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Gait Analysis and Gait Training in Patient With Total Hip or Total Knee Replacement

Gait Analysis and Gait Training in Subjects 1 Year After Total Hip or Total Knee Replacement by Means

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03849638
Acronym
WVPT
Enrollment
50
Registered
2019-02-21
Start date
2018-12-06
Completion date
2024-12-31
Last updated
2023-04-19

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

Conditions

Arthroplasty, Replacement, Hip, Arthroplasty, Replacement, Knee

Keywords

gait analysis, gait training, biofeedback

Brief summary

The main objective of the present study is the evaluation of the kinematic parameters of gait and distribution of the load, recorded thruogh a sensorized treadmill, on lower limbs in patients at 1 year from Total Hip Replacement or Total Knee Replacement. The secondary objective is to evaluate the effects of gait training with biofeedback by means of a sensorized treadmill in patients with asymmetry of the kinematic parameters of the step and of distribution of the load on the lower limbs.

Interventions

OTHERGait training with real time biofeedback

Patients presenting asymmetry of the kinematic parameters of the step to the evaluation with sensorized treadmill, will undergo gait training program. The training program consists of 20 session (1 session/day) of gait training. Daily gait training will last 30 minutes as distributed: * 5 minutes of heating at a comfortable speed for the patient * Three 5-minute sessions of gait training with biofeedback interspersed with a break of 5 minutes each.

Sponsors

Campus Bio-Medico University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Mini Mental State Examination ≥ 24 * 12 months after total hip or total knee replacement

Exclusion criteria

* impossibility to perform a walking test * disabling cardiovascular and osteo-arthro-muscular problems that can impair walking tests * central or peripheral neurological disorders that compromise the sensory-motor skills of the patient under examination and / or the degree of collaboration * patients who have not signed informed consent

Design outcomes

Primary

MeasureTime frameDescription
Gait Speedimmediately after treatmentmeters/second
Step Lengthimmediately after treatmentlength in meters
Ground Contact Timeimmediately after treatmentTime in seconds
Hip Kinematicsimmediately after treatmentangles (degrees) of hip ROM
Knee Kinematicsimmediately after treatmentangles (degrees) of knee ROM
Ankle Kinematicsimmediately after treatmentangles (degrees) of ankle ROM
Lower limb loadingimmediately after treatmentload percentage distribution on lower limbs

Countries

Italy

Contacts

Primary ContactFederica Bressi, MD
f.bressi@unicampus.it+390622541624

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026