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Training for Persons With Complete SCI for FES Cycling: a Case Series

Primary Purpose

Spinal Cord Injuries

Status
Unknown status
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Functional Electrical Stimulation
Sponsored by
Centre de Rééducation et Réadaptation Fonctionnelle La Châtaigneraie
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Spinal Cord Injuries

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • informed written consent
  • complete spinal cord injury AIS A or B
  • neurological level of lesion C6 - T12
  • post-lesion duration > 12 moths
  • paralysed muscles stimulable
  • joints of lower limb freely moveable
  • stable medical condition (absence of infectious respiratory or urinary event of cutaneous pathology confining the patient to bed and warranting treatment).

Exclusion Criteria:

  • Not affiliated to a social security scheme, beneficiary or not such a plan
  • Refusal to participate in the study (withdraw from study possible at any time)
  • Inability to give consent
  • body mass index higher or equal to 30
  • flaccid paralysis (denervation)
  • Inability to give consent
  • neurogenic para-osteoarthropathy
  • active thrombophlebitis
  • muscular disease
  • cardiovascular disease including coronary antecedent
  • bone mineral density T-score below -2.5
  • treatment with a drug known to have an effect on bone (< 3 months)
  • Aids in the lower limbs
  • Epilepsy
  • Orthostatic hypotension
  • Fractures of the lower limbs older (< 12 months)
  • Pacemakers or other implants contraindicating the use of FES
  • Pregnancy (women)

Sites / Locations

  • Centre de Rééducation et de Réadaptation Fonctionnelle La Châtaigneraie

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Subjects

Arm Description

Phase V1: 1 month of home-based FES-training using isometric contractions of quadriceps and hamstring muscles (3 times a week). Phase V2: 2 months of home-based FES-training on an ergo-cycle with arm support (3 times a week) Phase V3: 1 month of home-based FES-training on an ergo-cycle with arm support (1-2 times a week) and FES-cycling training overground on a tricycle (1-2 times a week) in the clinical setting. Optional (only for selected pilot): Phase V4: 2-4 months of home-based FES-training on an ergo-cycle with arm support (1-2 times a week) and FES-cycling training overground on a tricycle (1-2 times a week) in the clinical setting. This phase is focussing on optimizing the performance of the pilot and improving the mechanical efficiency of the tricycle. Phase V5: Participation on Cybathlon 2020

Outcomes

Primary Outcome Measures

Change in Maximum Cycling-Distance in [m]
Change in maximum distance cycled on flat ground on a tricycle
Change in Maximum Cycling-Speed in [km/h]
Change in maximum speed during cycling over flat ground on a tricycle
Change in Average Cycling-Speed in [km/h]
Change in average speed during cycling over flat ground on a tricycle
Change in Maximum Cycling-duration in [hh:mm:ss]
Change in maximum duration during cycling over flat ground on a tricycle
Change in Maximum Pedaling-Cadence in [RPM]
Change in maximum pedaling-cadence during cycling over flat ground on a tricycle
Change in Average Pedaling-Cadence in [RPM]
Change in average pedaling-cadence during cycling over flat ground on a tricycle
Ability to cycle 1200m in less than 8min
Qualification criterion Cybathlon 2020. It will be assessed it the pilot is able to cycle 1200m in less than 8min over flat ground on a tricycle.

Secondary Outcome Measures

Change of blood pressure during training
Blood pressure will be assessed before and after every training session. Mean change in blood pressure will be calculated along all training-sessions.
Change of heart rate during training
Heart rate will be assessed before and after every training session. Mean change in heart-rate will be calculated along all training-sessions.
Maximum heart rate during training
Maximum heart rate will be assessed during every training session. Mean and SD of the maximum heart-rate will be calculated along all training-sessions.
Average heart rate during training
Average heart rate will be assessed during every training session. Mean and SD of the average heart-rate will be calculated along all training-sessions.
Cutaneous status
Evaluation for absence of: skin lesions, pressure points, pressure ulcers, phlebitis, edema
Musculo-skeletal pain or inflammation
Evaluation for absence of: muscular pain, osteo-articular pain or inflammation
Psychological: Satisfaction
Evaluation of satisfaction [linear scale: 1 - 10; 1 = lowest satisfaction; 10 = highest satisfaction] will be assessed after every training session. Mean and SD of the satisfaction will be calculated along all training-sessions.
Psychological: Acceptability
Change in acceptability [questionnaire].
General Fatigue
Assessment of change in general fatigue via [Borg scale; Range: 6-20; 6 = No exertion, sitting and resting; 20 = Maximal exertion] will be assessed before and after every training session. Mean and SD of the change in fatigue will be calculated along all training-sessions.
Psycho-Social: Self-Esteem
Change in self-esteem via [Rosenberg Scale; Range: 10 - 40; 10 = lowest Self-Esteem; 40= Highest Self-Esteem].
Psycho-Social: Quality of Life
Change in quality-of-life via [questionnaire SF-36].
Cardio-Respiratory Fitness: Maximal Heartrate
Change of maximal heartrate via electrocardiogram
Cardio-Respiratory Fitness: VO2max
Change of VO2max
Musculo-skeletal changes: Thigh perimeter
Assessment of thigh perimeter [cm]. Measurement is taken 10cm and 20cm proximal to the proximal edge of the patella.
Musculo-skeletal changes: Bone mineral density
Bone mineral density via [DEXA]
Musculo-skeletal changes: Body composition
Body composition via [DEXA].
Occurrence of spasms: before training
Spasmic occurance will be assessed via [PENN Scale; Range: 0-4; 0 = No spasm; 4 = Spasms occuring more than 10 times per hour] before every training session. Mean and SD of the spasmic occurence will be calculated along all training-sessions.
Occurrence of spasms : after training
Spasmic occurance will be assessed via [PENN Scale; Range: 0-4; 0 = No spasm; 4 = Spasms occuring more than 10 times per hour] after every training session. Mean and SD of the spasmic occurence will be calculated along all training-sessions.

Full Information

First Posted
May 11, 2020
Last Updated
June 1, 2020
Sponsor
Centre de Rééducation et Réadaptation Fonctionnelle La Châtaigneraie
Collaborators
Institut National de Recherche en Informatique et en Automatique, Université Montpellier
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1. Study Identification

Unique Protocol Identification Number
NCT04412447
Brief Title
Training for Persons With Complete SCI for FES Cycling: a Case Series
Official Title
Training of Persons With Complete Spinal Cord Injury for Pedaling on a Tricycle, Induced by Electrical Stimulation of the Paralysed Muscles: a Case Series
Study Type
Interventional

2. Study Status

Record Verification Date
June 2020
Overall Recruitment Status
Unknown status
Study Start Date
October 1, 2019 (Actual)
Primary Completion Date
June 2020 (Anticipated)
Study Completion Date
September 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre de Rééducation et Réadaptation Fonctionnelle La Châtaigneraie
Collaborators
Institut National de Recherche en Informatique et en Automatique, Université Montpellier

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The main objective of this study is to validate the effectivity of a simple home-based training for cycling with functional electrical stimulation (FES). The training is designed to progressively increase strength and endurance of the paralysed muscles of a person with complete spinal cord injury. After a limited period of only several months, performance will be assessed during FES-assisted cycling on a recumbent tricycle over flat ground. The outcomes of this study should provide evidence for the effectivity of FES-cycling as potential rehabilitation method.
Detailed Description
People with spinal cord injuries suffer from numerous comorbidities, linked in particular to immobility and sedentariness. Studies have shown the benefits of training and reconditioning to adapted effort in spinal cord injured people. Among other innovative techniques, functional electrical stimulation (FES) is aimed primarily at mobilizing as many muscles as possible. Concerning electro-stimulated pedaling on a tricycle, it would allow individuals with paraplegia or tetraplegia to practise physical activity in perspective of experiencing pleasure during training. In 2016, our team carried out a pilot study aiming at using a recumbent tricylce powered by the lower limbs of a person with complete paraplegia under electrostimulation. The participant was trained for 12 months, whit the objective to participate at an international competition (Cybathlon 2016). This first study has opened up prospects and identified avenues for improvement. The main objective of this study is to significantly improve, over a limited period of time, the pedalling performance on a tricycle by using electrical stimulation of the sub-lesional muscles of people with spinal cord injuries. Secondary focusses will be: physical and psychological tolerance to training; influence on pain, cardio-respiratory functions, body composition regarding muscle trophicity and bone metabolism; psycho-social impact; impact of modification of stimulation parameters (frequency, phase width, intensity, waveform, contact location) in performance optimization and delay of muscle fatigue; performance impact of mechanical modifications performed on the tricycle. This is a prospective case study: patients suffering from a complete traumatic injury and followed at the Centre de Rééducation et de Réadaptation Fonctionnelle (CRRF) La Châtaigneraie (Menucourt) will be recruited by the investigating physician during a consultation for a period of approximately 6 months. The centre specialised in the management of acute and chronic neurological lesions. The eligibility criteria are predefined to ensure the participants safety. After verification of the criteria and before the start of the programme, an exercise test (monitoring of the evolution of VO2max) will be carried out in the Sports Medicine department of the CHI of Saint-Germain-en-Laye. The first phase (V1) consists of a one-month home-based isometric muscle training programme by electrostimulation followed by a two-month programme (phase V2) of home-based muscle training by electrostimulation on an ergocycle including one training per week at the CRRF. The home ergocycle electro-stimulation muscle training, will be continued once or twice a week and complemented in the third phase (V3) by training at the CRRF on a tricycle for one month. Only the patient selected to participate in the Cybathlon 2020 will continue with the final phase (V4), which includes, over a period of 2 to 4 months, muscle training by electrostimulation on an ergocycle at home, electrostimulation sessions on a tricycle up to 3 times a week at the CRRF. In this phase, the optimization of the stimulation and electrical patterns and the mechanics of the tricycle will take place in order to maximize the pilots overall performance. Finally, the pilot will take part in the tricycle FES-Cycling race at the Cybathlon 2020 in Zurich, i.e. an international competition and technological challenge, requiring to master 1200 metres in a maximum time of 8 minutes. The different training programs are based on sport-scientific principles and a physiotherapist will follow up on the home sessions. The collaborating teams (engineers and researchers from INRIA, the French National Institute for Research in Computer Science and Control) will measure performance in a bimonthly frequency. This research should demonstrate that the safety, acceptability, satisfaction, self-esteem and quality of life induced by the practice of FES-assisted pedalling, opens a new way of training in rehabilitation centres and at home with the perspective of improving certain physiological functions in the long-term.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spinal Cord Injuries

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Training of paralysed musculature of the lower limb by using electrical stimulation.
Masking
None (Open Label)
Allocation
N/A
Enrollment
2 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Subjects
Arm Type
Experimental
Arm Description
Phase V1: 1 month of home-based FES-training using isometric contractions of quadriceps and hamstring muscles (3 times a week). Phase V2: 2 months of home-based FES-training on an ergo-cycle with arm support (3 times a week) Phase V3: 1 month of home-based FES-training on an ergo-cycle with arm support (1-2 times a week) and FES-cycling training overground on a tricycle (1-2 times a week) in the clinical setting. Optional (only for selected pilot): Phase V4: 2-4 months of home-based FES-training on an ergo-cycle with arm support (1-2 times a week) and FES-cycling training overground on a tricycle (1-2 times a week) in the clinical setting. This phase is focussing on optimizing the performance of the pilot and improving the mechanical efficiency of the tricycle. Phase V5: Participation on Cybathlon 2020
Intervention Type
Device
Intervention Name(s)
Functional Electrical Stimulation
Intervention Description
Electrical stimulation of motor-nerves innervating the musculature of the lower limb.
Primary Outcome Measure Information:
Title
Change in Maximum Cycling-Distance in [m]
Description
Change in maximum distance cycled on flat ground on a tricycle
Time Frame
Change between 4 months of training (end of V3) and 6 months of training (end of V4)
Title
Change in Maximum Cycling-Speed in [km/h]
Description
Change in maximum speed during cycling over flat ground on a tricycle
Time Frame
Change between 4 months of training (end of V3) and 6 months of training (end of V4)
Title
Change in Average Cycling-Speed in [km/h]
Description
Change in average speed during cycling over flat ground on a tricycle
Time Frame
Change between 4 months of training (end of V3) and 6 months of training (end of V4)
Title
Change in Maximum Cycling-duration in [hh:mm:ss]
Description
Change in maximum duration during cycling over flat ground on a tricycle
Time Frame
Change between 4 months of training (end of V3) and 6 months of training (end of V4)
Title
Change in Maximum Pedaling-Cadence in [RPM]
Description
Change in maximum pedaling-cadence during cycling over flat ground on a tricycle
Time Frame
Change between 4 months of training (end of V3) and 6 months of training (end of V4)
Title
Change in Average Pedaling-Cadence in [RPM]
Description
Change in average pedaling-cadence during cycling over flat ground on a tricycle
Time Frame
Change between 4 months of training (end of V3) and 6 months of training (end of V4)
Title
Ability to cycle 1200m in less than 8min
Description
Qualification criterion Cybathlon 2020. It will be assessed it the pilot is able to cycle 1200m in less than 8min over flat ground on a tricycle.
Time Frame
After 6 months of training (end of V4)
Secondary Outcome Measure Information:
Title
Change of blood pressure during training
Description
Blood pressure will be assessed before and after every training session. Mean change in blood pressure will be calculated along all training-sessions.
Time Frame
through study completion (up to one year), an average throughout the study-duration
Title
Change of heart rate during training
Description
Heart rate will be assessed before and after every training session. Mean change in heart-rate will be calculated along all training-sessions.
Time Frame
through study completion (up to one year), an average throughout the study-duration
Title
Maximum heart rate during training
Description
Maximum heart rate will be assessed during every training session. Mean and SD of the maximum heart-rate will be calculated along all training-sessions.
Time Frame
through study completion (up to one year), an average throughout the study-duration
Title
Average heart rate during training
Description
Average heart rate will be assessed during every training session. Mean and SD of the average heart-rate will be calculated along all training-sessions.
Time Frame
through study completion (up to one year), an average throughout the study-duration
Title
Cutaneous status
Description
Evaluation for absence of: skin lesions, pressure points, pressure ulcers, phlebitis, edema
Time Frame
through study completion (up to one year)
Title
Musculo-skeletal pain or inflammation
Description
Evaluation for absence of: muscular pain, osteo-articular pain or inflammation
Time Frame
through study completion (up to one year)
Title
Psychological: Satisfaction
Description
Evaluation of satisfaction [linear scale: 1 - 10; 1 = lowest satisfaction; 10 = highest satisfaction] will be assessed after every training session. Mean and SD of the satisfaction will be calculated along all training-sessions.
Time Frame
through study completion (up to one year), an average throughout the study-duration
Title
Psychological: Acceptability
Description
Change in acceptability [questionnaire].
Time Frame
through study completion (up to one year), every 30 days
Title
General Fatigue
Description
Assessment of change in general fatigue via [Borg scale; Range: 6-20; 6 = No exertion, sitting and resting; 20 = Maximal exertion] will be assessed before and after every training session. Mean and SD of the change in fatigue will be calculated along all training-sessions.
Time Frame
through study completion (up to one year), an average throughout the study-duration
Title
Psycho-Social: Self-Esteem
Description
Change in self-esteem via [Rosenberg Scale; Range: 10 - 40; 10 = lowest Self-Esteem; 40= Highest Self-Esteem].
Time Frame
through study completion (up to one year), every 15 days
Title
Psycho-Social: Quality of Life
Description
Change in quality-of-life via [questionnaire SF-36].
Time Frame
through study completion (up to one year), every 30 days
Title
Cardio-Respiratory Fitness: Maximal Heartrate
Description
Change of maximal heartrate via electrocardiogram
Time Frame
Change between timepoint before first training, after 4 months of training (end of V3) and after 6 months of training (end of V4)
Title
Cardio-Respiratory Fitness: VO2max
Description
Change of VO2max
Time Frame
Change between timepoint before first training, after 4 months of training (end of V3) and after 6 months of training (end of V4)
Title
Musculo-skeletal changes: Thigh perimeter
Description
Assessment of thigh perimeter [cm]. Measurement is taken 10cm and 20cm proximal to the proximal edge of the patella.
Time Frame
Change between timepoint before first training and after end of study (end of V5, ~ 7 months)
Title
Musculo-skeletal changes: Bone mineral density
Description
Bone mineral density via [DEXA]
Time Frame
Change between timepoint before first training and after end of study (end of V5, ~ 7 months)
Title
Musculo-skeletal changes: Body composition
Description
Body composition via [DEXA].
Time Frame
Change between timepoint before first training and after end of study (end of V5, ~ 7 months)
Title
Occurrence of spasms: before training
Description
Spasmic occurance will be assessed via [PENN Scale; Range: 0-4; 0 = No spasm; 4 = Spasms occuring more than 10 times per hour] before every training session. Mean and SD of the spasmic occurence will be calculated along all training-sessions.
Time Frame
through study completion (up to one year), an average throughout the study-duration
Title
Occurrence of spasms : after training
Description
Spasmic occurance will be assessed via [PENN Scale; Range: 0-4; 0 = No spasm; 4 = Spasms occuring more than 10 times per hour] after every training session. Mean and SD of the spasmic occurence will be calculated along all training-sessions.
Time Frame
through study completion (up to one year), an average throughout the study-duration

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: informed written consent complete spinal cord injury AIS A or B neurological level of lesion C6 - T12 post-lesion duration > 12 moths paralysed muscles stimulable joints of lower limb freely moveable stable medical condition (absence of infectious respiratory or urinary event of cutaneous pathology confining the patient to bed and warranting treatment). Exclusion Criteria: Not affiliated to a social security scheme, beneficiary or not such a plan Refusal to participate in the study (withdraw from study possible at any time) Inability to give consent body mass index higher or equal to 30 flaccid paralysis (denervation) Inability to give consent neurogenic para-osteoarthropathy active thrombophlebitis muscular disease cardiovascular disease including coronary antecedent bone mineral density T-score below -2.5 treatment with a drug known to have an effect on bone (< 3 months) Aids in the lower limbs Epilepsy Orthostatic hypotension Fractures of the lower limbs older (< 12 months) Pacemakers or other implants contraindicating the use of FES Pregnancy (women)
Facility Information:
Facility Name
Centre de Rééducation et de Réadaptation Fonctionnelle La Châtaigneraie
City
Menucourt
ZIP/Postal Code
95180
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
34596097
Citation
Fattal C, Schmoll M, Le Guillou R, Raoult B, Frey A, Carlier R, Azevedo-Coste C. Benefits of 1-Yr Home Training With Functional Electrical Stimulation Cycling in Paraplegia During COVID-19 Crisis. Am J Phys Med Rehabil. 2021 Dec 1;100(12):1148-1151. doi: 10.1097/PHM.0000000000001898.
Results Reference
derived

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Training for Persons With Complete SCI for FES Cycling: a Case Series

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