TY - JOUR AU - Maarj, Muhammad AU - Pacey, Verity AU - Tofts, Louise AU - Clapham, Matthew AU - Gironès Garcia, Xavier AU - Coda, Andrea PY - 2022 DA - 2022/10/26 TI - Validation of an Electronic Visual Analog Scale App for Pain Evaluation in Children and Adolescents With Symptomatic Hypermobility: Cross-sectional Study JO - JMIR Pediatr Parent SP - e41930 VL - 5 IS - 4 KW - hypermobility syndrome KW - Ehlers-Danlos syndrome KW - hypermobility KW - hypermobile KW - mobile application KW - mobile app KW - pain measurement KW - pain KW - validation KW - validate KW - scale KW - measure KW - pain severity KW - pediatric KW - visual analogue scale KW - mHealth KW - mobile health KW - children KW - adolescent KW - youth KW - child KW - digital health tool AB - Background: Rapid advances in mobile apps for clinical data collection for pain evaluation have resulted in more efficient data handling and analysis than traditional paper-based approaches. As paper-based visual analogue scale (p-VAS) scores are commonly used to assess pain levels, new emerging apps need to be validated prior to clinical application with symptomatic children and adolescents. Objective: This study aimed to assess the validity and reliability of an electronic visual analogue scale (e-VAS) method via a mobile health (mHealth) App in children and adolescents diagnosed with hypermobility spectrum disorder/hypermobile Ehlers-Danlos syndrome (HSD/HEDS) in comparison with the traditional p-VAS. Methods: Children diagnosed with HSD/HEDS aged 5-18 years were recruited from a sports medicine center in Sydney (New South Wales, Australia). Consenting participants assigned in random order to the e-VAS and p-VAS platforms were asked to indicate their current lower limb pain level and completed pain assessment e-VAS or p-VAS at one time point. Instrument agreement between the 2 methods was determined from the intraclass correlation coefficient (ICC) and through Bland–Altman analysis. Results: In total, 43 children with HSD/HEDS aged 11 (SD 3.8) years were recruited and completed this study. The difference between the 2 VAS platforms of median values was 0.20. Bland–Altman analysis revealed a difference of 0.19 (SD 0.95) with limits of agreement ranging –1.67 to 2.04. An ICC of 0.87 (95% CI 0.78-0.93) indicated good reliability. Conclusions: These findings suggest that the e-VAS mHealth App is a validated tool and a feasible method of collecting pain recording scores when compared with the traditional paper format in children and adolescents with HSD/HEDS. The e-VAS App can be reliably used for pediatric pain evaluation, and it could potentially be introduced into daily clinical practice to improve real-time symptom monitoring. Further research is warranted to investigate the usage of the app for remote support in real clinical settings. SN - 2561-6722 UR - https://pediatrics.jmir.org/2022/4/e41930 UR - https://doi.org/10.2196/41930 UR - http://www.ncbi.nlm.nih.gov/pubmed/36287606 DO - 10.2196/41930 ID - info:doi/10.2196/41930 ER -