Chronic ankle instability is associated with changes in the nervous system that amount to increased difficulty in activating the stabilizing muscles of the ankle. Neuromuscular Electrical Stimulation involves using electricity to activate those muscles in bursts, and is commonly used to improve muscle function in those with ACL injury. This study will provide 5 treatments over 2 weeks in patients with Chronic Ankle Instability and determine if Electrical Stimulation can change neural excitability, balance, neuromuscular control, and perceived function in these individuals.
Individuals with joint injuries, including ankle sprain and anterior cruciate ligament (ACL) injury have been observed to exhibit changes in central nervous system function that potentially predispose them for further injury (Needle et al. 2017). In ankle sprains, repeated sensations of rolling and giving-way known as chronic ankle instability (CAI) emerges in nearly 50 percent of those with a history of ankle sprain (Holland et al. 2019), with symptoms tied to changes in central nervous system function. As the understanding of these pathologies have expanded, researchers have begun to attempt to identify neuromodulatory interventions capable of addressing injury-induced maladaptive neuroplasticity, thus improving function (Bruce et al. 2020, In Press). Among those with ACL injury, one of the most common interventions implemented to overcome muscle activation deficits includes neuromuscular electrical stimulation (NMES) (Lepley et al. 2015). This intervention is often used in the initial stages of post-surgical recovery to improve quadriceps function; however, it's use in other populations of joint injury (i.e. ankle sprain) is far more limited. Some previous research has looked at the effects of NMES on acute ankle sprains, as this is the timeframe in which muscle activation deficits would be most evident (Wainwright et al. 2019), but there is very limited evidence in those with CAI. It was potentially thought that activation deficits are less evident and strengthening may overcome these deficits in those with chronic injury; however, new insights have identified additional mechanisms by which NMES may be effective (Lepley et al. 2015). Aside from generating activation of a generally inactive muscle, NMES when performed at high intensities has been described to improve neuromuscular function through disinhibitory mechanisms. That is that increased somatosensation from the electrical stimulation raises the central nervous sytem's awareness of that muscle's activation, yielding decreased inhibition and ultimately increased neural excitability. Our previous research using cortically-directed interventions demonstrated that improving neural excitability yielded better function in patients with chronic ankle instability (Bruce et al. 2020). This study will follow a similar framework; however, determining if these changes can be induced via a peripheral intervention. These findings have the ability to reframe the current treatment for CAI. We are pursuing the following 2 specific aims: 1. To determine if NMES changes neural excitability (MEP size, H:M ratio, silent period) compared to a placebo treatment in participants with chronic ankle instability. H1: NMES will increase MEP size, H:M ratio, and decrease cortical silent period in individuals with CAI compared to the placebo treatment. 2. To determine if changes in neural excitability related to NMES or placebo treatment result in improved function (balance, muscle activation, outcomes) in participants with chronic ankle instability. H2: Increased neural excitability will yield improved balance (postural stability indices), muscle activation, and patient-reported function.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
26
5 sessions that consist of NMES over the peroneus longus muscle. This consists of a biphasic current with a phase duration of 240us delivered in a frequency of 75 pules per second, with a ramp-up time of 2-seconds, followed by a 50-s rest period (no stimulation). Each cycle will consist of 10 seconds of "on" time, and 50 seconds off, with 10 cycles being performed each session.
5 sessions that consist of 11-minutes of TENS over the skin of the peroneus longus. This consists of a biphasic current will be continuously applied at 100 pulses per second, with a phase duration of 100us for 10 minutes. The intensity will be turned up until the point the subjects feel the current (sensory threshold)
Leon Levine Hall for Health Sciences
Boone, North Carolina, United States
RECRUITINGTibialis Anterior corticospinal excitability
Motor evoked potential size of tibialis anterior
Time frame: Baseline, Week-2 (end of intervention), Week-4 (retention)
Soleus corticospinal excitability
Motor evoked potential size of soleus
Time frame: Baseline, Week-2 (end of intervention), Week-4 (retention)
Peroneus Longus corticospinal excitability
Motor evoked potential size of peroneus longus
Time frame: Baseline, Week-2 (end of intervention), Week-4 (retention)
Tibialis anterior reflexive excitability
H:M ratio of tibialis anterior
Time frame: Baseline, Week-2 (end of intervention), Week-4 (retention)
Soleus reflexive excitability
H:M ratio of soleus
Time frame: Baseline, Week-2 (end of intervention), Week-4 (retention)
Peroneus longus reflexive excitability
H:M ratio of peroneus longus
Time frame: Baseline, Week-2 (end of intervention), Week-4 (retention)
Dynamic postural stability index
Postural stability indices during a hop-to-stabilization task
Time frame: Baseline, Week-2 (end of intervention), Week-4 (retention)
Tibialis Anterior muscle activation
Mean electromyography from the tibialis anterior during a hop-to-stabilization task
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Time frame: Baseline, Week-2 (end of intervention), Week-4 (retention)
Soleus muscle activation
Mean electromyography from the soleus during a hop-to-stabilization task
Time frame: Baseline, Week-2 (end of intervention), Week-4 (retention)
Peroneus Longus muscle activation
Mean electromyography from the peroneus during a hop-to-stabilization task
Time frame: Baseline, Week-2 (end of intervention), Week-4 (retention)
Ankle Eversion Strength
Isometric ankle eversion strength
Time frame: Baseline, Week-2 (end of intervention), Week-4 (retention)
Side-to-side Hop Test
Time to complete 10 hops over 30 cm lines
Time frame: Baseline, Week-2 (end of intervention), Week-4 (retention)
Patient-reported outcomes
Foot \& Ankle ability measure, Disablement in the Physically Active Scale, Tampa Scale for Kinesiophobia
Time frame: Baseline, Week-2 (end of intervention), Week-4 (retention)
Foot & Ankle ability measure
Subjects complete FAAM questionnaire
Time frame: Baseline, Week-2 (end of intervention), Week-4 (retention)
Disablement in the Physically Active Scale
Subjects complete DPA questionnaire
Time frame: Baseline, Week-2 (end of intervention), Week-4 (retention)
Tampa Scale for Kinesiophobia
Subjects complete TSK-11 questionnaire
Time frame: Baseline, Week-2 (end of intervention), Week-4 (retention)