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(Stroke. 2005;36:2493.)
© 2005 American Heart Association, Inc.
Research Reports |
From the Department of Psychology (G.U., E.T., M.V.) and the Department of Physical Therapy, School of Health Related Professions (D.M.), University of Alabama at Birmingham; and the Division of Physical Therapy (K.M.), University of North Carolina at Chapel Hill.
Correspondence to Gitendra Uswatte, PhD, University of Alabama at Birmingham, 1530 3rd Ave S, CH415, Birmingham, AL 35294. E-mail guswatte{at}uab.edu
| Abstract |
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Methods Participants (n=41) in the first study completed MALs before and after CI therapy or a placebo control procedure. In addition, caregivers independently completed a MAL on the participants. Participants (n=27) in the second study completed MALs and wore accelerometers that monitored their arm movements for 3 days outside the laboratory before and after an automated form of CI therapy.
Results Validity of the participant MAL Quality of Movement (QOM) scale was supported. Correlations between pretreatment-to-posttreatment change scores on the participant QOM scale and caregiver MAL QOM scale, caregiver MAL amount of use (AOU) scale, and accelerometer recordings were 0.70, 0.73, and 0.91 (P<0.01), respectively. Internal consistency (
>0.81), test-retest reliability (r>0.91), stability, and responsiveness (ratio >3) of the participant QOM scale were also supported. The participant AOU and caregiver QOM and AOU scales were internally consistent, stable, and sensitive, but were not reliable.
Conclusions The participant MAL QOM scale can be used exclusively to reliably and validly measure real-world, upper-extremity rehabilitation outcome and functional status in chronic stroke patients with mild-to-moderate hemiparesis.
Key Words: arm function rehabilitation treatment outcome stroke
| Introduction |
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| Methods |
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Measures
The upper-extremity MAL-14 is a structured interview1,2 that elicits information about 14 activities of daily living (ADL; Table I, available online only at http://www.strokeaha.org). Patients are asked to rate how well (Quality of Movement [QOM] scale) and how much (Amount of Use [AOU] scale) they use their more impaired arm to accomplish each ADL. Both scales are anchored at 6 points by abbreviated phrases and longer definitions (online Table II); participants may select scores halfway between the anchors. Scale total scores are the mean of the item scores. In CI therapy studies from this laboratory, both scales are administered before and after treatment; the QOM scale alone is given daily during the intervention period. The MAL is also administered independently before and after treatment to an informant, who is usually a participants primary caregiver.
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The interview was conducted according to standardized procedures summarized in online Table III and described at length in a testing manual.6 One procedure of note is that after the initial MAL administration, the interviewer, using scripted phrases, probed responses that differ from those given on the previous testing administration to determine whether such scores reflect an actual change. The purpose of this procedure was to prevent errors in recall, misunderstanding of the scale levels, and enthusiasm about treatment gains (ie, a halo effect) resulting in final responses that are not veridical.
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Procedure
Study 1 participants and, if available, a caregiver (n=31) completed the MAL before (test 1) and after (test 2) receiving CI therapy (treatment group) or fitness training (control group). Study 2 participants completed the MAL before and after AutoCITE therapy; in addition, participants who lived in-town (n=10) wore accelerometers7 on each wrist for 3 days.
| Results |
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=0.87), and was reliable, stable, and very responsive (Table 2). Convergent validity of the patient QOM scale was supported. The Intraclass Correlation (ICC) type 2,18 between patient and caregiver scores for test 1 was 0.52 (P<0.01); for changes from test 1 to 2, it was 0.7 (P<0.0001). The patient AOU and caregiver QOM and AOU scales were internally consistent (Chronbach
>0.82), stable, and responsive but were not reliable (Table 2).
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Study 2 supported the concurrent validity of the patient QOM scale. The Pearson correlation between this scale and the accelerometer recordings7 for test 1 was 0.7 (P<0.05); for changes from test 1 to 2, it was 0.91 (P<0.01; Figure). Internal consistency was adequate (Chronbach
=0.81), and responsiveness was very high (Table 2).
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Because of concerns that probing responses (see Measures) might bias scores upward, initial item responses were recorded on each MAL administration for the last 13 study 2 participants. Examination of responses before and after probing revealed that the median change on the QOM scale was only 0.05 points (range, 0.0 to 0.1), which is 10 times smaller than what is considered a minimal clinically important difference.9
| Discussion |
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Our findings are mostly consistent with those from a recent study of the Dutch 26-item MAL (n=56), which found that the Dutch MAL was highly internally consistent, reliable, and stable.9 This study also reported that the pretreatment MAL and Action Research Arm (ARA)10 test scores were strongly correlated, but that pretreatment-to-posttreatment change on the MAL was not significantly correlated with change on the ARA and a single-item global change rating. This approach is flawed because the ARA is a measure of motor ability as opposed to use, and, as noted previously, CI therapy has differential effects on these 2 parameters. The single-item global change rating has not been described before its use by van der Lee et al,9 there is no information on its validity, and it is not clear whether it assesses arm motor ability or use or both.
A limitation of this article is that caregiver and accelerometry data were available for only a subsample of the participants in each study. However, comparison of study 1 subjects with and without caregiver data (n=31 and 10, respectively) showed that there were no significant differences between them in initial MAL scores or treatment gains on the MAL. There were also no significant differences on these parameters between study 2 subjects with and without accelerometry data (n=10 and 17, respectively). Nevertheless, it is possible that subjects for whom data were complete were not representative of the entire sample in some other important way, suggesting that confirmation of these results in a larger study would be valuable. A larger sample would also permit testing of whether differential reliability and validity was present for particular patient subgroups, such as men or women.
It is hoped that the availability of a valid measure of more-impaired arm use outside the laboratory will encourage stroke researchers to study this parameter more intensively than they have in the past. Neurorehabilitation trials typically assess impairment and functional independence.2 Exclusive attention to these domains does not permit evaluation of the effects of neurorehabilitation on actual use of the more-impaired extremity in daily life.2 This issue is particularly salient given the increasing emphasis on restoring function of the more-impaired extremity, as opposed to teaching compensatory strategies. In addition, relatively little is known about the relationship between patient characteristics at the impairment level and actual use of the more impaired extremity in daily life. Instruments, such as the MAL, might be used, in conjunction with existing measures of impairment, for cross-sectional or longitudinal studies that examine how these 2 domains of motor recovery are related.
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| Acknowledgments |
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| Footnotes |
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Received July 22, 2005; accepted August 15, 2005.
| References |
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