- Research article
- Open Access
- Open Peer Review
Multidimensional structure of the Groningen Frailty Indicator in community-dwelling older people
© Bielderman et al.; licensee BioMed Central Ltd. 2013
- Received: 25 April 2013
- Accepted: 15 August 2013
- Published: 22 August 2013
Due to the rapidly increasing number of older people worldwide, the prevalence of frailty among older adults is expected to escalate in coming decades. It is crucial to recognize early onset symptoms to initiate specific preventive care. Therefore, early detection of frailty with appropriate screening instruments is needed. The aim of this study was to evaluate the underlying dimensionality of the Groningen Frailty Indicator (GFI), a widely used self-report screening instrument for identifying frail older adults. In addition, criterion validity of GFI subscales was examined and composition of GFI scores was evaluated.
A cross-sectional study design was used to evaluate the structural validity, internal consistency and criterion validity of the GFI questionnaire in older adults aged 65 years and older. All subjects completed the GFI questionnaire (n = 1508). To assess criterion validity, a smaller sample of 119 older adults completed additional questionnaires: De Jong Gierveld Loneliness Scale, Hospital Anxiety Depression Scale, RAND-36 physical functioning, and perceived general health item of the EuroQol-5D. Exploratory factor analysis and Mokken scale analysis were used to evaluate the structural validity of the GFI. A Venn diagram was constructed to show the composition of GFI subscale scores for frail subjects.
The factor structure of the GFI supported a three-dimensional structure of the scale. The subscales Daily Activities and Psychosocial Functioning showed good internal consistency, scalability, and criterion validity (Daily Activities: Cronbach’s α = 0.81, Hs = .84, r = −.62; Psychosocial Functioning: Cronbach’s α = 0.80, Hs = .35, r = −.48). The subscale Health Problems showed less strong internal consistency but acceptable scalability and criterion validity (Cronbach’s α = .57, Hs = .35, r = −.48). The present data suggest that 90% of the frail older adults experience problems in the Psychosocial Functioning domain.
The present findings support a three-dimensional factor structure of the GFI, suggesting that a multidimensional assessment of frailty with the GFI is possible. These GFI subscale scores produce a richer assessment of frailty than with a single overall sum GFI score, and likely their use will contribute to more directed and customized care for older adults.
- Older adults
Frailty is characterized by a decline in reserve capacity in different domains of functioning, resulting in a decline in mobility, unintended weight loss, an elevated risk of morbidity, an increase in depression and anxiety, institutionalization, and premature death [1, 2]. Due to the rapidly increasing number of older people worldwide, the prevalence of frailty among older adults is increasing and expected to escalate in coming decades [3, 4]. In order to prevent the detrimental consequences of frailty, like the loss of balance and the decrease in muscle strength and walking speed, it is crucial to recognize early onset symptoms and then initiate appropriate care and specific preventive interventions. A number of review studies have shown that several interventions may be beneficial for older adults in different stages of frailty [5–8].
Early detection of frailty in older adults is feasible with appropriate screening instruments. These screening instruments measure frailty in various ways . Some measurements are based on a clinical assessment by a geriatrician others use performance-based tests or self-report questionnaires. A number of frailty assessment instruments have emerged in the last decade [1, 9–23]. These instruments are designed to screen older adults in a valid and feasible way. The majority of these screening instruments include items on physical frailty characteristics like mobility and nutritional status. Only some instruments include items in multiple frailty domains, like the Frailty Index, the Groningen Frailty Indicator, the Tilburg Frailty Indicator and the Edmunton Frail Scale . Especially frailty instruments used for case finding and screening, evaluate frailty dichotomously: persons are considered as either frail or not frail, regardless of the multiple dimensions measured by the instrument .
One of these multidimensional screening instruments is the Groningen Frailty Indicator (GFI). The GFI is a widely used screening instrument for identifying frail older adults [22, 24]. The GFI consists of 15 self-report items and is a feasible way to assess frailty in both community-dwelling and institutionalized older people [25, 26]. Psychometric studies examining the overall internal consistency of the GFI show a range of Cronbach’s α values, from α = 0.68 to α = 0.73, indicating moderate internal consistency [25–27]. Besides feasibility and reliability, the construct and discriminant validity of the GFI were examined in previous research .
However, the GFI is being used as a one-dimensional scale based on an overall sum score of 15 items. A person is considered to be frail when the GFI sum score is 4 points or higher [26, 27]. The sum score is used as a homogeneous indicator of frailty, without reference to specific problems like sensorimotor functioning, cognitive functioning, mobility, or psychosocial functioning. Consequently, a variety of different frailty-related problems can lead to a sum score of 4 points. We believe that the GFI has the potential to provide more differentiated information about the salience of specific frailty-related problems, and thus direct a more adequately focused program for the care and support frail older adults need. For this reason, an assessment of the various dimensions of frailty is obviously needed.
The main objective of this study was to evaluate the underlying dimensionality of the GFI questionnaire for screening frailty in community-dwelling older persons. In addition, we examined the criterion validity of the GFI subscales. Furthermore, we evaluated the composition of GFI subscale scores for subjects identified as frail based on the currently used cutoff score of 4 points.
A cross-sectional study design was used to evaluate the structural validity and criterion validity of the GFI questionnaire in older adults aged 65 years and older. In this study, data of older adults living in a small city in a centrally located region of the Netherlands were used (N = 1508). In a smaller sample (N = 119), we examined the criterion validity of the GFI subscales.
Study sample and data collection
In 2008, 3083 older adults (65 years and older) were approached by their local health authorities to fill in the GFI questionnaire. Besides, a smaller sample of 200 older adults was approached by community centers to fill in the GFI and additional questionnaires. In total, 1508 persons completed the GFI and 119 persons completed the additional questionnaires. Under Dutch legislation, ethical approval was not required in this cross-sectional non-obtrusive observational study. All subjects gave their consent to participate in the study.
The GFI is a 15-item screening instrument used to determine the level of frailty . Eight items have two response categories (yes / no), six items have three response categories (yes / sometimes / no), and one item has a Likert response category (1–10). All items were dichotomized to calculate GFI sum scores. A higher GFI sum score indicates a greater level of frailty, with a maximum score of 15. The GFI is displayed in Additional file 1.
To examine criterion validity, we used four additional scales or subscales: De Jong Gierveld Loneliness Scale , Hospital Anxiety Depression Scale (HADS) , physical functioning subscale of the RAND-36 , and the perceived general health item of the EuroQol-5D .
De Jong Gierveld Loneliness scale
The 6-item De Jong Gierveld scale was used to measure loneliness . This 6-item Likert scale is a reliable and valid instrument for measuring overall, emotional, and social loneliness in large surveys of older adults (Cronbach’s α = 0.61-0.73) . All items have five response categories (no! / no / more or less / yes / yes!). After recoding, higher scores indicate greater levels of loneliness.
The Dutch version of the 14-item HADS was used to assess the presence of anxiety and depressive states independent of coexisting general medical conditions . The HADS consists of an anxiety subscale (7 items) and a depression subscale (7 items). In a general population aged 65 years and over, the reliability of both the anxiety and depression subscales as the total scale varied with Cronbach’s α values between 0.71 and 0.8 . Higher scores represent greater anxiety and/or more depressive symptoms.
Self-reported physical functioning was assessed using the 10-item physical functioning subscale of the Dutch RAND 36-item Health Survey (RAND-36). The RAND-36 is a reliable and valid scale for measuring different aspects of health in different age groups [30, 33]. The overall scale contains eight subscales: physical functioning, social functioning, role limitations caused by physical health problems, role limitations caused by emotional problems, mental health, vitality, bodily pain, and general health perceptions . The physical functioning subscale is a reliable and valid scale for measuring limitations in daily activities due to health problems (Cronbach’s α = 0.92) . The respondent reports to what extent he feels limited in a particular activity (limited a lot / limited a little / not limited at all). Raw scores are transformed into index scores ranging from 0 to 100. After transformation, lower scores on the physical functioning subscale indicate more limitations in activities of daily living.
Perceived general health was assessed on a Likert scale of 1 to 10, where 10 represents excellent general health. This item represents one item in the overall EuroQol-5D questionnaire .
Descriptive statistics were used to report subject characteristics of the study sample.
Structural validity is defined as the degree to which the scores are an adequate reflection of the dimensionality of the construct to be measured . Structural validity was assessed using exploratory factor analysis. Exploratory principal component analysis followed by oblique rotation according to the direct oblimin criterion was conducted to explore factor structure. The number of factors was based on the scree plot evaluation, the size of the eigenvalues, and their confidence intervals. All factors with eigenvalues greater than one were retained. In case an item did not discriminate well between factors, decisions were made based on the content of the item and the results of the reliability analysis of the subscales. Reliability of the factor solution was determined by calculating internal consistency using Cronbach’s α with corresponding 95% Confidence Intervals (CI). A Cronbach’s α coefficient of ≥0.80 was considered “good,” 0.70 – 0.80 “acceptable,” 0.60 – 0.70 “questionable,” 0.50 – 0.60 “poor,” and <0.50 “unacceptable” [35, 36].
In addition, scale analysis of the GFI was applied using Mokken item response theory model of monotone homogeneity . Mokken scale analysis tests the homogeneity of the subsets of items of test batteries that are multidimensional by construction . A Loevinger’s scalability coefficient (H) of 0.30 - 0.39 indicates a weak scale, H 0.40 - 0.49 indicates a moderate scale, and H ≥ 0.50 indicates a strong scale .
Criterion validity is defined as the degree to which the scores are an adequate reflection of a “gold standard” . To establish criterion validity of the observed GFI subscales, the GFI subscales were compared to related reliable and valid scales considered to be gold standards of the individual dimensions. Positive relations were hypothesized between GFI subscale Psychosocial Functioning and HADS and the Jong Gierveld Loneliness scale. Negative relations were hypothesized between GFI subscale Daily Activities and RAND-36 physical functioning scale, and between GFI subscale Health Problems and Perceived general health (EuroQol-5D). Pearson correlations (two-tailed) between GFI subscales and related scales were calculated. A correlation of <0.30 was considered “low,” 0.30 – 0.60 “moderate,” and > 0.60 “high” .
A Venn diagram was constructed to show the composition of GFI subscale scores for all subjects identified as frail based on the currently used cutoff score of 4 points. The diagram provides information about the composition of a score of 4 (or more) points. Only subjects that perceived problems in 25% of the items of each subscale are represented in the Venn diagram. Differences between the groups within the Venn diagram were tested by using the Chi2 test for categorical data and ANOVA test for continuous data.
For frail older adults, frequency distributions for different age groups were calculated and tested for dependencies by using the Chi2 test and estimation of a log-linear model. We used the factors indicating age (in categories) and perceived problems in the subscales Daily Activities, Psychosocial Functioning, and Health Problems (score on 25% of the subscale items). To increase power, we treated the latter variables as ordinals.
Data from subjects were excluded from further analyses when more than five items (30%) of the GFI were missing. In total, 17 persons were excluded from further analyses because of missing data on the GFI. In the analyzed sample, 1277 persons had no missing data at all, 194 persons had one missing value, 27 persons had two missing values, 4 persons had three missing values and 6 persons had four or five missing values on the GFI. These remaining missing values were imputed by the logistic regression data imputation method .
Data were processed using the statistical software SPSS statistics 19 (SPSS Inc., Chicago, IL, USA) and the R statistical programming system (R Development Core Team, 2011). Statistical significance level was set to p = 0.05.
Characteristics of the participants (n = 1508)
Overall sample (n = 1508)
Main sample (n = 1389)
Smaller sample (n = 119)
t (df) †or Chi2(df) ‡
Mean age (y) ± SD
74.5 ± 6.9
74.3 ± 6.8
77.1 ± 7.7
−3.94 (135.5) †
Age groups, n (%)
65 – 69 y
20.01 (4) ‡
70 – 74 y
75 – 79 y
80 – 84 y
≥ 85 y
Gender, n (%)
30.81 (2) ‡
Educational level, n (%)
5.47 (2) ‡
Living situation, n (%)
29.37 (1) ‡
GFI, mean ± SD
3.0 ± 3.0
2.9 ± 3.0
3.4 ± 2.7
−1.77 (1506) †
As can be seen in Table 1, the smaller sample differed from the main sample in mean age, gender, and living situation. Compared to the main sample, the smaller sample consisted of persons with a higher average age (77 vs 74 years), relatively more females (71% vs 47%) and more single living persons (65% vs 40%). Educational level and GFI total scores of the smaller sample did not differ significantly from the main sample.
Factor structure of the GFI
Factor loadings and eigenvalues from the principal component analysis of the GFI scale ( n = 1508)
2. Walking outdoors
3. Dressing and undressing
4. Going to the toilet
5. Physical fitness
6. Vision problems
7. Hearing problems
8. Unintentional weight loss
9. Use of more than three medicines
10. Memory complaints
11. Experience of emptiness
12. Missing people around
13. Feeling abandoned
14. Feeling sad/dejected
15. Feeling nervous/anxious
Initial eigenvalues (95% CI)
Cumulative variance (%)
The rotated factors did not clearly discriminate item 5 (“How do you rate your physical fitness?”). Based on content and reliability analysis, this item was assigned to factor 3 (subscale Health Problems). Cronbach’s alpha decreased (from .81 to .77) when item 5 was assigned to factor 1 (subscale Daily Activities), and increased (from .47 to .57) when item 5 was assigned to factor 3 (subscale Health Problems).
The GFI subscales Daily Activities and Psychosocial Functioning showed good internal consistency, with Cronbach’s α = 0.81 (95% CI = 0.79-0.83) and Cronbach’s α = 0.80 (95% CI = 0.78-0.82), respectively. By contrast, the subscale Health Problems showed a poor internal consistency (Cronbach’s α = 0.57; 95% CI = 0.54-0.61). In all subscales, Cronbach’s α decreased when any of the items were deleted.
Scale analysis of GFI subscales
Scaling coefficients from Mokken scale analyses for items of the GFI subscales ( n = 1508)*
Daily activities (item 1–4)
Health problems (item 5–10)
Psychosocial functioning (item 11–15)
H i (95% CI)
H i (95% CI)
H i (95% CI)
Criterion validity of GFI subscales
Pearson correlations between the GFI subscales and related scales ( n = 119)
RAND-36 physical functioning
Perceived general health (EuroQol-5D) †
De Jong Gierveld Loneliness scale
r (95% CI)
r (95% CI)
r (95% CI)
r (95% CI)
Composition of GFI score for frail subjects
For almost half of the frail subjects (44.3%), the GFI score was composed of perceived problems in two domains. In only a limited number of subjects, the GFI score was composed of problems in both the Daily Activities and Psychosocial Functioning domains (3.0%), or composed of both the Daily Activities and Health Problems domains (5.5%). For 35.7% of the subjects, both the General Health and the Psychosocial Functioning domain contributed to the GFI scores.
In total, 28.9% of the subjects experienced problems in all three domains of frailty.
Percentages of frail persons (GFI ≥ 4) who experience problems in one, two, or three GFI domains (N = 540)*
One domain (N = 145)
Two domains (N = 239)
Three domains (N = 156)
F (df)†or Chi2(df)‡
Mean age (y) ± SD
73.54 ± 5.99
77.46 ± 6.84
80.71 ± 7.19
41.14 (2) †
65 – 69 y
70 – 74 y
75 – 79 y
80 – 84 y
≥ 85 y
No financial problems
Among frail subjects, the Chi2 test revealed dependency between age and the domains Daily Activities (Chi2 = 45.72; df = 4; p < 0.001) and Health Problems (Chi2 = 38.69; df = 4; p < 0.001). The data provided no support for an increase of psychosocial problems with increasing age (Chi2 = 5.04; df = 4; p = 0.284). ANOVA revealed interactions between age and Health Problems (p < 0.001), and age and Daily Activities (p < 0.001). Age did not interact with Psychosocial Functioning (p = 0.433).
In this study, we examined the structural validity and criterion validity of the GFI questionnaire in older adults. In addition, we evaluated the composition of GFI scores for frail older adults. Our findings support a three-dimensional factor structure of the GFI, in terms of the subscales Daily Activities (items 1–4), Psychosocial Functioning (items 11–15), and Health Problems (items 5–10). This model explains 50.6% of the overall variance. The internal consistency, scalability, and criterion validity of the GFI subscales Daily Activities (Cronbach’s α = .81, Hs = .84, r = −.62) and Psychosocial Functioning (Cronbach’s α = .80, Hs = .54, r = .67) are good. Consequently, both subscales identify problems in these frailty domains in a reliable and valid way. The internal consistency, scalability, and criterion validity of the GFI subscale Health Problems is less strong (Cronbach’s α = .57, Hs = .35, r = −.48). We surmise that the poor reliability and weak scalability of the Health Problems subscale is due to the heterogeneity of items pertaining physical health problems perceived by older adults. The Venn diagram showing the distribution of all subjects with a total GFI score of ≥4 revealed that 27% of older adults had problems in only one domain, 44% had problems in two domains, and 29% had problems in all three domains (see Figure 1). Furthermore, the present data suggest that 90% of the frail older adults experience problems in the Psychosocial Functioning domain.
In the literature, frailty is hypothesized to arise from multiple causes and to affect multiple domains of physical and cognitive functioning [9, 42, 43]. In different models of frailty, like the Functional Domains model (the accumulation of deficits), the Burden model (the index of health burden) and the Biologic Syndrome model (frailty as a biological syndrome) multidimensional screening instruments are considered to be most appropriate in screening frailty . Although the conceptualization of the multiple domains of frailty is generally used, there is no agreement about the included dimensions in frailty instruments [11, 15, 45].
In the assessment of frailty, screening instruments are mostly employed in a one-dimensional way. Originally, the GFI applied a cutoff point of a sum score of 4 points or higher, regardless of the number of domains in which an older adult faced problems. In addition, other screening instruments that distinguish different domains, like the Tilburg Frailty Indicator and the Edmunton Frail Scale, also use total sum scores to identify frail older adults [11, 46].
We suggest the results of our study may improve the adequacy of screening on frailty and will offer specific indications for intervening in the early onset of frailty. In this study, three separate dimensions of the GFI were established. These results lend support to the use of the GFI screening instrument as a multidimensional tool for the analysis of frailty. When we compare our multidimensional analysis with the originally used one-dimensional approach, as we showed in the Venn diagram, we now get a clearer picture of the underlying problems in the frailty sum scores. Therefore, we question the use of an overall cutoff point to identify frail older adults. It is clinically relevant to use the GFI as a multidimensional scale consisting of three subscales in order to direct the most appropriate care and to provide focused support to older adults facing problems in the different dimensions of frailty. Besides providing support for the use of the GFI screening instrument in a multidimensional way, the present study prompts a fundamental question about using an overall score without delineating specific frailty problems. The question is: Which combinations of pre-conditions are in fact essential for a valid assessment of frailty? The lack of a conceptual model in which frailty is specified results in overestimation and inconsistent identification of frailty in older adults. We propose exploring the possibility of using a conditional cutoff score, one based on both the sum score and the subscale scores. We believe this is necessary for establishing a more convergent diagnosis.
We suggest employing a multidimensional assessment of frailty with the GFI, one that uses a conditional cutoff point to establish a more convergent diagnosis of frailty. Because frailty is characterized by a decline in reserve capacity in different domains of functioning, we may consider a person to be frail if he or she obtains a GFI sum score of at least 4 points and reports problems in at least two domains of frailty.
A number of relevant methodological issues should be considered in interpreting the results of this study. First, the design was cross-sectional. Thus, we did not evaluate screening results of the GFI over time. Since frailty is a dynamic process that may be reversible, it is relevant to establish the sensitivity of the GFI as a screening instrument [47, 48]. So far, the GFI is not been used as an evaluative measurement instrument. Longitudinal studies should clarify the potential of the GFI as an evaluative measurement instrument to assess the changes in frailty status over time.
Second, item 5 of the GFI (“How do you rate your physical fitness?”) did not discriminate well among the factors. This finding may be explained by the fact that physical fitness is a multidimensional construct including multiple subcomponents. Furthermore, item 5 is a self-reported measure of physical fitness. It is known that levels of self-reported functioning may be influenced by affective functioning of an older adult . Therefore, the content of item 5 seems to be covered best by the subscale Health Problems, and reliability analysis supports its assignment (higher Cronbach’s α) to this subscale.
Third, a number of relevant personal characteristics were not taken into account in the analyses of our psychometric study. Since our data originated from epidemiological data collected by local health authorities, it contained a limited number of biographic and behavioral data. Therefore, in this study, we could not assess the impact of chronic diseases that may have been present, daily physical activity, physical fitness, and pharmaceutical consumption. It is likely relevant to control for these characteristics to gain more insight into applying the GFI.
The use of GFI subscale scores is directly relevant to the care of older adults. In our study, we identified three GFI subscales for assessing frailty more specifically. These GFI subscale scores produce a richer assessment of frailty than with the overall sum GFI score, and likely their use will contribute to more directed and customized care for older adults.
The authors are grateful to all participants for their willingness to participate in this study. Community centers in Groningen are acknowledged for their assistance in the recruitment of participants. This research has been funded by Hanze University of Applied Sciences Groningen.
- Fried LP, Tangen CM, Walston J, Newman AB, Hirsch C, Gottdiener J, Seeman T, Tracy R, Kop WJ, Burke G: Frailty in older adults: evidence for a phenotype. J Gerontol A Biol Sci Med Sci. 2001, 56 (3): 146-157. 10.1093/gerona/56.3.M146.View ArticleGoogle Scholar
- Fried LP, Ferrucci L, Darer J, Williamson JD, Anderson G: Untangling the concepts of disability, frailty, and comorbidity: implications for improved targeting and care. J Gerontol A Biol Sci Med Sci. 2004, 59 (3): 255-263. 10.1093/gerona/59.3.M255.View ArticlePubMedGoogle Scholar
- Ahmed N, Mandel R, Fain MJ: Frailty: an emerging geriatric syndrome. Am J Med. 2007, 120 (9): 748-753. 10.1016/j.amjmed.2006.10.018.View ArticlePubMedGoogle Scholar
- Etman A, Burdorf A, Van der Cammen TJM, Mackenbach JP, Van Lenthe FJ: Socio-demographic determinants of worsening in frailty among community-dwelling older people in 11 European countries. J Epidemiol Community Health. 2012, 66: 1116-1121. 10.1136/jech-2011-200027.View ArticlePubMedGoogle Scholar
- Peterson MJ, Giuliani C, Morey MC, Pieper CF, Evenson KR, Mercer V, Cohen HJ, Visser M, Brach JS, Kritchevsky SB: Physical activity as a preventative factor for frailty: the health, aging, and body composition study. J Gerontol A Biol Sci Med Sci. 2009, 64 (1): 61-68.View ArticlePubMedGoogle Scholar
- Chin A, Paw M, van Uffelen JG, Riphagen I, Van MW: The functional effects of physical exercise training in frail older people: a systematic review. Sports Med. 2008, 38 (9): 781-793. 10.2165/00007256-200838090-00006.View ArticleGoogle Scholar
- Theou O, Stathokostas L, Roland KP, Jakobi JM, Patterson C, Vandervoort AA, Jones GR: The effectiveness of exercise interventions for the management of frailty: a systematic review. J Aging Res 2011. 2011Google Scholar
- Eklund K, Wilhelmson K: Outcomes of coordinated and integrated interventions targeting frail elderly people: a systematic review of randomised controlled trials. Health Soc Care Community. 2009, 17 (5): 447-458. 10.1111/j.1365-2524.2009.00844.x.View ArticlePubMedGoogle Scholar
- De Vries N, Staal J, van Ravensberg C, Hobbelen J, Olde Rikkert M, Nijhuis-van der Sanden M: Outcome instruments to measure frailty: a systematic review. Ageing Res Rev. 2011, 10 (1): 104-114. 10.1016/j.arr.2010.09.001.View ArticlePubMedGoogle Scholar
- Carrière I, Colvez A, Favier F, Jeandel C, Blain H: Hierarchical components of physical frailty predicted incidence of dependency in a cohort of elderly women. J Clin Epidemiol. 2005, 58 (11): 1180-1187. 10.1016/j.jclinepi.2005.02.018.View ArticlePubMedGoogle Scholar
- Gobbens RJJ, van Assen MALM, Luijkx KG, Wijnen-Sponselee MT, Schols JMGA: The Tilburg Frailty Indicator: psychometric properties. J Am Med Dir Assoc. 2010, 11 (5): 344-355. 10.1016/j.jamda.2009.11.003.View ArticlePubMedGoogle Scholar
- Guilley E, Ghisletta P, Armi F, Berchtold A, d’Epinay CL, Michel JP, De Ribaupierre A: Dynamics of frailty and ADL dependence in a five-year longitudinal study of octogenarians. Res Aging. 2008, 30 (3): 299-317. 10.1177/0164027507312115.View ArticleGoogle Scholar
- Jones DM, Song X, Rockwood K: Operationalizing a frailty index from a standardized comprehensive geriatric assessment. J Am Geriatr Soc. 2004, 52 (11): 1929-1933. 10.1111/j.1532-5415.2004.52521.x.View ArticlePubMedGoogle Scholar
- Kiely DK, Cupples LA, Lipsitz LA: Validation and comparison of two frailty indexes: The MOBILIZE Boston Study. J Am Geriatr Soc. 2009, 57 (9): 1532-1539. 10.1111/j.1532-5415.2009.02394.x.View ArticlePubMedPubMed CentralGoogle Scholar
- Mitnitski AB, Mogilner AJ, Rockwood K: Accumulation of deficits as a proxy measure of aging. ScientificWorldJournal. 2001, 1: 323-336.View ArticlePubMedGoogle Scholar
- Puts MTE, Lips P, Deeg DJH: Sex differences in the risk of frailty for mortality independent of disability and chronic diseases. J Am Geriatr Soc. 2004, 53 (1): 40-47.View ArticleGoogle Scholar
- Ravaglia G, Forti P, Lucicesare A, Pisacane N, Rietti E, Patterson C: Development of an easy prognostic score for frailty outcomes in the aged. Age Ageing. 2008, 37 (2): 161-166. 10.1093/ageing/afm195.View ArticlePubMedGoogle Scholar
- Rolfson DB, Majumdar SR, Tsuyuki RT, Tahir A, Rockwood K: Validity and reliability of the Edmonton Frail Scale. Age Ageing. 2006, 35 (5): 526-529. 10.1093/ageing/afl041.View ArticlePubMedGoogle Scholar
- Rothman MD, Leo‒Summers L, Gill TM: Prognostic significance of potential frailty criteria. J Am Geriatr Soc. 2008, 56 (12): 2211-2216. 10.1111/j.1532-5415.2008.02008.x.View ArticlePubMedPubMed CentralGoogle Scholar
- Saliba D, Elliott M, Rubenstein LZ, Solomon DH, Young RT, Kamberg CJ, Roth C, MacLean CH, Shekelle PG, Sloss EM: The vulnerable elders survey: a tool for identifying vulnerable older people in the community. J Am Geriatr Soc. 2001, 49 (12): 1691-1699. 10.1046/j.1532-5415.2001.49281.x.View ArticlePubMedGoogle Scholar
- Scarcella P, Liotta G, Marazzi M, Carbini R, Palombi L: Analysis of survival in a sample of elderly patients from Ragusa, Italy on the basis of a primary care level multidimensional evaluation. Arch Gerontol Geriatr. 2005, 40 (2): 147-156. 10.1016/j.archger.2004.07.004.View ArticlePubMedGoogle Scholar
- Steverink N, Slaets J, Schuurmans H, Van Lis M: Measuring frailty: developing and testing of the Groningen Frailty Indicator (GFI). Gerontologist. 2001, 41 (1): 236-237.Google Scholar
- Studenski S, Hayes RP, Leibowitz RQ, Bode R, Lavery L, Walston J, Duncan P, Perera S: Clinical global impression of change in physical frailty: development of a measure based on clinical judgment. J Am Geriatr Soc. 2004, 52 (9): 1560-1566. 10.1111/j.1532-5415.2004.52423.x.View ArticlePubMedGoogle Scholar
- Frieswijk N, Buunk BP, Steverink N, Slaets JPJ: The interpretation of social comparison and its relation to life satisfaction among elderly people: does frailty make a difference?. J Gerontol B Psych Sci Soc Sci. 2004, 59 (5): 250-257. 10.1093/geronb/59.5.P250.View ArticleGoogle Scholar
- Metzelthin S, Daniëls R, Van Rossum E, De Witte L, van den Heuvel W, Kempen G: The psychometric properties of three self-report screening instruments for identifying frail older people in the community. BMC Publ Health. 2010, 10 (1): 176-183. 10.1186/1471-2458-10-176.View ArticleGoogle Scholar
- Peters LL, Boter H, Buskens E, Slaets JPJ: Measurement properties of the groningen frailty indicator in home-dwelling and institutionalized elderly people. J Am Med Dir Assoc. 2012, 13: 546-551. 10.1016/j.jamda.2012.04.007.View ArticlePubMedGoogle Scholar
- Schuurmans H, Steverink N, Lindenberg S, Frieswijk N, Slaets JPJ: Old or frail: what tells us more?. J Gerontol A Biol Sci Med Sci. 2004, 59 (9): 962-965. 10.1093/gerona/59.9.M962.View ArticleGoogle Scholar
- De Jong Gierveld J, van Tilburg T: Manual of the Loneliness Scale. 1999. 1999, Vrije Universiteit Amsterdam, Amsterdam: Department of Social Research Methodology, updated version 18.01.02Google Scholar
- Spinhoven P, Ormel J, Sloekers P, Kempen G, Speckens A, Hemert AM: A validation study of the Hospital Anxiety and Depression Scale (HADS) in different groups of Dutch subjects. Psychol Med. 1997, 27 (2): 363-370. 10.1017/S0033291796004382.View ArticlePubMedGoogle Scholar
- Van der Zee K, Sanderman R: RAND-36. 1993, Groningen: Northern Centre for Health Care Research, University of Groningen, the Netherlands, 1: 28-Google Scholar
- The EQG: EuroQol-a new facility for the measurement of health-related quality of life. Health Policy. 1990, 16 (3): 199-208.View ArticleGoogle Scholar
- De Jong GJ, Van Tilburg T: A shortened scale for overall, emotional and social loneliness. Tijdschr Gerontol Geriatr. 2008, 39 (1): 4-15. 10.1007/BF03078118.View ArticleGoogle Scholar
- Moorer P, Suurmeijer TPBM, Foets M, Molenaar I: Psychometric properties of the RAND-36 among three chronic disease (multiple sclerosis, rheumatic diseases and COPD) in the Netherlands. Qual Life Res. 2001, 10 (7): 637-645. 10.1023/A:1013131617125.View ArticlePubMedGoogle Scholar
- Mokkink LB, Terwee CB, Patrick DL, Alonso J, Stratford PW, Knol DL, Bouter LM, de Vet HC: The COSMIN study reached international consensus on taxonomy, terminology, and definitions of measurement properties for health-related patient-reported outcomes. J Clin Epidemiol. 2010, 63 (7): 737-745. 10.1016/j.jclinepi.2010.02.006.View ArticlePubMedGoogle Scholar
- Nunnally J: Psychometric methods. 1978, New York, NY: McGraw-HillGoogle Scholar
- George D, Mallery M: SPSS for Windows step by step: a simple guide and reference. 2003, Boston: Pearson Allyn & BaconGoogle Scholar
- Mokken RJ, Lewis C: A nonparametric approach to the analysis of dichotomous item responses. Appl Psychol Meas. 1982, 6 (4): 417-430. 10.1177/014662168200600404.View ArticleGoogle Scholar
- Hemker BT, Sijtsma K, Molenaar IW: Selection of unidimensional scales from a multidimensional item bank in the polytomous mokken I RT model. Appl Psychol Meas. 1995, 19 (4): 337-352. 10.1177/014662169501900404.View ArticleGoogle Scholar
- Mokken RJ: Handbook of modern item response theory. Nonparametric models for dichotomous responses. 1997, New York: Springer, 351-367.Google Scholar
- Cohen J: Statistical power analysis for the behavioral sciences (2nd ed.). 1988, Hillsdale, NJ: Lawrence Erlbaum AssociatesGoogle Scholar
- Van Buuren S, Groothuis-Oudshoorn K: MICE: Multivariate Imputation by chained equations in R. J Stat Softw. 2011, 45 (3): 1-67.Google Scholar
- Pialoux T, Goyard J, Lesourd B: Screening tools for frailty in primary health care: a systematic review. Geriatr Gerontol Int. 2012, 12 (2): 189-197. 10.1111/j.1447-0594.2011.00797.x.View ArticlePubMedGoogle Scholar
- Markle‒Reid M, Browne G: Conceptualizations of frailty in relation to older adults. J Adv Nurs. 2003, 44 (1): 58-68. 10.1046/j.1365-2648.2003.02767.x.View ArticleGoogle Scholar
- Cigolle CT, Ofstedal MB, Tian Z, Blaum CS: Comparing models of frailty: the health and retirement study. J Am Geriatr Soc. 2009, 57 (5): 830-839. 10.1111/j.1532-5415.2009.02225.x.View ArticlePubMedGoogle Scholar
- Walston J, Hadley EC, Ferrucci L, Guralnik JM, Newman AB, Studenski SA, Ershler WB, Harris T, Fried LP: Research agenda for frailty in older adults: toward a better understanding of physiology and etiology: summary from the American Geriatrics Society/National Institute on Aging Research Conference on Frailty in Older Adults. J Am Geriatr Soc. 2006, 54 (6): 991-1001. 10.1111/j.1532-5415.2006.00745.x.View ArticlePubMedGoogle Scholar
- Hábert R, Bravo G, Korner-Bitensky N, Voyer L: Predictive validity of a postal questionnaire for screening community-dwelling elderly individuals at risk of functional decline. Age Ageing. 1996, 25 (2): 159-167. 10.1093/ageing/25.2.159.View ArticleGoogle Scholar
- Wilson JF: Frailty–and its dangerous effects–might be preventable. Ann Intern Med. 2004, 141 (6): 489-492. 10.7326/0003-4819-141-6-200409210-00035.View ArticlePubMedGoogle Scholar
- Puts MTE: Frailty: Biological risk factors, negative consequences and quality of life. 2006, VU University Amsterdam: PhD dissertationGoogle Scholar
- Kempen GIJM, Van Heuvelen MJG, Van den Brink RHS, Kooijman AC, Klein M, Houx PJ, Ormel J: Factors affecting Contrasting Results between Self-reported and Performance-based Levels of Physical Limitations. Age Ageing. 1996, 25 (6): 458-464. 10.1093/ageing/25.6.458.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://0-www.biomedcentral.com.brum.beds.ac.uk/1471-2318/13/86/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.