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Walking test outcomes in adults with genetic neuromuscular diseases: a systematic literature review of their measurement properties.

European journal of physical and rehabilitation medicine
April 1, 2024
Nawale Hadouiri et al. (6 authors)
Systematic ReviewJournal ArticleHuman Study
Study Details

Study Goal

The researchers aimed to review walking tests and their measurement properties in adults with inherited or genetic neuromuscular diseases (NMDs) to help clinicians and researchers choose appropriate tests.

Results Summary

The review found that most walking outcomes were valid and reliable in NMDs, with the 6MWT being the most studied test. However, studies on responsiveness and minimal important differences were lacking or inadequate.

Population

Adults with inherited or genetic neuromuscular diseases (NMDs).

Effective Dosage

Not available

Duration

Not applicable (systematic review)

Interactions

None mentioned

Extracted Claims (4)
InterventionDirectionEndpointPopulationDosageImpactClaim #
walking tests and tools
no change
walking outcomes
adults with inherited or genetic NMDs
-
were found to be valid and reliable
#1
6MWT
no change
measurement properties
NMDs
-
was the most studied test
#2
studies evaluating construct validity, reliability and measurement error
no change
methodological design and statistical methods
-
-
were "very good"
#3
studies on responsiveness as minimal important difference or minimal important change
no change
measurement properties
-
-
were lacking or were found to have inadequate methodological and statistical methods
#4
Abstract

INTRODUCTION: Neuromuscular diseases (NMDs) include a large group of heterogeneous diseases. NMDs frequently involve gait disorders, which affect quality of life. Several walking tests and tools have been described in the literature, but there is no consensus regarding the use of walking tests and tools in NMDs or of their measurement properties for walking outcomes. The aim of this review is to present an overview of walking tests, including their measurement properties when used in adults with inherited or genetic NMDs. The aim is to help clinicians and researchers choose the most appropriate test for their objective. EVIDENCE ACQUISITION: A systematic review was conducted after consulting MEDLINE (via PubMed), EMBASE, Science direct, Google Scholar and Cochrane Central Register of Controlled Trials databases for published studies in which walking outcome measurement properties were assessed. The validity, reliability, measurement error and responsiveness properties were evaluated in terms of statistical methods and methodological design qualities using the COnsensus-based Standards for the selection of health Measurement Instruments (COSMIN) guidelines. EVIDENCE SYNTHESIS: We included 46 studies in NMDs. These studies included 15 different walking tests and a wide variety of walking outcomes, assessed with six types of walking tools. Overall, the 6MWT was the most studied test in terms of measurement properties. The methodological design and statistical methods of most studies evaluating construct validity, reliability and measurement error were "very good." The majority of outcome measurements were valid and reliable. However, studies on responsiveness as minimal important difference or minimal important change were lacking or were found to have inadequate methodological and statistical methods according to the COSMIN guidelines. CONCLUSIONS: Most walking outcomes were found to be valid and reliable in NMDs. However, in view of the growing number of clinical trials, further studies are needed to clarify additional measurement properties.

Medical Subject Headings (MeSH)
AdultHumansQuality of LifeReproducibility of ResultsWalkingGaitNeuromuscular DiseasesPsychometrics
Study Links
Quality Scores
SafetyNot Assessed
Efficacy75/10
Quality85/10
Citation Metrics
Total Citations1
Citations/Year1.0
Research Impact Scores
APT Score0.25
Weight Score2.70
Normalized Score0.67
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