Exoskeleton Training for Spinal Cord Injury Neuropathic Pain (ExSCIP): Protocol for a Phase 2 Feasibility Randomised Trial

Status: Recruiting
Location: See location...
Intervention Type: Other, Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this feasibility trial is to learn if exoskeleton or robotic walking works to reduce nerve (neuropathic) pain after spinal cord injury. This study asks is: * Providing walking practice through use of a robotic device (exoskeleton) three times per week for twelve weeks possible to deliver? * Would people sign up and stick to the programme? * And will it help to reduce neuropathic pain levels after spinal injury? Researchers will compare robotic walking and a relaxation program to see if robotic walking works to reduce neuropathic pain levels after spinal injury. Participants will: * Complete a number of questionnaires and tests related to their pain before the trial. * Complete robotic walking or a relaxation program three times per week for twelve weeks. * Complete the same questionnaires and tests after the trial finishes and 6 months after. * Complete an interview telling researchers about their experiences of the trial.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 90
Healthy Volunteers: f
View:

• Individuals who are 18 years and over.

• Confirmed traumatic SCI (injury resulted from an external physical impact and not an acute or chronic disease process) of \>6 months duration with complete or incomplete paraplegia or tetraplegia.

• Individuals with above confirmed traumatic SCI who have below-level NP (≥ 3 levels below neurological level and/or extending to at-level region) starting after the SCI and persisting for \> 3 continuous months, despite pharmacotherapy.

• NP will be confirmed based on a neurological examination, a score of ≥4 on the Douleur Neuropathique 4 (DN4) (48) and a comprehensive pain history supported by the use of the ISCIP Pain Classification. They endorse one or more of the following pain descriptors to assist in confirmation of below level NP 'hot-burning', 'tingling', 'pricking', 'pins and needles', 'sharp', 'shooting', 'squeezing', 'painful cold' and 'electric shock-like' (45).

• Moderate and severe NP as confirmed above will be described as pain ≥ 3 and ≥ 6 on the 0-10 Numerical Rating Scale (NRS) for NP (averaged over a week).

• Exoskeleton naive

• Stable medication regimen

• Have the capacity to provide informed consent.

Locations
Other Locations
Ireland
University College Dublin
RECRUITING
Dublin
Contact Information
Primary
Olive Lennon, PhD
olive.lennon@ucd.ie
+3537166508
Time Frame
Start Date: 2024-12-20
Estimated Completion Date: 2026-11-30
Participants
Target number of participants: 40
Treatments
Experimental: Exoskeleton (Intervention)
Exoskeleton walking delivered three times per week for twelve weeks. Each session will be one hour duration.
Active_comparator: Relaxation (Comparator)
An equally dosed blended relaxation program delivered online for two sessions per week and in-person one session per week.
Related Therapeutic Areas
Sponsors
Leads: University College Dublin
Collaborators: University of Aarhus, Royal College of Surgeons, Ireland

This content was sourced from clinicaltrials.gov