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Efficacy of adding a physiotherapy rehabilitation programme to arthroscopic management of femoroacetabular impingement syndrome: a randomised controlled trial (FAIR)
  1. Kim L Bennell1,
  2. Libby Spiers1,
  3. Amir Takla2,
  4. John O’Donnell3,
  5. Jessica Kasza4,
  6. David J Hunter5,6,
  7. Rana S Hinman1
  1. 1Department of Physiotherapy, The University of Melbourne, Centre for Health, Exercise and Sports Medicine, School of Health Sciences, Melbourne, Victoria, Australia
  2. 2Ivanhoe Sports and Physiotherapy Clinic, Melbourne, Victoria, Australia
  3. 3St Vincent’s Private Hospital, East Melbourne, Victoria, Australia
  4. 4Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Victoria, Australia
  5. 5Department of Rheumatology, Royal North Shore Hospital, Sydney, New South Wales, Australia
  6. 6Institute of Bone and Joint Research, Kolling Institute, University of Sydney, Sydney, New South Wales, Australia
  1. Correspondence to Dr Kim L Bennell; k.bennell{at}unimelb.edu.au

Abstract

Objectives Although several rehabilitation programmes following hip arthroscopy for femoracetabular impingement (FAI) syndrome have been described, there are no clinical trials evaluating whether formal physiotherapy-prescribed rehabilitation improves recovery compared with self-directed rehabilitation. The objective of this study was to evaluate the efficacy of adding a physiotherapist-prescribed rehabilitation programme to arthroscopic surgery for FAI syndrome.

Design Randomised controlled trial.

Methods People aged ≥16 years with FAI syndrome scheduled for hip arthroscopy were recruited and randomly allocated to physiotherapy (PT) or control. The PT group received seven PT sessions (one preoperative and six postoperative) incorporating education, manual therapy and a progressive rehabilitation programme of home, aquatic and gym exercises while the control group did not undertake PT rehabilitation. Measurements were taken at baseline (2 weeks presurgery) and 14 and 24 weeks postsurgery. The primary outcomes were the International Hip Outcome Tool (iHOT-33) and the sport subscale of the Hip Outcome Score (HOS) at week 14.

Results Due to slower than expected recruitment and funding constraints, recruitment was ceased after 23 months. Thirty participants (14 PT and 16 control) were randomised and 28 (14 PT and 14 control; 93%) and 22 (11 PT and 11 control; 73%) completed week 14 and 24 measurements, respectively. For the 14-week primary outcomes, the PT group showed significantly greater improvements on the iHOT-33 (mean difference 14.2 units; 95% CI 1.2 to 27.2) and sport subscale of the HOS (13.8 units; 95% CI 0.3 to 27.3). There were no significant between-group differences at week 24.

Conclusions An individual PT treatment and rehabilitation programme may augment improvements in patient-reported outcomes following arthroscopy for FAI syndrome. However, given the small sample size, larger trials are needed to validate the findings.

Trial registration number Trial registered with the Australian New Zealand Clinical Trials Registry :ACTRN12613000282785, Results.

  • FAI
  • hip
  • exercise
  • arthroscopy
  • physical therapy

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Strengths and limitations of this study

  • Our study was designed with attention to key methodological features to minimise bias including randomisation, concealed allocation and intention-to-treat analysis.

  • The primary outcomes were reliable and valid patient-reported measures suitable for young active individuals with femoracetabular impingement syndrome.

  • The delivery of the physiotherapy intervention by multiple physiotherapists enhances the generalisability of the findings.

  • The results cannot necessarily be generalised to other physiotherapy protocols with different content and number of physiotherapy sessions.

  • The trial recruited fewer than expected participants and hence given the small sample size, the results should be considered preliminary and require replication in a larger study.

Introduction

Femoroacetabular impingement (FAI) syndrome is a common cause of hip/groin symptoms and impaired performance in younger sporting populations1–3 and a potential precursor to hip osteoarthritis.4–6 FAI syndrome results from morphological hip abnormalities where the proximal femur and non-bony connective tissue abut against the acetabular rim.2

Hip arthroscopy is often used to manage FAI syndrome7 with case series generally reporting favourable outcomes.8 9 Use of postoperative rehabilitation is variable and dependent on surgeon’s preferences and patient access to services.10 Furthermore, content of rehabilitation programmes vary considerably.10 Although several rehabilitation programmes following hip arthroscopy have been described,10–13 there are no clinical trials evaluating whether formal physiotherapy (PT)-prescribed rehabilitation improves recovery compared with self-directed rehabilitation.

Thus, the objective of this clinical trial was to evaluate the efficacy of a progressive physiotherapist-prescribed rehabilitation programme in individuals undergoing hip arthroscopy for FAI syndrome. The primary hypothesis was that those receiving physiotherapist-prescribed rehabilitation would report significantly greater improvements in health-related quality-of-life and function in sport at 14 weeks postsurgery than those in the control group not undergoing PT rehabilitation.

Methods

We conducted a parallel-design two-arm randomised controlled trial (RCT) with outcomes assessed at baseline (within 2 weeks prior to surgery), at 14 weeks postsurgery (immediately following the PT intervention) and at 24 weeks postsurgery (figure 1). Ethical approval was obtained from the institutional Human Research Ethics Committee (#1238190). Participants provided written informed consent. The trial protocol has been published.12 Part way through recruitment, the original upper age limit of 35 years was removed, and patients undergoing bilateral surgery were included to improve generalisability and expedite recruitment. The funding organisation did not have a role in the collection, analysis or interpretation of data, or in approval of publication of this manuscript.

Figure 1

Participant flow through the trial. FAI, femoracetabular impingement.

Individuals aged ≥16 years with FAI syndrome (diagnosed by an orthopaedic surgeon based on clinical/imaging findings) with hip/groin symptoms for ≥3 months and scheduled for hip arthroscopy were recruited from the private surgical practices of three orthopaedic surgeons in Melbourne, Australia. Exclusion criteria included: (1) radiographic evidence of hip osteoarthritis more than mild in severity defined as Tönnis >grade 114; (2) professional athlete; (3) other concurrent injury/condition affecting ability to undertake rehabilitation; (4) unable to attend a study physiotherapist if randomised to the PT group; (5) unwilling to refrain from formalised PT rehabilitation; and (6) unable to understand English.

Potentially eligible patients were identified by study surgeons and provided with study information. An independent research assistant confirmed eligibility via subsequent telephone screening. Consenting participants completed baseline questionnaires electronically approximately 2 weeks before surgery. Participants were then consecutively randomised into either the physiotherapist-prescribed rehabilitation (PT) group or the control group.

A study biostatistician prepared the randomisation schedule (computer-generated random permuted blocks of 6–8, stratified by orthopaedic surgeon and unilateral/bilateral surgery). Consecutively numbered, sealed, opaque envelopes containing group allocation were prepared by an independent researcher. Envelopes were stored in a locked location and opened in sequence to reveal group allocation by a different researcher not involved in recruitment or data handling.

It was not possible to blind participants (who were also deemed to be assessors given that outcome measures were self-reported) or physiotherapists providing the intervention. However, surgeons performing hip arthroscopy, the physiotherapists providing inpatient management and the biostatistician were blinded to group allocation.

All participants underwent hip arthroscopic surgery for FAI syndrome performed by an experienced hip orthopaedic surgeon. Unstable articular cartilage flaps were debrided and exposed subchondral bone was treated by microfracture if <400 sq mm. Superficial labral tears were debrided, and tears that were unstable or >50% deep were repaired. Partial or complete teres tears were debrided with a radiofrequency probe. Cam impingement lesions were treated by femoral osteochondroplasty. Pincer impingement lesions were treated when both radiological and intraoperative pathological evidence confirmed the diagnosis.

Immediate postoperative care was consistent for both groups and included: ice and compression; one inpatient visit by the hospitals’ physiotherapist for provision of a gait aid; surgeons’ usual written educational material; and use of a non-steroidal anti-inflammatory drug. A follow-up visit with the surgeon occurred approximately 2 weeks postsurgery. Patients were advised to use crutches until pain-free walking, likely 5 days or less, and to avoid hip flexion past 90° and positions that could cause impingement and/or increase inflammation for approximately 6 weeks.

The protocol for the physiotherapist-prescribed rehabilitation has been previously described.12 It was a progressive semistructured accelerated programme based on the Takla-O’Donnell protocol, developed and refined by two of the authors over 10 years and currently used in their clinical practice (see table 1, online supplementary material 1, online supplementary material 2).12 Participants in the PT group attended seven 30 min individual appointments with a study physiotherapist: one preoperative visit (after baseline assessment) within 2 weeks prior to surgery and six postoperative visits commencing at week two (approximately 2, 4, 6, 8, 10 and 12 weeks postsurgery). Six physiotherapists with ≥2 years of musculoskeletal experience were trained to provide the intervention.

Supplementary Material

Supplementary material 1

Supplementary Material

Supplementary material 2
Table 1

The physiotherapy intervention

The PT programme included both mandatory and optional components and comprised of standardised PT assessments/reassessments, education and advice, manual therapy techniques, daily home exercise programme, unsupervised gym and aquatic programme at a local community facility at least twice weekly and graduated return to sport and physical activity. Individual progression of the programme was guided by the assessment findings and the surgical intervention, such as whether microfracture was used. PT treatment and gym/pool access were provided free of charge to the PT group participants.

Education: education and advice was the key component of the preoperative treatment session and an important part all postoperative session. Participants were given a handout summarising information about postoperative joint protection, including activities to avoid or modify. Advice was given about return to driving and work, and the importance of the home exercise programme was emphasised.

Manual therapy: trigger point massage was used at each postsurgical treatment session to release muscle tension, assist with pain relief and improve hip range of motion. Lumbar spine mobilisation (passive accessory intervertebral movements) was used when the PT assessment indicated it was needed.

Home exercise programme: the daily home exercise programme aimed to improve local stabilisation of the hip joint by retraining and strengthening the deep hip rotator muscles. This muscle retraining followed seven stages, with participants moving to the next stage once they achieved effective activation and endurance of the muscles as determined by the therapist. Exercises to reduce the risk of adhesions and maximise hip range of movement were also prescribed. Exercise sheets were provided to study participants (see online supplementary material 1).

Gym and aquatic programme: participants were provided with access to local community gym and pool facilities (YMCA centres) and asked to attend at least twice weekly following the first postoperative PT session. Participants walked in the pool and used a stationary bike and cross-trainer, progressing to swimming and lower body resistance exercise.

Return to sport: this included provision of functional and sport-specific drills. Preliminary components of sporting activity generally commenced 6–8 weeks postsurgery, with training in the actual sporting environment starting 10–12 weeks postsurgery.

The control group received no physiotherapist-prescribed rehabilitation programme. Participants were asked to refrain from seeing a physiotherapist for the first 3 months after surgery. Participants gradually increased their physical activity levels and returned to exercise/sport based on information provided by the surgeon. As such, participants performed self-directed rehabilitation.

Physiotherapist protocol adherence was maximised through provision of a treatment manual, attendance at a 1-day training course and telephone meetings. Physiotherapists used standardised treatment recording forms, which were audited by research staff.

Age, sex, occupation, sporting involvement, duration of hip symptoms, previous treatments, medication use, surgical findings and surgical intervention were obtained from questionnaires and the surgical report.

The International Hip Outcome Tool (iHOT-33) measures health-related quality-of-life in young active patients with hip disorders15 and covers: symptoms and functional limitations (16 items); sports and recreational activities (six items); job-related concerns (four items); and social, emotional and lifestyle concerns (seven items). It uses a 100 mm horizontal visual analogue scale where a higher score represents better quality-of-life. This tool has good test–retest reliability, demonstrated face, content and construct validity and is highly responsive to clinical change.15 16 The minimum clinically important difference (MCID) for this patient population is 6.1.15

The Hip Outcome Scale (HOS) assesses the degree of difficulty in performing tasks in: activities of daily living (ADLs; 17 items) and sport (nine items).17 Items are scored on a 5-point Likert scale with scores summed and converted to a percentage. In younger patients undergoing hip arthroscopy, the HOS has excellent test–retest reliability,16 evidence of content, construct and concurrent validity18 19 and is responsive to clinical change.20 The MCID for the sport subscale is 6.0.20

The Copenhagen Hip and Groin Outcome Score (HAGOS) assesses hip and groin disability,21 including pain (10 items), symptoms (7 items), physical function in daily living (5 items), physical function in sport and recreation (8 items), participation in physical activities (2 items) and hip and/or groin-related quality-of-life (5 items). Items are scored on a 5-point Likert scale and a normalised score (100 indicating no symptoms and 0 indicating extreme symptoms) is calculated. In young to middle-aged patients with chronic hip/groin pain, the HAGOS has good to excellent test–retest reliability16 21 and evidence of construct validity and responsiveness to change.21

At each reassessment, participants rated their perceived overall change in their hip/groin problem (compared with baseline) on a seven-point ordinal scale (much worse to much better).22

A modified Tegner Activity Scale23 (scores 0–10 with 10 indicating professional/international level competition) and the Heidelberg Sports Activity Score (HSAS)24 (0–220, higher score indicating greater sports activity) were administered to grade participants’ level of sport/recreation and occupational physical activity.

The number of PT visits attended was recorded for the PT group. The PT group maintained a log-book to record home exercise, gym and pool activity. The number of exercise sessions completed was calculated as a percentage of those prescribed by the physiotherapist. In addition, participants self-rated their adherence to the rehabilitation programme at 14 weeks postsurgery on an 11-point numeric rating scale (0 being ‘not at all’ to 10 being ‘completely as instructed’).

Information on adverse events, cointerventions and medication use was collected from all participants during the intervention phase using a log-book and by self-report questionnaire at 14 and 24 weeks postsurgery.

Primary endpoints were change from baseline to 14 weeks postsurgery in: (1) the iHOT-33 and (2) sports subscale of the HOS. Between-participant SDs have not been widely reported in the literature for these questionnaires so the study was powered to detect a moderate effect size of 0.5. Given this, the required sample for a two-tailed comparison of the groups using analysis of covariance with baseline values as covariates and an assumed correlation between participant measures at baseline and 14 weeks of 0.625 when d=0.5, power is 0.8 and type I error is .05 was 41 participants per group.

Analysis was by a blinded biostatistician (JK) using Stata (V.13.1) software on an intention-to-treat basis. Testing was two sided with a significance level set at p<0.05. Due to minimal missing data (2 out of 30 participants for week 14 outcomes), a complete case analysis was performed rather than analysis using multiple imputation. Between-group differences in mean change from baseline to each time point were compared using linear regression modelling adjusting for baseline levels of the outcome measure and including physiotherapist as a random effect to account for clustering. Ratings of global change were dichotomised a priori as improved (‘moderately’ or ‘much’ better) and not improved (‘slightly’ better and below) and between-group comparisons made using log binomial regression and presented as relative risks.

Results

Participants were recruited between July 2013 and June 2015. Figure 1 shows participant flow through the trial. Due to difficulty recruiting participants, we terminated recruitment prior to the target number. Of 108 patients screened, 78 (72%) were ineligible or did not wish to participate. In total, 30 participants (14 PT, 16 control) were randomised and 28 (14 PT, 14 control; 93%) and 22 (11 PT, 11 control; 73%) completed week 14 and 24 measurements, respectively. Cross-over occurred from control to PT, with three (19%) participants seeking PT rehabilitation prior to week 14. Characteristics of treatment groups and intraoperative findings and surgical procedures (table 2) were similar between groups, except for slightly more acetabular rim lesions and microfractures in the PT group.

Table 2

Baseline characteristics and intraoperative findings and surgical management by group, reported as mean (SD), unless otherwise stated

Table 3

Mean (SD) scores on continuous outcome measures across time according to group

At week 24, there were no significant differences between groups for changes in any primary or secondary outcome (table 3). A similar proportion of participants in both groups reported overall improvement (PT: 9/11, 82% vs controls 8/10, 80%; relative risk 1.0; 95% CI 0.67 to 1.6).

Table 4

Mean (95% CI) changes within groups, and adjusted mean (95% CI) difference in changes between groups, for continuous outcome measures, adjusting for baseline values of outcome and physiotherapist

All participants in the PT group attended all seven PT appointments. The mean (SD) percentage of prescribed exercise sessions completed was excellent at 88.8 (10.0)%. On a scale of 0–10, mean (SD) self-rated adherence was 8.3 (1.2) for the overall programme. For individual programme components, self-rated adherence was 8.6 (1.4) for home exercises, 5.9 (3.5) for the pool programme and 7.2 (2.4) for the gym programme.

Two participants in the PT group reported mild adverse events comprising muscle soreness from exercise and back pain. Use of other cointerventions was minimal and included analgesia (PT: n=2, control: n=2). The three participants who crossed over from the control group sought massage in addition to PT, while another two consulted a health professional in the first 14 weeks after surgery (osteopathy and yoga, n=1; chiropractic, n=1).

Discussion

One of the major advantages of hip arthroscopic surgery for FAI syndrome is the relative speed of recovery compared with open surgery.26 Any additional intervention that further speeds recovery would add to this perceived advantage. We found that a physiotherapist-prescribed rehabilitation programme led to greater improvements of a clinically relevant magnitude for both primary outcomes at 14 weeks postsurgery compared with a patient-managed protocol with only minor input from an inhospital physiotherapist and the surgeon. At 24 weeks, the results were inconclusive given the small sample size. The findings provide preliminary evidence supporting the value of a PT rehabilitation programme in speeding progress of postoperative recovery.

Our study was designed with attention to key methodological features to minimise bias including randomisation, concealed allocation and intention-to-treat analysis. The primary outcomes were reliable, and valid patient-reported measures were suitable for young active individuals with FAI syndrome.16 The delivery of the PT intervention by multiple physiotherapists enhances the generalisability of the findings. Furthermore, as the protocol involved a relatively small number of PT visits (n=7) and emphasised a home rehabilitation programme, it would be reasonably inexpensive to implement.

The study has several limitations. The sample size was small and did not reach our intended target due to difficulty recruiting participants. As this study was conducted in private practice, the surgeons were responsible for identifying potentially eligible patients during their consultation and directing them to the research assistant for further discussion about the study. As this relied on busy surgeons, a number of potentially eligible patients may have been missed. In future studies, it is recommended that the responsibility for participant identification rests with the researchers rather than the surgeons as far as possible. We also modified our eligibility criteria part way through the study to remove the upper age limit of 35 years and include those with bilateral surgery, which bolstered recruitment. Thus, future studies should consider the effect that eligibility criteria have on recruitment. Our recruitment rate of 28% of those screened was in fact reasonable, but a larger number of surgeons and/or a longer time frame would have been needed to reach our target. These were constrained by funding and timelines. Over 50% of potentially eligible individuals were unwilling to refrain from postoperative PT rehabilitation and were excluded. Inclusion of a control group whereby the participants consulted a physiotherapist for education and advice rather than a control group with no contact with a physiotherapist may have facilitated participation by patients who were unwilling to refrain from seeing a physiotherapist after surgery. While the dropout rate at the primary time point at 14 weeks was acceptable at 7%, the dropout rate by week 24 was much larger at 27%. The reasons for the dropout are unclear as these participants did not respond to numerous efforts to contact them via various means (eg, telephone, SMS and email). A small financial incentive for completion of questionnaires was provided at the 14-week time point. A similar incentive at the 24-week time point may have improved overall retention rates. Nevertheless, with our small sample, we were still able to demonstrate statistically and clinically significant differences in primary outcomes between groups at our primary time point of 14 weeks with the smaller sample than planned because the effect size of PT was larger than we assumed in our initial sample size calculation. By necessity, patients and physiotherapists were unblinded. We did not include objective measures of physical performance or impairments, so we cannot determine the effect of the intervention on these. Our results cannot be generalised to different rehabilitation programmes with more intensive PT contact and slower progression or to high-level competitive athletes whose functional requirements are greater. We excluded patients who planned to consult a physiotherapist for their rehabilitation due to their high risk of crossover and potential negative expectations about outcomes if they were allocated to the control group. It is possible that this subgroup may respond differently to the PT programme than those who were willing to participate and had some degree of equipoise about PT rehabilitation. Similarly, given the small sample size, we did not formally investigate whether other factors such as age and bilateral surgery moderate outcomes.

Two recent systematic reviews10 13 have highlighted the absence of RCTs investigating the efficacy of adding rehabilitation to hip arthroscopic management of FAI syndrome and as such we cannot directly compare our results to other RCTs. Instead studies have been either observational case series or case reports. Grzybowki et al13 identified 18 such studies and found considerable heterogeneity in rehabilitation programmes as well as poor reporting of specific programme parameters. Differences are apparent in timing of functional progression, often dictated by surgeon-imposed postoperative restrictions related to weight-bearing and hip range of motion, use of therapeutic techniques such as continuous passive motion machines, bracing and types of exercises. Consistent with several other programmes, ours emphasised strategies to improve hip range and muscle strength.10 13 We also aimed to retrain and strengthen the deep hip rotator muscles, which have a short lever arm and have been suggested to provide fine control of hip joint stability, acting as the ‘rotator cuff’ of the hip joint.27 28 Comparisons of our results with those of observational studies are somewhat constrained by differences in terms of outcome measures, follow-up time points post-FAI surgery and patient demographics, particularly age and level of sporting activity. Many studies included older patients to those in our sample and follow-up time points were often longer than 24 weeks, although one study found maximal improvement at this time with no further improvement at 2 years.29 Nonetheless, the levels of impairment seen at baseline in our sample and the magnitude of improvement seen in our treatment group are relatively consistent with those reported in observational studies.15 29–33 For example, we found a 93% improvement in the iHOT-33 at week 14 and a 110% improvement at week 24 that is similar to the approximate 90% and 82% improvement at 3 months and the 107% and 97% at 6 months in men and women, respectively, in the study by Joseph et al.29 However, no conclusions can be drawn about the superiority of one rehabilitation protocol over another at this stage.

The mechanisms that led to the greater improvements with the PT-prescribed rehabilitation programme are speculative. First, although not measured, the improvements may be due in part to improved hip range-of-motion and muscle strength (aims of the rehabilitation programme), as impairments in these have been reported in people with FAI syndrome34 35 and have been related to function.34 Second, it is possible that the education, advice and support provided by the physiotherapist and the structured progressive programme gave patients confidence to better manage their recovery.36 Third, patients may have been more adherent to performing rehabilitation exercises and activities given the regular contact with the physiotherapist. Last, as self-reported outcomes were used and patients and physiotherapists were not blind to group allocation, it is possible that initial treatment benefits were related, at least partly, to participant expectations and placebo effects.37

There was no significant difference between groups at 24 weeks postsurgery. It is possible that benefits of an initial PT programme become less apparent once contact with the physiotherapist ceases. However, the sample size was small and further reduced by the 24-week time point, so that statistical power was limited and sufficient only to detect large treatment effects. Furthermore, three controls crossed-over and sought PT rehabilitation and another two consulted a health professional but were included in the analysis as per intention-to-treat. This may have attenuated differences between groups. Thus, there is potential for a type II error, particularly as the mean between-group difference for change in the iHOT-33 favoured the PT group and exceeded the MCID. Therefore, while it is possible that PT rehabilitation may be beneficial over the longer term, this requires further confirmation.

Although greater improvements in the PT group were noted in a number of functional outcomes, these did not translate into greater increases in levels of sporting and occupational activity, as measured by the modified Tegner and the HSAS. However, this might reflect a limitation of these measures as both are relatively crude and likely not sensitive enough to detect small changes. Return to previous sporting level was not specifically assessed due to difficulties in reliably and accurately measuring this in a heterogeneous cohort such as ours.

As our study used patient-reported outcome measures whose clinimetric properties have been demonstrated in this patient population, our results also provide a baseline against which other protocols can be measured. Such comparisons could point to possible improvements in rehabilitation strategies that can then be introduced and rigorously tested.

Conclusion

Our results suggest that this particular PT rehabilitation programme, as part of the overall arthroscopic management of FAI syndrome, might improve patient-reported outcomes compared with self-directed rehabilitation at 14 weeks postsurgery but not at 24 weeks. However, given the small sample size due to early termination of the study, the results should be considered preliminary and require replication in a larger study before they can inform clinical practice.

Acknowledgments

Dr Margaret Staples performed the sample size calculation and prepared the randomisation schedule. The YMCA provided the participants in the PT group with free gym and pool access during their 3-month postsurgery treatment period. The orthopaedic surgeons who recruited research participants were Mr Parminder Singh and Mr Andrew Chia. Mr Phong Tran and Mr Cam Fary also identified potential participants but these did not pass screening. The study physiotherapists who provided the PT treatments were: Tony Beecroft, Moonee Ponds/Blackburn; Cara Peake, Ivanhoe; Craig Mansfield, Bendigo; Christian Becker, Narre Warren; Simon Ata, Ivanhoe; and Michael Rafla, Blackburn/Richmond.

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Footnotes

  • Contributors AT, JOD, KLB and RSH conceived the project; KLB and JOD procured the project funding; KLB and RSH coordinated the trial. KLB, RSH, AT, JOD, LS and DJH assisted with protocol design. AT and LS designed the physiotherapy protocol and, along with KLB, trained the physiotherapists. LS recruited the participants and managed the project. KLB wrote the first draft of this manuscript. JK performed the statistical analyses. All authors participated in the trial design, provided feedback on drafts of this paper and read and approved the final manuscript.

  • Funding This trial was funded by the National Health and Medical Research Council (program grant #631717), St Vincent’s Private Hospital Fitzroy Campus and the Australian Hip Arthroscopy Education and Research Foundation. Kim Bennell (#1058440) and David Hunter (#1079777) are supported by NHMRC Fellowships, and Rana Hinman is supported by an Australian Research Council Future Fellowship (FT130100175).

  • Competing interests AT and JOD developed the physiotherapy protocol that was tested and used this in their private clinical practices. JOD is the founder of the Australian Hip Arthroscopy Education and Research Foundation that provided financial support of the project. None of the other authors have any competing interests.

  • Ethics approval University of Melbourne Human Research Ethics Committee (HREC #1238190).

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data sharing statement Statistical code: Available from Dr Kasza (email: jessica.kasza@monash.edu). Data set: available from Dr Bennell (email: k.bennell@unimelb.edu.au).

  • Correction notice This paper has been amended since it was published Online First. Owing to a scripting error, some of the publisher names in the references were replaced with 'BMJ Publishing Group'. This only affected the full text version, not the PDF. We have since corrected these errors and the correct publishers have been inserted into the references.

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