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In-home Versus Hospital Preoperative Training for Patients Undergoing Total Knee Replacement

In-home Versus Hospital Preoperative Training for Patients Undergoing Total Knee Replacement

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03100890
Acronym
home_ATR
Enrollment
67
Registered
2017-04-04
Start date
2017-04-12
Completion date
2019-11-01
Last updated
2022-11-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Knee Osteoarthritis

Brief summary

In this work the importance of the potentiation and recovery of the balance with a physiotherapeutic intervention that begins in the early preoperative phase is compared with the conventional postoperative rehabilitation. The objective is to evaluate the influence of a muscle enhancement protocol in which a specific work of balance is included, with the physical benefits that this entails for the evolution of the patient. It also seeks to verify if the teaching and recommendation of exercises at home as preparation and conditioning for the intervention of ATR is effective, and to what extent, compared to a guided training in the hospital.

Interventions

OTHERPreoperative training (hospital)

Preoperative hospital training

OTHERPreoperative training (home)

Preoperative in-home training

Sponsors

Hospital Politècnic i Universitari la Fe de València
CollaboratorUNKNOWN
University of Valencia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
60 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Subjects with severe knee osteoarthritis that have not been operated before of total knee replacement. * The score in Berg scale must be greater than 21. * The score of the Mini-Mental State Examination must be equal or greater than 20. * Once the informed consent is read and explained, patients must accept and agree to participate in the study.

Exclusion criteria

* Post-surgical infection of the operated knee. * Pathology of central origin (i.e. cerebellar) that could interfere with balance or strength * Vestibular pathology that could interfere with balance

Design outcomes

Primary

MeasureTime frameDescription
Knee injury and Osteoarthritis Outcome Score (KOOS)change from baseline to the week before surgery, 2 and 6 weeks after surgerySelf-reported functionality assessment
Berg Balance Scale (BBS)change from baseline to the week before surgery, 2 and 6 weeks after surgeryOverall state of balance. Balance among older people with impairment in balance function by assessing the performance of functional tasks from the total score achieved in the 14 items test

Secondary

MeasureTime frameDescription
Timed Up and Go Test (TUG)change from baseline to the week before surgery, 2 and 6 weeks after surgeryDynamic balance assessment. Also points at the risk of falling. Time of getting up from a chair, walk three meters, come back and sit again, measured in seconds
Knee Range of Mobility (ROM)change from baseline to the week before surgery, 2 and 6 weeks after surgeryKnee Range of Mobility (Flexion, Extension) in degree
Quadriceps Strengthchange from baseline to the week before surgery, 2 and 6 weeks after surgeryElectronic dynamometer in Newton
Euro Quality of Life 5 Dimensionchange from baseline to the week before surgery, 2 and 6 weeks after surgeryQuality of Life assessment

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 8, 2026