Bias and precision in visual analogue scales: a randomized controlled trial.
Fiche publication
Date publication
novembre 1999
Journal
American journal of epidemiology
Auteurs
Membres identifiés du Cancéropôle Est :
Pr BRIANCON Serge, Pr GUILLEMIN Francis
Tous les auteurs :
Paul-Dauphin A, Guillemin F, Virion JM, Briançon S
Lien Pubmed
Résumé
Various types of visual analogue scales (VAS) are used in epidemiologic and clinical research. This paper reports on a randomized controlled trial to investigate the effects of variations in the orientation and type of scale on bias and precision in cross-sectional and longitudinal analyses. This trial was included in the pilot study of the SU.VI.MAX (supplementation by antioxidant vitamins and minerals) prevention trial in France in 1994. Six types of VAS (simple, middle-marked, graphic rating, graduated, graduated-numbered, and numerical rating) and two orientations (horizontal and vertical) were used to measure three symptoms of ear, nose, and throat infection at 2-month intervals in 870 subjects. Differences between scales were analyzed by comparing variances (Levene's test) and means (variance-covariance analysis for repeated measures). Scale characteristics were shown to influence the proportion of zero and low values (i.e., there was a floor effect), but not mean scores. The precision of measurements varied cross-sectionally according to the type of scale, but no differences were observed in the precision of measurement of change over time. In conclusion, the characteristics of VAS seem to be important in cross-sectional studies, particularly when symptoms of low or high intensity are being measured. Researchers should try to reach a consensus on what type of VAS to use if studies are to be compared.
Mots clés
Adult, Bias (Epidemiology), Clinical Trials as Topic, standards, Cross-Sectional Studies, Female, Health Surveys, Humans, Male, Middle Aged, Pain Measurement, Reproducibility of Results, Research Design, Respiratory Tract Infections, classification, Sensitivity and Specificity
Référence
Am. J. Epidemiol.. 1999 Nov;150(10):1117-27