“…Outcome measures related to quality of life were utilised within 12 studies, with the most common outcome measures used being the 12-Item Short Form Survey (SF-12) (Duthon et al, 2011;Habets et al, 2017;Mansur et al, 2017;Murawski et al, 2014;Stenson et al, 2018), EuroQol 5 Dimension 5 Level Questionnaire (EQ-5D-5L) (Chester et al, 2008;De Marchi et al, 2018;Habets et al, 2017;Hasani et al, 2020) and 36-Item Short Form Survey (SF-36) (Hutchison et al, 2011;Maffulli et al, 2019;Petersen, Welp & Rosenbaum, 2007). Similarly, psychosocial outcomes were poorly measured, being utilised on 11 occasions, with the most common outcome measures being the Pain Catastrophizing Scale (PCS) (Chimenti et al, 2020;Eckenrode, Kietrys & Stackhouse, 2019;Hasani et al, 2020;Post et al, 2020;Vallance et al, 2020), Tampa Kinesiophobia Scale (TKS) (Chimenti et al, 2020;Hasani et al, 2020;Post et al, 2020;Vallance et al, 2020), Pain Disability Index (PDI) (Mayer et al, 2007;Scott, Huisman & Khan, 2011) and Pain Efficacy Scale (PES) (Mayer et al, 2007;Scott, Huisman & Khan, 2011).…”