Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Up to 25 individuals living with chronic incomplete spinal cord injury (iSCI) who can stand but have limited ability to elicit a step without physical assistance or upper limb (U/L) support will be recruited for this study. The first objective of the study will aim to investigate the orthotic effect (i.e., immediate effect) of FES on the reactive stepping response. The second objective is to investigate the therapeutic effect of a novel balance intervention, perturbation-based balance training (PBT) combined with FES (i.e., PBT+FES) on reactive stepping ability, measures of postural sway during quiet standing (i.e., biomechanical measures), and scores on clinical measures of balance and walking.
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Perturbation-based balance training with FES | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Perturbation-based balance training with functional electrical stimulation | Behavioral | The PBT program will consist of repetitive practice of reactive stepping for one hour. The participants will be equipped with the Odstock 2-Channel stimulator on one or both sides depending on their deficits. One channel of stimulation may be applied to the common fibular nerve to elicit a flexor withdraw reflex and elicit a step. The second channel of stimulation may be applied to the quadriceps muscles to assist with the supporting phase of the reactive step, as required. Participants will experience about 60 perturbations per session during balance exercises. To create a perturbation, the researcher will apply unexpected pushes or pulls to a safety harness around the participant's trunk. Throughout the hour-long session, participants will complete challenging balance tasks, customized to their ability level, during standing and walking. The training will be supervised by a licensed physiotherapist and administered by a licensed physiotherapist or registered kinesiologist. |
| Measure | Description | Time Frame |
|---|---|---|
| Lean-and-release test | Test of reactive stepping and balance in the forward direction | Up to 7 weeks |
| Biomechanical measures of postural control | Measurement of centre of pressure during quiet standing | Up to 7 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Mini-Balance Evaluation Systems Test | Assesses four balance control systems | Up to 7 weeks |
| Activities-specific Balance Confidence Scale | Assesses balance efficacy |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Contraindications for EMS. Electrical stimulation will not be used if:
severe spasticity is present in the legs;
the person has contractures in the lower limbs that prevent achieving a neutral hip and ankle position, or extended knee;
there is a history of prior lower limbs fragility fracture;
the leg muscles are unresponsive to electrical stimulation (i.e., peripheral nerve damage in the legs).
Pressure sores on pelvis or trunk, where safety harness will be donned.
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Lyndhurst Centre, Toronto Rehabilitation Institute-UHN | Toronto | Ontario | M4G 3V9 | Canada |
Not provided
| ID | Term |
|---|---|
| D013119 | Spinal Cord Injuries |
| ID | Term |
|---|---|
| D013118 | Spinal Cord Diseases |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
| D020196 | Trauma, Nervous System |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
|
| Up to 7 weeks |
| Gait parameters | Step length (cm), gait speed (m/s), double support time (%) | Up to 7 weeks |
| Falls Efficacy Scale International | Assesses the degree of concern about fear of falling | Up to 7 weeks |
| Semi-structured interview | Queries the participants' perceived challenges and benefits of the PBT+FES program | 3 months post |
| D014947 | Wounds and Injuries |