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Dev Med Child Neurol ; 55(11): 1038-45, 2013 Nov.
Article in English | MEDLINE | ID: mdl-23902233

ABSTRACT

AIM: An international Clinical Outcomes Group consisting of clinicians, scientists, patient advocacy groups, and industries identified a need for a scale to measure motor performance of the upper limb. We report the steps leading to the development of the Performance of the Upper Limb (PUL), a tool specifically designed for assessing upper limb function in ambulant and non-ambulant patients with Duchenne muscular dystrophy (DMD). METHOD: The development of the PUL followed a number of steps, from the systematic review and a preliminary study exploring the suitability of the existing measures, to the application of a pilot version in a multicentric setting, with Rasch analysis of the preliminary results, leading to a revised pro forma. RESULTS: The PUL was specifically designed for DMD, with a conceptual framework reflecting the progression of weakness and natural history of functional decline in DMD. Modern psychometric methods were used to create a scale with robust internal reliability, validity, and hierarchical scalability; males with DMD and their families were involved iteratively throughout the process of the clinician-reported outcome assessment tool development to establish clinical meaningfulness and relevance of individual PUL items to activities of daily living. INTERPRETATION: The module was developed using innovative approaches and will be useful for designing clinical trials.


Subject(s)
Disability Evaluation , Movement Disorders/diagnosis , Muscular Dystrophy, Duchenne/pathology , Psychometrics , Upper Extremity/physiopathology , Activities of Daily Living , Humans , Movement Disorders/etiology , Muscular Dystrophy, Duchenne/complications , Reproducibility of Results , Sensitivity and Specificity , Walking
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