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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02817399
Other study ID # 16022015
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 2016
Est. completion date January 2018

Study information

Verified date January 2018
Source Medical Corps, Israel Defense Force
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to examine the short term effect of functional electrical stimulation treatment versus neuro-muscular electrical stimulation on gait quality for patient after anterior cruciate ligament reconstruction.


Description:

Background: Quadriceps weakness is common following anterior cruciate ligament (ACL) reconstruction. The inadequate quadriceps strength contributes to altered gait patterns following ACL reconstruction. Neuromuscular electrical stimulation (NMES) has been shown to reduce quadriceps atrophy post-ACL reconstruction. However, the effect of functional electrical stimulation (FES), a modulation of NMES which enables quadriceps stimulation synchronized with gait, has not been tested. Objective: The aim of this study is to evaluate the effectiveness of FES to improve the gait pattern of patients post ACL reconstruction. Methods: Fifty six Individuals post-ACL reconstruction will be randomly placed into FES or NMES treatment group. All patients will receive a standard exercise program three sessions weekly. In addition, each group will receive a different electrical stimulation treatment: Neuromuscular Electrical Stimulation (NMES) or Functional Electrical Stimulation (FES). Outcome measures will include spatiotemporal gait measures (e.g., gait speed, single limb support, and asymmetry index), as well as isometric quadriceps strength. Measures will be taken a week before the surgery, a week after it, and one month from the beginning of rehabilitation. Strength and gait pattern will be measured. Isometric Quadriceps strength will measured using the Biodex isokinetic system, and gait analysis will be carried out through the spatio-temporal Optogait system.


Recruitment information / eligibility

Status Completed
Enrollment 23
Est. completion date January 2018
Est. primary completion date January 1, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 30 Years
Eligibility - Inclusion Criteria: - Intended patients for ACL reconstruction procedure - Age 18-30 - Committed for three sessions per week for 4 weeks - Exclusion Criteria: - Previous surgery at the same knee - Chronic knee swelling - Knee injury - History of recurrent ankle sprains, Achilles tendinopathy, or lower limb

Study Design


Related Conditions & MeSH terms

  • Rupture
  • Rupture of Anterior Cruciate Ligament

Intervention

Device:
Functional electrical stimulation
Electrical stimulation that cause muscle contraction while walking
Neuro-muscular electrical stimulation
Electrical stimulation that cause muscle contraction in a stationary position
Procedure:
Active exercises
Subjects will receive training exercise according to ACL reconstruction protocol

Locations

Country Name City State
Israel Zrifin Rishon LeZion Doar Tsvai

Sponsors (2)

Lead Sponsor Collaborator
Medical Corps, Israel Defense Force Ariel University

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percentages of single support at each leg The test will perform with the Optogait system (a device for the Gait Analysis). Single support phase within the gait cycle during which the body mass is carried by a single limb. This parameter calculated by percentage of stride (normally about 40%). One year
Secondary strength symmetry The method of assessment for this Outcome Measure is by calculated the differences between the right Quadriceps strength and the left Quadriceps strength One year
Secondary Gait speed Measured by kilometer per hour One year
Secondary Step length Measured by length of the average step for each leg One year
Secondary Quadriceps strength Measured by maximal peak torque in each leg (through Biodex Isokinetic dynamometer) One year
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