Methods
Study participants
Fifty adult male professional rugby union athletes aged between 18 and 35 years (22.8±5.1) were recruited at the start of a full playing season (First of July 2019) and were considered relatively well rested after a minimum of 5 weeks break between playing seasons. The participants were injury free and considered available for full training at the time of testing.
Study design
This study investigates the association between a clinician assessed IRS system and PCI sustained during one full playing season. Due to the COVID-19 pandemic shortening the season, deviation from the original protocol occurred, so PCI data were collected across the first 9 months of the season instead of the originally planned 11 months. PCI was defined as any non-contact injury to the foot (palmar aspect), calf complex (including the achilles tendon), adductor muscle group, hamstring muscle group, gluteal muscle group, lumbar spine and thoracic spine regions that led to time loss in training and/or matches. PCI included soft tissue disruption categorised using the British Athletics Muscle Injury Classification,28 which details tissue disruption of all types between grades 0 and 4; discopathy, neuropathy, tendonopathy, and overload injuries were also included. Contact injuries from direct impact were excluded from the study as direct impact injuries are not generally deemed to be affected by biomechanics.
The IRS
A visual representation of the testing procedure is presented in figure 1 and an example of the IRS system criteria in figure 2. This novel testing protocol is clinician assessed and it is not documented in the empirical literature. However, the assessment method uses a modified approach that used EMG in assessing prone hip extension (PHE), which demonstrated good levels of reliability and validity.27 The modification translated into this study sees the replacement of EMG with palpable assessment of gluteal muscle tone, the addition of prone knee flexion (PKF) and observation of biomechanics retrospectively analysed using two-dimensional video analysis. Biomechanics are assessed against the IRS system in the performance of combined PHE and PKF (figure 1), subsequently providing greater comparison to the gait cycle than PHE alone, where PHE and PKF are performed concurrently.20 Participants can score a maximum of 10 points following the IRS system criteria—the more biomechanical change observed from the participants anatomical prone starting position, the higher the score. The five compensatory criteria include: (1) loss of palpable coactivation in either gluteal muscle, (2) lumbar spine extension, (3) lift of the anterior superior iliac spine from the plinth, (4) an increase in hip external rotation (5) an increase in hip abduction. If the athlete displays a compensatory movement pattern for one of the five criteria, 1 point would be scored per limb, left (maximum 5 points) and right (maximum 5points) with a maximum of 10 points achievable.
Figure 1Still image views of longitudinal (left) and transverse (right) views of biomechanical deficit and limb asymmetry when using the IRS system: starting position (A), testing left limb (B) and testing right limb (C).
Figure 2IRS system criteria.
As the IRS system is novel, a repeatability pilot was performed prior to the data collection and results were analysed using Fleiss Kappa to assess inter-rater reliability (IRR). The lead researcher educated and familiarised four assessors in the IRS system. Each clinician had a minimum of 5 years experience in musculoskeletal medicine. The clinicians were blinded and asked to analyse a small pilot group (four participants), against the IRS system. Results from this pilot study were interpreted as suggested by McHugh,29 whereby (R≥0.90—excellent, R=0.80–0.89—very good, R=0.60–0.79—good, R=0.40–0.59—moderate and R=0.21–0.39—minimal). Completing this pretrial pilot demonstrated good levels of IRR (R=0.651, p<0.001) and allowed for some minor adjustments in the logistics around participant testing, reflected in the testing procedure section.
Testing procedure
Each participant started in a prone position on a treatment plinth with arms placed by their side or above their head (as in figure 1) to negate the use of upper limb stabilisation during testing. The testing clinician then placed their index finger and thumb of one hand on the horizontal plateau of the gluteus maximus to assess palpable gluteal activation.30 Prior to testing, each participant was read the same script by the testing clinician, Tense both buttock muscles and maintain this contraction for the duration of the movement, until told the test is over. Now bend your left knee to 90 degrees and lift that knee off the bed. The testing practitioner would then say, The test is over. The participant then relaxes, resuming the prone starting position. The opposite side would then be tested with the same instructions where left knee was replaced with right knee. Each participant was given a 2 min testing window and participants were tested consecutively. The testing clinician retrospectively assessed each participant through the combined PHE and PKF movement against the IRS criteria, using video analysis. The only live score recorded during the testing protocol was palpable gluteal activation as muscle tone was deemed unrecordable by video analysis. All scores were recorded on a laptop using spreadsheet software.
Setting and equipment
Equipment included: a password-protected external hard drive; computer compatible with spreadsheet software and the SPSS V.2531 for analysis; height-adjustable treatment plinth (plinth height was maintained throughout); three high-resolution video-recording cameras (Panasonic HC-V770 50× Zoom 4k Full HD) with tripods, capable of recording in two dimensions at perpendicular angles, where the horizontal centre line of the camera was lined up with the horizontal surface of the treatment plinth. The plinth height from the surface to the floor was set to 75 cm. Cameras were set up at 150 cm away from the edge of the treatment plinth to the lens. Video cameras were synchronised to record simultaneously from two angles at the start of testing. Recording angles included a lateral view of both left and right sides of the participants and a caudal to cephalad view. Footage was cropped to allow for time efficiency when assessing IRS by deleting plinth transfer footage between participants using video analysis software.32 This method of video augmentation in movement analysis is well validated33 34 and has proven reliable when qualitatively assessing human biomechanics against quantitative criteria.35–37
Data collection
Participant’s IRS data were collected by a senior team physiotherapist and participant’s PCI data were collected over the course of the season by an independent member of the team’s therapy staff. Data collection for IRS took place within the physiotherapy room of an English premiership rugby union club. Participants were required to spend a maximum of 2 min each (including transfer time) in a prone position on the treatment plinth. Testing for all participants took approximately 2 hours including equipment setup. Data were collected from all participants on day 1 of preseason testing. The number and location of PCIs for each participant were then recorded for the duration of the 9-month English premiership rugby playing season using digital spreadsheet software as part of departmental injury surveillance. This was standardised using the definition of PCI as outlined in the study design, and the same individual was responsible for data recording to ensure continuity and avoid potential for bias.
Outcome measures
The two main outcome measures for this study were PCI (dependent variable) and the IRS (independent variable). The IRS was measured quantitatively from analysis of the qualitative data collected against the IRS and cross-referenced against the recorded video by the lead researcher. The number of PCIs sustained by each player across a 9 month playing season was captured at the end of the season. Participant age was also compared against the number of PCIs sustained for use in data comparison against the already established injury risk identifier.
Statistical analysis
Data analysis using SPSS version 2531 was used for data comparisons and assessment of correlation. Prior to statistical analysis both IRS and PCI variables were assessed for homogeneity of variance and normal distribution using the Kolmogorov-Smirov and Shapiro-Wilk tests. As assumptions of homogeneity and normal distribution were not met, a Spearman’s correlation coefficient (SCC) was conducted where R was interpreted as (R≥0.90—very strong, R=0.70–0.89—strong, R=0.40–0.69—good, R=0.10–0.39—weak and R=0–0.09—negligible).38 As age is proven to be a significant predictor of injury, it was considered a confounder; hence, appropriate adjustment was made to control this factor in the statistical analysis.
To reduce the likelihood of any type 1 errors within the group (N=50), a critical alpha (p) of <0.05 was used. Finally, a non-parametric linear regression was conducted to demonstrate whether there was a linear relationship between PCI and IRS, and if so to what degree the variables were related. To ensure methodological rigour throughout the study adheres to STROBE (Strengthening The Reporting of OBservational Studies in Epidemiology)39 reporting guidelines.
Patient and public involvement
Participants were first involved in research during the first day of data collection when informed consent was obtained, and their IRS was recorded. The research question and outcome measures were developed by the authors, and participants were informed of these using a patient information sheet prior to data collection. Participants were not involved in study design, recruitment or conduction and they were not asked to assess the burden or time required to participate in the study. In the dissemination of the results, the participants received their individual IRS followed by a discussion around their PCI risk with advice around reducing this risk.