About this trial
Many types of pain can occur in Multiple Sclerosis (MS), one of the most common types is neuropathic pain. Neuropathic pain is directly related to the disease's demyelination process and is associated with dysesthetic pain, allodynia, hyperalgesia. For neuropathic pain in MS, there are numerous physical therapy and rehabilitation interventions focused on proprioception, balance reaction time management. Loss of proprioception is commonly observed in MS, this loss results from the demyelination of the central somatosensory pathways. Proprioception-the ability to perceive the position of the body and limbs relative to the environment-is also related to balance performance. Balance problems can be detected in the early stages of the disease, even if the patient has no disability. Another effect of MS is observed in reaction time. In MS, which is characterized by demyelination, axonal damage, a slowing of nerve conduction velocity leads to a decrease in information processing speed, resulting in prolonged reaction times. Neuromuscular training models designed to train the Central Nervous System (CNS) can be used to address these effects.Motor Imagery (MI) is one of the neuromuscular training models.
Imagery can be defined as the use of all one's senses to create a mental image of an activity. MI is referred to as a brain-training method and utilizes the neuromatrix theory to inhibit pain. MI training aims to retrain the neural networks that activate the neuromatrix so that they become less sensitive to stimuli that would not normally cause pain. Lateralization is a method used in conjunction with MI to distinguish between the right and left sides of the painful area. The imagery phase involves visualizing the positions and movements of the painful areas. MI is a neuromuscular training model, and another neuromuscular training method is Sensorimotor (SM) training.
It is known that SM, which applies repetitive sensorimotor stimulation, passively improves sensorimotor performance. Known as perceptual learning, this approach involves simple exposure to SM stimulation for several hours. While the term "perceptual" encompasses various senses, including sight and hearing, the term "sensorimotor training" is used here specifically to refer to methods focused on SM stimulation. SM training typically does not require participants to actively focus on external stimuli, which makes it easily applicable in neuro-rehabilitation settings. It does not focus solely on increasing muscle strength in a specific area; rather, it aims to improve movement quality and patterns by training the CNS. This training model, which emphasizes the importance of sensory input in developing motor skills, plays an effective role in improving balance, enhancing functionality, and reducing pain. Studies demonstrating the effectiveness of SM interventions in MS are available. The literature shows that both MI and SM have effects on neuropathic pain, proprioception, balance, and reaction time in individuals with MS. These two methods involve different neurophysiological mechanisms. For example, MI sends a "top-down" message to the brain. It first uses laterality (right/left distinction), then imagery, and prepares the brain for movement. SM, however, sends a "bottom-up" message to the brain. It focuses primarily on sensory input. Furthermore, while MI is an approach that aims to activate central motor networks without peripheral afferent input, SM supports central motor control processes by enhancing peripheral sensory input. In addition to these differences, it is known that both methods actually train CNS.The literature shows that both MI and SM have effects on neuropathic pain, proprioception, balance, and reaction time in individuals with MS. These two methods involve different neurophysiological mechanisms. For example, MI sends a "top-down" message to the brain. It first uses laterality (right/left distinction), then imagery, and prepares the brain for movement. SM, however, sends a "bottom-up" message to the brain. It focuses primarily on sensory input. Furthermore, while MI is an approach that aims to activate central motor networks without peripheral afferent input, SM supports central motor control processes by enhancing peripheral sensory input. There are only a few studies comparing these two methods.No studies have been found in the literature that compare these two methods in patients with MS and examine their effects.
The aim of our study is to examine the effects of MI and SM training administered to individuals with MS. Motor control in patients with MS is a process resulting from the interaction of central and peripheral mechanisms. For this reason, it is believed that comparing the relative effects of central-focused (MI) and peripheral-focused (SM) approaches could contribute to the development of rehabilitation interventions.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
18-45 years of age,
Having received a definitive MS diagnosis according to the 2024 McDonald criteria,
Not having had a relapse in the past 3 months,
Having an EDSS score of ≤ 6.00,
Disqualifiers
The presence of any other orthopedic or neurological condition that could interfere with participation in the study,
A level of spasticity in the lower extremities of ≥ 1+ on the Modified Ashworth Scale,
The presence of any hearing, vision, or cognitive impairment that could interfere with the assessments,
Receiving additional treatment beyond routine medication,
Trial design
Parallel
Treatments tested in this trial
Motor imagery
BehavioralThe patient will participate in motor imagery training two days a week for eight weeks.
Sensorimotor Training
BehavioralThe patient will participate in sensorimotor training two days a week for eight weeks.
Conventional therapy
BehavioralThe patient will participate in conventional therapy two days a week for eight weeks.
Treatment groups
Trial outcomes
Primary outcomes
Assessment of Neuropathic Pain
Algometer will be used. Each patient will be taught how to distinguish between tactile and painful stimuli. PPT will be recorded as the amount of pressure required to elicit a sensation of pain distinct from pressure or discomfort. Patients will be asked to say "stop" as soon as they feel a distinct sensation of pain; at that point, the algometer's pressure will be released immediately and the piston will be retracted by the evaluator.
Assessment of Neuropathic Pain
The Leeds Neuropathic Symptoms and Signs Assessment (S-LANSS) will be used. The S-LANSS consists of a 5-item questionnaire regarding pain symptoms and a 2-item clinical symptom scale that includes self-administered sensory tests for the presence of allodynia and reduced sensitivity to needle pricks. Responses to each item are binary (yes or no), and each item is weighted differently based on the odds ratio of a positive response to that item, in order to predict whether the pain is primarily neuropathic. Possible scores range from 0 to 24, and a score of 12 or higher suggests neuropathic pain.
Reaction Time Assesments
Kinovea software will be used. The feature that allows the video to continue without disrupting the flow of time while slowing it down will be utilized. A video recording capturing the reaction to taking a step will be made and uploaded to the Kinovea software.
Balance Assessment
HUR SmartBalance BTG4 balance platform will be used.Postural stability and stability limits will be measured and recorded.
Secondary outcomes
Motor Imagery Ability Assessment
The Kinesthetic and Visual Imagery Questionnaire (KVIQ) kinesthetic score will be used. During the assessment, participants are first instructed to visualize the requested movement and are then asked to actually perform it. After physically performing the movement, participants are asked to visualize themselves performing the same movement as if they were actually doing it. Participants rate the quality of the visual image in their imagination on a scale of 1 to 5, where 1 means "no image" and 5 means "as clear as the real thing.
Mental Chronometer
The mental chronometer will be administered in conjunction with the Timed Up and Go test.Participants will be asked to imagine walking at their normal pace from the chair to a wooden block 3 meters away, walking around the wooden block, walking back to the chair, sitting down, and letting the researcher know when they have sat down. The time between the researcher's "start" command and the participant's statement "I'm seated" will be recorded by the researcher using a stopwatch. The temporal alignment between the actual and imagined movements will be calculated as the delta time using the formula: "(actual movement - imagined movement) / \[(actual movement + imagined movement) / 2\] × 100."
Cognitive Functions Assessment
The Brief International Cognitive Assessment Battery (BICAMS) will be used.The scale consists of three subscales: processing speed, as assessed by the Symbol Number Modalities Test; verbal memory, as assessed by the California Verbal Learning Test-II; and visual memory, as assessed by the Short Visual-Spatial Memory Test.
Fatigue Assessment
The Fatigue Severity Scale will be used.The scale's questions are scored using a 7-point Likert scale ranging from "strongly disagree (1)" to "strongly agree (7)." The scale score is calculated as the average of the responses to the questions asked.
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