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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03834324
Other study ID # 6054
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 3, 2013
Est. completion date March 1, 2018

Study information

Verified date February 2019
Source University of Southampton
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Neuroscience research that has identified potential for recovery (neuroplasticity) following incomplete SCI has changed clinical practice away from compensation strategies towards optimizing recovery. Important factors include: repetitive exercise, Functional Electrical Stimulation (FES) and appropriate feedback. The iCycle combines repetitive exercise with FES and provides feedback on performance in a virtual cycle race. Unlike previous devices, performance in the race is determined only by voluntary effort (i.e. not torque generated by FES plus voluntary effort). In this study with incomplete SCI participants we will test the iCycle with six inpatients to refine the protocol and make technical improvements. We will then conduct an ABA pilot study (n=10) in which a 3G-connected iCycle is used in people's own homes. We will compare usual care (A) with iCycle exercise (B). Changes in neural connectivity (TMS evoked EMG potentials), muscle strength and walking will be measured as well qualitative analysis of users' views.


Description:

Background: Functional Electrical Stimulation (FES) cycling can benefit health and may lead to neuroplastic changes following incomplete spinal cord injury (SCI). Our hypothesis is that greater neuroplastic effects occur when electrical stimulation of peripheral nerves is combined with voluntary drive. In this pilot study, we will investigate the effects of a one-month training programme using a novel device, the iCycle, in which voluntary effort (cortical drive) is encouraged by virtual reality biofeedback during FES cycling. Methods: Eleven participants (C1-T12) with incomplete SCI (5 sub-acute; 6 chronic) will be recruited and undergo 12-sessions of iCycle training. Function will be assessed before and after training using the bilateral ISNC-SCI motor score neurological (motor) function, Oxford power grading, Modified Ashworth Score, Spinal Cord Independence Measure, the Walking Index for Spinal Cord Injury and 10m-walk test. Power output will be measured during training.


Recruitment information / eligibility

Status Completed
Enrollment 11
Est. completion date March 1, 2018
Est. primary completion date April 29, 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: 1. using a wheelchair for at least two hours per day Exclusion Criteria: 1. cardiac pacemaker 2. pressure sores or unresolved skin problems 3. unhealed lower limb fractures 4. pregnancy 5. active heterotrophic ossification (lower limbs) 6. severe osteoporosis 7. complex regional pain syndrome 8. metal implants near electrode sites 9. lower limb malignancy 10. T6 and below spinal malignancy 11. uncontrolled autonomic dysreflexia 12. history of knee dislocation/subluxation 13. allergy to electrodes 14. cognitive difficulties 15. severe spasticity (Ashworth scale 4 or 5 in muscle groups that would prevent smooth pedalling) or 16. neurological degenerative diseases.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
FES
Functional Electrical Stimulation during cycling with Virtual Reality Feedback

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
University of Southampton University College, London

References & Publications (1)

Duffell LD, Paddison S, Alahmary AF, Donaldson N, Burridge J. The effects of FES cycling combined with virtual reality racing biofeedback on voluntary function after incomplete SCI: a pilot study. J Neuroeng Rehabil. 2019 Nov 27;16(1):149. doi: 10.1186/s1 — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary International Standards for Neurological Classification of Spinal Cord Injury (ISNC-SCI). Neurological Classification Change between baseline and 4 weeks
Primary International Standards for Neurological Classification of Spinal Cord Injury (ISNC-SCI). Neurological Classification Change between baseline and 8 weeks
Secondary Oxford scale motor power grading Muscle strength Change between baseline and 4 weeks
Secondary Oxford scale motor power grading Muscle strength Change between baseline and 8 weeks
Secondary Modified Ashworth Score (MAS) Spasticity / stiffness Change between baseline and 4 weeks
Secondary Modified Ashworth Score (MAS) Spasticity / stiffness Change between baseline and 8 weeks
Secondary Spinal Cord Independence Measure (SCIM) ADL Change between baseline and 4 weeks
Secondary Spinal Cord Independence Measure (SCIM) ADL Change between baseline and 8 weeks
Secondary Walking Index for Spinal Cord Injury (WISCI II) Walking ability Change between baseline and 4 weeks
Secondary Walking Index for Spinal Cord Injury (WISCI II) Walking ability Change between baseline and 8 weeks
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