ESCAIP: Functional Electrical Stimulation in Chronic Ankle Instability

Sponsor
Shmuel Springer (Other)
Overall Status
Recruiting
CT.gov ID
NCT04314960
Collaborator
(none)
22
1
1
23.3
0.9

Study Details

Study Description

Brief Summary

Individuals with chronic ankle instability (CAI) display neuromuscular deficits such as altered control of posture and gait when compared with healthy controls. These deficits may be attributed to muscle inhibition occurring after a surrounding joint structure has been damaged. Functional electrical stimulation (FES) is the application of high-intensity intermittent electrical stimuli to generate muscle contractions that may overcome inhibition, and which is coupled with a functional task such as gait.

The current study aims to investigate the short and immediate effects of FES on gait parameters and postural control in subjects with CAI. Prior to intervention, treadmill gait will be evaluated using a motion analysis system, and postural control will be evaluated in a series of tests that measure balance, reaction time to ankle perturbation and stabilization ability after jump-landing. Then, a 20 minutes gait training with an FES device will be applied. Immediate effects of the training on gait parameters will be assessed. For medium-term effects evaluation, subjects will return for additional 7 training sessions (2 per week for 4 weeks), following by a complete measurements acquisition as prior to intervention. At six months follow-up, subjects will be contacted for collecting subjective outcomes.

Condition or Disease Intervention/Treatment Phase
  • Device: Functional electrical stimulation device (NESS L300Plus, Bioness, Valencia, CA)
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
22 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Immediate and Long-term Effects of Gait Training With Functional Electrical Stimulation in Subjects With Chronic Ankle Instability
Actual Study Start Date :
Jun 23, 2020
Anticipated Primary Completion Date :
Jun 1, 2022
Anticipated Study Completion Date :
Jun 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: CAI subjects

Subjects in this group will receive eight 20-minutes gait training sessions with functional electrical stimulation.

Device: Functional electrical stimulation device (NESS L300Plus, Bioness, Valencia, CA)
Functional electrical stimulation (FES) is the application of high-intensity intermittent electrical stimuli to generate muscle contractions that may bypass spinal and supraspinal inhibition, and which is coupled with a functional task such as gait. Gait training will be conducted on a treadmill.

Outcome Measures

Primary Outcome Measures

  1. Immediate change in ankle inversion angle during heel strike [immediately after the intervention]

    Ankle inversion angle at heel strike (in degrees) will be measured using Qualisys motion analysis system. Change will be measured between pre-intervention to immediately after first intervention session to assess immediate effects of the intervention.

  2. Change in ankle inversion angle during heel strike at 4 weeks [through intervention completion, approximately at 4 weeks]

    Ankle inversion angle at heel strike (in degrees) will be measured using Qualisys motion analysis system. Change will be measured between pre-intervention and after completing the entire intervention.

  3. Immediate change in peroneal muscle electromyography [immediately after the intervention]

    Peroneal muscle activity will be measured (in millivolts) using Trigno EMG system during the 5% of gait cycle prior to heel strike. Change will be measured between pre-intervention to immediately after first intervention session to assess immediate effects of the intervention.

  4. Change in peroneal muscle electromyography at 4 weeks [through intervention completion, approximately at 4 weeks]

    Peroneal muscle activity will be measured (in millivolts) using Trigno EMG system during the 5% of gait cycle prior to heel strike. Change will be measured between pre-intervention and after completing the entire intervention.

Secondary Outcome Measures

  1. Change in Star excursion balance test (SEBT) score [through intervention completion, approximately at 4 weeks]

    The SEBT has been previously described as a postural control test that can differ between subjects with CAI and healthy controls. The test is performed with the subjects standing barefoot in the middle of a grid formed by eight tape measures extending out at 45° from each other. While the subject is balancing on one leg that is placed in the middle of the grid, the other leg has to reach as far as possible in each direction. The reached distance in centimeters is recorded, with the greater distance representing better postural stability. An average scores is calculated and normalized to the length of the subject's leg in centimeters.

  2. Time to stabilization (TTS) [through intervention completion, approximately at 4 weeks]

    TTS is the time required to normalize ground reaction forces (GRF) after following a jump-landing. To measure TTS, subjects will be required to perform a single-leg drop-jump from a 40-cm box onto a force plate (Kistler, Switzerland) and keep balancing on a single leg for 20 seconds. GRF recordings will be analyzed to determine TTS in seconds in the ML and AP planes, as was previously described. Shorter duration demonstrates better postural stability. Subjects will be allowed at least 3 practice trials, following by 5 successful jumps landings. A rest period of 30 seconds will be allowed between jumps. If a subject will not be able to stabilize for at least 20 seconds, the trial will be repeated. Lower values indicate better postural control.

  3. Peroneal reaction time (PRT) [through intervention completion, approximately at 4 weeks]

    PRT is the time duration between and ankle inversion perturbation and beginning of peroneal muscle activation which is recognized using EMG. Subjects will stand on an inversion stimulator. In an unknown time, a sudden inversion perturbation will occur. Time measurement between perturbation time and muscle activation time is measured in seconds. Lower values indicate better postural control.

Other Outcome Measures

  1. Foot and Ankle Ability Measure (FAAM) - questionnaire [through intervention completion, approximately at 4 weeks]

    A self-reported functional outcome measure utilized to track subjective changes in perceived pain and ankle function Score ranges between 0-100. Higher scores represent higher levels of function, with score of 100 represents no disability.

  2. Cumberland Ankle Instability Tool (CAIT) - questionnaire [through intervention completion, approximately at 4 weeks]

    A self-reported outcome measure designated for people with chronic ankle instability. Will also serve as an inclusion criteria. Score ranges between 0-30, with lower scores indicate less ankle instability.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 45 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. A history of at least one significant ankle sprain:

  2. At least 12 months prior to participating in the study

  3. Was characterized by inflammatory symptoms (i.e. pain and swelling)

  4. Caused at least one day of decreased physical activity

  5. At least 3 months since the last acute ankle sprain that results in inflammatory symptoms and at least one interrupted day of desired physical activity.

  6. History of the previously injured ankle 'giving way' at least twice during the last 6 months, and/or 'feelings of instability' and/or recurrent sprain.

  7. Being able to bear full weight on the injured lower extremity with no more than mild discomfort.

  8. Scoring<24 in the Cumberland Ankle Instability Tool (CAIT)

Exclusion Criteria:
  1. A history of previous surgeries to a musculoskeletal structure in either lower limb.

  2. A history of a fracture requiring re-alignment

  3. Any acute injury to a lower limb in the last 3 months.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ariel University Ariel Israel 40700

Sponsors and Collaborators

  • Shmuel Springer

Investigators

  • Principal Investigator: Shmuel Springer, PhD, Ariel University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Shmuel Springer, Chair, Physiotherapy Department, Neuromuscular & Human Performance Laboratory, Ariel University
ClinicalTrials.gov Identifier:
NCT04314960
Other Study ID Numbers:
  • AU-HEA-SS-20200308a
First Posted:
Mar 19, 2020
Last Update Posted:
Sep 2, 2020
Last Verified:
Sep 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Product Manufactured in and Exported from the U.S.:
Yes
Keywords provided by Shmuel Springer, Chair, Physiotherapy Department, Neuromuscular & Human Performance Laboratory, Ariel University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 2, 2020