Efficacy of real-time feedback exercise therapy in patients following total hip arthroplasty: a pilot cluster-randomized controlled trial
摘要
The prevalence of hip osteoarthritis is increasing and frequently requires total hip arthroplasty (THA). However, a standardized rehabilitation protocol to ensure sustainable functional recovery from THA has yet to be established. Therefore, this study compared the effects of real-time feedback-assisted home-exercise versus standard written instructions on the functional performance of patients following unilateral THA.
MethodsThis study was designed as a cluster-randomized controlled pilot trial with two parallel groups. Data from three-dimensional movement analysis, clinical examination, body-composition, activity monitoring and questionnaires were collected at baseline four weeks post-surgery, and follow-ups at three- and six-months post-surgery. Baseline measurements were followed by an eight-week supervised group exercise therapy. For home-exercise the control-group received printed instructions, whereas the intervention-group was provided a real-time feedback prototype.
ResultsA total of 22 patients, aged 52 to 73 years (mean 62.9), participated in the study, 21 completed the intervention and thereof, 19 could be assessed at six-months post-surgery. No statistically significant differences were found for the primary outcomes frontal knee, pelvis and trunk range-of-motion during level walking, nor the secondary outcomes Harris Hip Score (HHS), SF-12 and IPAQ short form. Both groups improved their mean walking speed, cadence, step length, isometric knee flexion force of operated limb, SF-12 physical domain and HHS.
ConclusionReal-time feedback assisted home-exercise after THA did not differ when compared to commonly used written instructions in improving function and quality of life. However, patients in the real-time feedback group reported greater motivation and self-confidence regarding exercise performance, which was not reflected in the recorded numbers of home-exercise sessions.
Trial registrationThe study was prospectively registered on 7th December 2023 at ClinicalTrials.gov NCT06161194.