- Research article
- Open Access
- Open Peer Review
Assessment of fall-related self-efficacy and activity avoidance in people with Parkinson's disease
BMC Geriatricsvolume 10, Article number: 78 (2010)
Fear of falling (FOF) is common in Parkinson's disease (PD), and it is considered a vital aspect of comprehensive balance assessment in PD. FOF can be conceptualized differently. The Falls-Efficacy Scale (FES) assesses fall-related self-efficacy, whereas the Survey of Activities and Fear of Falling in the Elderly (SAFFE) assesses activity avoidance due to the risk of falling. This study aimed at investigating the validity and reliability of FES and SAFFE in people with PD.
Seventy-nine people with PD (mean age; 64 years, SD 7.2) completed the Swedish version of FES(S), SAFFE and the physical functioning (PF) scale of the 36-Item Short-Form Health Survey (SF-36). FES(S) and SAFFE were administered twice, with an 8.8 (SD 2.3) days interval. Assumptions for summing item scores into total scores were examined and score reliability (Cronbach's alpha and test-retest reliability) were calculated. Construct validity was assessed by examining the pattern of Spearman correlations (rs) between the FES(S)/SAFFE and other variables, and by examining differences in FES(S)/SAFFE scores between fallers and non-fallers, genders, and between those reporting FOF and unsteadiness while turning.
For both scales, item mean scores (and standard deviations) were roughly similar and corrected item-total correlations exceeded 0.4. Reliabilities were ≥0.87. FES(S)-scores correlated strongest (rs, -0.74, p < 0.001) with SAFFE-scores, whereas SAFFE-scores correlated strongest with PF-scores (rs, -0.76, p < 0.001). Both scales correlated weakest with age (rs ≤ 0.08). Experiencing falls, unsteadiness while turning, and FOF was associated with lower fall-related self-efficacy and higher activity avoidance.
This study provides initial support for the score reliability and validity of the FES(S) and SAFFE in people with PD.
People with Parkinson's disease (PD) run an increased risk of falling, and most falls occur while walking or turning [1–5]. Some factors associated with an increased risk of falling are longer PD duration, limitations in activities of daily living (ADL) and more severe motor symptoms [2, 6–11]. Latt et al. identified abnormal posture, freezing of gait, frontal impairment, impaired balance and reduced knee extensor strength as independent risk factors for future falls . Age does not appear associated with an increased fall risk in people with PD [2, 6, 8, 10, 13].
Fear of falling (FOF) and decreased balance confidence is more common in people with PD than in healthy controls [14–16]. In a study investigating 119 people with PD, 59% of the participants reported having FOF . FOF is even more common and pronounced among fallers, and it can cause ADL restrictions and social isolation [8–11, 14, 17, 18]. After adjusting for prior falls and PD-specific impairments, FOF has been shown to be a significant predictor of future falls . It has therefore been recommended to include FOF when assessing balance performance in persons with PD [15, 20].
Conceptually, the construct of FOF has been described as an ongoing concern about falling, a loss of balance confidence, a low fall-related efficacy, or as activity avoidance [21–25]. These differences in conceptualization are also reflected in available assessment tools. For example, Tinetti et al. developed the Falls Efficacy Scale (FES) to assess "the degree of perceived efficacy at avoiding a fall during each of 10 relatively nonhazardous activities of daily living" . The Survey of Activities and Fear of Falling in the Elderly (SAFFE), on the other hand asks about activity avoidance due to the risk of falling [24, 25].
Although FOF is considered a vital aspect of comprehensive balance assessment in PD, the measurement properties of FES and SAFFE do not appear to have been investigated in PD. This is unfortunate since traditional indices of such properties (e.g. scaling assumptions, reliability and validity) are sample dependent.
A reliable score contains little measurement error and is reproducible. This can be assessed in various ways, of which Cronbachs alpha and test-retest reliability are the most common . Construct validity relates to the extent an instrument produces scores that are representative of the variable it is intended to represent. It includes convergent validity and divergent validity, which can be assessed by examining the pattern of correlations with other variables. In terms of FOF, scores exhibiting relatively strong associations with related aspects (e.g. physical functioning and mobility), but weaker associations with aspects less strongly associated with FOF (e.g. demographic variables) could thus be interpreted in support of convergent and divergent validity, respectively. Construct validity also includes whether scores distinguish between groups that are expected to differ in relation to the investigated construct , e.g. fallers and non-fallers.
The aim of this study was to investigate the measurement properties of the self-completed versions of the Swedish FES and SAFFE in people with PD.
Data were collected from two samples including 79 people with clinically diagnosed idiopathic PD  (Table 1). All participants were recruited from a Swedish university hospital, where the patients are regularly evaluated (clinical tests and questionnaires) as either in- or outpatients. Selection of participants was done by the treating neurologist or by a specialist nurse working within the same movement disorder team. Dementia was an exclusion criterion for both samples.
One sample consisted of 50 people with varying degrees of motor complications and/or gait disturbances, receiving out-patient care at two movement disorder neurologists' clinics during one year. Eight patients declined participation and five patients were unable to attend the study visit. The remaining 37 participants responded to the included questionnaires and they were also assessed clinically.
An additional sample consisted of 42 people, who had received and four who were on the waiting list for Deep Brain Stimulation (DBS) in the subthalamic nucleus. They were invited to participate in a postal survey. A total of 93 patients were eligible, but 47 were excluded for the following reasons: age >75 years, dementia, or previous inclusion in the first sample. Forty-six patients were invited to participate in the survey and 42 consented (Table 1).
Items in the FES(S) are framed "How confident are you that you can....without falling?" [22, 23]. The definition of self-efficacy is based on Banduras work, who defines perceived self-efficacy as a "judgment of one's capability to accomplish a certain level of performance" . FES(S) includes 13 activities rated from 0 (not confident at all) to 10 (completely confident), yielding a total score between 0 and 130 (higher scores = better balance confidence in performing the activities) . Compared to the original FES, the FES(S) thus contains three additional items (getting in and out of bed, grooming, and toileting) .
SAFFE focuses on undesirable consequences of FOF, i.e. activity restriction [24, 25]. The underlying assumption is that fear itself is harmless unless it leads to sedentary behavior or restriction of important activities . SAFFE includes 17 activities with three response options: never avoid, sometimes avoid, and always avoid (scored 1-3, respectively) . Thus, the possible score range is 17-51 and higher scores denote greater avoidance.
In addition, the Physical Functioning (PF) scale of the 36-Item Short-Form Health Survey (SF-36)  was used. PF comprises ten physical activity items with an emphasis on mobility. The score can range from 0 to100, and higher scores denote better physical functioning. Participants were also asked whether they had fallen during the past six months (No/Yes), if they were afraid of falling (No/Yes), and if they experienced unsteadiness while turning (No/Yes). When completing the questionnaires, the participants also rated their present mobility as either "good", "good but hyperkinetic" or "bad".
Demographic data was collected through self report (Table 1). Participants then completed the FES(S), SAFFE and PF. When completing FES(S) and SAFFE, they were instructed to make a general estimation when rating.
The participants in the outpatient sample were also assessed clinically. Assessments were scheduled at a time point when they typically felt at their best. Following completion of self-reported questionnaires at time 1, they were assessed with gait tests and the Unified PD Rating Scale (UPDRS). Timed gait tests included the 10 meter walk test (gait speed, m/s) and the Timed Up & Go (TUG) . The ten meter walk test was performed both in comfortable and fast gait speed (starting order randomized). A practice trial was followed by a test trial. TUG was only performed in comfortable gait speed. One practice trial was followed by two test trials (best value analyzed). Assessments also included parts II (Activities of daily living, ADL) and III (motor examination) of the UPDRS . After completing the assessments, participants in the outpatient clinic sample were given an envelope with a second set of the FES(S) and SAFFE to be completed a week later, during a period of good mobility. Each envelope was marked with the applicable date.
Participants in the postal survey were mailed a questionnaire package including the same demographic questions as in the clinic sample, together with the FES(S), SAFFE and PF. A second questionnaire package was sent out three days after their first responses had been received.
The study was approved by the by the Advisory Committee for Research Ethics in Health Education (Lund), and all participants gave their written informed consent.
First, we explored if the assumptions for summing item scores into total FES(S) and SAFFE scores were met . That is, whether item mean scores and standard deviations were roughly similar and if the corrected item-total correlations exceeded 0.3. Whether the items appear to represent a common variable was considered supported if corrected item-total correlations were ≥0.4 .
Internal consistency (analyzed by inter-item correlations) and Cronbach's alpha was calculated for scores at time 1 and time 2. Test-retest reliability was analyzed by the intraclass correlation (ICC) coefficient between scores obtained at time 1 and 2. ICC was calculated by using random effect two-way ANOVA with absolute agreement (ICC2.1) . Reliability values ≥0.8 are recommended . Any systematic change in mean scores between time 1 and time 2 was scrutinized by ANOVA. In addition, the standard error of measurement (SEM) was estimated using the formula SEM = SDbaseline × √(1 - ICC).
Floor- and ceiling effects were determined based on participants with computable total scores: The number of participants that score at maximum (or minimum)/the total number of participants, multiplied by 100 .
Construct validity of FES(S) and SAFFE was assessed by examining the pattern of Spearman correlations (rS) with other variables and differences between subgroups of people. The strongest correlation was anticipated to be between FES(S) and SAFFE since balance confidence, fall-related self-efficacy and activity avoidance all relate to FOF [21–25]. We further anticipated that FES(S) and SAFFE scores would correlate stronger with PF, timed gait tests, UPDRS parts II (ADL) and III (motor symptoms) than with PD-duration and age, of which the latter was anticipated to exhibit the weakest correlation. We expected that FES(S) and SAFFE scores would differ (Mann-Whitney U test) between fallers and non-fallers, genders, and between those reporting FOF and unsteadiness while turning (yes/no). Those affirming the question about previous falls, FOF or being unsteady were anticipated to have a higher degree of FOF than those responding no. In addition, women were anticipated to have a higher degree of FOF than men , i.e. higher SAFFE scores and lower FES(S) scores.
All analyses were performed using SPSS 15 (SPSS Inc., Chicago, IL). Two-tailed p-values <0.05 were considered statistically significant. Due to the exploratory nature of the study we did not correct for multiple testing.
Item and total scores at time 1 and time 2 are presented in Tables 2 and 3. At the first administration, one participant left the FES(S) blank. Mean (SD) FES(S) item scores ranged between 6.2-8.1 (2.6-3.3), and corrected item-total correlations ranged between 0.73-0.89 (Table 2). The average inter-item correlation at time 1 was 0.72 (min-max, 0.46-0.93) and at time 2 it was 0.84 (min-max, 0.69-0.95). Total FES(S) scores could be computed for 88% and 93% of the responding participants at times 1 and 2, respectively. The median (q1-q3) total scores at time 1 and time 2 were 99 (64-121) and 104 (60-126), respectively. Floor and ceiling effects were ≤10.6% at both occasions (Table 2).
At the first administration, three participants left SAFFE blank. Mean (SD) SAFFE item scores ranged between 1.3-2.0 (0.5-0.8), and corrected item-total correlations ranged between 0.60-0.83 (Table 3). The average inter-item correlation at time 1 was 0.55 (min-max, 0.27-0.82) and at time 2 it was 0.57 (min-max, 0.34-0.77). Total SAFFE scores could be computed for 93% and 90% of the responding participants at times 1 and 2, respectively. The median (q1-q3) total SAFFE scores at time 1 and time 2 were 24 (18-33) and 24 (18-30). The best possible SAFFE score was attained by 18% of the sample at time 1 and by 19% at time 2; none had the worst possible score (Table 3).
At time 1, 64 out of 79 (81%) participants considered their mobility as "good" or "good but hyperkinetic" when completing the questionnaires. Fourteen rated their mobility as bad. One had missing data.
Score reliabilities and SEM for FES(S) and SAFFE are presented in Table 4. Cronbach's alpha was ≥0.95 for both questionnaires. Seventy-six out of the 79 (96%) participants completed FES(S) and SAFFE twice. However, data from four participants were excluded from the test-retest analyses due to a long delay between times 1 and 2 (≥25 days). An additional participant was excluded due to having undergone DBS-surgery between administrations. For the remaining 71 participants, the mean number of days between test and retest was 8.8 (SD, 2.3). Test-retest reliability (ICC) was 0.87 for FES(S) and 0.92 for SAFFE. None of the scores differed between test occasions (FES(S): F, 0.093; P = 0.762, SAFFE: F, 0.686; P = 0.411). The SEM was 12.3 for the FES(S) and 2.4 for SAFFE.
FES(S) scores correlated strongest with SAFFE scores (rs, -0.74; p < 0.001). This was followed by significant (p < 0.001) correlations with PF (rs, 0.66), fast gait speed (rs, 0.63), TUG (rs, -0.61), UPDRS parts II (rs, -0.58) and III (rs, -0.46). Weaker correlations were found between FES(S) and comfortable gait speed (rs, 0.30), PD-duration (rs, -0.28) and age (rs, -0.07).
SAFFE scores correlated strongest with PF (rs, -0.76; p < 0.001), followed by significant (p ≤ 0.001) correlations with FES(S) (rs, -0.74), TUG (rs, 0.67), fast gait speed (rs, -0.64), comfortable gait speed (rs, -0.52), UPDRS parts II (rs, 0.52) and III (rs, 0.50). Weaker correlations were attained with PD-duration (rs, 0.28) and age (rs, 0.08).
Those reporting previous falls, FOF or unsteadiness had significantly (p ≤ 0.017) lower FES(S) scores and higher SAFFE scores than those not reporting these experiences (Table 5). Women scored lower on FES(S) and higher on SAFFE than men (Table 5).
Discussion and Conclusions
This study provides initial support for the scoring assumptions, validity and reliability of the FES(S) and SAFFE among people with PD. This has important clinical implications since FOF is an integral aspect of comprehensive balance assessment in PD.
Our observations provide support for the reliability of SAFFE and FES(S) scores when investigating FOF in people with PD, as alpha and ICC values of both exceeded the recommendations of 0.80 . Cronbach's alpha was ≥ 0.95, and it has been recommended to be at least 0.90 in a clinical application . High alpha values and inter-item correlations may also indicate a redundancy of items , suggesting that there may be room for item reduction of the scales, particularly in the FES(S). However, further studies in larger samples addressing this issue more specifically are needed before any firm recommendations can be made. Previous studies investigating the measurement properties of FES(S) and SAFFE have not specifically evaluated people with PD. Hellström and Lindmark investigated the reliability of FES(S) in patients with stroke  and found a test-retest reliability of 0.97 (ICC), which is higher than that found here. This may be due to differences in study designs. In the study by Hellstrom and Lindmark the FES(S) was interviewer administrated, whereas it was self-administered in this study. Test-retest reliability for SAFFE has been investigated in the elderly, but over a six month period, with a Spearman correlation coefficient of 0.75 . The time interval (6 months) between test and retest could thus explain the relatively low reliability in that study. This is a particularly relevant aspect since FOF may change over time and may be influenced by external events such as having experienced a fall or a near fall. People with PD have a high risk of falling  and about 60 to 75% experience near falls [4, 41].
Floor and ceiling effects were below or close to the recommendation of <15-20% [37, 42]. This suggests that both scales can be useful in detecting differences over time or between groups. However, measurement errors also need to be taken into consideration as differences in scores need to exceed the measurement error. Several indices have been introduced for the evaluation of measurement errors expressed in absolute values. In this study, we used the SEM which expresses the error of the hypothetical (unknown) "true score" based on the observed raw scores . Although not unchallenged, a number of studies have suggested that the SEM is a reasonable estimate of the minimal important difference . Our FES(S) results suggest that a meaningful change should exceed 12.3 points. The corresponding value for SAFFE was 2.4 points. In order to facilitate interpretation of change scores on an individual level, modern psychometric methods such as Rasch analysis could be used in future studies .
The corrected item-total correlations exceeded 0.4 for both FES(S) and SAFFE, which can be taken as support that items of the respective scale represent a common variable . This is an important aspect of validity but it does not tell us what the common variable is. Results from evaluations of construct validity may, however be helpful in this respect. In the present study, the hypothesized patterns of correlations and differences in FOF scores were empirically supported, which provides support for the validity of both FES(S) and SAFFE. However, they do not appear interchangeable. FES(S) correlated the strongest with SAFFE, whereas SAFFE correlated marginally stronger with PF. The correlation coefficient between FES(S) and SAFFE was -0.74. Accordingly, about 55% of the variance in scores on one scale can be explained by scores on the other. This illustrates that although fall-related self-efficacy and activity avoidance are related, they are not interchangeable constructs, and scale selection should be based on the objectives at hand.
FES(S) and SAFFE scores were more strongly correlated with PF-scores and clinical gait tests than to parkinsonian motor symptoms (UPDRS III). This is probably due to the fact that people with PD typically fall while walking [2, 3]. Walking has in fact been reported in connection with 54% of all falls in PD .
As expected, both FES(S) and SAFFE scores were able to distinguish between those with and without falls, FOF and unsteadiness while turning. Two thirds of those with severe PD experience instability while turning during an everyday task . Turning is furthermore associated with "freezing episodes" (i.e. motor blocks) , which are associated with falls [2, 7, 47]. FOF has previously been reported to be more common and pronounced in people with PD who fall than in non-fallers [8–10, 17, 18]. Both the FES(S) and SAFFE-scores were able to distinguish between those who reported FOF as well as previous falls. That is, fallers and those reporting FOF had lower fall-related self-efficacy and avoided activities more often due to the risk of falling. Activity avoidance in itself can result in sedentary behaviour which implies the importance of including this construct when evaluating people with PD. Although Koller et al. described that people with PD who fall confined their ambulation , this was not evaluated in a systematic way. Bloem et al. described that a restriction of activities due to FOF was more common among people with PD than in controls, but they did not use a standardized questionnaire incorporating a broad variety of activities . To our knowledge, this is the first time activity avoidance in relation to falls has been systematically evaluated in people with PD. The SAFFE items with the highest scores ("more avoidance") were items 8 (go out when it is slippery), 10 (go to a place with crowds), 13 (walk half a mile) and 15 (travel by public transportation). This suggests an impact not only on activity performance but also on participation. The present results furthermore show that people with PD who were unsteady, had experienced previous falls and/or reported a FOF avoided more activities due to the risk of falling. Taken together, these findings indicate the importance of taking this construct into consideration both when evaluating and treating people with PD.
There are some methodological concerns that can affect the external validity of the present findings. For example, demented patients were excluded, and participants had quite a long duration of PD. In addition, the survey sample consisted of selected patients and the clinical sample was not randomly selected. It is also conceivable that responses may be influenced by whether respondents with PD are "on" or "off" while completing questionnaires, which could not be controlled for here since data collection was conducted by postal surveys. However, the high test-retest coefficients argue against this being a major source of bias. Finally, it should be borne in mind that the data presented here was collected through self report and it is unknown whether responses are influenced by mode of administration. The equivalence between self completion and interviewer based administration of the FES(S) and SAFFE needs to be assessed in additional studies.
This study presents initial support for the validity and reliability of the scores of FES(S) and SAFFE in people with PD. Further studies are needed to support or refute the present findings as well as providing firmer evidence for the interpretation of change scores.
Pickering RM, Grimbergen YA, Rigney U, Ashburn A, Mazibrada G, Wood B, Gray P, Kerr G, Bloem BR: A meta-analysis of six prospective studies of falling in Parkinson's disease. Mov Disord. 2007, 22 (13): 1892-1900. 10.1002/mds.21598.
Gray P, Hildebrand K: Fall risk factors in Parkinson's disease. J Neurosci Nurs. 2000, 32 (4): 222-228. 10.1097/01376517-200008000-00006.
Ashburn A, Stack E, Ballinger C, Fazakarley L, Fitton C: The circumstances of falls among people with Parkinson's disease and the use of Falls Diaries to facilitate reporting. Disability and rehabilitation. 2008, 30 (16): 1205-1212. 10.1080/09638280701828930.
Stack E, Ashburn A: Fall events described by people with Parkinson's disease: implications for clinical interviewing and the research agenda. Physiotherapy research international. 1999, 4 (3): 190-200. 10.1002/pri.165.
Stack EL, Ashburn AM, Jupp KE: Strategies used by people with Parkinson's disease who report difficulty turning. Parkinsonism Relat Disord. 2006, 12 (2): 87-92. 10.1016/j.parkreldis.2005.08.008.
Wood BH, Bilclough JA, Bowron A, Walker RW: Incidence and prediction of falls in Parkinson's disease: a prospective multidisciplinary study. J Neurol Neurosurg Psychiatry. 2002, 72 (6): 721-725. 10.1136/jnnp.72.6.721.
Lim I, van Wegen E, Jones D, Rochester L, Nieuwboer A, Willems AM, Baker K, Hetherington V, Kwakkel G: Identifying fallers with Parkinson's disease using home-based tests: who is at risk?. Mov Disord. 2008, 23 (16): 2411-2415. 10.1002/mds.22209.
Matinolli M, Korpelainen JT, Korpelainen R, Sotaniemi KA, Matinolli VM, Myllyla VV: Mobility and balance in Parkinson's disease: a population-based study. Eur J Neurol. 2009, 16 (1): 105-111. 10.1111/j.1468-1331.2008.02358.x.
Landers MR, Backlund A, Davenport J, Fortune J, Schuerman S, Altenburger P: Postural instability in idiopathic Parkinson's disease: discriminating fallers from nonfallers based on standardized clinical measures. J Neurol Phys Ther. 2008, 32 (2): 56-61.
Robinson K, Dennison A, Roalf D, Noorigian J, Cianci H, Bunting-Perry L, Moberg P, Kleiner-Fisman G, Martine R, Duda J, et al: Falling risk factors in Parkinson's disease. NeuroRehabilitation. 2005, 20 (3): 169-182.
Koller WC, Glatt S, Vetere-Overfield B, Hassanein R: Falls and Parkinson's disease. Clinical neuropharmacology. 1989, 12 (2): 98-105. 10.1097/00002826-198904000-00009.
Latt MD, Lord SR, Morris JG, Fung VS: Clinical and physiological assessments for elucidating falls risk in Parkinson's disease. Mov Disord. 2009, 24 (9): 1280-1289. 10.1002/mds.22561.
Balash Y, Peretz C, Leibovich G, Herman T, Hausdorff JM, Giladi N: Falls in outpatients with Parkinson's disease: frequency, impact and identifying factors. J Neurol. 2005, 252 (11): 1310-1315. 10.1007/s00415-005-0855-3.
Bloem BR, Grimbergen YA, Cramer M, Willemsen M, Zwinderman AH: Prospective assessment of falls in Parkinson's disease. J Neurol. 2001, 248 (11): 950-958. 10.1007/s004150170047.
Adkin AL, Frank JS, Jog MS: Fear of falling and postural control in Parkinson's disease. Mov Disord. 2003, 18 (5): 496-502. 10.1002/mds.10396.
Mak MK, Pang MY: Balance self-efficacy determines walking capacity in people with Parkinson's disease. Mov Disord. 2008, 23 (13): 1936-1939. 10.1002/mds.22251.
Dennison AC, Noorigian JV, Robinson KM, Fisman DN, Cianci HJ, Moberg P, Bunting-Perry L, Martine R, Duda J, Stern MB: Falling in Parkinson disease: identifying and prioritizing risk factors in recurrent fallers. American journal of physical medicine & rehabilitation/Association of Academic Physiatrists. 2007, 86 (8): 621-632.
Mak MK, Pang MY: Balance confidence and functional mobility are independently associated with falls in people with Parkinson's disease. J Neurol. 2009, 256 (5): 742-749. 10.1007/s00415-009-5007-8.
Mak MK, Pang MY: Fear of falling is independently associated with recurrent falls in patients with Parkinson's disease: a 1-year prospective study. J Neurol. 2009, 256 (10): 1689-1695. 10.1007/s00415-009-5184-5.
Franchignoni F, Martignoni E, Ferriero G, Pasetti C: Balance and fear of falling in Parkinson's disease. Parkinsonism Relat Disord. 2005, 11 (7): 427-433. 10.1016/j.parkreldis.2005.05.005.
Powell LE, Myers AM: The Activities-specific Balance Confidence (ABC) Scale. J Gerontol A Biol Sci Med Sci. 1995, 50A (1): M28-34.
Tinetti ME, Richman D, Powell L: Falls efficacy as a measure of fear of falling. Journal of gerontology. 1990, 45 (6): P239-243.
Tinetti ME, Mendes de Leon CF, Doucette JT, Baker DI: Fear of falling and fall-related efficacy in relationship to functioning among community-living elders. Journal of gerontology. 1994, 49 (3): M140-147.
Lachman ME, Howland J, Tennstedt S, Jette A, Assmann S, Peterson EW: Fear of falling and activity restriction: the survey of activities and fear of falling in the elderly (SAFE). The journals of gerontology. 1998, 53 (1): P43-50.
Yardley L, Smith H: A prospective study of the relationship between feared consequences of falling and avoidance of activity in community-living older people. The Gerontologist. 2002, 42 (1): 17-23.
Hobart JC, Lamping DL, Thompson AJ: Evaluating neurological outcome measures: the bare essentials. J Neurol Neurosurg Psychiatry. 1996, 60 (2): 127-130. 10.1136/jnnp.60.2.127.
Streiner D, Norman G: Validity. Health measurement scales - a practical guide to their development and use. 2008, Oxford: Oxford University Press, 247-276. Fourth
Gibb WR, Lees AJ: The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease. J Neurol Neurosurg Psychiatry. 1988, 51 (6): 745-752. 10.1136/jnnp.51.6.745.
Hellstrom K, Lindmark B: Fear of falling in patients with stroke: a reliability study. Clinical rehabilitation. 1999, 13 (6): 509-517. 10.1191/026921599677784567.
Bandura A: Social foundations of thought and actions: a social cognitive theory. 1986, Englewoods Cliffs: NJ:Prentice Hall
Ware JE, Sherbourne CD: The MOS 36-item short-form health survey (SF-36). I. Conceptual framework and item selection. Medical care. 1992, 30 (6): 473-483. 10.1097/00005650-199206000-00002.
Morris S, Morris ME, Iansek R: Reliability of measurements obtained with the Timed "Up & Go" test in people with Parkinson disease. Phys Ther. 2001, 81 (2): 810-818.
Fahn S, Elton R, et al: Unified Parkinson's Disease Rating Scale. Recent developments in Parkinson's disease. Edited by: Fahn S, Marsden CD, Calne D, Goldstein M. 1987, Florham Park, N J:MacMillan Healthcare Information, 2: 153-163. 293-304
Ware JE, Harris WJ, Gandek B, et al: MAP-R for Windows: multitrait/multi-item analysis program-revised user's guide. 1997, Boston: Health Assessment Lab
Shrout PE, Fleiss JL: Intraclass correlations: uses in assessing rater reliability. Psychological bulletin. 1979, 86 (2): 420-428. 10.1037/0033-2909.86.2.420.
Nunnally JC, Bernstein IH: Psychometric theory. 1994, New York: McGraw-Hill, Third
McHorney CA, Tarlov AR: Individual-patient monitoring in clinical practice: are available health status surveys adequate?. Qual Life Res. 1995, 4 (4): 293-307. 10.1007/BF01593882.
Delbaere K, Crombez G, Vanderstraeten G, Willems T, Cambier D: Fear-related avoidance of activities, falls and physical frailty. A prospective community-based cohort study. Age and ageing. 2004, 33 (4): 368-373. 10.1093/ageing/afh106.
Bland JM, Altman DG: Cronbach's alpha. BMJ: British Medical Journal. 1997, 314 (7080): 572-572.
Boyle GJ: Does item homogeneity indicate internal consistency or item redundancy in psychometric scales?. Personality and Individual Differences. 1991, 12 (3): 291-294. 10.1016/0191-8869(91)90115-R.
Ashburn A, Stack E, Pickering RM: A community-dwelling sample of people with Parkinson's disease: characteristics of fallers and non-fallers. Age & Ageing. 2001, 30 (1): 47-53.
Holmes WC, Shea JA: Performance of a new, HIV/AIDS-targeted quality of life (HAT-QoL) instrument in asymptomatic seropositive individuals. Qual Life Res. 1997, 6 (6): 561-571. 10.1023/A:1018464200708.
Wyrwich KW, Bullinger M, Aaronson N, Hays RD, Patrick DL, Symonds T: Estimating clinically significant differences in quality of life outcomes. Qual Life Res. 2005, 14 (2): 285-295. 10.1007/s11136-004-0705-2.
Hobart JC, Cano SJ, Thompson AJ: Effect sizes can be misleading: is it time to change the way we measure change?. J Neurol Neurosurg Psychiatry. 2010, 81 (9): 1044-1048. 10.1136/jnnp.2009.201392.
Stack E, Jupp K, Ashburn A: Developing methods to evaluate how people with Parkinson's Disease turn 180 degrees: an activity frequently associated with falls. Disability and rehabilitation. 2004, 26 (8): 478-484. 10.1080/09638280410001663085.
Giladi N, McMahon D, Przedborski S, Flaster E, Guillory S, Kostic V, Fahn S: Motor blocks in Parkinson's disease. Neurology. 1992, 42 (2): 333-339.
Michalowska M, Fiszer U, Krygowska-Wajs A, Owczarek K: Falls in Parkinson's disease. Causes and impact on patients' quality of life. Functional neurology. 2005, 20 (4): 163-168.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2318/10/78/prepub
The authors wish to thank the participants for their cooperation; Jan Reimer, Stina Bladh, Martina Eliasson, Åsa Högstedt and Christine Toreld for assistance with data collection; and Klas Wictorin, Jan Reimer and Anna-Lena Törnqvist Jensen for assistance with patient selection. The study was supported by the Swedish Research Council, the Swedish Parkinson Academy, Skane County Council's Research and Development Foundation, and the Faculty of Medicine at Lund University, Lund, Sweden. This study was accomplished within the context of the Centre for Ageing and Supportive Environments (CASE), Lund University, Sweden, funded by the Swedish Council for Working Life and Social Research, and within the context of the Neuroscience Caring and Outcomes Research (NeuroCORE) group, Department of Health Sciences, Lund University, Sweden.
The authors declare that they have no competing interests.
MHN participated in conception and design, acquisition of data, analysis and interpretation of data and drafted the manuscript. A-MH participated in analysis and interpretation of data and in revising the manuscript. PH participated in conception and design, acquisition of data, interpretation of data and in revising the manuscript. All authors read and approved the final manuscript.