This is the protocol of a systematic review that aims to explore outcomes relevant for people living with type 1 diabetes mellitus and their caregivers.
Objectives: Gain an overview of expected response rates (RRs) to patient-reported outcome measures (PROMs) in clinical quality registry-based studies and long-term cohorts in order to better evaluate
Supplementary Tables 1-6 for Understanding the Patient Experience of Living with Notalgia Paresthetica: A Qualitative Interview Study of Symptoms and Impacts
*: disease severity was assessed on a visual analogue scale (0–10) with 10 indicating the most severe disease; CD: celiac disease; IQR: interquartile range. The MOS-SF36 scores are presented both as r
