions and nursing home placements in older adults with cognitive difficulties, they contribute significantly to the overall health care burden for Canada.

This study is distinctive due to the fact the intervention will target cognition with the outcome to improve mobility, balance, gait performance, and risk of falls. If we can demonstrate the effect of cognitive enhancers on fall risk and gait performance, these results will reveal a previously unrecognized benefit of this pharmacological therapy, which could in turn serve to decrease this burden. We are a unique position to conduct this project based on our previous research program expertise with gait assessment as well as our record of research involving elderly people with MCI

By characterizing and understanding the effects of cognitive enhancers on fall risk in older adults with cognitive impairments, we will be able to pave the way for a new approach to fall prevention in this population. This RCT study will provide, for the first time, information regarding the effect of a medication designed to augment cognitive functioning have on the risk of falls in older adults with Mild Cognitive Impairment. We will expect a significant reduction in the risk of falls in this vulnerable population as a function of the reduced gait variability achieved by treatment with cognitive enhancers. In this vein, we would establish that medications that augment cognitive function could be a complementary therapeutic option for reducing fall risk in people with MCI. This may contribute to a new approach to prevent and treat fall risk in this population, which will lead to improving the autonomy and quality of life of seniors in early stage of dementia.

References

  1. Canadian Study of Health and Aging Working Group: Canadian study of health and aging: study methods and prevalence of dementia. CMAJ. 1994, 150: 899-913.

    Google Scholar 

  2. Third Canadian Consensus Conference on Diagnosis and Treatment of Dementia. [http://www.cccdtd.ca/pdfs/Final_Recommendations_CCCDTD_2007.pdf]

  3. Thomas VS, Darvesh S, MacKnight C, Rockwood K: Estimating the prevalence of dementia in elderly people: a comparison of the Canadian Study of Health and Aging and National Population Health Survey approaches. Int Psychogeriatr. 2001, 13 (Supp 1): 169-175. 10.1017/S1041610202008116.

    Article  PubMed  Google Scholar 

  4. Rosano C, Brach J, Longstreth WT, Newman AB: Quantitative measures of gait characteristics indicate prevalence of underlying subclinical structural brain abnormalities in high-functioning older adults. Neuroepidemiology. 2006, 26: 52-60. 10.1159/000089240.

    Article  PubMed  Google Scholar 

  5. Tinetti ME, Speechley M, Ginter SF: Risk factors for falls among elderly persons living in the community. N Engl J Med. 1988, 319: 1701-1707.

    Article  CAS  PubMed  Google Scholar 

  6. Morris JC, Rubin EH, Morris EJ, Mandel SA: Senile dementia of the Alzheimer's type: an important risk factor for serious falls. J Gerontol. 1987, 42: 412-417.

    Article  CAS  PubMed  Google Scholar 

  7. Woollacott M, Shumway-Cook A: Attention and the control of posture and gait: a review of an emerging area of research. Gait Posture. 2002, 16: 1-14. 10.1016/S0966-6362(01)00156-4.

    Article  PubMed  Google Scholar 

  8. Yogev-Seligmann G, Hausdorff JM, Giladi N: The role of executive function and attention in gait. Mov Disord. 2008, 23: 329-342. 10.1002/mds.21720.

    Article  PubMed  Google Scholar 

  9. Aggarwal NT, Wilson RS, Beck TL, Bienias JL, Bennett DA: Mild cognitive impairment in different functional domains and incident Alzheimer's disease. J Neurol Neurosurg Psychiatry. 2005, 76: 1479-1484. 10.1136/jnnp.2004.053561.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Burns A, Zaudig M: Mild cognitive impairment in older people. Lancet. 2002, 360: 1963-1965. 10.1016/S0140-6736(02)11920-9.

    Article  PubMed  Google Scholar 

  11. Petersen RC, Smith GE, Waring SC, Ivnik RJ, Tangalos EG, Kokmen E: Mild cognitive impairment: clinical characterization and outcome. Arch Neurol. 1999, 56: 303-308. 10.1001/archneur.56.3.303.

    Article  CAS  PubMed  Google Scholar 

  12. Petersen RC, Thomas RG, Grundman M, Bennett D, Doody R, Ferris S, Galasko D, Jin S, Kaye J, Levey A, et al: Vitamin E and donepezil for the treatment of mild cognitive impairment. N Engl J Med. 2005, 352: 2379-2388. 10.1056/NEJMoa050151.

    Article  CAS  PubMed  Google Scholar 

  13. Winblad B, Palmer K, Kivipelto M, Jelic V, Fratiglioni L, Wahlund LO, Nordberg A, Backman L, Albert M, Almkvist O, et al: Mild cognitive impairment – beyond controversies, towards a consensus: report of the International Working Group on Mild Cognitive Impairment. J Intern Med. 2004, 256: 240-246. 10.1111/j.1365-2796.2004.01380.x.

    Article  CAS  PubMed  Google Scholar 

  14. Lopez OL, Jagust WJ, DeKosky ST, Becker JT, Fitzpatrick A, Dulberg C, Breitner J, Lyketsos C, Jones B, Kawas C, et al: Prevalence and classification of mild cognitive impairment in the Cardiovascular Health Study Cognition Study: part 1. Arch Neurol. 2003, 60: 1385-1389. 10.1001/archneur.60.10.1385.

    Article  PubMed  Google Scholar 

  15. Petersen RC, Doody R, Kurz A, Mohs RC, Morris JC, Rabins PV, Ritchie K, Rossor M, Thal L, Winblad B: Current concepts in mild cognitive impairment. Arch Neurol. 2001, 58: 1985-1992. 10.1001/archneur.58.12.1985.

    Article  CAS  PubMed  Google Scholar 

  16. Liu-Ambrose TY, Ashe MC, Graf P, Beattie BL, Khan KM: Canadian study of health and aging: study methods and prevalence of dementia. Phys Ther. 2008, 88: 1482-1491.

    Article  PubMed  PubMed Central  Google Scholar 

  17. Hausdorff JM, Yogev G, Springer S, Simon ES, Giladi N: Walking is more like catching than tapping: gait in the elderly as a complex cognitive task. Exp Brain Res. 2005, 164: 541-548. 10.1007/s00221-005-2280-3.

    Article  PubMed  Google Scholar 

  18. Lundin-Olsson L, Nyberg L, Gustafson Y: "Stops walking when talking" as a predictor of falls in elderly people. Lancet. 1997, 349: 617-10.1016/S0140-6736(97)24009-2.

    Article  CAS  PubMed  Google Scholar 

  19. Beauchet O, Dubost V, Gonthier R, Kressig RW: Dual-task-related gait changes in transitionally frail older adults: the type of the walking-associated cognitive task matters. Gerontology. 2005, 51: 48-52. 10.1159/000081435.

    Article  PubMed  Google Scholar 

  20. Ble A, Volpato S, Zuliani G, Guralnik JM, Bandinelli S, Lauretani F, Bartali B, Maraldi C, Fellin R, Ferrucci L: Executive function correlates with walking speed in older persons: the InCHIANTI study. J Am Geriatr Soc. 2005, 53: 410-415. 10.1111/j.1532-5415.2005.53157.x.

    Article  PubMed  Google Scholar 

  21. Bootsma-van der Wiel A, Gussekloo J, de Craen AJ, van Exel E, Bloem BR, Westendorp RG: Walking and talking as predictors of falls in the general population: the Leiden 85-Plus Study. J Am Geriatr Soc. 2003, 51: 1466-1471. 10.1046/j.1532-5415.2003.51468.x.

    Article  PubMed  Google Scholar 

  22. Camicioli R, Howieson D, Lehman S, Kaye J: Talking while walking: the effect of a dual task in aging and Alzheimer's disease. Neurology. 1997, 48: 955-958.

    Article  CAS  PubMed  Google Scholar 

  23. Camicioli R, Bouchard T, Licis L: Dual-tasks and walking fast: Relationship to extra-pyramidal signs in advanced Alzheimer disease. J Neurol Sci. 2006, 248: 205-209. 10.1016/j.jns.2006.05.013.

    Article  PubMed  Google Scholar 

  24. Petersen RC: Mild cognitive impairment as a diagnostic entity. J Intern Med. 2004, 256: 183-194. 10.1111/j.1365-2796.2004.01388.x.

    Article  CAS  PubMed  Google Scholar 

  25. Ritchie K, Touchon J: Mild cognitive impairment: conceptual basis and current nosological status. Lancet. 2000, 355: 225-228. 10.1016/S0140-6736(99)06155-3.

    Article  CAS  PubMed  Google Scholar 

  26. Montero-Odasso M, Bergman H, Phillips NA, Wong C, Sourial N, Chertkow H: The effect of executive and memory dysfunction in gait performance in a cognitive impairment population. J Am Geriatric Soc. 2006, 54: S154-

    Article  Google Scholar 

  27. Hausdorff JM: Gait variability: methods, modeling and meaning. J Neuroeng Rehabil. 2005, 2: 19-10.1186/1743-0003-2-19.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Herman T, Giladi N, Gurevich T, Hausdorff JM: Gait instability and fractal dynamics of older adults with a "cautious" gait: why do certain older adults walk fearfully?. Gait Posture. 2005, 21: 178-185. 10.1016/j.gaitpost.2004.01.014.

    Article  CAS  PubMed  Google Scholar 

  29. Paleacu D, Shutzman A, Giladi N, Herman T, Simon ES, Hausdorff JM: Effects of pharmacological therapy on gait and cognitive function in depressed patients. Clin Neuropharmacol. 2007, 30: 63-71. 10.1097/01.wnf.0000240949.41691.95.

    Article  CAS  PubMed  Google Scholar 

  30. Guideline for the prevention of falls in older persons. American Geriatrics Society, British Geriatrics Society, and American Academy of Orthopaedic Surgeons Panel on Falls Prevention. J Am Geriatr Soc. 2001, 49: 664-672. 10.1046/j.1532-5415.2001.49115.x.

  31. Oliver D, Connelly JB, Victor CR, Shaw FE, Whitehead A, Genc Y, Vanoli A, Martin FC, Gosney MA: Strategies to prevent falls and fractures in hospitals and care homes and effect of cognitive impairment: systematic review and meta-analyses. BMJ. 2007, 334: 82-10.1136/bmj.39049.706493.55.

    Article  PubMed  Google Scholar 

  32. Shaw FE, Bond J, Richardson DA, Dawson P, Steen IN, McKeith IG, Kenny RA: Multifactorial intervention after a fall in older people with cognitive impairment and dementia presenting to the accident and emergency department: randomised controlled trial. BMJ. 2003, 326: 73-10.1136/bmj.326.7380.73.

    Article  PubMed  PubMed Central  Google Scholar 

  33. Shaw FE: Prevention of falls in older people with dementia. J Neural Transm. 2007, 114: 1259-1264. 10.1007/s00702-007-0741-5.

    Article  CAS  PubMed  Google Scholar 

  34. Seltzer B, Zolnouni P, Nunez M, Goldman R, Kumar D, Ieni J, Richardson S: Efficacy of donepezil in early-stage Alzheimer disease: a randomized placebo-controlled trial. Arch Neurol. 2004, 61: 1852-1856. 10.1001/archneur.61.12.1852.

    Article  PubMed  Google Scholar 

  35. Assal F, Allali G, Kressig RW, Herrmann FR, Beauchet O: Galantamine improves gait performance in patients with Alzheimer's disease. J Am Geriatr Soc. 2008, 56: 946-947. 10.1111/j.1532-5415.2008.01657.x.

    Article  PubMed  Google Scholar 

  36. Pahapill PA, Lozano AM: The pedunculopontine nucleus and Parkinson's disease. Brain. 2000, 123 (Pt 9): 1767-1783. 10.1093/brain/123.9.1767.

    Article  PubMed  Google Scholar 

  37. Bohnen N, Kaufer D, Hendrickson R, Ivanco L, Moore R, DeKosky S: Effects of donepezil on motor function in patients with Alzheimer disease. J Clin Psychopharmacol. 2004, 24: 354-356. 10.1097/01.jcp.0000126665.88905.6a.

    Article  PubMed  Google Scholar 

  38. Montero-Odasso M, Wells J, Borrie M: Can cognitive enhancers reduce the risk of falls in people with dementia? An open-label study with controls. J Am Geriatr Soc. 2009, 57: 359-360. 10.1111/j.1532-5415.2009.02085.x.

    Article  PubMed  Google Scholar 

  39. Powell LE, Myers AM: The Activities-specific Balance Confidence (ABC) Scale. J Gerontol A Biol Sci Med Sci. 1995, 50A: M28-M34.

    Article  CAS  PubMed  Google Scholar 

  40. Altman R, Alarcon G, Appelrouth D, Bloch D, Borenstein D, Brandt K, Brown C, Cooke TD, Daniel W, Feldman D, et al: The American College of Rheumatology criteria for the classification and reporting of osteoarthritis of the hip. Arthritis Rheum. 1991, 34: 505-514. 10.1002/art.1780340502.

    Article  CAS  PubMed  Google Scholar 

  41. Altman RD: Criteria for the classification of osteoarthritis of the knee and hip. Scand J Rheumatol Suppl. 1987, 65: 31-39. 10.3109/03009748709102175.

    Article  CAS  PubMed  Google Scholar 

  42. Altman RD, Block DA, Brandt KD, Cooke DV, Greenwald RA, Hochberg MC, Howell DS, Ike RW, Kaplan D, Koopman W, et al: Osteoarthritis: definitions and criteria. Ann Rheum Dis. 1990, 49: 201-10.1136/ard.49.3.201-a.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  43. Yesavage JA, Brink TL, Rose TL, Lum O, Huang V, Adey M, Leirer VO: Development and validation of a geriatric depression screening scale: a preliminary report. J Psychiatr Res. 1982, 17: 37-49. 10.1016/0022-3956(82)90033-4.

    Article  PubMed  Google Scholar 

  44. Yesavage JA: Geriatric Depression Scale. Psychopharmacol Bull. 1988, 24: 709-711.

    CAS  PubMed  Google Scholar 

  45. Chertkow H: Mild cognitive impairment. Curr Opin Neurol. 2002, 15: 401-407. 10.1097/00019052-200208000-00001.

    Article  PubMed  Google Scholar 

  46. Nasreddine ZS, Phillips NA, Bedirian V, Charbonneau S, Whitehead V, Collin I, Cummings JL, Chertkow H: The Montreal Cognitive Assessment, MoCA: a brief screening tool for mild cognitive impairment. J Am Geriatr Soc. 2005, 53: 695-699. 10.1111/j.1532-5415.2005.53221.x.

    Article  PubMed  Google Scholar 

  47. Muir SW, Berg K, Chesworth B, Speechley M: Use of the Berg Balance Scale for predicting multiple falls in community-dwelling elderly people: a prospective study. Phys Ther. 2008, 88: 449-459.

    Article  PubMed  Google Scholar 

  48. Speechley M, Belfry S, Borrie MJ, Jenkyn KB, Crilly R, Gill DP, McLean S, Stolee P, Vandervoort AA, Jones GR: Risk factors for falling among community-dwelling veterans and their caregivers. Can J Aging. 2005, 24: 261-274.

    Article  PubMed  Google Scholar 

  49. Hittmair-Delazer M, Semenza C, Denes G: Concepts and facts in calculation. Brain. 1994, 117 (Pt 4): 715-728. 10.1093/brain/117.4.715.

    Article  PubMed  Google Scholar 

  50. Verghese J, Kuslansky G, Holtzer R, Katz M, Xue X, Buschke H, Pahor M: Walking while talking: effect of task prioritization in the elderly. Arch Phys Med Rehabil. 2007, 88: 50-53. 10.1016/j.apmr.2006.10.007.

    Article  PubMed  PubMed Central  Google Scholar 

  51. Myers AM, Powell LE, Maki BE, Holliday PJ, Brawley LR, Sherk W: Psychological indicators of balance confidence: relationship to actual and perceived abilities. J Gerontol A Biol Sci Med Sci. 1996, 51: M37-M43.

    Article  CAS  PubMed  Google Scholar 

  52. Lord SR, Clark RD, Webster IW: Postural stability and associated physiological factors in a population of aged persons. J Gerontol. 1991, 46: M69-M76.

    Article  CAS  PubMed  Google Scholar 

  53. Montero-Odasso M, Casas A, Hansen K, Gutmanis I, Wells J, Borrie M: Test-Retest Reliability of Quantitative Gait Analysis in People with Mild Cognitive Impairment. Canadian Journal of Geriatric Medicine & Psychiatry. 2007, 10: 33-34.

    Google Scholar 

  54. Bilney B, Morris M, Webster K: Concurrent related validity of the GAITRite walkway system for quantification of the spatial and temporal parameters of gait. Gait Posture. 2003, 17: 68-74. 10.1016/S0966-6362(02)00053-X.

    Article  PubMed  Google Scholar 

  55. van Uden CJ, Besser MP: Test-retest reliability of temporal and spatial gait characteristics measured with an instrumented walkway system (GAITRite). BMC Musculoskelet Disord. 2004, 5: 13-10.1186/1471-2474-5-13.

    Article  PubMed  PubMed Central  Google Scholar 

  56. Youdas JW, Hollman JH, Aalbers MJ, Ahrenholz HN, Aten RA, Cremers JJ: Agreement between the GAITRite walkway system and a stopwatch-footfall count method for measurement of temporal and spatial gait parameters. Arch Phys Med Rehabil. 2006, 87: 1648-1652. 10.1016/j.apmr.2006.09.012.

    Article  PubMed  Google Scholar 

  57. Gill DP, Zou GY, Jones GR, Speechley M: Injurious falls are associated with lower household but higher recreational physical activities in community-dwelling older male veterans. Gerontology. 2008, 54: 106-115. 10.1159/000116113.

    Article  PubMed  Google Scholar 

  58. Gill DP, Jones GR, Zou GY, Speechley M: The Phone-FITT: a brief physical activity interview for older adults. J Aging Phys Act. 2008, 16: 292-315.

    PubMed  Google Scholar 

  59. Birks J: Cholinesterase inhibitors for Alzheimer's disease. Cochrane Database Syst Rev. 2006, CD005593-1

  60. Birks J, Harvey RJ: Donepezil for dementia due to Alzheimer's disease. Cochrane Database Syst Rev. 2006, CD001190-2

  61. Altman DG, Schulz KF, Moher D, Egger M, Davidoff F, Elbourne D, Gotzsche PC, Lang T: The revised CONSORT statement for reporting randomized trials: explanation and elaboration. Ann Intern Med. 2001, 134: 663-694.

    Article  CAS  PubMed  Google Scholar 

  62. Moher D, Schulz KF, Altman DG: The CONSORT statement: revised recommendations for improving the quality of reports of parallel-group randomised trials. Lancet. 2001, 357: 1191-1194. 10.1016/S0140-6736(00)04337-3.

    Article  CAS  PubMed  Google Scholar 

  63. Tinetti ME, Baker DI, McAvay G, Claus EB, Garrett P, Gottschalk M, et al: A multifactorial intervention to reduce the risk of falling among elderly people living in the community. N Engl J Med. 1994, 331: 821-827. 10.1056/NEJM199409293311301.

    Article  CAS  PubMed  Google Scholar 

  64. Ganz DA, Higashi T, Rubenstein LZ: Monitoring falls in cohort studies of community-dwelling older people: effect of the recall interval. J Am Geriatr Soc. 2005, 53: 2190-2194. 10.1111/j.1532-5415.2005.00509.x.

    Article  PubMed  Google Scholar 

  65. Hochberg Y, Sharper A: Bonferroni Procedure for Multiple Tests of Significance. Biometrika. 1988, 75: 800-8002. 10.1093/biomet/75.4.800.

    Article  Google Scholar 

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Acknowledgements

This study is funded by Physician's Services Incorporated Foundation of Ontario, Canada. Dr. Manuel Montero-Odasso is the first recipient of the Schulich Clinician Scientist Award (2009–2011). We are grateful for the detailed review of the protocol from Dr. Denise Goens, Clinical Research Office at University of Western Ontario. Our gratitude also goes to Kevin Hansen, MA, for his assistance with the manuscript.

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Authors and Affiliations

  1. Department of Medicine, Division of Geriatric Medicine, Parkwood Hospital, University of Western Ontario, London, ON, Canada

    Manuel Montero-Odasso, Jennie L Wells & Michael J Borrie

  2. Department of Epidemiology and Biostatistics, University of Western Ontario, London, ON, Canada

    Manuel Montero-Odasso & Mark Speechley

  3. Lawson Health Research Institute, London, ON, Canada

    Manuel Montero-Odasso, Jennie L Wells, Michael J Borrie & Mark Speechley

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  1. Manuel Montero-Odasso
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  2. Jennie L Wells
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Correspondence to Manuel Montero-Odasso.

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The authors declare that they have no competing interests.

Authors' contributions

MMO conceived the study, and drafted the original protocol. JLW, MJB, and MS participated in the design of this study protocol. All authors read and approved the final manuscript.

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Montero-Odasso, M., Wells, J.L., Borrie, M.J. et al. Can cognitive enhancers reduce the risk of falls in older people with Mild Cognitive Impairment? A protocol for a randomised controlled double blind trial. BMC Neurol 9, 42 (2009). https://doi.org/10.1186/1471-2377-9-42

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BMC Neurology

ISSN: 1471-2377

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