Abstract
Collection of Patient Reported Outcomes in Vitiligo: A Study Announcement by the VR Foundation
A six-month data collection project from Vitiligo Research Foundation (VRF) is set to begin on November 1, 2015. It involves academic institutions, small-to-medium sized clinics, patient organizations and service providers. A self-reported patient questionnaire structure, along with possible conceptual and methodological difficulties, is reviewed in this communication paper.
Author(s):
Yan Valle
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