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Modified Fatigue Impact Scale (MFIS)
Modified Fatigue Impact Scale (MFIS)
Freely available at the NMSS website: Modified Fatigue Impact Scale (MFIS)
Supplemental: Amyotrophic Lateral Sclerosis (ALS), Friedreich's Ataxia (FA), Multiple Sclerosis (MS)
Exploratory: Myalgic encephalomyelitis/Chronic fatigue syndrome (ME/CFS)
|Short Description of Instrument||
Construct measured: Impact of fatigue on patient's daily life.
Generic vs. disease specific: Generic.
Means of administration: Self-report or by a trained interviewer.
Intended respondent: Patient.
# of items: 21.
# of subscales and names of sub-scales: 3 – Physical, cognitive and psychosocial functioning.
# of items per sub-scale: N/A.
Administration: 5-10 minutes
Background: The MFIS is a modified form of the Fatigue Impact Scale (Fisk et al, 1994) based on items derived from interviews with MS patients concerning how fatigue impacts their lives. This multidimensional instrument includes physical, cognitive, and psychosocial subscales and assesses the impact of fatigue on a variety of daily activities. The full-length MFIS consists of 21 items while the abbreviated version has 5 items. The abbreviated version can be used if time is limited but the full-length version has the advantage of generating subscales. The MFIS is one of the components of the MSQLI.
Scoring: The total score for the Modified Fatigue Impact Scale (MFIS) is the sum of the scores for the 21 items. Individual subscale scores can also be generated by calculating the sum of specific sets of items. Users should refer to the MSQLI User's Manual for detailed scoring instructions for both the full length 21-item MSSS and abbreviated 5-item version. Each item is scored between 0 (never) and 4 (almost always). Total score varies between 0-84 and are obtained by adding scores for each of the sub-scales. The sub-scales scores are 0-36 (physical), 0-40 (cognitive) and 0-8 (psychosocial).
Strengths/Weaknesses: The MFIS is easy to administer and focuses on the ways in which fatigue affects everyday life. As such it has high face validity for patients. The availability of the three subscales may be useful to investigators interested in testing hypotheses concerning these different areas of function. However, the three subscales tend to correlate highly with one another, which limits their usefulness to some extent.
Advantages: This scale is free to use. It might be useful for comparison with people with MS. This form is part of a modular instrument MSQLI, which contains a free version of the health status (SF-36), perceived deficits questionnaire (PDQ) and other questionnaires, some of them could be useful in ME/CFS, though others would be very very specific to MS. The sub-scales, may be useful to investigators interested in testing hypotheses concerning these different areas of function.
Limitations: This scale has not been validated in ME/CFS. It measures the impact and not the severity of fatigue and there are no questions on post-exertional malaise. This scale could be potentially used alongside a scale exploring severity.
MS Psychometric Properties: NOTE: Limited data on psychometric properties in North American MS populations are available. Summary of demonstrated properties below includes data from both N. American and European MS studies.
Reliability: Cronbach's alpha [MSQLI field test population]: Total MFIS = .81, Cognitive subscale = .95, Physical subscale = .91, psychosocial subscale = .81, and abbreviated version = .80; Cronbach's alpha [four-country European study (Kos et al., 2005)]: Total MFIS = .92, Cognitive subscale = .92, Physical subscale = .88, psychosocial subscale = .65; Reproducibility: ICC = .91 (Kos et al., 2005); Convergent Validity: MFIS correlates with the Fatigue Severity Scale: Spearman r =.68, p<.0001 in an RRMS predominate Spanish population (TÉllez et al., 2005); r =.66, p<.0001 in a four-country European study (Kos et al., 2005); Kendall's Tau-b = 0.729, Dutch MFIS. (Kos et al., 2003) Divergent Validity: Does not diverge from Beck Depression Inventory (Spearman r = .7, p<.0001); divergence from EDSS (r = .30, p<.0001; r = 0.15, p =.02 after adjusting for BDI) (TÉllez et al., 2005) Sensitivity: Dutch MFIS sensitive to change (z = -3.401, p =. 001) following a four-week rehabilitation program; no floor or ceiling effect detected.
Administration: Administration time is approximately 5-10 minutes for the full-length version and 2-3 minutes for the abbreviated version. The MFIS is a structured, self-report questionnaire that the patient can generally complete with little or no intervention from an interviewer. However, patients with visual or upper extremity impairments may need to have the MFIS administered as an interview. Interviewers should be trained in basic interviewing skills and in the use of this instrument.
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