Electrical Stimulation for Spasticity in Spinal Cord Injury

Not Applicable

Active, not recruiting

• Conditions: Spinal Cord Injuries
• Interventions: Other: TENS

• Registration Number: NCT05103436
• Lead Sponsor: University of Alberta

Brief Summary

This study examines the immediate and long-term effects of lumbosacral TENS on spasticity and residual voluntary force control in spinal cord injury in comparison to no TENS. Participants in the intervention group will receive 2 months of TENS. Participants in the control group will receive TENS after a 2-month delay. Modified Ashworth score and pendulum test will be used to assess spasticity and force control. Electrophysiological measures will be used to assess the activity profile of motorneurons.

Detailed Description

Transcutaneous electrical nerve stimulation (TENS) has been used to control pain in stroke, MS, cerebral palsy and spinal cord injury (SCI) and its effect on spasticity reduction, although not used clinically, has been examined recently. In the few SCI studies done to date, the TENS electrodes have been placed on the nerve to the muscle under study and initial reports show a consistent decrease in spasticity measures, like the Modified Ashworth Score (MAS) and reflexes, during or hours after the TENS application. Recently, study team members from the ReYu Recovery Centre in Edmonton have observed that when TENS is applied with both electrodes over the lower back (lumbosacral TENS), varying amounts of immediate and long-term spasticity relief are produced in both legs.

The investigators have observed 3 clients from ReYU and all have shown immediate reductions in spasticity for at least 2 joints in both legs. The effect of the lumbosacral TENS varied from an immediate dramatic reduction to a more moderate reduction when applied over several days. This study will examine the immediate and longer-term (2 months) effect of using spinal TENS in reducing spasticity of the lower limbs in a larger number of participants with SCI. The investigators want to understand how spinal TENS affects spinal circuits and motoneurons below the lesion to reduce spasticity to observe improvement in its effect in those with more moderate responses. Lumbosacral TENS has the potential for a non-pharmacological, on-demand control of SCI spasticity to greatly improve the quality of life of those affected.

Study Timeline

• Study First Submitted: 2021-10-07
• Study First Submitted QC: 2021-10-20
• Study First Posted: 2021-11-02
• Study Start: 2022-05-04
• Status Verified: 2024-12
• Last Update Submitted: 2024-12-10
• Last Update Posted: 2024-12-12
• Primary Completion: 2026-12-31
• Study Completion: 2026-12-31

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

• SCI adults 18 years and older
• injury levels between C5-T12

Exclusion Criteria

• severe head injury
• uncontrolled autonomic dysreflexia
• other medical conditions precluding TENS

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Intervention Group	TENS	Participants will receive 2 months of TENS (1 hr AM, 1 hr PM/day, 50 Hz, below pain/motor threshold, using an EMS 7500 TENS unit) immediately upon entry to the study.

Primary Outcome Measures

Name	Time	Method
Change in Modified Ashworth Score	Pre Intervention. 1, 2 and 4 months follow up. In addition, spasticity will be measured every 2 weeks to assess stability of the effects.	Clinical assessment of spasticity. Scores range from '0' to '4'. Minimum score is '0' meaning no increase in tone. Maximum score is '4' meaning limb is ridged in flexion and extension. The lower the score the better the outcome.

Secondary Outcome Measures

Name	Time	Method
Change in Knee Pendulum Angle	Pre Intervention. 1, 2 and 4 months follow up.	Clinical assessment of passive knee motion to assess spasticity.
Change in EMG	Pre Intervention. 1, 2 and 4 months follow up.	Assessment of motor control. Participants are asked to match their muscle contraction force to a target force profile. EMG data will be used to calculate the smoothness of muscle force.
Change in Manual Muscle Testing	Pre Intervention. 1, 2 and 4 months follow up.	Clinical assessment of muscle strength from grade '0' to '5', where '0' means no strength and '5' means normal strength.
Change in International Standard for Neurological Classification of SCI (ISNCSI)	Pre Intervention. 1, 2 and 4 months follow up.	Neurological Examination of participant. The Impairment Scale has 5 grades from A to E. Grade A is complete injury and grade E is normal. It is based on the strength of 10 key muscle groups in the upper and lower extremities, sensory response to light touch and pin prick at 28 key sensory points on each side of the whole body, and anal responses.

Trial Locations

Locations (1)

University of Alberta - 524 HMRC; 🇨🇦 Edmonton, Alberta, Canada