Gait Asymmetry Assessed Using Portable Gait Analysis System

Sponsor
University Hospital, Basel, Switzerland (Other)
Overall Status
Completed
CT.gov ID
NCT02489188
Collaborator
(none)
150
1
52
2.9

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Procedure: arthroplasty
  • Other: manual therapy
  • Procedure: lumbar spinal stenosis decompression

Detailed Description

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

Study Design

Study Type:
Observational
Actual Enrollment :
150 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Gait Asymmetry in Orthopaedic Conditions of the Lower Extremity Assessed Using Portable and Laboratory Based Systems: Cross-sectional Observational Single-centre Pilot Study
Actual Study Start Date :
Jun 1, 2015
Actual Primary Completion Date :
Sep 30, 2019
Actual Study Completion Date :
Sep 30, 2019

Arms and Interventions

Arm Intervention/Treatment
ankle osteoarthritis

patients with ankle osteoarthritis scheduled for arthroplasty

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

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

knee osteoarthritis

patients with knee osteoarthritis scheduled for arthroplasty

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

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

hip osteoarthritis

patients with hip osteoarthritis scheduled for arthroplasty

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

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

lumbar spinal stenosis

patients with lumbar spinal stenosis scheduled for lumbar spinal stenosis decompression

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

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

muscle contracture

patients with functionally limited range of motion at the knee because of muscle contracture scheduled for manual therapy

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

healthy subjects

healthy subjects

Outcome Measures

Primary Outcome Measures

  1. symmetry index [up to 6 months]

    gait asymmetry assessed using a portable and laboratory gait analysis systems

Secondary Outcome Measures

  1. change in symmetry index [up to 6 months]

    changes in gait asymmetry assessed using a portable and laboratory gait analysis systems

  2. maximum isokinetic joint moment [Nm] [up to 6 months]

    isokinetic muscle strength

  3. relative electromyographic (EMG) intensity [up to 6 months]

    electromyographic activity normalised to activity during maximum voluntary contraction

  4. differences between maximum flexion and extension [degrees] [up to 6 months]

    passive range of motion

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 70 Years
Sexes Eligible for Study:
All
Accepts 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Hospital Basel Basel Basel Stadt Switzerland 4031

Sponsors and Collaborators

  • University Hospital, Basel, Switzerland

Investigators

  • Principal Investigator: Annegret Mündermann, PhD, University Hospital, Basel, Switzerland

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
University Hospital, Basel, Switzerland
ClinicalTrials.gov Identifier:
NCT02489188
Other Study ID Numbers:
  • 2015-139
First Posted:
Jul 2, 2015
Last Update Posted:
Nov 15, 2019
Last Verified:
Nov 1, 2019
Keywords provided by University Hospital, Basel, Switzerland
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 15, 2019