A Novel Combined Neuromodulation Therapy to Enhance Balance and Neuroplasticity

Spinal Cord Injuries Clinical Trial

Official title:

A Novel Combined Neuromodulation Therapy to Enhance Balance and Neuroplasticity After Incomplete SCI

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT05940636
• Other study ID #: 23-5262
• Status: Not yet recruiting
• Phase: N/A
• Start date: September 2023
• Est. completion date: July 2025

Study information

• Verified date: July 2023
• Source: University Health Network, Toronto
• Contact: Kei Masani, PhD
• Phone: 416-597-3422
• Email: k.masani[@]utoronto.ca
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Many people with partial damages in their spinal cord (iSCI) have physical impairments such as muscle paralysis in legs which make standing balance difficult. Poor balance control often leads to falls, injuries, and hospitalization. Therefore, improvement of standing balance is an important therapeutic goal for these individuals. Our team has shown that a therapy called visual feedback training (VFT) can improve standing balance by allowing individuals with iSCI to actively participate and follow visual feedback of their body sway on a screen like a computer game. We have also found that the application of low-energy electrical pulses to weak muscles called functional electrical stimulation (FES) during VFT can enhance the training effects. Recently, transcutaneous spinal cord stimulation (TSCS) has been discussed as a promising technique to further promote the rehabilitation effects after SCI by enhancing the connectivity between the brain and spinal cord and within the spinal pathways. However, to date, the potential of combining the two techniques (TSCS+FES) to improve the standing balance remains unknown. In this study, through the completion of a clinical trial, we will investigate the effects of an intervention that combines lumbar TSCS with FES of ankle muscles during VFT on the functional and neurophysiological outcomes in individuals living with iSCI. Participants will be randomly allocated to receive combined TSCS with FES or FES alone during VFT for 12 training sessions over 4 weeks. We expect that the new therapy would further improve balance and strengthen the neural connections between the brain and muscles. The expected changes in the neural connections will be measured by recording electrical signals from the lower limb muscles following stimulation of the motor region of the brain. Results of this study will be used for a larger-scale study in people with iSCI to improve balance and reduce falls during their daily life activities.

Description:

This is a single-center, randomized controlled trial to test the effects of a novel neuromodulation program on balance performance and neuroplasticity in individuals with iSCI. Participants will be randomly assigned to 2 equal groups labeled as (1) FES with VFT, and (2) combined neuromodulation with VFT. They will complete 8 training sessions over 4 weeks (2 sessions/week). For the FES with VFT group, participants will receive visual feedback regarding their center of pressure location during four games with varying levels of difficulty and FES will be applied bilaterally to SOL and TA via a closed-loop system. Each exercise will be completed 3 times per training session. For the combined neuromodulation with VFT group, the sub-motor threshold, open-loop TSCS will be coupled with closed-loop FES of ankle muscles during VFT. For this purpose, 2 electrical stimulators, one for each leg will stimulate SOL and TA muscles bilaterally while open-loop tonic lumbar TSCS will be applied at an intensity producing paresthesia in most of the lower-limb dermatomes. The range of FES stimulation intensity will vary between the minimal contraction threshold and 80% of the maximal tolerable threshold for each participant during games depending on the instant location of the participant's center of pressure and the location of the desired target during the game. All dependent variables will be assessed prior, immediately after, and 6-weeks after the end of intervention.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 20
• Est. completion date: July 2025
• Est. primary completion date: November 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

1. A traumatic or non-traumatic, non-progressive motor iSCI [American Spinal Injury Association Impairment Scale (AIS) rating of C or D];

2. More than 1-year post-injury;

3. =18 years old;

4. BBS score <46;

5. Free of any other condition besides SCI that significantly affects walking or balance (e.g., no vestibular disorder, significant vision loss, stroke)

Exclusion Criteria:

1. Neurological lesion levels below T12 ;

2. Severe spasticity in the legs;

3. Contractures in the lower extremities that prevent achieving a neutral hip and ankle position, or extended knee;

4. Peripheral nerve damage in the legs (i.e. leg muscles unresponsive to electrical stimulation);

5. A pressure sore (>grade 2) on the pelvis or trunk where the safety harness is applied;

6. Pregnancy;

7. History of epilepsy;

8. Contraindications for electrical stimulation (i.e. implanted electronic device, active cancer or radiation in past months, epilepsy, skin rash/wound at a potential electrode site)

Related Conditions & MeSH terms

• Fall
• Paresis
• Spinal Cord Injuries

Intervention

Other:
• Activity-based rehabilitation+electrical stimulation
Balance training will occur three times per week for four weeks, totaling 12 two-hour sessions. In both groups, you will be asked to stand on a force plate while playing visual feedback training (VFT) games as part of the standing balance training. A force plate is similar to a bathroom scale that you can stand on which measures your body sway during movement. Visual feedback training (VFT) is a type of activity that includes weight-shifting movements in the upright stance. VFT will be done in both groups. There will be different games as shown in figure 1 and the order of the games will be randomly chosen in each session. During each game, there will be targets that will be presented on the screen and you will have to navigate toward them . You will be able to rest between games as needed.

Locations

Country	Name	City	State
Canada	Toronto Rehabilitation Institute-Lyndhurst Center	Toronto	Ontario

Sponsors (1)

Lead Sponsor	Collaborator
University Health Network, Toronto

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Mini-Balance Evaluation Systems Test (mini-BESTest)	evaluates different components of postural control including anticipatory, reactive postural control, sensory orientation, and dynamic gait. It has high test-retest reliability, concurrent and convergent validity in individuals with iSCI.	pre- immidiately post- 6 weeks follow up
Primary	10-meter Walk Test (10MWT)	performance-based measure to assess mobility and walking speed over a short distance.	pre- immidiately post- 6 weeks follow up
Primary	Motor evoked potentials (MEP)	To measure neuroplasticity, we will record changes in the MEPs for the SOL and TA induced by TMS over the leg representation of the motor cortex	pre- immidiately post- 6 weeks follow up
Secondary	Activities-specific Balance Confidence (ABC) Scale	self-reported questionnaire that evaluates balance confidence while performing 16 different mobility tasks such as walking around the house, sweeping the floor, climbing up and down the stairs, walking on a ramp and negotiating escalators	pre- immidiately post- 6 weeks follow up
Secondary	Falls Efficacy Scale - International (FES-I)	16-item self-reported questionnaire that measures fear of falling during basic and demanding daily life activities	pre- immidiately post- 6 weeks follow up