6533b7d4fe1ef96bd12633f3

RESEARCH PRODUCT

In-home versus hospital preoperative balance and proprioceptive training in patients undergoing TKR; rationale, design, and method of a randomized controlled trial.

José-maría BlascoCeledonia Igual-camachoSergio Roig-casasúsSergio Roig-casasús

subject

MaleBalancemedicine.medical_specialtylcsh:Diseases of the musculoskeletal systemSports medicinemedicine.medical_treatmentCost-Benefit AnalysisPsychological interventionlaw.invention03 medical and health sciencesStudy Protocol0302 clinical medicineRheumatologyRandomized controlled trialQuality of lifelawPreoperative CaremedicineHumansOrthopedics and Sports Medicine030212 general & internal medicineDynamic balanceArthroplasty Replacement KneePostural BalancePhysiotherapyBalance (ability)AgedAged 80 and overRehabilitationbusiness.industryRecovery of FunctionMiddle AgedOsteoarthritis KneeProprioceptionHome Care ServicesHospitalizationTotal knee replacementSensorimotorTotal knee arthroplastyBerg Balance ScalePhysical therapyFemalelcsh:RC925-935Preoperative interventionbusiness030217 neurology & neurosurgeryPhysical Conditioning Human

description

Abstract Background Severe knee osteoarthritis, as well as the surgical procedure of total knee replacement that aims to reduce its symptoms, cause great deterioration on the proprioceptive system. Taking this fact into account, and considering that balance abilities positively influence the capacity to perform basic functional tasks, this trial aims to find the short and mid-term effects of a preoperative balance and proprioceptive training when conducted by patients undergoing total knee replacement. Along with the effects, it is intended to determine whether in-home based training can be as effective as hospital training. The results will help to conclude whether the possible benefits may outweigh the health costs. Methods Seventy-five participants will take part. The trial will include in-home and supervised hospital experimental training compared to a non-active control group in order to estimate the actual effect of the proposal against the benefits due exclusively to the surgical procedure. Interventions last 4 weeks prior to surgery, and the follow-up will be at 2w, 6w, and 1y following the operation. The primary outcomes are in agreement with the goals: self-reported functionality in terms of KOOS and overall balance in terms of the Berg Balance Scale. The secondary outcomes will include the measurements of static and dynamic balance abilities, pain, function, and quality of life. Discussion It is expected for the results of this trial to provide relevant information in order to decide if a specific intervention is cost-effective to be implemented in clinical practice. Trial registration Clinicaltrials.gov identifier NCT03100890 . Registered in April 4, 2017.

10.1186/s12891-017-1887-4https://pubmed.ncbi.nlm.nih.gov/29221471