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Gait Asymmetry Assessed Using Portable Gait Analysis System

Gait Asymmetry in Orthopaedic Conditions of the Lower Extremity Assessed Using Portable and Laboratory Based Systems: Cross-sectional Observational Single-centre Pilot Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02489188
Acronym
Asymmetry
Enrollment
150
Registered
2015-07-02
Start date
2015-06-30
Completion date
2019-09-30
Last updated
2019-11-15

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

Conditions

Ankle Osteoarthritis, Hip Osteoarthritis, Knee Osteoarthritis, Lumbar Spine Stenosis, Muscle Contracture

Keywords

gait asymmetry, joint angles

Brief summary

To date, detailed analysis of movement patterns in orthopaedic conditions are mainly performed in research projects. Because these tests are time consuming, they are not feasible in clinical routine or in standard examinations. Novel technologies allow capturing detailed movement patters within a few minutes. The aim of this regional study is to compare aspects of movement tasks measured using a mobile gait analysis system to those measured using laboratory based systems and to determine aspects of gait patterns relevant for different orthopaedic conditions. Moreover, the researchers will investigate if these relevant aspects can be altered using surgical treatment or manual therapy.

Detailed description

This is a cross-sectional study. Pre- and post-treatment data will only be collected in patients undergoing routine orthopaedic treatment.

Interventions

PROCEDUREarthroplasty

patients, who are scheduled for arthroplasty, will be measured before and on average 6 months after surgery

OTHERmanual therapy

patients, who are scheduled for manual therapy, will be measured before, immediately and on average 1 week after treatment

PROCEDURElumbar spinal stenosis decompression

patients, who are scheduled for lumbar spinal stenosis decompression, will be measured before and on average 6 months after surgery

Sponsors

University Hospital, Basel, Switzerland
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Age ≥ 40 years, for patients: diagnosed osteoarthritis at the ankle, knee or hip, lumbar spinal stenosis or limited range of motion at the knee

Exclusion criteria

* Body mass index \> 35kg/m2 * Use of walking aids * Inability to walk for 6 minutes * Neuromuscular disorders affecting gait * Cardiovascular disease * Inability to follow procedures due to psychological disorders or dementia

Design outcomes

Primary

MeasureTime frameDescription
symmetry indexup to 6 monthsgait asymmetry assessed using a portable and laboratory gait analysis systems

Secondary

MeasureTime frameDescription
change in symmetry indexup to 6 monthschanges in gait asymmetry assessed using a portable and laboratory gait analysis systems
maximum isokinetic joint moment [Nm]up to 6 monthsisokinetic muscle strength
relative electromyographic (EMG) intensityup to 6 monthselectromyographic activity normalised to activity during maximum voluntary contraction
differences between maximum flexion and extension [degrees]up to 6 monthspassive range of motion

Countries

Switzerland

Outcome results

None listed

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