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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT03403413
Other study ID # F2177-P
Secondary ID RX002177
Status Terminated
Phase N/A
First received
Last updated
Start date January 1, 2017
Est. completion date December 31, 2018

Study information

Verified date April 2020
Source VA Office of Research and Development
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The primary goal of this pilot study is to explore the feasibility of cyclic vibration (CV) of the lower extremity muscles to improve walking in individuals with gait deficits from multiple sclerosis (MS).


Description:

This pilot study is designed to test the efficacy and safety of vibration at correcting the typical gait deficits that involve strength and coordination of multiple joints (hip, knee and ankle) in pre- and early swing phases of the gait cycle.

Aim 1: Develop a real-time control algorithm, timed by sensor detected gait events, to provide vibration emulating electromyographic (EMG) activity of target muscles during normal gait and verify its functionality in an able-body volunteer. Further, recruit 12 subjects (6 for CV and 6 controls) with gait deficits at the hip, knee and ankle from MS. Impose vibration during the gait cycle so that it emulates muscle activity pattern of normal gait. Perform baseline quantitative gait analyses to determine the spatio-temporal parameters, foot-to-floor clearance, kinematics, kinetics and patterns of EMG activity during walking with and without vibration in treatment group and without vibration in control group.

Aim 2: Implement 12 sessions (3/week for a month) of gait training with cyclic vibration emulating normal muscle activity of lower extremities in treatment group and gait training without vibration in control group and repeat baseline gait assessment to test the following hypotheses.

Hypothesis 1. Vibration of hip, knee and ankle muscles improves walking speed and foot-to-floor clearance through increased hip and knee pre-swing flexion and improved hip-knee coordination.

Hypothesis 2. Gait training with cyclic muscle vibration induces carryover effects that maintain improved walking after vibration is discontinued.

Hypothesis 3. Muscle vibration produces no untoward sensations or adverse physiological responses.


Recruitment information / eligibility

Status Terminated
Enrollment 5
Est. completion date December 31, 2018
Est. primary completion date December 31, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- MS diagnosis reviewed and confirmed by neurologist per the revised McDonald criteria [ ]

- EDDS>3

- Age 18-70

- Fixed gait deficiency defined as being present for at least 3 months without improvement

- Hip, knee and ankle muscle weakness or increased extensor tone with difficulty to initiate a step

- Ability to ambulate at least 10ft with contact guard.

- Muscle vibration without untoward sensation.

- Sufficient upper extremity function to use walking aids (walkers, crutches, canes).

- Poor hip-knee-ankle coordination during swing

- Hip, knee and ankle joint range within normal limits.

- Ability to clearly understand written and oral direction in English to provide consent.

- BMI < 30

- Absence of psychological and cognitive problems or chemical dependency

- No acute orthopedic or medical complications

Exclusion Criteria:

- Presence of demand pacemakers.

- Edema of the affected limb/s.

- Uncontrolled seizures/epilepsy.

- Severe depression.

- Botulin toxin treatment within 12 months.

- Peripheral neuropathy.

- Respiratory disease.

- Chronic pain.

- Rapidly progressive course suggestive of Marburg variant, Hurst encephalomyelitis or PPMS with three or more system involvement.

- Concurrent treatment with Tysabri.

- Cardiac arrhythmias with associated hemodynamic instability.

- Lower extremity injuries that limit range of motion or function

- Joint problems (hip or leg) that limit range of motion or cause pain with movement

- Women during pregnancy

- Patients with a relapse in the 3 months prior to presentation for study evaluation

- Patients with more than two relapses within the past 12 months

Study Design


Related Conditions & MeSH terms


Intervention

Device:
muscle vibration during walking
Baseline assessment of gait followed by 12 sessions (3/week for a month) of gait training with cyclic muscle vibration during walking emulating normal muscle activity of lower extremities in treatment group. Gait assessment both with and without muscle vibration were collected at follow-up after 12 sessions of gait training with muscle vibration.

Locations

Country Name City State
United States Louis Stokes VA Medical Center, Cleveland, OH Cleveland Ohio

Sponsors (1)

Lead Sponsor Collaborator
VA Office of Research and Development

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary 10MWT speed (m/s) baseline and after twelve 1 hour sessions in four weeks of gait training with muscle vibration. Outcome measures were tested both with and without muscle vibration and repeated measures were collected and averaged.
Primary Kinematics Peak hip, knee and ankle flexion during swing baseline and after twelve 1 hour sessions in four weeks of gait training with muscle vibration. Repeated measures were collected and averaged
Primary Toe Clearance Toe clearance between foot and the ground during swing baseline and after twelve 1 hour sessions in four weeks of gait training with muscle vibration. Repeated measures were collected and averaged
Primary Walking Distance Volitional walking distance at baseline and after gait training with vibration baseline and after twelve 1 hour sessions in four weeks of gait training with muscle vibration. Repeated measures were collected and averaged
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