Validation of the 25 level modified shuttle test in children with cystic fibrosis

Abstract

AbstractObjectiveTo evaluate the validity and reliability of the modified shuttle 25‐level test (MST‐25) in children with cystic fibrosis (CF).MethodsA prospective single center study in clinically stable children with CF. Participants undertook two testing conditions on different days: (1) 2xMST‐25 tests; (2) cardiopulmonary exercise test (CPET). Test order was randomized. Nadir oxygen saturation (SpO2), peak heart rate (HR), breathlessness (modified Borg), rate of perceived exertion (RPE), energy expenditure (EE) and metabolic equivalents (MET) from the MST‐25 and CPET were compared to assess validity, while outcomes from 2xMST‐25 tests were compared for reliability. CPET was performed using breath‐by‐breath analysis and EE from the MST‐25 obtained using the SenseWear Armband.ResultsStrong correlations were found between MST‐25 distance and peak oxygen uptake, peak work and minute ventilation on CPET (all r > 0.7, p < 0.01). Moderate correlations were found between MST‐25 distance and CPET for METs (r = 0.5) and HR (r = 0.6). Weak associations between tests were evident for nadir SpO2 (r = 0.1), modified Borg (rs = 0.2) and RPE (rs = 0.2). Test−retest reliability was excellent for MST‐25 distance (ICC 0.91), peak EE (ICC 0.99) and peak METs (ICC 0.90). Good reliability was achieved for HR (ICC 0.84) and modified Borg score (ICC 0.77), while moderate reliability for nadir SpO2 (ICC 0.64) and RPE (ICC 0.68) was observed.ConclusionThe MST‐25 is a valid and reliable field test for the assessment of exercise capacity in children with CF. The MST‐25 can be used to accurately monitor exercise capacity and prescribe exercise training, particularly when CPET is not available.