Abstract

BackgroundFemoroacetabular impingement has been recognized as a common cause of hip pain and dysfunction, especially in athletes. Femoroacetabular impingement can now be better treated by hip arthroscopy but it is unclear what postoperative rehabilitation of hip arthroscopy should look like. Several rehabilitation protocols have been described, but none presented clinical outcome data. These protocols also differ in frequency, duration and level of supervision. We developed a rehabilitation protocol with supervised physical therapy which showed good clinical results and is considered usual care in our treatment center. However, it is unknown whether, due to the relatively young age and low complication rate of hip arthroscopy patients, rehabilitation based on self-management might lead to similar results. The aims of this pilot study are (1) to determine feasibility and acceptability of the self-management intervention, (2) to obtain a preliminary estimate of the difference in effect between physical therapy aimed at self-management versus usual care physical therapy in patients who undergo hip arthroscopy for femoroacetabular impingement.Methods/DesignThirty participants (aged 18–50 years) scheduled for hip arthroscopy will be included and randomized (after surgery) to either self-management or usual care physical therapy in this assessor-blinded randomized controlled trial. After surgery, the self-management group will perform a home-based exercise program three times a week and will receive physical therapy treatment once every 2 weeks for 14 weeks. The usual care group will receive physical therapy treatment twice a week for 14 weeks and will perform an additional home-based exercise program once a week. Assessment will occur preoperatively and at 6, 14, 26 and 52 weeks after surgery. Primary outcomes are feasibility, acceptability and preliminary effectiveness. Feasibility and acceptability will be determined by the willingness to enroll, recruitment rate, adherence to treatment, patient satisfaction, drop-out rate and adverse events. Preliminary effectiveness will be determined using the following outcomes: the International Hip Outcome Tool 33 and hip functional performance as measured with the Single Leg Squat Test 14 weeks after surgery.DiscussionThe results of this study will be used to help decide on the need, feasibility and acceptability of a large-scale randomized controlled trial.Trial registrationThis protocol was registered with the Dutch Trial Registry (NTR5168) on 8 May 2015.Electronic supplementary materialThe online version of this article (doi:10.1186/s13063-016-1222-7) contains supplementary material, which is available to authorized users.

Highlights

  • Femoroacetabular impingement has been recognized as a common cause of hip pain and dysfunction, especially in athletes

  • The results of this study will be used to help decide on the need, feasibility and acceptability of a large-scale randomized controlled trial

  • Participants in the selfmanagement group who report a deterioration on the International Hip Outcome Tool 33 (IHOT-33) at 6 weeks after surgery compared to the baseline/preoperative measurement or who experience complications from surgery, as described in Fig. 1, will be offered a transition to the usual care physical therapy group

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Summary

Discussion

This study provides a protocol for a pilot randomized controlled study into the feasibility, acceptability and preliminary effectiveness of two physical therapy rehabilitation strategies, self-management versus usual care physical therapy, in patients who undergo hip arthroscopy for FAI. This study will identify feasibility and acceptability by means of willingness to enroll, the number of eligible patients, recruitment rate, adherence to treatment, patient satisfaction, possible drop-out rates and adverse events [22] It will obtain a preliminary estimate of the difference in effect of the two physical therapy rehabilitation strategies in order to assist in future power calculations for a larger RCT [22]. The initial outcomes (IHOT-33 and SLST) used to determine a preliminary estimate of the difference in effect are reliable and valid for use in a population of hip arthroscopy patients and are translated and validated into the Dutch language [29–31, Tak et al, 2015 unpublished data] These outcomes are widely recommended for use in this particular population and will provide data for comparison with other studies such as the aforementioned trial by Bennell et al [21, 29,30,31].

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