NCT03300986

Brief Summary

This study aims to look at how changes to a person's functional electrical stimulation might change how they walk. Functional electrical stimulation (FES) is commonly used to help people with foot drop from upper motor neurone conditions such as stroke or multiple sclerosis. This group of people have muscle weakness which makes it difficult to lift the foot, which causes trips and falls. FES reduces foot drop by using a portable device to apply short electrical pulses to the nerve which lifts the foot. The FES device stimulates this nerve only during the swing phase, when the foot is off the floor. Typically this is achieved by using a foot-switch, which detects when the heel leaves the floor. Stimulation begins a short interval of time after the heel leaves the floor, ramps up from zero to set stimulation for the individual, and at another period of time after the heel hits the floor, stimulation ramps down from set amount to zero. There are four time intervals described here which can be varied by the clinician on the device:-

  • Delay (the time between heel lift and the start of stimulation)
  • Ramp up (the time for stimulation to reach full strength)
  • Extension (the time between heel strike and the ramp down)
  • Ramp down (the time for stimulation to reach zero from full strength) These intervals are usually set by experienced clinicians using a qualitative assessment of the patient's walking and trial-and-error. A literature review has found no published studies which compare walking with different timing. This knowledge would be useful for clinicians, who could use this information as a starting point in finding the best timing parameters for each patient.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
10

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Apr 2016

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2016

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2017

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

May 2, 2017

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

August 11, 2017

Completed
2 months until next milestone

First Posted

Study publicly available on registry

October 4, 2017

Completed
Last Updated

October 4, 2017

Status Verified

September 1, 2017

Enrollment Period

11 months

First QC Date

August 11, 2017

Last Update Submit

September 28, 2017

Conditions

Outcome Measures

Primary Outcomes (1)

  • Gait analysis will be measured according to routine protocol

    Gait analysis will measured in accordance with the Plug-In-Gait model guide. This measures 16 points on the subjects left and right leg.

    Gait will be assessed over one visit of three hours.

Study Arms (1)

Functional Electrical Stimulation (FES) users

Eligibility Criteria

Age18 Years - 100 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The population for this study is adult users of standard FES for foot drop, registered with the Leeds FES service. Any upper motor neurone lesion can be the primary condition.

You may qualify if:

  • Upper motor neurone lesion causing foot drop
  • Currently use single-channel Odstock Medical ODFS functional electrical stimulator
  • Age 18 or older
  • Attending Leeds FES Service follow-up clinics

You may not qualify if:

  • FES user for less than three months
  • Lower limb prosthesis
  • Cannot walk 5m with walking aids
  • Cannot walk twenty 5m walks within a three-hour period
  • Use FES less than once per week

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Gait Disorders, Neurologic

Condition Hierarchy (Ancestors)

Neurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 11, 2017

First Posted

October 4, 2017

Study Start

April 1, 2016

Primary Completion

March 1, 2017

Study Completion

May 2, 2017

Last Updated

October 4, 2017

Record last verified: 2017-09